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Birth and Neonatal Death Registrations in Jordan

Authors:

Abstract

Assessing the magnitude and etiologies of perinatal deaths and their risk factors begins with accurately defining and reporting these deaths. This chapter examines to what extent births and neonatal deaths are underreported and discusses the challenges facing the current registration system in Jordan. Irrespective of where the event occurs, reporting a birth or death in Jordan to the Civil Status and Passports Department is initiated by a family member. Stillbirths in Jordan are not routinely registered. Moreover, the majority of neonatal deaths are underreported, and the causes of neonatal death are very likely recorded inaccurately. There are several reasons for this, but avoidable reasons center around the death notification, including the causes of death, which is not usually completed by the attending physician as physicians are not well trained on assigning causes of death; they are often not aware of the definitions of and distinctions between direct causes, underlying causes, and contributing causes of death. The majority of neonatal deaths in Jordan and all stillbirths go unreported and are not registered in Jordan. The underreporting is mainly attributable to a dysfunctional reporting system and the fact that families, not the health system, are responsible for registering births and deaths. Greater investment of resources is needed to improve vital registration and the health information system in Jordan. Timely actions are required at two levels: at the institutional level immediately after a stillbirth or an infant death has occurred and at a national level from data received from institutional levels. Since a high proportion of deaths occur in, or have been in contact with, the health system, investments in its ability to report neonatal deaths are therefore warranted. Clear policies and guidelines are required to ensure data collection activity is accurate, timely, comprehensive, and accessible to policy makers.
Birth and Neonatal Death Registrations
in Jordan
Yousef S. Khader, Mohammad Alyahya, and Anwar Batieha
Contents
Introduction ....................................................................................... 2
Limitations in Mortality Data: Underreporting .. ................................................ 3
Registration of Births and Deaths in Jordan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. 5
Registration of Births in Jordan .............................................................. 5
Registration of Deaths in Jordan .............................................................. 6
Problems in Registration of Births and Deaths in Jordan ....................................... 6
Completeness of Neonatal Death Registration ................................................... 7
Conclusions ....................................................................................... 8
Recommendations to Improve the Process of Birth Registration . . .. . . . . . . . . .. . . . . . . . . . . .. . . . . . 10
Recommendations to Improve the Process of Death Registration . . . . .......................... 10
References .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .. . . . . . . . . . 11
Abstract
Assessing the magnitude and etiologies of perinatal deaths and their risk factors
begins with accurately dening and reporting these deaths. This chapter examines
to what extent births and neonatal deaths are underreported and discusses the
challenges facing the current registration system in Jordan. Irrespective of where
the event occurs, reporting a birth or death in Jordan to the Civil Status and
Passports Department is initiated by a family member. Stillbirths in Jordan are not
routinely registered. Moreover, the majority of neonatal deaths are underreported,
and the causes of neonatal death are very likely recorded inaccurately. There are
Y. S. Khader · A. Batieha (*)
Department of Community Medicine, Public Health and Family Medicine, Faculty of Medicine,
Jordan University of Science & Technology, Irbid, Jordan
e-mail: yskhader@just.edu.jo;batieha@just.edu.jo
M. Alyahya
Department of Health Management and Policy, Faculty of Medicine, Jordan University of Science
and Technology, Irbid, Jordan
e-mail: msalyahya@just.edu.jo
© Springer Nature Switzerland AG 2019
I. Laher (ed.), Handbook of Healthcare in the Arab World,
https://doi.org/10.1007/978-3-319-74365-3_116-1
1
several reasons for this, but avoidable reasons center around the death notica-
tion, including the causes of death, which is not usually completed by the
attending physician as physicians are not well trained on assigning causes of
death; they are often not aware of the denitions of and distinctions between
direct causes, underlying causes, and contributing causes of death.
The majority of neonatal deaths in Jordan and all stillbirths go unreported
and are not registered in Jordan. The underreporting is mainly attributable to
a dysfunctional reporting system and the fact that families, not the health system,
are responsible for registering births and deaths. Greater investment of resources
is needed to improve vital registration and the health information system in
Jordan. Timely actions are required at two levels: at the institutional level
immediately after a stillbirth or an infant death has occurred and at a national
level from data received from institutional levels. Since a high proportion of
deaths occur in, or have been in contact with, the health system, investments in its
ability to report neonatal deaths are therefore warranted. Clear policies and
guidelines are required to ensure data collection activity is accurate, timely,
comprehensive, and accessible to policy makers.
Keywords
Neonatal deaths · Stillbirths · Registration · Underreporting · Causes of perinatal
deaths
Introduction
Perinatal death rate is widely recognized as a key indicator of population health
status. It is a broad denition which combines neonatal deaths and stillbirths during a
given year per 1000 births (Lawn et al. 2011; World Health Organization 2016a).
Assessing the magnitude and etiologies of these important events and predicting its
risk factors begin with accurately dening and reporting perinatal deaths (Bareld
2016). Although generally accepted by the larger medical community, WHO de-
nitions are not the basis for perinatal data collection in many countries. Countries
may have their own legal denitions of live births, stillbirths, or infant deaths, which
differ from those recommended by WHO (World Health Organization 2016a; AIHW
et al. 2016; Manning et al. 2014). The criteria for registering these important events
also vary, and the time within which an event must be registered varies between
events and among countries. The reporting of stillbirths, which is an alternative
outcome to live birth, is frequently not explicitly dened or included in national
statistical data; perinatal data is often collected as a by-product of administrative or
legal processes. Timing of registration is usually longer for live births and stillbirths
compared to registration of deaths of live-born infants and adults. As a consequence,
stillbirths and neonatal deaths are not reported accurately because births may not be
recorded prior to early death (World Health Organization 2016b).
Neonatal mortality improvement requires improvement so as to build a trustwor-
thy ofcial reporting system for births and deaths. Tackling underreporting and
2 Y. S. Khader et al.
evaluating the proles of unregistered deaths will reduce the decision-making based
on invalid information. In doing so, the challenges in neonatal health can be
recognized, and resources may be distributed according to real needs instead of
overly optimistic indicators. In this chapter, we analyze to what extent births and
neonatal deaths are underreported and discuss the challenges of the current registra-
tion system in Jordan.
Limitations in Mortality Data: Underreporting
Reliability of data depends on accurate reporting and recording of births and
deaths, and failure to report the birth of a baby who dies soon afterward leads to
underestimated mortality rates. Underreporting and misclassication are common,
originating both with the parent and with the recording process. Misclassication of
live births and deaths can also occur; there may be a misunderstanding of the
denition of live birth and fetal death or a misunderstanding of the purpose of
reporting. Live births are more likely to be reported compared to fetal or early
neonatal deaths, and a nonviable fetus may systematically be reported as a stillbirth
(World Health Organization 2016b; Atlas 2013; Deb-Rinker et al. 2015).
Countries around the world are increasingly interested in collecting data on
perinatal deaths because of the burden of 2.6 million stillbirths and 2.61 million
neonatal deaths that are estimated to occur every year (UNICEF 2015; United
Nations Inter-agency Group for Child Mortality Estimation (UN IGME) 2017).
In most countries, however, especially those that continue to have high perinatal
mortality rates, there are no effective civil registration and vital statistics systems for
capturing all births and deaths and assigning causes of death. Half of the worlds
children do not receive a birth certicate; and almost all stillbirths and half of all
neonatal deaths are not currently registered. Developing national systems for
reporting births and perinatal deaths is a matter of human rights and a prerequisite
for improving stillbirths and neonatal mortality rates (World Health Organization
2016a; Lawn et al. 2014; Målqvist et al. 2008).
It has been argued that the potential of reporting the infant as being alive may be
associated with the perception of the infants survivability (Oza et al. 2014); a young
gestational age and low birth weight reduce survival rates and also reporting death.
Vital statistics, which are derived from birth and death certicates, are available for
more than half of the world countries, but only about 50% of those datasets (mostly
from the wealthiest countries) are reliable (Oza et al. 2014; Oestergaard et al. 2011).
Comparison between vital statistics and surveys carried in different countries,
especially in developing ones, showed that signicant numbers of infant and early
deaths remain undocumented. For example, a recent study used the Ethiopian Mini
Demographic and Health Survey (EMDHS) data and found that the rate of stillbirths
was 85 per 1000 total births. This rate was signicantly higher than what has been
previously reported (26 stillbirths per 1000) (Lakew et al. 2017; Cousens et al.
2011). Another prospective study carried out in a Nepali district found that the
perinatal mortality rate was 60 per 1000 births and the neonatal mortality rate was
Birth and Neonatal Death Registrations in Jordan 3
38 per 1000 live births (Manandhar et al. 2010). Yet, at the time of the study, the
most recent ofcial estimates of perinatal deaths and neonatal deaths were 45/1000
births and 33/1000 live births, respectively (Population Division 2007). This reects
a discrepancy between reporting of vital events and the ndings of community
survey studies; vital statistics underestimate the true magnitude of perinatal mortality
rates. Furthermore, incomplete reporting or misreporting of vital registration data is
not uncommon even in developed countries (Farquhar et al. 2015; Seske et al. 2017).
Results from a study aimed to recognize the limitations of combining fetal and
neonatal death records and to nd opportunities for improving fetal death registra-
tion in New York City showed that fetal death records frequently lack important
information including demographic, medical, and cause of death (Lee et al. 2014).
The results conrmed the ndings of previous studies concerning completeness
of fetal death registration (Lee et al. 2014; Duke et al. 2008). Another US retrospec-
tive cohort study was conducted to evaluate the reliability of infant death certicate
information regarding cause of death in comparison with related autopsy data and
conrmed a considerable disconnect between infant cause of death data derived from
vital records and autopsy data (Seske et al. 2017).
According to the WHO, perhaps 40% or more of early neonatal deaths and
stillbirths may go unreported in ofcial data. Underreporting is also a problem in
birth registration. There may be various reasons for why children are registered late
or not at all. In some countries the responsibility to register newborns is put on the
families, who often have a poor understanding of the necessity of registration. Many
parents simply do not see an urgent need for the procedure and, particularly in
remote areas, simply do not have easy access to registrars. According to a UNICEF
study, less than half of the families in Vietnam had registered their child within the
legally prescribed time period (UNICEF 2000). If the responsibility to report births
and deaths was instead placed on the institutions where these events occurred, more
reliable statistics could be produced.
Inconsistency between various terminologies used to evaluate pregnancy could
also lead to underreporting at several levels. In this sense, livebirth, perinatal death,
neonatal death, stillbirth, fetal death, and abortion terms have denitions which may
overlap based on the country or the health facility. For example, the WHO recom-
mends reporting of livebirths weighing at least 500 g or born after 22 weeks
of gestation (World Health Organization 2016b). Another well-recognized difculty
in the registration of neonatal deaths is the matter of dening early neonatal deaths
from stillbirths. To distinguish whether a baby dies intrapartum or shows signs of life
immediately after delivery can be difcult, and establishing the boundary can be
a source of confusion. In some countries where neonatal survivability is uncertain,
the baby remains unnamed and unreported, and if death occurs early in neonatal life,
it will not be registered as a live birth. Similarly, due to variations in the timing of
the death during the neonatal period and national reporting standards, a live birth
with less than 28 weeks of gestation will be recorded as an abortion case rather than
a live birth (Pathirana et al. 2016).
To avoid this, perinatal mortality has often been used as a measure that combines
the stillbirth rate with the early neonatal mortality rate. Especially in a setting with
4 Y. S. Khader et al.
a large proportion of home deliveries, perinatal mortality has been widely used as an
indicator especially where there is a large proportion of home deliveries, thereby
avoiding the trouble of denition. However, considering the differences in etiology
between stillbirths and neonatal deaths, and the subsequent possible preventive
interventions, there is an argument for stratifying them (Kramer et al. 2002).
Underreporting of births and deaths may have severe consequences for policy
formulation, health planning, research, and resource allocation at all levels in the
pursuit of improved neonatal survival. Without statistics based on local data, it will
be difcult to target interventions to reach those in greatest need. Pregnant women
will not take adequate precautions before delivery since pregnancy may be perceived
as a normal part of life and not as a potentially hazardous situation (Mesko et al.
