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Ten years of clinical experience with cyanoacrylate glue for venous access in a 1300-bed university hospital

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In the past decade, cyanoacrylate glue has been progressively introduced into the clinical practice of venous access devices used for different purposes. Glue has been used to increase device stabilisation (to reduce the risk of catheter dislodgement), to seal the exit site (to both reduce local bleeding and decrease the risk of bacterial contamination) and to close skin incisions required for the insertion of tunnelled catheters or totally implanted venous ports. For many of these purposes, the efficacy and cost-effectiveness of cyanoacrylate glue has been demonstrated, while some indications are still controversial. This article reports on 10 years of clinical experience with cyanoacrylate glue in a large university hospital, and provides a narrative review of the scientific evidence on the benefits of glue in venous access that has been accumulating over the past decade.
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© 2022 MA Healthcare Ltd
S4 British J ournal of Nursi ng, 2022, Vol 31, No 8 (IV and Vas cular Ac cess Sup plement)
VENOUS ACCESS SECUREMENT
Ten years of clinical experience with
cyanoacrylate glue for venous access
in a 1300-bed university hospital
Mauro Pittiruti, Maria Giuseppina Annetta, Bruno Marche, Vito DAndrea and
Giancarlo Scoppettuolo
In the past two decades, dierent types of cyanoacrylate
glue (CG)—octyl-CG, butyl-CG and octyl-butyl-CG—
have been used in surgical practice to close skin incisions,
to repair lacerations of internal organs, to stop oesophageal
bleeding and to secure prostheses for inguinal hernias
(Singer and Thode, 2004).
Since 2000, octyl-CG has been widely used in the authors’
university hospital for closing skin incisions after minor surgical
procedures as an alternative to sutures and staples, with several
advantages in terms of control of local bleeding, to provide a
barrier to bacteria and for cosmetic results (Gurnaney et al,
2011; Auyong et al, 2017; Chalacheewa et al,2021).
In 2007, Wilkinson et al reported for the rst time the use
of CG to stabilise centrally inserted central venous catheters
(CICCs) as an alternative to sutures. The same authors reported
the eectiveness of CG in reducing dislodgment of epidural
catheters (Wilkinson et al 2007; Wilkinson and Fitz-Henry,
2008).
The benefits of CG include not only the sutureless
stabilisation of the catheter but also a potential antibacterial
activity, as proven in vitro—in particular for octyl-CG—
especially against Gram-positive bacteria (Bhende et al, 2002;
Narang et al, 2003; Wilkinson et al, 2008).
In the authors’ 1300-bed university hospital, most central
lines are inserted by a multiprofessional, multidisciplinary
vascular access team. The authors started to use CG 10 years
ago, mainly as a haemostatic strategy in patients at a high risk
of local bleeding.
In 2012, they reported for the rst time the eectiveness of
CG in reducing bleeding from exit sites within the rst 24
hours of peripherally inserted central catheter (PICC) placement.
They studied 45 adult patients requiring the insertion of
polyurethane PICCs without reverse tapering; no signicant
local bleeding at 1 hour and after 24 hours was recorded. Both
octyl-butyl-CG and butyl-CG were used, and no local reactions
were reported (Pittiruti et al, 2012).