2003). Initiatives by local actors or NGOs will not be backed up by statistics, and
local authorities will not act to solve problems that they perceive not to have. On the
contrary, local health authorities might even encourage underreporting in order to
gain approval and rewards from central authorities.
To register the death of a newborn is, however, not only a matter of statistics
but also a matter of human rights. The right to birth registration is part of the UN
Convention on the Rights of the Child (Pais 2002), but despite this fact, newborns
not reported to have died are often not even registered as being born. The imple-
mentation and enforcement of human rights depend on civil registration, something
that is not well known or recognized in many parts of the world (Jewkes and Wood
1998). Acknowledging and reporting a neonatal death strengthens the position and
rights of the living by acknowledging that every child is a human being from the
moment of birth. The UN Millennium Project states that in order to improve
the situation of womens and childrens health in the world, human rights need to
be highlighted and enforced (Freedman and Millénaire 2005). Pursuing a true
representation of child survival is an integral part of this effort (Filippi et al. 2006).
Registration of Births and Deaths in Jordan
Birth registration as dened by UNICEF is the continuous, permanent, and universal
reporting process, within the civil registry system, of the incidence and main
characteristics of births based on the legal requirements of a country. In Jordan,
99% of live births are registered through the civil registration system which is
a centralized system (UNICEF 2013). The Department of Civil Status and Passport
(under the Ministry of Interior) is responsible for all civil registrations in the country.
There are 74 subofces spread around the country, and ofces within the Department
of Civil Status and Passport are linked to a computer network, operated by the
network management center.
Registration of Births in Jordan
Usually the notication of a birth is prepared by a health institution and in a limited
number of cases by a local government ofcial such as a village chief (i.e.,
Birth and Neonatal Death Registrations in Jordan 5
Al-Mukhtar). To document the birth of a baby (issuing a birth certication), the
notication should be submitted to the registrar of the Department of Civil Status and
Passport. The notication report has no legal value other than being informative
(Department of Civil Status and Passport 2018).
Current legislation on birth registration requires that all births occurring in Jordan
(including to foreign citizens) should be reported to the civil registration administra-
tion within 30 days of birth. For the registration of births occurring in the country, the
family member, family book (or passport for foreigners), and proof from the hospital
have to be presented. The government imposes a ne for late registration. Birth
certicates for births reported after 30 days but within 1 year are ned 10 Jordanian
Dinars (JD), equivalent to about US $14. Births reported after 1 year requires a court
decision to be registered, and a 10 JD ne should be paid. While this ne enforces and
encourages parents to register their babies on time, it can also put a burden on families
that nd it difcult to register, such as those living in remote areas that are poorly
served by government services. For Jordanians born outside the country, a similar
process is followed, but the time periods described earlier are extended to 90 days
instead of 30 days and to 2 years instead of 1 year. A birth certicate from the country
in which the baby was born can be exchanged with a Jordanian birth certicate
irrespective of the time elapsed. Reporting of births is carried out by the babys family
member or a family member (Department of Civil Status and Passport 2018).
Once a birth certicate is issued, each child is given a unique and unchangeable
national identication number (NID). This unique ofcial number is used in
government transactions. Moreover, the NID is also used to securely access
a patients centric health record which can be retrieved from any automated health
institution through the Hakeem program across the country. The Hakeem
program was launched in 2009 to facilitate efcient, high-quality healthcare services
through the nationwide implementation of an electronic health record solution
(HER) (Solution EH 2018).
Registration of Deaths in Jordan
The death registration process is similar to the process of birth registration. Deaths
occurring within the country have to be reported with the following documents: the
presence of a qualied family member, family book and NID for Jordanians who
die within Jordan (or passport for foreigners), and proof from the hospital or other
eligible agencies. Deaths should be reported within 1 week of death; death certi-
cates for deaths reported after 7 days but within 1 year are ned 10 JD. A court
decision is needed to register deaths reported after 1 year.
Problems in Registration of Births and Deaths in Jordan
Irrespective of where the event occurs, the reporting of a birth or death to the Civil
Status and Passports Department is initiated by a family member. Families report
births to preserve the babys privileges, such as health insurance, vaccination,
6 Y. S. Khader et al.
admission to school, inheritance, and so on. However, if the baby dies shortly after
birth, then families may have no interest in reporting the birth or the death. Similarly,
deaths of people who have no property are unlikely to be reported. According to the
latest analytical study conducted in 2015, the infant mortality rate for males and
females were 18.4 and 15.8 infant deaths per 1000 live births (Statistcs Do 2016).
While the infant mortality rate (per 1000 live births) was reported at 15.0 for the
same year according to the 2016 UNICEF report (UNICEF 2016). These conicting
gures reect the fact that the death registration system in Jordan does not cover all
events. The problem of underreporting is also magnied because people are largely
unaware of the need for early reporting, and the ne for late reporting is too small to
deter people.
The cause/s of death are likely to be recorded inaccurately. There are several
reasons for this, but important, avoidable reasons include:
(a) The death notication, including the causes of death, is not usually completed by
the attending physician.
(b) Physicians are not well trained on how to assign causes of death; they are often
not aware of the denitions of and distinctions between direct causes, underlying
causes, and contributing causes of death.
A new registration system was launched in March 2018. Each individual birth
and death will be recorded so that trends can be identied. The dataset of the new
system will enable multivariable analysis to produce an initial report on perinatal
mortality and therefore make necessary changes to prevent future losses. The goal of
such a system is not only to accurately report perinatal deaths but also to collaborate
with the wider maternity community and enhance maternal healthcare services in
Jordan.
Completeness of Neonatal Death Registration
Under-registration of births and deaths in Jordan may have a substantial impact on
reported neonatal and infant death rates and distort international mortality compar-
isons. There is a need for valid health statistics and data reporting on child births and
deaths as such ofcial gures are important for policy formation, planning,
and allocation of funds. They are also necessary for the design and monitoring
of interventions aimed at improving child survival. According to a workshop report
by the Civil Administration in 2005, about 1.5% of births were not registered
because the babies died early, and a further 80% of infant deaths were not recorded.
A tendency to under-register female deaths was also observed since registered
female deaths accounted for only 40% of all registered deaths.
There is currently little data available on stillbirths in Jordan. According to the
WHO estimation in 2000, the stillbirth rate was 13 per 1000. With a neonatal
mortality rate reaching 17 per 1000, the perinatal mortality rate was estimated as
26 per 1000 live births. In 2002, a survey conducted in the Deir-Alla district of
Birth and Neonatal Death Registrations in Jordan 7
Jordan found that 72.2% of child deaths including stillbirths were not registered
(Al Rabee and Al Kafajei 2006).
The Jordan Neonatal Mortality Study (Batieha et al. 2016) is a national prospec-
tive study in which a total of 21,928 women who gave birth (a total 22,591 births) in
18 selected hospitals during the study period were followed up for 28 days to verify
the status of their newborns (dead or alive) and to identify causes and predictors of
neonatal death. The study provided a unique opportunity to assess the completeness
of registration of stillbirths and neonatal deaths by the Department of Civil Status
and Passport. To analyze the extent to which neonatal deaths were unregistered,
268 out of 327 neonatal deaths identied during the study period were cross-checked
with the Department of Civil Status and Passport registry to determine how many
were captured. The babys national number was used for cross-checking, and when it
was unavailable, the name of the mother and other information such as residency,
fathers name, and hospital of child birth were used for cross-checking. The neonatal
deaths were cross-checked 28 months after the babiesdeaths, with the vast
majority being checked 67 months after death. The same procedure was used to
cross-check for stillbirths.
No stillbirth was registered in the Department of Civil Status and Passport
registry. Of the total 268 neonatal deaths identied in the prospective study,
207 (77.2%) neonatal deaths were not registered, 22 (8.2%) were still registered as
alive, and 39 (14.6%) neonatal deaths were accurately registered as dead. Overall,
the rate of under-registration of neonatal deaths was 85.4% (95% CI: 81.289.6%).
The rate of under-registration of neonatal deaths according to different variables
including region, type of hospital, timing of death, gender of the baby, gestational
age, birth weight, mothers employment status and education, and fathers education
is shown in Table 1. The rate of under-registration of neonatal deaths varied
signicantly according to gestational age (p-value =0.021) and fathers level of
education (p-value =0.006). The rate of under-registration of neonatal deaths was
the highest (90.4%) for preterm babies (31 gestational weeks). The corresponding
rates were 84.0% for older preterm babies (3236 gestational weeks) and 76.4% for
full-term babies (37 gestational weeks). Neonatal deaths in babies born to fathers
with 12 years of education were more likely to be unregistered compared to
neonatal deaths of babies born to fathers with >12 years of education (88.4%
vs. 73.6%). On the other hand, the data does not support the claim that female deaths
are more likely to go unregistered compared to male deaths. The rate of under-
registration of female neonatal deaths (83.3%) was not signicantly different from
the rate of under-registration of male neonatal deaths (86.9%). The registered cause
of neonatal deaths was appropriately recorded for only 3 of the 39 registered deaths.
Conclusions
The majority of neonatal deaths in Jordan and all stillbirths go unreported and are not
registered in Jordan. The underreporting is mainly attributable to a dysfunctional
reporting system and the fact that families, not the health system, are responsible for
8 Y. S. Khader et al.
Table 1 Rates of under-registration of neonatal deaths in the Department of Civil Status and
Passport registry, Jordan
Not registered as dead
(N=229) N (%)
Registered as dead (N=39)
N (%)
P-
value
Region 0.478
North 83 (88.3) 11 (11.7)
Middle 129 (83.2) 26 (16.8)
South 17 (89.5) 2 (10.5)
Type of hospital 0.062
Private 13 (76.5) 4 (23.5)
Public 131 (88.5) 17 (11.5)
Military 73 (85.9) 12 (14.1)
Teaching 12 (66.7) 6 (33.3)
Mothers education
(years)
0.089
12 171 (87.7) 24 (12.3)
>12 58 (79.5) 15 (20.5)
Fathers education
(years)
0.006
12 190 (88.4) 25 (11.6)
>12 39 (73.6) 14 (26.4)
Mothers occupation 0.365
Housewife 207 (84.8) 37 (15.2)
Employed 22 (91.7) 2 (8.3)
Gender of baby 0.420
Male 139 (86.9) 21 (13.1)
Female 90 (83.3) 18 (16.7)
Timing of neonatal
death
0.411
Early neonatal
death
194 (86.2) 31 (13.8)
Late neonatal
death
35 (81.4) 8 (18.6)
Birth weight (g) 0.059
<1000 62 (89.9) 7 (10.1)
1000 to <1500 56 (88.9) 7 (11.1)
1500 to <2500 67 (87.0) 10 (13.0)
2500 44 (74.6) 15 (25.4)
Gestational age
(weeks)
0.021
31 132 (90.4) 14 (9.6)
3236 42 (84.0) 8 (16.0)
37 55 (76.4) 17 (23.6)
Birth and Neonatal Death Registrations in Jordan 9
registering births and deaths. Greater investment of resources is needed to make
systemic improvements in vital registration data and for the collection of routine
information in Jordan. Timely actions are required at two levels: at the institutional
level immediately after a stillbirth or an infant death has occurred and at the national
level as a result of data received from the institutional level. Since a high proportion
of deaths occur in babies born in (or have been in contact with) the health system,
investments in its ability to report neonatal deaths are warranted. Clear policies and
guidelines are required to ensure data collection is timely, accurate, comprehensive,
and customized for the purposes required.
Recommendations to Improve the Process of Birth Registration
The following are recommendations to improve the process of birth registration:
There is a need for legislation that obliges hospitals and other places where
deliveries occur to directly report births to the Department of Civil Status and
Passport in a timely manner. Knowing that about 99% of all deliveries occur in
hospitals, such legislation, if properly implemented, would boost the complete-
ness and timely coverage of births in Jordan. An electronic system automatically
connecting the Department of Civil Status and Passport with hospitals would be
ideal for the registration process
Community awareness programs are needed to capture the remaining roughly 1%
of births that are unreported. Implementation of public awareness programs on
the importance of birth registration and an accurate system of vital records should
be initiated at the national and local levels.