The ecacy of CG in reducing the risk of bleeding was
further studied in a group of adult patients requiring polyurethane
CICCs and PICCs without reverse tapering, in a non-intensive
care ward in the authors’ hospital. The exit site of 65 central
Mauro Pittiruti, Vascular Access Specialist and Vascular
Access Team Member, Department of Surgery, Fondazione
Policlinico Universitario A Gemelli, Catholic University, Rome Italy,
mauropittiruti@me.com
Maria Giuseppina Annetta, Vascular Access Specialist and
Vascular Access Team Member, Department of Anesthesia and
Intensive Care, Fondazione Policlinico Universitario A Gemelli,
Catholic University, Rome Italy
Bruno Marche, Vascular Access Specialist and Vascular Access
Team Member, Department of Hematology, Fondazione Policlinico
Universitario A Gemelli, Catholic University, Rome Italy
Vito D’Andrea, Neonatologist, Neonatal Intensive Care Unit,
Fondazione Policlinico Universitario A Gemelli, Catholic University,
Rome Italy
Giancarlo Scoppettuolo, Infectious Disease Specialist, and
Consultant for the Vascular Access Team, Department of Infectious
Disease, Fondazione Policlinico Universitario A Gemelli, Catholic
University, Rome Italy
Accepted for publication: January 2022
ABSTRACT
In the past decade, cyanoacrylate glue has been progressively introduced
into the clinical practice of venous access devices used for different
purposes. Glue has been used to increase device stabilisation (to reduce
the risk of catheter dislodgement), to seal the exit site (to both reduce
local bleeding and decrease the risk of bacterial contamination) and to
close skin incisions required for the insertion of tunnelled catheters or
totally implanted venous ports. For many of these purposes, the efcacy
and cost-effectiveness of cyanoacrylate glue has been demonstrated,
while some indications are still controversial. This article reports on
10years of clinical experience with cyanoacrylate glue in a large university
hospital, and provides a narrative review of the scientic evidence on the
benets of glue in venous access that has been accumulating over the
pastdecade.
Key words: Cyanoacrylate glue Tissue adhesive Peripheral venous
access Peripherally inserted central catheter Central venous access
Securement Skin closure
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catheters (45 PICCs, 11 dialysis catheters and nine CICCs) was
assessed at 1 hour and 24 hours after insertion. No local bleeding
occurred. No local adverse reaction or damage to the
polyurethane was reported (Scoppettuolo et al, 2013).
In the same year, the authors also carried out a randomised
clinical study to evaluate the ecacy of two methods of sealing
exit sites—metallic powder (Statseal, Biolife) versus octyl-butyl-
CG—in patients in the intensive care unit. Thirty polyurethane
PICCs without reverse tapering with double (5 Fr) and triple
(6 Fr) lumen were randomised to be sealed with either metallic
powder or with CG.
Bleeding was assessed at 1 hour and 24hours after placement
and weekly thereafter. All catheters were removed after 3 weeks,
and cultures of both the subcutaneous tract of the catheter and
the catheter tip were performed. There was no early bleeding
at 1 hour, but there were two later bleedings (one in each
group) at 24 hours. All cultures of the subcutaneous tract were
negative. One PICC in the metallic powder group had a tip
culture test positive for Candida albicans, although the blood
culture was negative.
The authors concluded that both methods were eective
in reducing bleeding at the exit site, and that the compliance
of nurses and patients was higher for the glue. Preliminary data
about the cultures suggested that sealing the exit site (with
either method) was effective in reducing extraluminal
contamination (Annetta et al, 2013).
Two experimental in vitro studies further conrmed the
antimicrobial activity of CG. In 2012, the in vitro ecacy of
octyl-CG and butyl-CG for the securement of intravenous
catheters was studied (Simonova et al, 2012). While butyl-CG
was associated with stronger securement than octyl-CG, both
compounds showed signicant antibacterial activity against
Staphylococcus aureus and S.epidermidis. Another in-vitro study
(Rushbrook et al, 2014) demonstrated the bactericidal property
of octyl-CG against Gram-positive bacteria (but not against
Escherichia coli, Pseudomonas aeruginosa or C.albicans).
In 2014-2015, three more clinical studies analysed the ecacy
of CG in secur ing vascular access devices. Two randomised
studies addressed the use of CG for peripheral arterial catheters.
While the rst study was inconclusive (Edwards et al, 2014),
the second demonstrated that CG was associated with the
lowest risk of catheter failure and was more cost-eective than
other strategies, including bordered transparent dressings and/
or sutureless securement devices (Reynolds et al, 2015). Similar
results were reported in a randomised clinical study on short
peripheral cannulas (SPCs) (Marsh et al, 2015).
Meanwhile, further clinical studies carried out at the authors’
hospital demonstrated the high ecacy of both butyl-CG and
butyl-octyl-CG in reducing bleeding at the exit site. In a
prospective study on 45 PICCs without reverse tapering, the
risk of bleeding was reduced from 40% to zero in the rst hour
and from 15% to zero at 24 hours after insertion (Scoppettuolo
et al, 2015).
A wider retrospective study on 1429 central venous catheters
was also conducted in the university hospital (Pittiruti et al,
2016). This study included: 348 non-tunnelled PICCs inserted
in patients at a high risk of bleeding (those with chronic renal
failure, hepatic dysfunction or coagulation disorders or receiving
antithrombotic treatment); 165 non-tunnelled CICCs and
femorally inserted central catheters (FICCs) in patients at high
risk of local bleeding (including dialysis catheters); 114 tunnelled
central catheters (PICCs, CICCs and FICCs, cued or non-
cued); and 802 ports (both chest ports and PICC ports). At
the end of the study, the authors concluded that CG was 100%
eective in preventing post-insertion bleeding from the exit site
in every type of central venous access device, even in patients
at high risk of bleeding, in both children and adults. The use of
glue for sealing the exit site of PICCs was found to be not only
eective but also highly cost-eective, given that early bleeding
woul d often mean an unscheduled dressing change was neede d.
Considering the results of this retrospective study and the
evidence accumulated in previous years (2012-2015), the
university hospital’s policies were modied. In 2016, the ocial
hospital policies on the insertion and management of venous
access devices recommended the use of cyanoacrylate glue for
three main indications:
Sealing the exit site of all PICCs soon after insertion (Figure1)
Sealing the exit site of other types of central venous access
devices (CICCs, and FICCs) in patients at a high risk of
local bleeding
Closing the skin incisions required for the implantation of
tunnelled central catheters (Figure 2) and ports (Figure 3).
Expanding the indications: 2016-2019
After the 2016 hospital policies were introduced, the use of
CG in venous access was implemented signicantly in the
hospital (2000 vials/year for an estimated 7000 central venous
catheters inserted per year by the vascular access team).
Concerned that CG might potentially damage catheters,
the authors carried out an in-vitro study analysing the chemical
and physical interactions between octyl-butyl-CG and 12 brands
of PICCs (11 made of polyurethane and one of silicone). The
samples were analysed after 4, 8 and 12 weeks of contact with
the glue. The conclusion was that the long-term use of octyl-
butyl-CG was not associated with any damage to polyurethane
catheters, although it may alter the physical properties of silicone
(Di Puccio et al, 2018). Considering that use of silicone catheters
AB
Figure 1. Tunnelled peripherally inserted central catheters: glue is used both to
seal the exit site (a) and to close the puncture site (b)
a b
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because of a synergistic eect on the reduction of several
complications (infection, dislodgment and bleeding) (Judge et
al, 2018; Ortiz-Miluy et al, 2019).
The cost-eectiveness of CG (for both peripheral and central
venous catheters) was related mainly to its haemostatic eect,
with the elimination of a need for dressing changes 24 hours
after insertion, leading to signicant cost savings (Nicholson
and Hill, 2019).
The authors also agreed that CG should be used in all central
venous access devices requiring tunnelling (for closing the skin
incision at the puncture site) or requiring subcutaneous
placement of a reservoir (for closing the skin incision at the
pocket) (Martin et al, 2017).
The present: 2020-2021
Over the past 2 years, many more clinical studies have focused
on CG for both central and peripheral catheters and in dierent
patient populations.
Regarding CICCs, a randomised clinical trial involving 121
adult patients (Mitchell et al, 2020) conrmed that CG was
not optimal for the purpose of securement only. However, as
had been abandoned at the hospital since 2010, the ndings
of this study werereassuring.
In the following years, further clinical studies focused on
CG as securement device.