Requiring the national identication number (NID) as a prerequisite for receiving
healthcare, vaccinations in health facilities, and other benets can also
help improve birth registration. To avoid denying essential health services to
the baby, the health facility can take the opportunity to report the birth to the
Department of Civil Status and Passport while simultaneously providing the
services.
Birth registration should be carried out free of charge. Fees may be charged for
issuance of a birth certicate.
Recommendations to Improve the Process of Death Registration
To improve the process of death registration, the following changes are
recommended:
The legislation and electronic system proposed above to improve birth registra-
tion should be extended to cover registration of deaths.
Introduce reporting requirements for fetal demise or stillbirth.
10 Y. S. Khader et al.
Strict adherence to obtaining a burial permit should be enforced by
municipalities.
In order to consider preventable factors, there is a need for a classication system
to identify the most important factors or health conditions which might lead to or
cause the death of an infant. Moreover, physicians should be trained on how to
identify the correct causes of death.
Institutionalize basic training regarding concepts of death certication practices in
medical school and postgraduate training curricula.
Conduct training for both healthcare providers involved in certifying births and
death and the coders responsible for assigning the International Classication of
Diseases-10th revision (ICD-10) codes.
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... 4,9,10 One possible reason for the lack of data are the poor quality of birth and death registration systems and the lack of death auditing in many LMICs. [11][12][13] Facility-based review of neonatal deaths and stillbirths has proven to be feasible and useful in different health care institutions, as it detects the medical causes of these deaths and highlights any gaps or challenges in the institution. Hence, death review audit can motivate stakeholders and policy makers to improve the overall provision of healthcare for pregnant women and their fetuses/newborn babies by identifying the avoidable and modifiable factors, as well as any opportunities for improvement. ...
... 6,23,24 Further, there have been inaccuracies in reporting the exact causes of neonatal deaths and stillbirths in Jordan. 6,11,23 One study showed that the majority of neonatal deaths in Jordan are preventable, highlighting the urgent need for the provision of high-quality intrapartum and postpartum care. 24 In addition, there is a lack of evidence regarding the contribution of the three aforementioned delays to stillbirths and neonatal deaths in Jordan. ...
... Since Jordan lacks a credible system for registering neonatal deaths and stillbirths and their causes, accurate mortality measures and quality indicators are lacking. 11 Also, neonatal death and stillbirth auditing is unavailable in most hospitals in Jordan. 13,25 Consequently, this study aimed to establish DRCs in five major hospitals; identify the modifiable factors that could be contributing to stillbirths and neonatal deaths; assess the delays in pregnant women recognizing the need for care, seeking care, and receiving care; and describe the specific actions and interventions taken by the participating hospitals to avoid or minimize the related preventable deaths. ...
Article
Objective This study employed the “three-delay” model to investigate the types of critical delays and modifiable factors that contribute to the neonatal deaths and stillbirths in Jordan. Study Design A triangulation research method was followed in this study to present the findings of death review committees (DRCs), which were formally established in five major hospitals across Jordan. The DRCs used a specific death summary form to facilitate identifying the type of delay, if any, and to plan specific actions to prevent future similar deaths. A death case review form with key details was also filled immediately after each death. Moreover, data were collected from patient notes and medical records, and further information about a specific cause of death or the contributing factors, if needed, were collected. Results During the study period (August 1, 2019–February 1, 2020), 10,726 births, 156 neonatal deaths, and 108 stillbirths were registered. A delay in recognizing the need for care and in the decision to seek care (delay 1) was believed to be responsible for 118 (44.6%) deaths. Most common factors included were poor awareness of when to seek care, not recognizing the problem or the danger signs, no or late antenatal care, and financial constraints and concern about the cost of care. Delay 2 (delay in seeking care or reaching care) was responsible for nine (3.4%) cases. Delay 3 (delay in receiving care) was responsible for 81 (30.7%) deaths. The most common modifiable factors were the poor or lack of training that followed by heavy workload, insufficient staff members, and no antenatal documentation. Effective actions were initiated across all the five hospitals in response to the delays to reduce preventable deaths. Conclusion The formation of the facility-based DRCs was vital in identifying critical delays and modifiable factors, as well as developing initiatives and actions to address modifiable factors. Key Points
... The scarcity of data in Jordan on stillbirths and neonatal mortality, especially early mortality is generally linked to the fact that some births are not registered (10,11). In addition, the existing sources of data on neonatal mortality are likely to be biased or incomprehensive. ...
... Assessing the magnitude and etiology of these important events and predicting their risk factors begin with accurately defining and reporting perinatal deaths (23,24). A strategy for regionalized and cohesive perinatal network should be developed (10,11) to reduce perinatal morbidity and mortality and improve survival for pre-term infants and other high-risk newborns. Mortality data should be available by geographical area, rural or urban, place of death, timing, underlying cause, and other data such as socio-economic status (25). ...
... However, not all births are registered in Jordan, especially if the birth results in stillbirth or early neonatal death before discharge from the hospital and the majority of neonatal deaths are not reported either (10,11). About 30% of children <5 years do not have a birth certificate (42), and parents do not usually issue a death certificate for the majority of neonatal deaths (36). ...
Article
Full-text available
Background: It has been estimated that 27.8 million neonates will die worldwide between 2018 and 2030 if no improvements in neonatal and maternal care take place. The aim of this study was to determine the rate, risk factors, and causes of neonatal mortality in Jordan. Methods: In August 2019, an electronic stillbirths and neonatal deaths surveillance system (JSANDS) was established in in three large cities through five hospitals. Data on all births, neonatal mortality and their causes, and other characteristics in the period between August 2019 and January 2020 were exported from the JSANDS and analyzed. Results: A total of 10,328 births [10,226 live births (LB) and 102 stillbirths] were registered in the study period, with a rate of 14.1 deaths per 1,000 LBs; 76% were early neonatal deaths and 24% were late deaths. The odds of deaths in the Ministry of Health hospitals were almost 21 times (OR = 20.8, 95% CI: 2.8, 153.1) higher than that in private hospitals. Low birthweight and pre-term babies were significantly more likely to die during the neonatal period compared to full-term babies. The odds of neonatal mortality were significantly higher among babies born to housewives compared to those who were born to employed women (OR = 2.7; 95% CI: 1.2, 6.0). Main causes of neonatal deaths that occurred pre-discharge were respiratory and cardiovascular disorders (43%) and low birthweight and pre-term (33%). The main maternal conditions that attributed to these deaths were complications of the placenta and cord, complications of pregnancy, and medical and surgical conditions. The main cause of neonatal deaths that occurred post-discharge were low birthweight and pre-term (42%). Conclusions: The rate of neonatal mortality have not decreased since 2012 and the majority of neonatal deaths occurred could have been prevented. Regular antenatal visits, in which any possible diseases or complications of pregnant women or fetal anomalies, need to be fully documented and monitored with appropriate and timely medical intervention to minimize such deaths.
... One reason for such inaccurate estimates is the lack of reliable national surveillance system to register stillbirths and neonatal deaths and their causes in Jordan [6]. Similarly, there is a lack of facility-based death auditing in maternity and children hospitals in Jordan. ...
... Attention to Human Rights during DRC Meetings. All participants identified several factors that can highlight the deprived woman's right and welfare, including unplanned pregnancy, in which the husband has the power to decide 6 BioMed Research International on behalf of the wife, low income, early marriage and adolescent pregnancy, low women educational level, and socioeconomic characteristics. Specifically, almost all DRC members became more aware that human rights issues in general and teenage pregnancy in specific are global issues. ...
Article
Full-text available
Background. Facility-based death review committee (DRC) of neonatal deaths and stillbirths can encourage stakeholders to enhance the quality of care during the antenatal period and labour to improve birth outcomes. To understand the benefits and impact of the DRCs, this study was aimed at exploring the DRC members’ perception about the role and benefits of the newly developed facility-based DRCs in five pilot hospitals in Jordan, to assess women empowerment, decision-making process, power dynamics, culture and genderism as contributing factors for deaths, and impact of COVID-19 lockdown on births. Methods. A descriptive study of a qualitative design—using focus group discussions—was conducted after one year of establishing DRCs in 5 pilot large hospitals. The number of participants in each focus group ranged from 8 to10, and the total number of participants was 45 HCPs (nurses and doctors). Questions were consecutively asked in each focus group. The moderator asked the main questions from the guide and then used probing as needed. A second researcher observed the conversation and took field notes. Results. Overall, there was an agreement among the majority of DRC members across all hospitals that the DRC was successful in identifying the exact cause of neonatal deaths and stillbirths as well as associated modifiable factors. There was also a consensus that the DRC contributed to an improvement in health services provided for pregnant women and newborns as well as protecting human rights and enabling women to be more interdependent in taking decisions related to family planning. Moreover, the DRC agreed that a proportion of the neonatal deaths and stillbirths occurring in the hospitals could have been prevented if adequate antenatal care was provided and some traditional harmful practices were avoided. Conclusions. Facility-based neonatal death review audit is practical and can be used to identify exact causes of maternal and neonatal deaths and is a valuable tool for hospital quality indicators. It can also change the perception and practice of health care providers, which may be reflected in improving the quality of provided healthcare services. 1. Introduction Accurate rates of neonatal deaths and stillbirths are insufficiently calculated and documented in low- and middle-income countries. A secondary analysis of data over ten years from 40 low- and middle-income countries showed that only 23 countries have counted stillbirths and predischarge neonatal deaths where the rate of stillbirths per 1000 deliveries ranged from 5.8 to 116.5, and the rate of predischarge neonatal deaths ranged from 1.8 to 21 [1]. Physicians and nurses working in maternity hospitals in Jordan reported poor attitude towards perinatal death audit due to lack of time, inadequate documentation of patient information in hospital records, and lack of available health information systems in Jordanian hospitals [2]. Consequently, rates and causes of neonatal mortality and stillbirths lack precise estimations in Jordan [3–5], where the majority of such deaths can be avoided or at least minimized if adequate and comprehensive quality intrapartum and postpartum care provided [3]. One reason for such inaccurate estimates is the lack of reliable national surveillance system to register stillbirths and neonatal deaths and their causes in Jordan [6]. Similarly, there is a lack of facility-based death auditing in maternity and children hospitals in Jordan. Therefore, a newly developed electronic surveillance system, Jordan Stillbirths and Neonatal Deaths (JSANDS), has been implemented in five Jordanian hospitals since August 2019. The JSANDS was developed by lead researchers at a Jordanian university in partnership with the Ministry of Health in Jordan. It is a secure on-line system to collect, organize, analyse, and disseminate trustworthy data on neonatal deaths, stillbirths, and associated causes and modifiable factors. Also, the JSANDS (http://www.jsands.jo/) registers births to use them as a denominator for mortality measures and adopted the ICD-10 (International Classification of Diseases, Tenth Revision) to identify and classify main and secondary causes of neonatal deaths and stillbirths as well as maternal causes of deaths. The JSANDS is fully described in a conference paper (Khader, Alyahya, Batieha, & Taweel, 2019). Facility-based audit/review of neonatal deaths and stillbirths can encourage stakeholders to enhance the quality of care during the antenatal period and labour thus improve birth outcomes [7, 8]. One way to accomplish this is through the recognition of modifiable risk factors and the development of initiatives to improve care [9–11]. In specific, audit committee members discuss each neonatal death or stillbirth carefully to provide a better understanding of root causes thus allow them to prevent similar deaths in the future [7, 12]. A recent national study analysed 10,328 births registered at the JSANDS in five hospitals over the six-month period [13]. The rate of neonatal deaths was 14.1 deaths per 1,000 live births with significantly higher deaths in the Ministry of Health hospitals than those in private hospitals. This is because private hospitals usually receive low-risk pregnancies. Major causes of neonatal deaths were cardiovascular and respiratory disorders, preterm births, and low birthweight. The most common maternal conditions that contributed to these deaths were complications of pregnancy, placenta, and cord, as well as medical and surgical conditions such as preeclampsia and gestational diabetes [13]. As part of a larger ongoing project, a facility-based death review committee (DRC) was established in five large hospitals in Jordan in June 2019 in order to identify the causes contributing to stillbirths and neonatal deaths; to assess the delays in recognizing, seeking, and receiving care by pregnant women and their newborns; and to describe the specific actions and initiatives taken by DRC members to prevent or reduce similar preventable deaths. Recognizing modifiable factors of stillbirths and neonatal mortality can help in developing actions to improve the antenatal and intranatal care especially for high-risk pregnancies [14]. The DRC committee within each of the 5 hospitals consisted of obstetricians & gynecologists, pediatricians/neonatologists, a NICU head nurse, a labour head nurse, and senior staff from each department. Training was conducted for all DRC members in July 2019 on how to obtain accurate and complete data bout each death and how to manage and report DRC meetings. The assigned roles of the newly appointed five DRC members included the following: collecting information on the underlying causes of death, discussing and analyzing root causes and modifiable factors of neonatal deaths and stillbirths, and then developing and implementing actions and recommendations to address the modifiable factors and following up on the progress of the implemented actions. To enable the DRC role more fully, prenatal care in Jordan needs to be adequately sought by pregnant women and documented. It is a service that is covered by health insurance for all Jordanian women. Overall, antenatal care (ANC) in Jordan is of a high quality; the vast majority (94%) have at least four antenatal visits and 98% give birth within a healthcare institution providing qualified and experienced medical care [15]. Conversely, not all hospitals in Jordan provide the same level of high-quality ANC, and there is a substantial disparity in available resources among geographical regions and the diverse health sectors in the country [16]. For instance, a study was aimed to examine maternal and neonatal services in 32 Jordanian maternity hospitals [16] found that all hospitals—except one private—provide ANC. Health services such as hemoglobin and blood pressure measurements were available and provided thoroughly in all hospitals. Though, some services such as iron and folic acid supplementation, urine stick (sugar, protein), fasting blood sugar measurement, breastfeeding, and family planning counselling were not fully implemented antenatally and not provided in some hospitals. Regardless, all services were provided adequately in university teaching hospitals. Such services were more commonly provided in the Ministry of Health hospitals compared to private and Royal Medical Services ones. The quality of ANC in Jordan is particularly important in high-risk pregnancies. A report by the Jordanian Ministry of Health [17] found that the vast majority of maternal deaths received ANC services were either from public or private health sectors. Of the 62 maternal deaths, only 42 had a record of ANC visits, whereas 24% of maternal deaths had 1 to 3 ANC visits, 39.1% had 4 to 7 visits, and 37.0% had at least 8 visits. Only 8.5% of the maternal deaths had received ANC services from public primary healthcare institutions. According to the Jordanian healthcare systems, ANC services provided for high-risk pregnant women usually occur at the secondary and tertiary levels [17]. Unfortunately, Jordanian pregnant women usually seek postnatal care services to check up on the newborn’s health but not theirs [18]. On the other hand, a study was conducted to understand prenatal and intrapartum health service utilization among Syrian women refugees in Jordan [19]. The majority of women (82%) reported seeking ANC with an average of at least six ANC visits, and almost all births occurred in a health facility. Unlike Jordanian women who usually have a health insurance that covers birth in a maternity hospital (private or public), a large number of Syrian women (33%) reported to pay out of pocket costs for intrapartum care [19]. In an attempt to understand the benefits and impact of the DRCs, the current study was aimed at exploring the DRC members’ perception about the role and benefits of the newly developed facility-based DRCs in the five pilot hospitals in Jordan; assessing the DRC members’ perception of women empowerment, decision-making process, power dynamics, culture, and genderism as contributing factors for deaths; and assessing the impact of COVID-19 lockdown on births. 2. Methods A descriptive study of a qualitative design, using focus group discussions, was conducted after one year of establishing DRCs in 5 pilot large hospitals; three of them were public Ministry of Health (MOH) hospitals, one is university teaching, and one is private. All death review committee (DRC) members across the five hospitals were invited to participate in this study. The DRCs within each hospital met monthly since August 2019 to review all neonatal deaths and stillbirths that occurred during the month preceding the DRC meeting. The DRCs used a specific form (mortality audit and action items form), developed by the JSANDS team, to record the main causes of antepartum stillbirths, intrapartum stillbirths ,and neonatal deaths; identify critical delays and modifiable factors; and to identify specific actions and a follow-up plan. The form summarizes all deaths that occur during the month preceding the DRC meeting. The meeting benefits from a form filled for each individual death by attending nurses and doctors. The two forms were used as guides by the DRC members to initiate and facilitate the discussion. Data were abstracted from the patient notes and medical records as well as from the JSANDS system. More information about the exact cause of death or the contributing risk factors was collected from mothers, family members, relatives, and other health care providers. Five focus group discussions were conducted with the DRC members, one in each hospital. The number of participants in each focus group ranged from 8 to10, and the total number of participants was 45 HCPs (nurses and doctors) who were members of the developed facility-based DRC in the five hospitals. All participants were a multidisciplinary group of pediatricians, obstetricians, gynecologists, medical residents, and two hospital directors, as well as nurses or midwives who acted as focal points in the selected hospitals (senior head nurses of labour and NICU departments, and senior staff nurses and two midwives who used the JSANDS system since its implementation). Focus group discussions were held in a quiet meeting room in each hospital and lasted 45 to 90 minutes. The same moderator facilitated all five FGs to maintain consistency. Questions guide was developed by the researchers and used to moderate the FG discussions with enough time provided by the moderator to motivate discussion among members. The moderator was responsible for asking the main questions listed on the guide and used probing, if needed, and then directed and facilitated the group discussion, and a second researcher observed the conversation and took field notes. All focus groups were audio-recorded with prepermission granted from all DRC members. Ethical approval was gained from the Institutional Review Board at Jordan University of Science and Technology. Participation in the focus group discussions was voluntary, and DRC members were informed that they have the right to withdraw at any point without penalties. A directed (deductive) content analysis approach was adopted in this study, in which analysis was based on preidentified questions that were asked by the moderator and, then, answered by the DRC members [20]. This deductive approach enabled the moderator to focus on the research questions and provided predictions about some of the study variables and, thus, helped in determining initial coding and relationships between codes [20]. After the complete transcription of the focus group discussions, data analysis began by identifying key concepts as initial coding categories. The focus group questions were used as a guide to analyse data, in which researchers identified all examples of a particular predetermined code. Finally, coded data were then categorized into themes and subthemes. In particular, the moderator and the researcher came up with initial themes after reading the transcript and then recoded them after thorough discussions and rereading of the transcript to finally come up with a consensus on the themes and the subthemes. We used the deductive content analysis approach as we had an idea about the potential responses from the participants [21]. 3. Results All quotes mentioned by the DRC members in this article reflect real observations as well as actions and interventions made since the establishment of these committees. Thematic analysis identified six major themes, described below. 3.1. Roles of DRC In each of the participating hospital and before piloting the JSANDS, there is a death review committee—mostly embedded with maternal deaths—that is established to meet regularly to identify root causes of all stillbirths and neonatal deaths, especially preventable ones. However, among the five hospitals, only two meet regularly to discuss neonatal deaths but not stillbirths. After establishing a new DRC within each of the five hospitals, DRC members met regularly and utilized the data entered into the JSANDS system to help in identifying the root causes of stillbirths and neonatal deaths as well as contributing modifiable factors and delays. A pediatrician stated: “we repeatedly review all cases and try to get the specific cause of death if possible and if there was a delay.” Similarly, a pediatric resident noted: “when we meet now, we identify exactly where the problem is and how we can improve it in order to avoid such deaths…in fact, being a member of the DRC motivated us to walk the talk.” However, the majority of participants admitted that the first few DRC meetings were challenging in a way that they could not spot the exact underlying cause of fetal or newborn death. The most common stated reason was that they were not accustomed to analyse data and thoroughly review each death to find out the root cause responsible for deaths. A pediatric nurse argued: “we’re not used to dig deep into the exact cause of death.” A gynecologist noted: “the beginning was hard and challenging.” He added: “we already had a DRC before commencing the JSANDS project, though it used to focus on maternal deaths and was not activated as it should’ve…we don’t meet very often, and even when we meet, we don’t have enough data to give us a complete picture on what went wrong.” Almost all DRC members commenting on the usual “shallow” practice in documenting the cause of death before establishing the DRC. A pediatrician working in a private hospital explained the usual practice of documenting the cause of death before establishing the DRC: “before the DRC formation, only the doctor who is in-charge of the death tries to write a general cause of death in the death certificate without discussing the case with any one of his colleagues.” In specific, before establishing the DRC and its monthly meetings, obstetricians and pediatricians used to relate prematurity as a cause to all premature neonatal deaths or stillbirths without any further investigation to identify the exact cause of prematurity. However, the majority of DRC members highlighted the change in their practice in an attempt to correctly identify the cause and modifiable factors contributing to deaths. For instance, a pediatrician observed: “Before establishing the DRC in our hospital, there were some aspects that we used not to pay attention to…but when we began to complete the forms needed for the DRC, we’ve changed our practice in a way that we now set with the mother more often after her baby’s death to discuss all the circumstances that could’ve led to the delay/death… this is something we didn’t do before DRC establishment.” A hospital director—reflecting on his experience as being the head of the DRC within the hospital he works at—noted: “when I look back since last year when we first established the DRC, there’s a tangible difference and improvement in identifying the root cause of death as well as coming up with effective and feasible actions to overcome similar preventable deaths.” A head pediatric nurse also shared her experience: “regular DRC meetings helped us to focus on the root causes of death, and identify the most common causes… this motivated us to think thoroughly of how to prevent such deaths especially neonatal deaths, which I believe are largely preventable.” 3.2. Benefits and Impact of DRC 3.2.1. Improved Communication between Labour and Neonatal Intensive Care Unit Staff Overall, all pediatricians and obstetricians participating in the DRC committee became more interested in stillbirth and newborns admitted to the NICU and monitor and follow up with them more closely. All members agreed that the formation of the DRC and the regular review meetings enhanced the collaboration and coordination between nursing and medical staff in labour and NICU and between pediatricians and obstetricians, thus influenced decisions taken. An obstetrician proudly shared a success story reflecting on the benefits of early and timely communication and consultation between obstetricians and pediatricians during the antenatal period. He answered: “One example is the quadruplets that we delivered in the hospital without any complications due to the previous consultation and knowledge of the pediatrician about the health status of the mother and fetuses throughout pregnancy.” He added: “before establishing the DRC, we had similar triplet situation, but we didn’t know exactly what to do as there was no knowledge from the pediatrician about the maternal history during antenatal period…that’s why we lost one newborn, who could’ve been saved if we communicated with the pediatrician earlier.” He added: “awareness is the main pillar to provide quality and timely care.” A senior pediatrician—commenting on the usual practice before DRC developments—explained: “before DRC establishment, we never had to deal or care for a fetus with IUFD as we literally don’t see them…we even don’t know anything about them and we’re not interested to be honest… we didn’t literally know about anything happen outside our NICU ward.” A midwife added: “we now discuss stuff and agree on things, but before DRC meetings, we were disconnected…as if we’re separate hospitals!” Therefore, the majority of the participants agreed that pediatricians have become more interested in stillbirths that occur in their hospital, and the obstetricians also became more aware of and interested in newborns who were admitted to NICU, because they knew that they would set together to discuss the same cases, whether stillbirth or neonatal death, in the same DRC meeting. 