A randomised trial involving 380 SPCs inserted in 360 adult
patients demonstrated that, when using CG, catheter failure
was 10% lower and dislodgement was 7% lower than when
standard dressings were used (Bugden et al, 2016). On the other
hand, a randomised trial involving 221 cardiac surgical patients
showed that CG with a standard transparent dressing was not
eective for the securement of CICCs; however, when CG
was added to standard care (sutures and polyurethane dressing),
dislodgments were reduced from 4% to 0% in comparison with
standard care only (Rickard et al, 2016). A single-centre study
involving 124 PICCs in patients with cancer showed that
securement by CG and standard transparent dressing was
associated with the lowest risk of catheter failure (Chan et al,
2017). In a larger randomised trial involving 1807 patients that
analysed dierent strategies of SPC securement in adults, the
results were inconclusive, but some adverse events (skin damage)
were reported in the CG group (Rickard et al, 2018).
At this time, other studies focused on paediatric patients.
In a randomised trial involving 101 PICCs in children (Kleidon
et al, 2017), CG was eective both in reducing catheter
dislodgements and in decreasing local bleeding. A randomised
trial comparing securement devices in 48 tunnelled central
venous catheters in children (Ullman et al, 2017) was associated
with inconclusive results. In another randomised trial involving
108 children with non-tunnelled central venous devices,
securement by CG only was less eective than securement by
sutures or sutureless devices (Ullman et al, 2019).
However, in a clinical study car ried out in the university
hospital’s paediatric intensive care unit, an insertion bundle for
avoiding extraluminal bacterial contamination of CICCs
(cyanoacrylate glue with a sutureless device, tunnelling and a
transparent dressing) was associated with a 90% reduction in
catheter-related bloodstream infections from 15 to 1.5 episodes
per 1000 catheter days (Biasucci et al, 2018).
This potential antimicrobial activity of CG was conrmed
in several experimental studies (Bull et al, 2018; Prince et al,
2018; Waller et al, 2019). In one of these studies (Bull et al,
2018), the eectiveness of CG to inhibit bacter ial growth at
the extracorporeal membrane oxygenation (ECMO) cannulation
site and in secur ing ECMO cannulas was evaluated in vitro.
Bull et al (2018) concluded that combining CG at the cannula
insertion site with a sutureless securement device could be an
eective strategy to prevent or minimise both infection and
linedislodgement.
The role of glue in venous access was discussed in a meeting
organised by the authors’ team in 2019, based on the literature
and on an audit of their exper ience. They concluded that
securement of central venous access devices by CG only was
not eective and that, for CICCs, FICCs and PICCs, CG should
be used not for securement but for the purpose of reducing
local bleeding and bacterial contamination. For long-term
central venous access, the combined use of CG, tunnelling and
subcutaneous anchorage was judged to be especially benecial
Figure 3. Glue used for closing the skin incision made for
brachial port implantation
AB
Figure 2. Glue used for centrally inserted central catheters (a) and for tunnelled
femorally inserted central catheters (b), on both the exit site and the puncture site
a b
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another trial with 150 adult patients showed, when added to
standard securement, CG may reduce the incidence of early
dressing change (Prachanpanich et al, 2021).
Findings seem to be dierent for SPC. A large, randomised
trial involving 350 adult patients (Bahl et al, 2021) suggested
that a transparent dressing combined with CG may improve
survival of an SPC if the line is expected to be used for more
than 48hours. In a randomised study with 330 children, both
integrated securement dressings and CG were more eective
than bordered transparent dressings in reducing catheter failure
(Kleidon et al,2020). Nonetheless, the greatest change in
practice in the past 2years has been the introduction of CG
into neonatal intensive care units.
Butyl-CG and octyl-butyl-CG have proven to be safe and
eective for the securement of epicutaneo-caval catheters (ECC)
(Barone and Pittiruti, 2020; D’Andrea et al, 2021; van Rens,
2021). The local application of small quantities of CG seems
to be harmless even in premature newborns, while it is highly
eective in reducing dislodgement and preventing bleeding
and oozing at the puncture site.
Data also suggest that CG may be associated with a reduction
in the risk of central-line bloodstream infection in neonates,
probably by reducing bacterial contamination via the
extraluminal route. One of the authors’ protocols on the use
of CG for umbilical venous catheters (UVCs) in pre-term
neonates is being investigated. Preliminary results suggest that
the addition of CG to a standard UVC securement may reduce
catheter dislodgment and tip migration (Pittiruti et al, 2020).