3.2.2. Increased Knowledge and Accountability Almost all DRC members agreed that being part of the regular DRC meetings enhanced their knowledge about various causes of stillbirths and neonatal deaths and improved their responsibility and accountability of the work they provide. Steps perceived to improve knowledge were regular, thorough, and interactive discussions of each death from all members of the DRC, who have different experiences and specialties. Specialized scientific knowledge was usually shared by specialists about the root causes of deaths, thus enriched some other DRC members’ awareness and understanding, particularly nurses and junior members. Additionally, using specific forms and checklists adopted from the ICD-10 after each death and during the meetings required collecting detailed information about each death, thus improved awareness of causes of deaths that could have been prevented by either family and/or hospital care at prenatal, antenatal, or postnatal periods. Most importantly, immediate and prospective multidisciplinary discussions of neonates born with critical conditions could enable pediatricians to prevent deaths or lessen the severity of the health condition with the least complications. A senior nurse, who is also the head of NICU, shared her experience with being a member of the DRC: “I gained a lot of trusted knowledge and treasured information about maternal and newborn medical cases and complications through discussing them at the DRC meetings with experienced specialists in the field.” All participating DRC members acknowledged that regular meetings helped in creating a culture of increased DRC members’ responsibility and accountability, resulting in documentation of a detailed cause of death rather than merely writing broad causes on the death note or certificate. One pediatrician commented: “we always used to register the cause of death as “Stop of heart and lungs” … that’s it…now, after being part of the DRC, more focus on the root causes is needed…so specialists became more accountable and responsible…they know that other people will dig deep into the exact cause of death… so it’s better for them to have it right or otherwise they’ll be on the spot and questioned by the DRC members and probably hospital administration for their negligence.” Another emerged benefit of the DRC regular meetings was the quality and completeness of data from the JSANDS, which enabled DRC members to spot and recognize trends and patterns in certain anomalies and/or diseases within a certain period or a geographical area. One pediatrician noted: “we noticed many cases in the last month of spina befida…much more than what we usually see in other months…the electronic data on the JSANDS showed that very clearly.” A midwife added: “when I prepare the documents and the forms just before the meetings, I look at the pattern of death and start to compare it with other areas and then discuss it at the meeting to be able to do something about it.” Another tangible benefit that results from the preparations for the DRC meetings and the recommendations of the meetings was that HCP’s daily work and tasks have become more organized, comprehensive, and thorough. 3.2.3. Challenges, Actions and Initiatives for Improved Health Services Overall, all DRC members commented that the majority of women do not hold a pregnancy card with them. However, if the pregnant woman seeks ANC at a private clinic that does not belong to a hospital, then she has a card kept at that clinic. If the woman seeks ANC in a medical “outpatient” clinic belongs to a hospital, then she has a pregnancy record—mostly computerized—through electronic health record systems within the hospital. The major challenge is when the woman seeks birth in a hospital that she did not receive ANC at. In this case, she does not have a pregnancy card with her identifying maternal health condition and the fetus’ health status during pregnancy. Similarly, one of the most challenging situations that healthcare providers face in maternity hospitals is that most of the deliveries seeking hospitals are either emergency cases or unbooked births. Visiting private ANC clinics during pregnancy while giving birth in public hospitals can lead to the discontinuity and fragmentation in maternal and fetal healthcare services [18]. One pediatrician admitted: “sometimes, we face some critical issues especially if the baby is sick and, for example, need blood ASAP, this is where we know that it would’ve been great if we have a complete maternal history such as blood group type…any information could save the baby or the mother.” He added: “neither the obstetrician nor the pediatrician know much about maternal history, this is where we sometimes have to intervene without being fully certain about the outcome of our medical intervention or treatment.” The participants thus emphasized the importance of documenting maternal history during ANC and prehospital care as the current practice lacks maternal history. One gynecologist argued: “landing women give birth with no information whatsoever about them or the fetus…she probably sought a private doctor during antenatal care, but we have no clues about her medical condition.” In regard to actions taken by the DRC, the majority of participants identified several actions and initiatives. They all agreed that most of the actions recommended by the DRC were effective and taken seriously and had an obvious role in improving health services. In particular, there was a consensus amongst DRC members that the resulting actions and initiatives have been reflected in a better customized quality of care for pregnant and labouring women as well as neonates. An obstetrician working in a private hospital proudly commented on the action being taken by the DRC in regard to folic acid supplements during pregnancy: “we now see pregnant women coming to the outpatient clinic already on folic acid from the beginning of pregnancy…this reflects the high awareness of women as a result of the health education classes that we conducted in our outpatient clinic to avoid congenital abnormalities of the fetus.” All other DRC members agreed and encouraged mothers to take folic acid at preconception. Another important initiative was conducting counselling sessions for women who lost a newborn or just had a stillbirth to take complete medical and antenatal history to help in identifying possible causes of death. A pediatrician commented: “while interviewing the mother, we focus on all verbal and non-verbal cues for an accurate identification of the cause of death.” Another midwife added: “during counselling, we aim at increasing women awareness about the exact cause of death of her child so they try to avoid similar deaths in subsequent pregnancies.” The obtained data from the women’s interview are utilized as a baseline for taking decisions during DRC meetings. Such counselling was not conducted before establishing the committee. A pediatric nurse tried to highlight the group of women who needed counselling the most. She affirmed: “this purposive counselling is most helpful for women who don’t usually have their antenatal care visits in the hospital or those who don’t have antenatal care at all.” She added: “this is something new that we didn’t do before… if we figure out what happened, we then try to find out why it happened.” A pediatrician happily shared his experience with the outcome of extreme premature babies after being part of the DRC, which enabled a more thorough care for this vulnerable population: “recently, we began to notice that the outcome improved… for example, before we started to meet regularly, we were accustomed to accept the death of extreme premature and very low birth weight (800 to 1200 g)… but now- Thanks God- the outcome is excellent for 1000, 900, and even 700 gram babies because we now intervene immediately without any delays…it’s as if we, somehow, transform stillbirths into alive neonates.” Another issue discussed by some of the DRC members was the way the DRC actions successfully tackled the “chronic” shortage in medical equipment and staff. A pediatrician admitted: “one of the benefits of the DRC is that it made us look at the shortage in medical care provided in the NICU and try to develop strategies and actions to overcome the shortages, such as lack of training especially among medical residents on some procedures…” As a result, advanced training sessions about ventilators and CPAP (continuous positive airway pressure) were conducted for residents and nurses in all five hospitals. This action was reported to improve the quality of nursing services and the overall outcome. A pediatric nurse noted, “premature babies who weigh 900 grams are now admitted to the NICU for two months without any sign of sepsis…meaning that we’ve become more competent while administering procedures.” Similarly, a pediatrician at the private hospital proudly added: “Now the Neonatal resuscitation program course has become an essential part and a hospital policy for all staff in the NICU.” Lack of ANC was identified as the most common factor that contributes to preventable deaths. An obstetrician gave an example of the actions taken by the DRC to overcome the problem of lack of ANC and associated medical records for pregnant women and those whose labour is imminent. He stated: “so far, we tried to cover some of the comprehensive health centres of disadvantaged communities and allocated medical residents and a specialist (obstetrician) to pick up early cases of high-risk pregnancies, and then refer these pregnant women to us at the hospital to provide early quality care in a hope to decrease chance of death.” When they were asked about the DRC sustainability and moving forward, the majority admitted that the permanency of DRC is important as it helps HCPs identify the exact and most common cause of death in the hospital and, thus, work towards decreasing similar deaths. Another reason to continue the meetings is that they could feel the difference now in the quality of care. Therefore, the majority stated that they will continue having regular monthly meetings even when the JSANDS project comes to an end. Some participants in two hospitals mentioned that part of the accreditation of the hospital is to have a DRC, so they will continue conducting these meetings. Nonetheless, all DRC members agreed that the DRC needs to be supported by the MOH and other relevant stakeholders. A pediatrician argued: “we can reach out to the MOH as it’s the one who would adopt the JSANDS and keep the DRC meetings going.” She added: “we would tell the stakeholders within the MOH our suggestions and recommendations to decrease deaths in disadvantaged neighborhoods that particularly have poor ANC and low socioeconomic status such as Bedouins and Syrians.” Another pediatrician suggested: “we’ll make recommendations to provide those disadvantaged populations with proper equipment and adequate trained medical staff to avoid deaths.” An obstetrician suggested: “we would like to have a DRC at a national level to discuss all neonatal deaths and stillbirths across Jordan regardless of the place where the death occurred (private, public, and military), and then develop recommendations that are taken seriously by stakeholders… I mean not merely recommendations without any subsequent action.” 3.3. Perceived Preventability of Deaths When they were asked about the perceived percentage of preventable stillbirths and neonatal deaths within their hospital, the answers were inconsistent. The majority answered that around 10% of neonatal deaths could be prevented. An obstetrician justified his answer of 10% or less of preventable deaths by saying: “the problem here is in the unbooked patients who only approach us at the time of delivery…there are a lot of such cases unfortunately.” In regard to stillbirths, some members argued that very few stillbirths can be prevented, especially that the most common causes are RDS and congenital abnormalities. An obstetrician, however, reported that the percentage of stillbirths that can be prevented could reach 30% in the hospital he works at. Conversely, another senior medical resident in the same hospital argued: “the most common cause of stillbirths between 24-28 weeks is congenital abnormality and we cannot prevent it even if diagnosed early…in fact, we need antenatal care in a tertiary hospital in order to identify the exact abnormality.” Likewise, a senior pediatric nurse stated: “preventable cases are around 40-45%... I’m sorry to admit that.” The majority of DRC members across all hospitals agreed that poor ANC and lack of coordination between maternity hospitals and primary ANC clinics and the private sector are the major reasons behind preventable neonatal deaths and probably stillbirths. One obstetrician argued: “if women received good and regular antenatal care, I believe we still can prevent many more cases as we could pick up any problem and intervene immediately.” He added: “it’s like giving stillbirths a dose of fresh air.” Though financial status and monthly income were stated as factors that influenced poor ANC. Regardless, almost all members agreed—with enthusiasm—that the DRC meetings would still help in preventing future deaths if the actions arise from the committee become active and implemented correctly. Members of the DRC in the private hospital noted that the percentage of preventable deaths is even lower than those in the other participating hospitals considering that they do not see complicated cases such as triplets. One obstetrician admitted: “as we work in a private hospital, only stable cases come to have birth here…known complicated cases don’t usually come to us…if it happens and come to us, we transfer them to a comprehensive hospital directly as the resources are better there with less cost.” Another midwife explained: “most people can’t financially afford having their child hospitalized in the NICU of a private hospital for a long period of time.” 3.4. Attention to Human Rights during DRC Meetings All participants identified several factors that can highlight the deprived woman’s right and welfare, including unplanned pregnancy, in which the husband has the power to decide on behalf of the wife, low income, early marriage and adolescent pregnancy, low women educational level, and socioeconomic characteristics. Specifically, almost all DRC members became more aware that human rights issues in general and teenage pregnancy in specific are global issues. This awareness results from thoroughly discussing the possible modifiable factors that could contribute to death during their regular monthly meetings. One obstetrician raised attention: “there’s a written chapter in WHO that sheds light on high-risk pregnancy.” He added: “human rights are somehow linked with the sustainable developmental goals, therefore all pregnant women should have free comprehensive access to high quality antenatal care to minimize the complications as much as possible.” A senior resident doctor stated: “the woman deserves to receive the best medical care possible during pregnancy…this is part of her welfare that needs to be promoted and protected.” A head nurse gave an example of deprived human rights: “A 21 years-old woman just had a caesarian section now…she has been living with her parents for the last 4 months due to a conflict with her husband…he didn’t even come to the hospital to check up on her and his child…I guess this is a clear case of neglect and unattained human rights.” According to the majority of midwives, women go through the worst of their life during pregnancy due to lack of husband’s support, stress of the responsibilities of their other children, and poor socioeconomic status especially when it requires women to work in the farm for long hours. One mentioned outcome of these factors is anemia during the antenatal period, which can have negative health consequences on both the woman and her fetus. Moreover, the participants gave many examples of protecting women and newborn’s human rights from their experience with the DRC meetings. One example shared by a midwife: “we try to reach out for every woman, especially those who are marginalized and live in poor neighborhoods during pregnancy to provide the best antenatal care for her and the fetus.” She added: “through early detection