Finally, the antibacterial activity of CG has been further
conrmed by two recent studies. In one clinical study on 102
PICCs, local application of CG at the exit site soon after
insertion was compared with the local application of a
chlorhexidine-releasing sponge dressing. Both strategies were
eective in controlling bacterial colonisation; however, CG was
more eective in reducing local bleeding and more cost-eective
than the sponge dressing in the rst week after PICC insertion
(Gilardi et al, 2021).
In an experimental study, the antimicrobial properties of
two formulations of octyl-butyl-CG were compared in terms
of bacterial inhibition at peripheral ECMO cannula insertion
sites: both were capable of inhibiting bacterial growth and
migration of S. epidermidis (Pearse et al, 2021).
As a result, in the past 2 years, several evidence-based
documents have included specic recommendations about the
use of CG in venous access.
In 2020, the Italian Association of Pediatric Hematology
and Oncology guidelines recommended the use of CG at the
exit site of all central venous catheters in children. The rationale
for this recommendation is that glue is safe, allows rapid and
complete haemostasis at the exit site, reduces the incidence of
dressing change and decreases micromovements of the catheter,
so it may be useful in preventing thrombosis and infection. The
use of glue alone may not reduce the risk of catheter dislodgment
but, when used in with other securement devices, it may improve
the dwell time of central devices (Cellini et al, 2020).
The 2021 Standards of the Infusion Nursing Society include
CG as an option for securing SPCs, combined with a standard
transparent dressing or an integrated securement dressing, in
both adult and paediatric patients (Gorski et al, 2021).
Finally, the Consensus on European Recommendations on
the Proper Indication and Use of Peripheral venous access
devices stipulate securing ‘integrated’ SPCs and long peripheral
catheters (LPCs) using either a bordered transparent dressing
with an integrated securement system or a standard bordered
transparent dressing after application of cyanoacrylate glue at
the exit site. According to this consensus, local application of
CG should also be considered in any patient at high risk of
bleeding (Pittiruti et al, 2021).
Conclusion
In summary, there is now enough evidence on CG in
severalareas.
CG is an eective securement only for SPC (Kleidon et al,
2020; Bahl et al, 2021) and ECC (D’Andrea et al, 2021; Van
Rens et al, 2021); it should be used not alone but in combination
with a transparent semipermeable membrane.
CG is a safe, eective and cost-eective strategy for avoiding
the risk of early bleeding and oozing after the insertion of any
peripheral or central venous catheter (Pittiruti et al, 2012; 2016;
Scoppettuolo et al, 2013; Guido et al, 2020).
In all central venous access devices, CG may reduce the risk
of infection by decreasing bacter ial contamination via the
extraluminal route (Annetta et al, 2013; Biasucci et al, 2018,
Bull et al, 2018; Gilardi et al, 2021), but its antibacter ial use
should be limited to the rst week (Corley et al, 2017; Gilardi,
et al 2021), since there is not enough evidence to show that
weekly replacement of glue is harmless.
CG is an eective and cost-eective replacement for sutures
when a skin incision needs to be closed (ie in tunnelled venous
access devices and in ports)(Pittiruti et al, 2016; Martin et al,2017).
Based on such evidence, in 2021 the Italian Group of Long-
Term Venous Access Devices (GAVeCeLT) released specic
recommendations for the use of CG (Ta b l e 1 )(Pittiruti and
Scoppettuolo, 2021).