and intervening of the problem or health condition of the mother or the fetus, we ensure the best chance of survival.” Furthermore, many participants denote the case of communication with and cooperation among pediatricians and obstetricians to discuss medical cases in pregnancy as a reflection of protecting human rights of mother and baby. 3.5. DRC Members’ Perception of Women Empowerment, Decision-Making Process Power Dynamics, Culture, and Genderism Women’s empowerment is defined in this section as “promoting sense of self-worth, their ability to determine their own choice of and their right to influence social change for themselves and others” [22]. Education is one of the most important means to empower women with the knowledge, skills, and self-confidence necessary to participate fully in the development process [23]. In this sense, Bedouins and Syrians are less educated thus less empowered and feel lack of confidence in taking decisions. When asked about the degree of women empowerment, especially in the area of family planning and the decision of the timing and number of children, there were many conflicting answers. Some participants agreed that it depends on the woman’s age, level of education, and the husband’s educational status. The higher the women’s level of education, the more likely they are empowered and have an active role in family planning issues. A pediatric nurse observed: “if she’s young, you’ll know straightaway that she’s not empowered at all…she’s convinced easily by her mother’s decision exactly like a generation snowball….mother to mother kind of habit.” Conversely, the majority of DRC members had a consensus that Bedouins and Syrians living in Jordan still have their women not empowered at all, and the sole decision about pregnancy, birth, and child care is mainly with the father and mother-in-law. This issue highlights sociocultural impact in the decision-making process and power dynamics within married couples. Likewise, almost all DRC members agreed that Jordanian women are somehow more educated and more empowered and take shared decisions with their husbands as compared to Syrian women who are less educated and less empowered, thus have no active role in the decision-making process regarding family planning issues. A pediatric nurse explained, “Syrian women usually get married at a very young age…I remember one woman who came to us at the age of 23 years with 8 previous pregnancies and only two alive children…when I asked her why she kept having stillbirths, she answered that it was her destiny nothing else…she didn’t blame anyone because she didn’t know better, I guess!” A physician continued: “a big difference exists between Jordanian women and Syrians in terms of health awareness and influence on the decision of number of children.” Male dominance in regards to the decision of pregnancy and birth was obvious, especially in rural areas and among less empowered women. Almost all DRC members agreed that males usually have the power in the decision-making process about pregnancy and labour. An obstetrician noted: “the real situation in our country is about how many boys and girls you have…even if you have ten girls, you still need to have a boy…regardless of women’s educational level.” He added: “the number of boys the woman has largely affects the decision about the use of family planning methods…if she has no boys or only one boy, she might be reluctant to use long lasting method and vice versa.” Therefore, according to the DRC members, traditional beliefs and culture were reported as the most common delay or preventable factor that contributes to death. A pediatrician shared a sad story about a severely dehydrated baby, who was not fed for three days at all and ended up with acute renal failure because the grandmother forced the mother to wait for the breast milk to come despite the fact that there was no breast milk at all with several unsuccessful attempts. Another example of the impact of wrong beliefs and lack of power, according to a midwife: “if the mother was concerned about reduction in fetal movement, then the Mother-in-law would tell her that this is normal and no need to seek medical care…unfortunately, this will end up in having stillbirths, which could’ve been prevented if the mother had more power in taking an independent decision.” Furthermore, a pediatric nurse also shared an example of the impact of wrong practices on the mortality rate of neonates: “we still have babies whose parents attempted to treat them with some traditional remedies such as putting salt on the baby’s whole body and garlic to treat jaundice…when they come to us, we can’t bear the strong smell of garlic coming out from the newborn.” When we asked the participants if they witnessed cases of domestic violence associated with family planning, the majority assured that there are few cases but they do not see it very often for a number of reasons. One of the identified reasons was the reluctance of the woman to tell the medical staff, mainly midwives, about their experience with domestic violence, because she is afraid of the husband’s reaction if he finds out. Another mentioned reason was the inability of the medical staff to recognize cases of domestic violence. One midwife noted: “We discovered some cases of domestic violence…we therefore asked the family protection agency to come and provide us with lectures to increase our awareness about how to recognize it and deal with it.” Another midwife added: “we now contact the family protection agency if we suspect any case of domestic violence on women.” On the other hand, participants who work in the private hospital had a different experience with the socioeconomic characteristics of pregnant women. They all agreed that most of the women who come to the private hospital are from middle to high socioeconomic status, thus are empowered enough to take an active role in the decision-making process regarding family planning. An obstetrician observed: “so we don’t usually see husbands impose their decisions on women…women are usually educated and you feel them empowered…these are usually the type of women who come to the private sector.” An obstetrician reflected on the shared decision among couples who seek private hospitals for antenatal care: “I have started to notice that husbands increasingly accompany women to most of their medical appointments…I guess this reflects interest and good communication among couples.” Finally, when we asked DRC members about their role in ensuring women and babies’ human rights, all participants mentioned that several actions and initiatives have been developed to overcome maternal complications and preventable deaths, thus ensuring human rights. An example of successfully developed actions across all hospitals that ensure women’s human rights is the conduction of health educational classes for women to increase their awareness about danger signs during pregnancy and to enable them to recognize these signs and seek immediate medical care without any delays. Such classes were reported to enable women to be more independent in taking the right decisions during pregnancy, birth, and when caring for their newborns. A midwife commented: “these awareness classes are particularly important as the most common cause of stillbirth and maternal complications are delays in either recognizing care or seeking care.” 3.6. Impact of COVID-19 Lockdown on Births In March 17, 2020, the Jordanian government took several steps to prevent the spread of COVID-19 pandemic. Of these steps are the following: social distancing, seizing all inbound and outbound movements and international travel, and improved the Defense Law, which assigned the authority to the Minister of Defense to formulate orders according to the pandemic situation in the country and worldwide [24]. Accordingly, a curfew was ordered nationally to guarantee total isolation and a lockdown on arrivals from pandemic countries to Jordan prior to the 17th of March, 2020 [25]. Several issues were identified by the majority of DRC members when they were asked about the impact of COVID-19 lockdown on pregnant women in terms of the access to and quality of ANC and birth. First, some DRC members noticed an increase in stillbirths during the lockdown. An obstetrician said: “We noticed that in the month of April, the cases of stillbirths increased as most outpatient maternal antenatal clinics were cancelled…so only women who come to the emergency department were seen by doctors.” Second, access to ANC was restricted across the country. A midwife explained: “all medical centers where some women follow up with them during antenatal period had been closed for more than two months…this restricted women’s choice of seeking medical help except for cases of emergencies.” Some other DRC members attributed the high number of stillbirths and neonatal deaths during the quarantine to lack in transportation and limited access to hospitals. A physician shared a story: “parents brought a newborn to the emergency room already dead, then we transferred him to forensic medicine, where we discovered a delay in seeking care.” A pediatric nurse said: “people complain that there was a delay in the ambulance for almost 1 to 2 hours due to the high demand on civil defense leading to having complications while waiting for the ambulance.” Conversely, the COVID-19 lockdown did not affect one of the hospitals as much as the remaining hospitals, because they did not have any case of COVID-19 in that governorate; however, all antenatal clinics were closed due to national lockdown. Therefore, pregnant women in that governorate, similar to those in other parts of Jordan, sought emergency departments for any alarming medical conditions. An obstetrician said: “though the antenatal clinics were closed, we still provided comprehensive care for any pregnant woman who approached the emergency department to try and compensate for the ‘cancelled’ antenatal appointments.” She added: “we would run all necessary tests and procedures to make sure the woman and her fetus are okay.” Third, several anemia cases among pregnant women have been reported due to the lack of medical follow-up during the COVID-19 lockdown period. A midwife said: “since the lockdown, every day we give 8-10 units of blood for labouring women due to severe anemia ….one of the reasons is fear from going to hospital during Covid-19 and cancelling all outpatient clinics and appointments in the country.” Fourth, the lockdown was reported by the majority of DRC members to improve the quality of care and services for women giving birth. An obstetrician noted: “The lockdown affected us in two ways; the first was an improvement of staff commitment to save patients despite the fact that we only received top emergency cases who didn’treceive adequate antenatal care…the second was that every woman who approached us to give birth gets to have a separate room with a midwife available all the time during the whole process of labour.” Finally, while the percentage of births decreased in the MOH hospitals, COVID-19 lockdown increases labour cases in the private hospital as women were afraid to seek public hospitals to not catch the virus, especially that one big unit teaching hospital was dedicated for COVID-19 cases. 4. Discussion The current qualitative study sheds the light on the role, benefits, and challenges of the facility-based DRC in five Jordanian hospitals where the JSANDS was piloted. Overall, there was an agreement among the majority of DRC members across all hospitals that the DRC was successful in identifying the exact cause of neonatal deaths and stillbirths as well as associated modifiable factors contributing to such deaths. Additionally, there was a consensus that the DRC regular meetings and resulting initiatives contributed to an improvement in health services provided for pregnant women and newborns. Such developed initiatives and actions were reported to ensure protecting human rights and enabling women to be more interdependent in taking decisions related to family planning. Moreover, the DRC agreed that a proportion of the neonatal deaths and stillbirths that occur in the hospitals could have been prevented if adequate ANC was provided and some traditional harmful practices were avoided. There is an increased awareness of the importance to review and investigate perinatal mortality cases for substandard care [26]. Perinatal death audit can help in identifying the main causes of death, modifiable factors, and areas of improvement, as well as a decrease in the early neonatal deaths [27]. A recent prospective study was conducted in Kampala to assess the effects of perinatal death audit on perinatal outcomes [27]. A total of 526 perinatal deaths were reviewed with 27% of fresh stillbirths, 23.8% of macerated stillbirths, and 49.2% of early neonatal deaths. Interestingly, 43.2% of cases had uncertain cause of death with 35.3% of cases received a low-quality level of care, especially among neonatal deaths [27]. The death audit team noticed a delay between the decision and the actual time to perform a cesarean section, which might have increased the risk of hypoxia. Thus, some of the causes of hypoxia and possible perinatal deaths and cerebral palsy in neonates could be due to intrapartum events such as delay in making decisions to perform cesarean section as well as the lack of neonatal resuscitation skills. Such events can have a profound impact on neonatal asphyxia and can deteriorate the health condition of the neonate. In order to resolve this issue, the death review team recommended to involve a physician during patient preparation [27]. It was also noticed that the medical staff were not very competent in the neonatal resuscitation skills thus led to perinatal deaths [27]. Lawn et al. (2011) also confirmed that rates of full-term unexpected intrapartum stillbirths are a measure of the quality of intrapartum care provided in a unit, in which the main factors are inadequate monitoring of the fetus, labour risk assessment, and management. To overcome this issue, all the staff working in the obstetrics department were retrained on the neonatal resuscitation skills. Additionally, the delivery of high-risk women was conducted under the supervision of senior medical staff. Moreover, CPAP and surfactants were introduced [27]. All activities and initiatives recommended by the death audit team were assessed periodically to ensure sustainability [27]. Moreover, a recent literature review reported that 10–60% of stillbirths and neonatal deaths were associated with a minimal level of care [28]. Their conclusion was based on identifying three types of perinatal audits; national, local, and confidential [28] that collect perinatal mortality data in order to identify the causes of death and related modifiable factors. The national audit was used to compare different maternal units and to create a national rate for perinatal mortality. The local audit is a hospital-based perinatal mortality review to identify the causes of stillbirths and neonatal deaths to prevent future deaths. Hence, it is important to establish a collaborative multidisciplinary approach for this target. Congruent with the emerged themes in our study, local audit provides recommendations and actions based on the audit, and it is crucial to establish a nonblaming culture and focus on the goal of improvement using errors as a learning lesson [28]. The WHO also stressed the importance of nonblaming