Table 1. Italian Group of Long-Term Venous Access Devices
recommendations on the use of glue in venous access
1. Use cyanoacrylate glue
As an additional securement of peripheral venous access devices at a high risk
ofdislodgement
Particularly in peripheral catheter s with expected duration >48 hours
For sealing the exit site of any central venous access device soon after insertion
to avoid post-procedural local bleeding , prevent unscheduled dressing changes and
protect the exit site from bacterial contamination during the rst week
Use chlorhexidine-releasing sponge dressing (in non-tunnelled central catheters)
after the rst week
For closing any skin incision related to venous access procedures (skin incisions for
tunnelling or for subcutaneous port placement)
Never use stitches
2. Remember to p refer butyl- cyanoacryla te or octyl-butyl- cyanoacrylate
3. Use a minimal amount o f cyanoacr ylate glue and only at the time of insertion
Source: Pittiruti and S coppet tuolo (2021)
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VENOUS ACCESS SECUREMENT
In spring 2021, a revised version of the university hospital
policies was issued. This document recommends the use of
butyl-CG or octyl-butyl-CG for venous access, while octyl-CG
is considered appropriate for skin closure after minor surgical
procedures only. Its recommendations include:
Consider using CG for sealing the exit site of SPCs in
neonates, in children and in any patient at high risk of local
bleeding, before covering with a semipermeable transparent
membrane (Figure 4)
Use CG for sealing the exit site of all ECCs in neonates,
before covering with a semipermeable transparent membrane
(Figure 5)
Always use CG for sealing the exit site of any LPC, any
midline catheter (Figure 6), and any central venous catheter
(PICC, FICC or CICC), in both children (Figure 7) and
adults (Figure 8), in addition to standard sutureless securement
and coverage with a transparent semipermeable membrane
Always use CG for closing any skin incision related to venous
Figure 7. Glue used for sealing the exit site of a centrally
inserted central catheter in a small infant
Figure 8. Glue used for sealing exit site of dialysis catheter
Figure 4. Glue used to seal the exit site of a short peripheral
cannula
Figure 6. Glue used to seal the exit site of a midline
catheter
Figure 5. Glue used to secure of an epicutaneo-cava catheter
in a pre-term neonate
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catheters and skin incisions for reservoir placement during
port insertions).
In the authors’ hospital, the vascular access team is currently
using approximately 10 000 vials per year of butyl-CG or octyl-
butyl-CG; no adverse eects related to CG have been reported
in the last decade.
Prospective extensions of the use of glue (still to be supported
by evidence) include UVC, peripheral arterial catheters and
any SPC, as well as in patients at a low risk of bleeding/
dislodgment. In addition, the safety and cost-eectiveness of
weekly replacement of glue over the exit site of central venous
access devices needs to be evaluated by future studies. BJN
Declaration of interest: none
Annetta MG, Pittiruti M, Scoppettuolo G et al. Randomized clinical study on
the ecacy of metallic powder vs cyanoacrylate glue in sealing the exit
site of the peripherally inserted central catheters: preliminary results. Oral
presentation at the Annual Meeting of the Association for Vascular Access,
Nashville, 20-23 September 2013
Auyong DB, Cantor DA, Green C, Hanson NA. The eect of xation technique
on continuous interscalene nerve block catheter success: a randomized,
double-blind trial. Anesth Analg. 2017;124(3):959–965. https://doi.
org/10.1213/ANE.0000000000001811
Bahl A, Gibson SM, Jankowski D, Chen NW. Short peripheral
intravenous catheter securement with cyanoacrylate glue compared
to conventional dressing: a randomized controlled trial. J Vasc Access.
2021:11297298211024037 (epub ahead of print). https://doi.
org/10.1177/11297298211024037
Barone G, Pittiruti M. Epicutaneo-caval catheters in neonates: new insights
and new suggestions from the recent literature. J Vasc Access. 2020;21(6):
805–809. https://doi.org/10.1177/1129729819891546
Bhende S, Rothenburger S, Spangler DJ, Dito M. In vitro assessment
of microbial barrier properties of Dermabond topical skin
adhesive. Surg Infect (Larchmt). 2002;3(3):251–257. https://doi.
org/10.1089/109629602761624216
Biasucci DG, Pittiruti M, Taddei A et al. Targeting zero catheter-related
bloodstream infections in pediatric intensive care unit: a retrospective
matched case-control study. J Vasc Access. 2018;19(2):119–124. https://doi.