culture while dealing with mortality audits [12]. Similarly, a study was conducted in Bangladesh to identify the effect of maternal and neonatal death review in terms of improving maternal and neonatal health [29]. The maternal and neonatal death review initiated several activities including awareness workshops, pregnancy registration, ANC, birth planning, and community clinic reactivation. The community involvement indicated an improvement in antenatal coverage, delivery in clinics, postpartum care, and referral of complications, leading to a substantial decline in maternal and neonatal deaths [29]. The maternal and neonatal death review is considered a constitutive method to identify the causes of death, thus improving the quality of maternal and neonatal healthcare services especially in areas with high mortality rates in rural communities, thus drives policy makers to improve community healthcare services through adopting community-based activities [29]. Conversely, another recent review was aimed to provide an overview of the facility-based maternal and perinatal mortality and morbidity audits in sub-Saharan Africa [30]. The review found a variation among countries in the process of data collection and a difficulty in the evaluation and interpretation of the data. It also found that some DRC did not conduct regular meetings either because the hospital staff did not understand the importance of such death audits or were not committed. Additionally, the reports written during the meetings were poor and incomplete, with no thorough discussion about the root causes of death, modifiable factors, and action plans and recommendations because they do not have access to accurate and complete data or to avoid the blaming culture within the hospital [30]. Hence, similar to the JSANDS that provided the DRC members with accurate and complete data in our study, adopting an electronic system may be helpful to facilitate data analysis, and to generate tables, graphs, and maps [12]. Therefore, it is of high importance to undertake continuous monitoring and evaluation of the perinatal death audits and the subsequent relevant recommendations and actions. The DRC members in our study stressed the importance of regularity and sustainability of the meetings and the support by stakeholders. A systematic review was conducted in 2020 [31] to assess the impact and cost effectiveness of different types of death audits and reviews in reducing maternal, perinatal, and child mortality. Only two RCT studies met the inclusion criteria: ([32, 33]. This review reported that the impact of adopted interventions by the DRC members was low and had little to no impact on stillbirth rates as well as the neonatal mortality rate after 24 hours of birth [31]. A possible reason was the lack of monitoring and evaluation of the DRC and resulting initiatives. The 2016 WHO report “making every baby count” recommends that mortality audits should include the right stakeholders who can initiate the program. It reports that the quality improvement committee can provide support in the formulation of facility-level steering committee that could be joined with the maternity death review committee. The role of steering committee includes auditing policy implementation, providing technical assistance, as well as continuous assessment and follow-up for recommendations progress [12]. Similar to the recommendations made by the DRC committee in our qualitative findings, the WHO also recommends that the audit findings should be shared with different parties such as the Ministry of Health and regional policy makers to facilitate the implementation of actions recommended by the DRC to prevent similar future deaths [12]. Correspondingly, it is crucial to generate a quality improvement indicator to evaluate the progress of improvement through a periodic evaluation of the entered data [12]. Our findings also stressed on the importance of conducting counselling sessions to the parents of a dead newborn or stillbirth to enable them to understand what and why the death exactly happened in an attempt to help them in the grieving process. Similarly, available literature recommends that perinatal mortality reviews need to involve a thoughtful consideration of the clinical and emotional care provided to the grieving parents [34]. A report titled as “Perinatal deaths in Australia 1993–2012” [35] included guidelines to help parents overcome their grieving and plan for future pregnancy, and enable physicians to identify the root causes of perinatal deaths and related modifiable factors as well as provide appropriate counselling for families regarding future pregnancy [35]. Although the DRC members in our qualitative study did not explicitly tackle all the barriers they face, a recent literature identified barriers to implement perinatal audits and reviews included lack of financial staff support, staff turnover, and fear of consequences and legal claims [28]. Another study was conducted in Uganda to identify the factors that influenced the use of maternal and perinatal death review (MPDR) program [36]. The modifiable death factors identified were late in referral, followed by health system issues, then lack of training on (MPDR) program for committee members [36]. Other identified factors included the following: lack of supportive supervision, no implementation of committee recommendations, workload accompanied with staff shortage, and limited financial resources to implement the recommendations when the death is linked to community delays [36]. In order to overcome these barriers, there is a need to nominate leaders and audit committee members to guarantee regular and high-quality review meetings, establish a nonblaming culture and legal protection, develop a multidisciplinary death review committee members, develop prenatal mortality tools, and use electronic perinatal mortality systems that foster the objectives of perinatal mortality and generate action plans [28]. Also, assessment of training needs and provision of continuous medical, evidence-based training for healthcare professionals is important to correctly implement the recommendations of the DRC [36]. 5. Conclusions The current qualitative study sheds the light on the role, benefits, and challenges of the facility-based DRC in five Jordanian hospitals where the JSANDS have been piloted. Overall, there was an agreement among the majority of DRC members across all hospitals that the DRC was successful in identifying the exact cause of neonatal deaths and stillbirths as well as associated modifiable factors contributing to such deaths. Additionally, there was a consensus that the DRC contributed to an improvement in health services provided for pregnant women and newborns as well as protecting human rights and enabling women to be more interdependent in taking decisions related to family planning. Moreover, the DRC agreed that a proportion of neonatal deaths and stillbirths occurs in the hospitals could have been prevented if adequate ANC was provided and some traditional harmful practices were avoided. In conclusion, the facility-based neonatal death review audit is practical and can be used to identify the exact causes of maternal and neonatal deaths and is considered a valuable tool for hospital quality indicators. Furthermore, the facility death review can change the perception and practice of health care providers to improve the quality of provided healthcare services [10]. Data Availability The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. Conflicts of Interest The authors declare that they have no competing interests. Authors’ Contributions Y.K. is the principal investigator and performed the conceptualization, methodology, project administration, and funding acquisition. N.A.A. performed the data collection, writing, original draft preparation, reviewing, and editing. K.K.S. performed the data collection, writing, reviewing, and editing. M.A. performed the data collection, writing, reviewing, and editing. A.B. performed the data collection, writing, reviewing, and editing. All authors have approved the final version of the manuscript. Acknowledgments We would like to thank all nurses and doctors in the five participating hospitals for their support, especially those who have been members of the death review committees. This research is supported and funded by the International Development Research Centre/Canada (IDRC) and the United Nations International Children’s Emergency Fund (UNICEF). The funding source had no role other than financial support.
... Currently, in Jordan's HIS, the evaluation of various types of data shows that birth registrations are almost complete (99%), while death registrations represent 75%. According to Khader, Alyahya et al. [8], some neonatal deaths and stillbirths are not fully registered due to a malfunctioning reporting system that places the responsibility of registration on families [9]. ...
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Background This study is based on extensive evidence-based assessments. The aim of this paper is to evaluate how well Jordan’s health information system (HIS) incorporates social determinants of health inequity (SDHI) and to propose suggestions for future actions. Methods An extensive evidence-based assessment was performed. A meta-synthesis of the inclusion of the SDHI in the HIS in Jordan was conducted. After searching and shortlisting, 23 papers were analyzed using Atlas.ti 9.0 employing thematic analysis technique. Results The HIS in Jordan is quite comprehensive, comprising numerous data sources, various types of information, and data from multiple producers and managers. Nevertheless, the HIS confronts several obstacles and fails to ensure the timely and secure publication of available data. The assessment of the inclusion of the SDHI in the HIS showed that the HIS allows for the measurement of progress in relation to social policies and actions but has a very limited database for supporting the inclusion of health inequity measures. One reason for the difficulty in identifying fairness is that certain crucial information necessary for this task cannot be obtained through the available institutional HIS or population survey tools. Additionally, relevant modules for fairness may be missing from population surveys, possibly due to a failure to fully utilize the capabilities of the institutional HIS. Conclusion There are opportunities to make use of Jordan’s dedication to fairness and its already established strong HIS. Some social determinants of health exist in the HIS, but much more data, information, and effort are needed to integrate the SDHI into the Jordanian HIS. A proposal from a regional initiative has put forward a comprehensive set of indicators for integrating SDHI into HIS, which could aid in achieving health equity in Jordan.
... In terms of the assessment of different types of data in the HIS of Jordan, the registration of vital events is currently assessed to be nearly complete (99%) for birth registration, while death registration stands at 75%. Khader, Alyahya et al. [8] reported that the registration for some neonatal deaths and stillbirths is not complete. This was attributed to the dysfunctional reporting system which leaves the responsibility of births and deaths to the families. ...
... Therefore, repeated pregnancy and childbirth cause damage to the blood vessels in the uterine wall. And more and more will affect the circulation of food to the fetus and can cause disturbances and obstacles to the growth of the fetus in the womb.[10][11][12][13][14][15] Pregnant women at a young age in terms of the biological development of reproductive organs are not fully optimized. ...
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Background: Attention to efforts to reduce neonatal mortality is important because neonatal mortality contributes to 74% of under-five deaths in Aceh. Of all neonatal mortality, 81% occurred in the 0-6 day age group (early neonates). This study aims to determine the analysis of the determinants of early neonatal mortality at the Datu Beru Takengon General Hospital, Central Aceh Regency. Methods: The research design is an observational case-control approach. 84 case subjects and 84 control subjects were included in this study. Univariate, bivariate, and multivariate data analysis was performed to determine the determinants of early neonatal mortality, p<0.05. Results: Asphyxia increases the risk of premature neonatal mortality by 6.8 times. Low birth weight infants increase the risk of early neonatal by 8.4 times. Prematurity increases the risk of early neonatal mortality by 7.1 times. A parity of more than 3 times increases the risk of early neonatal mortality by 8.9 times, and maternal gestational age of fewer than 20 years increases the occurrence of early neonatal mortality by 14.2 times. Conclusion: Asphyxia, low birth weight, prematurity, parity with risk, and a young mother's gestational age are risk factors that contribute to early neonatal mortality.
... The scarcity of data in Jordan on neonatal mortality, especially early mortality is generally linked to the fact of that some births are not registered. 15,16 In addition, the existing sources of data on neonatal mortality are likely to be biased. In the absence of reliable and standardised vital registration and administrative data in many countries, modelling of NMR remains necessary for public health policy and priority setting and monitoring. ...
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Background It has been estimated that 27.8 million neonates will die between 2018 and 2030 if no improvements in neonatal mortality take place. The aim was to determine the rate, determinants, and causes of neonatal mortality in Jordan. Methods In August 2019, an electronic stillbirths and neonatal deaths surveillance system (JSANDS) was established in in three large cities through five hospitals. Data on all births, neonatal mortality and their causes, and other characteristics in the period between August 2019 – January 2020 were exported from the JSANDS and analysed. Results A total of 10328 births were registered in the study period, with a rate of 14.1 deaths per 1000 LBs; 76% were early neonatal deaths and 24% were late deaths. 25%of all deaths occurred in the first day of life. Multivariable analysis showed that the odds of neonatal deaths was 20.8 (95% CI 2.8,153.1) in Ministry of Health hospitals compared to private hospitals, OR 31.8 (95% CI 18.8,53.8) for very low birth (< 1500gram) neonates, OR 13 (95% CI 7.8,21.6) in preterm births compared to full-term births, and OR 2.7 (95% Cl 1.2,6.0) among housewives compared to employed women. Main causes of neonatal deaths that occurred pre-discharge were respiratory and cardiovascular disorders (43%) and low birthweight and preterm (33%). The main maternal conditions that attributed to these deaths were complications of the placenta and cord, complications of pregnancy, and medical and surgical conditions. The main cause of neonatal deaths that occurred post-discharge were low birthweight and preterm (42%). Conclusions The rate of neonatal mortality have not decreased since 2012 and the majority of neonatal deaths occurred could have been prevented. Regular antenatal visits, in which any possible diseases or complications of pregnant women or foetal anomalies, need to be fully documented and monitored with appropriate and timely medical intervention to minimize such deaths.
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Background Stillbirth is one of general medical issues that could contribute significantly to creating nations like Ethiopia. This study aimed to determine the prevalence and related factors of stillbirth among deliveries at Amhara region, Ethiopia. Methods The study used the Ethiopian Mini Demographic and Health Survey (EMDHS) data collected from 2555 eligible Amhara region women in 2014. Bi-variable and multi-variable binary logistic regression analysis was used. ResultsThe prevalence of stillbirth outcomes became 85 per 1000 (total live birth). Besides, majority of women did not attend any formal education and had no antenatal care follow up. Women whose age at first birth below 18 years were 1859(72.8%) and the mean preceding birth interval were 33.6 months. Even women who attended primary and above education were about 50% and they were less likely to have had stillbirth outcomes than those who had no education (AOR: 0.505, 95% CI 0.311–0.820) and women having higher household wealth index were less likely to have had stillbirth outcomes as it is compared to the reference category. Moreover, women having preceding birth interval above 36 months were about 89% of less likely to end up stillbirth outcomes as compared to women having preceding birth interval below 24 months (AOR: 0.109, 95% CI 0.071–8.0.168). Conclusions It could be inferred that a stillbirth result is one of the general medical issues in Amhara Region. Among different factors considered in this study, age, age at first birth, wealth index, birth order number and preceding birth interval in months were found to be significantly associated factors for stillbirth. Therefore, more awareness of early birth, widening birth interval, enhancing maternal care (for aged women) and early birth order number could be recommended.
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Introduction Infant mortality rate is a sensitive metric for population health and well-being. Challenges in achieving accurate reporting of these data can lead to inaccurate targeting of public health interventions. We analyzed a cohort from a pediatric tertiary care referral medical center to evaluate concordance between autopsy cause of death (COD) and death certificate documentation for infants <1 year of age. We predicted that infant COD as documented through vital records would not correspond to that as determined by autopsy. Methods We conducted a retrospective review comparing causes of infant death reported through Ohio Department of Health documents to those on Cincinnati Children’s Hospital Medical Center autopsy reports over an 8-year period from January 1, 2006 through December 31, 2013. Results We analyzed 276 total cases of which 167 (61.5 %) represented infants born preterm. Autopsy reports identified 55 % of cases had a congenital anomaly. Additionally, 34 % of all cases had primary or contributing COD related to infection and 14.5 % of all cases indicated chorioamnionitis. We identified 156 (56.5 %) death certificates discordant with autopsy COD of which 52 (33.3 %) involved infection and 24 (15.4 %) involved congenital anomalies. Discussion There are opportunities to improve COD reporting through training for providers, and improvement of established state certification systems. Future strategies to reduce infant mortality will be better informed through enhancements in vital records COD reporting.
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More than 40% of all deaths in children under 5 years of age occur during the neonatal period: the first month of life. Immunization of pregnant women has proven beneficial to both mother and infant by decreasing morbidity and mortality. With an increasing number of immunization trials being conducted in pregnant women, as well as roll-out of recommended vaccines to pregnant women, there is a need to clarify details of a neonatal death. This manuscript defines levels of certainty of a neonatal death, related to the viability of the neonate, who confirmed the death, and the timing of the death during the neonatal period and in relation to immunization of the mother.
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Objectives To determine the proportion of maternal and perinatal mortality and morbidity cases, identified by the Perinatal and Maternal Mortality Review Committee (PMMRC), that are also reported within the annual serious adverse events (SAEs) reports published by the Health Quality and Safety Commission (HQSC). Setting Nationally collated data from the PMMRC and HQSC, New Zealand. Participants Analysis of maternal and perinatal mortality and morbidity data 2009–2012. Interventions Every SAE report published by the HQSC from 2009 to 2012 was scrutinised for maternal and perinatal cases using the case history provided by district health boards (DHB). Further detail of each case was requested from each DHB to establish whether they had been identified as maternal or perinatal mortalities or morbidities by the PMMRC. Primary outcome measure The proportion of maternal and perinatal mortality and morbidity cases identified by HQSC SAE reports, compared with PMMRC reporting. Results 58 maternal and perinatal SAEs were identified from the SAE reports 2009–2012. Of these, 50 fit under the PMMRC reporting definitions, all of which were also reported by the PMMRC. In the same time frame, the PMMRC captured 536 potentially avoidable maternal and perinatal mortalities and morbidities that fitted the HQSC SAE definition. Fewer than 9% of maternal and perinatal SAEs are captured by the HQSC SAE reporting process. Conclusions The rate of maternal and perinatal adverse event reporting to the HQSC is low and not improving annually, compared with PMMRC reporting of eligible events. This is of concern as these events may not be adequately reviewed locally, and because the SAE report is considered a measure of quality by the DHBs and the HQSC. Currently, the reporting of SAEs to the HQSC cannot be considered a reliable way to monitor or improve the quality of maternity services provided in New Zealand.
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Background: Variation in birth registration criteria may compromise international comparisons of fetal and infant mortality. We examined the effect of birth registration practices on fetal and infant mortality rates to determine whether observed differences in perinatal and infant mortality rates were artifacts of birth registration or reflected true differences in health status. Methods: A retrospective population-based cohort study was done using data from Canada, United States, Denmark, Finland, Iceland, Norway, and Sweden from 1995-2005. Main outcome measures included live births by gestational age and birth weight; gestational age-and birth weight-specific stillbirth rates; neonatal, post-neonatal, and cause-specific infant mortality. Results: Proportion of live births <22 weeks varied substantially: Sweden (not reported), Iceland (0.00 %), Finland (0.001 %), Denmark (0.01 %), Norway (0.02 %), Canada (0.07 %) and United States (0.08 %). At 22-23 weeks, neonatal mortality rates were highest in Canada (892.2 per 1000 live births), Denmark (879.3) and Iceland (1000.0), moderately high in the United States (724.1), Finland (794.3) and Norway (739.0) and low in Sweden (561.2). Stillbirth:live birth ratios at 22-23 weeks were significantly lower in the United States (79.2 stillbirths per 100 live births) and Finland (90.8) than in Canada (112.1), Iceland (176.2) and Norway (173.9). Crude neonatal mortality rates were 83 % higher in Canada and 96 % higher in the United States than Finland. Neonatal mortality rates among live births ≥28 weeks were lower in Canada and United States compared with Finland. Post-neonatal mortality rates were higher in Canada and United States than in Nordic countries. Conclusions: Live birth frequencies and stillbirth and neonatal mortality patterns at the borderline of viability are likely due to differences in birth registration practices, although true differences in maternal, fetal and infant health cannot be ruled out. This study emphasises the need for further standardisations, in order to enhance the relevance of international comparisons of infant mortality.
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The days immediately after birth are the most risky for human survival, yet neonatal mortality risks are generally not reported by day. Early neonatal deaths are sometimes under-reported or might be misclassified by day of death or as stillbirths. We modelled daily neonatal mortality risk and estimated the proportion of deaths on the day of birth and in week 1 for 186 countries in 2013. We reviewed data from vital registration (VR) and demographic and health surveys for information on the timing of neonatal deaths. For countries with high-quality VR we used the data as reported. For countries without high-quality VR data, we applied an exponential model to data from 206 surveys in 79 countries (n=50 396 deaths) to estimate the proportions of neonatal deaths per day and used bootstrap sampling to develop uncertainty estimates. 57 countries (n=122 757 deaths) had high-quality VR, and modelled data were used for 129 countries. The proportion of deaths on the day of birth (day 0) and within week 1 varied little by neonatal mortality rate, income, or region. 1·00 million (36.3%) of all neonatal deaths occurred on day 0 (uncertainty range 0·94 million to 1·05 million), and 2·02 million (73.2%) in the first week (uncertainty range 1·99 million to 2·05 million). Sub-Saharan Africa had the highest risk of neonatal death and, therefore, had the highest risk of death on day 0 (11·2 per 1000 livebirths); the highest number of deaths on day 0 was seen in southern Asia (n=392 300). The risk of early neonatal death is very high across a range of countries and contexts. Cost-effective and feasible interventions to improve neonatal and maternity care could save many lives. Save the Children's Saving Newborn Lives programme. Copyright © 2014 Oza et al. Open Access article distributed under the terms of CC BY. Published by .. All rights reserved.
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Accurately defining and reporting perinatal deaths (ie, fetal and infant deaths) is a critical first step in understanding the magnitude and causes of these important events. In addition to obstetric health care providers, neonatologists and pediatricians should have easy access to current and updated resources that clearly provide US definitions and reporting requirements for live births, fetal deaths, and infant deaths. Correct identification of these vital events will improve local, state, and national data so that these deaths can be better addressed and prevented.
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In this Series paper, we review trends since the 2005 Lancet Series on Neonatal Survival to inform acceleration of progress for newborn health post-2015. On the basis of multicountry analyses and multi-stakeholder consultations, we propose national targets for 2035 of no more than 10 stillbirths per 1000 total births, and no more than 10 neonatal deaths per 1000 livebirths, compatible with the under-5 mortality targets of no more than 20 per 1000 livebirths. We also give targets for 2030. Reduction of neonatal mortality has been slower than that for maternal and child (1–59 months) mortality, slowest in the highest burden countries, especially in Africa, and reduction is even slower for stillbirth rates. Birth is the time of highest risk, when more than 40% of maternal deaths (total about 290 000) and stillbirths or neonatal deaths (5·5 million) occur every year. These deaths happen rapidly, needing a rapid response by health-care workers. The 2·9 million annual neonatal deaths worldwide are attributable to three main causes: infections (0·6 million), intrapartum conditions (0·7 million), and preterm birth complications (1·0 million). Boys have a higher biological risk of neonatal death, but girls often have a higher social risk. Small size at birth—due to preterm birth or small-for-gestational-age (SGA), or both—is the biggest risk factor for more than 80% of neonatal deaths and increases risk of post-neonatal mortality, growth failure, and adult-onset non-communicable diseases. South Asia has the highest SGA rates and sub-Saharan Africa has the highest preterm birth rates. Babies who are term SGA low birthweight (10·4 million in these regions) are at risk of stunting and adult-onset metabolic conditions. 15 million preterm births, especially of those younger than 32 weeks' gestation, are at the highest risk of neonatal death, with ongoing post-neonatal mortality risk, and important risk of long-term neurodevelopmental impairment, stunting, and non-communicable conditions. 4 million neonates annually have other life-threatening or disabling conditions including intrapartum-related brain injury, severe bacterial infections, or pathological jaundice. Half of the world's newborn babies do not get a birth certificate, and most neonatal deaths and almost all stillbirths have no death certificate. To count deaths is crucial to change them. Failure to improve birth outcomes by 2035 will result in an estimated 116 million deaths, 99 million survivors with disability or lost development potential, and millions of adults at increased risk of non-communicable diseases after low birthweight. In the post-2015 era, improvements in child survival, development, and human capital depend on ensuring a healthy start for every newborn baby—the citizens and workforce of the future.
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We aimed to compare demographic, medical, and cause-of-death information reported for third-trimester fetal and neonatal death vital records collected in New York City (NYC) before and after implementation of the revised fetal death certificate to identify: (1) the limitations of combining fetal and neonatal death records for the purpose of perinatal death prevention; and (2) improvement opportunities for fetal death vital records registration. Using Chi squared tests, we compared data completeness and cause-of-death information between third-trimester NYC fetal (n = 1,930) and neonatal deaths (n = 735) from 2007 to 2011. We also compared fetal death data before and after the 2011 implementation of the 2003 United States (US) Standard Report of Fetal Death and an electronic reporting system. Compared with neonatal deaths, fetal death data were generally less complete (P < 0.0001). Fetal death data much more frequently reported an ill-defined cause of death (67 vs. 5 %). Most ill-defined reported causes of fetal death (73 %) were attributed to stillbirth synonyms (e.g., "fetal demise"). Ill-defined causes of fetal death decreased from 68 to 61 % (P < 0.01) after 2011. Both data completeness and ill-defined causes of death varied widely by hospital. In NYC, fetal deaths lack demographic, medical, and cause-of-death information compared with neonatal deaths, with implications for research that uses combined perinatal mortality data sets. Electronic implementation of the US Standard Report of Fetal Death minimally improved cause-of-death information. Substantial variability by hospital suggests opportunities for improvement exist.