org/10.5301/jva.5000797
Bugden S, Shean K, Scott M et al. Skin Glue reduces the failure rate of
emergency department-inserted peripheral intravenous catheters: a
randomized controlled trial. Ann Emerg Med. 2016;68(2):196–201. https://
doi.org/10.1016/j.annemergmed.2015.11.026
Bull T, Corley A, Smyth DJ, McMillan DJ, Dunster KR, Fraser JF. Extracorporeal
membrane oxygenation line-associated complications: in vitro testing of
cyanoacrylate tissue adhesive and securement devices to prevent infection
and dislodgement. Intensive Care Med Exp. 2018;6(1):6. https://doi.
org/10.1186/s40635-018-0171-8
Cellini M, Bergadano A, Crocoli A et al. Guidelines of the Italian Association
of Pediatric Hematology and Oncology for the management of the central
veno us acc ess dev ices i n ped iatri c p atients with onco-hematol ogica l dise ase.
J Vasc Access. 2020:1129729820969309 (epub ahead of print). https://doi.
KEY POINTS
Glue is effective for securement only for short peripheral cannulas
and epicutaneo-cava catheters and when used with a transparent
semipermeable membrane
At all central venous access devices, glue is effective in minimising local
bleeding and is cost-effective as it reduces unscheduled dressing changes
Glue is probably effective in minimising bacterial contamination for all
central venous access devices but should be used only in the rst week as
replacing it every week may be harmful
To close skin incisions, glue is effective and cost-effective for all venous
access procedures
© 2022 MA Healthcare Ltd
British Journal of Nur sing, 2022, Vol 31, No 8 (IV and Vascular A ccess S uppleme nt) S13
VENOUS ACCESS SECUREMENT
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Fraser JF. Cyanoacrylate tissue adhesives—eective securement
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feasibility. Anaesth Intensive Care. 2012;40(3):460–466. https://doi.
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amjsurg.2003.11.017
Ullman AJ, Kleidon T, Gibson V et al. Innovative dressing and securement of
tunneled central venous access devices in pediatrics: a pilot randomized
controlled trial. BMC Cancer. 2017;17(1):595. https://doi.org/10.1186/
s12885-017-3606-9
Ullman AJ, Long D, Williams T et al. Innovation in central venous access
device security: a pilot randomized controlled trial in pediatric critical care.
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neonatal PICC use: a 4-year observational study. Adv Neonatal Care. 2021
(epub ahead of print). https://doi.org/10.1097/ANC.0000000000000963
Waller SC, Anderson DW, Kane BJ, Clough LA. In vitro assessment of microbial
barrier properties of cyanoacrylate tissue adhesives and pressure-sensitive
adhesives. Surg Infect (Larchmt). 2019;20(6):449–452. https://doi.
org/10.1089/sur.2018.280
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for securing central venous catheters. Anaesthesia. 2007;62(9):969–970.
https://doi.org/10.1111/j.1365-2044.2007.05240.x
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glue. Anaesthesia. 2008a;63(3):324. https://doi.org/10.1111/j.1365-
2044.2008.05468.x
Wilkinson JN, Chikhani M, Mortimer K, Gill SJ. The antimicrobial eect of
Histoacryl skin adhesive. Anaesthesia. 2008b;63(12):1382–1384. https://doi.
org/10.1111/j.1365-2044.2008.05775.x
bleeding of the exit site after PICC placement (abstract from second World
Congress on Vascular Access (WoCoVA), Amsterdam, 27-29 June 2012). J
Va s c A cc e s s 2 0 12 ; 1 3 : 2 7 A . h t tp s : / / d o i. o r g / 1 0 .5 3 0 1 / J VA . 20 1 2 . 9 3 6 2
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and central venous access device insertion. J Ass Vasc Access. 2016;21(4):249.
https://doi.org/10.1016/j.java.2016.10.026
Pittiruti M, D’Andrea V, Pinna G, Costa S, Vento G. Securing umbilical venous
catheter with glue: why not? (abstract from sixth World Congress on Vascular
Access (WoCoVa 2020—June 17–19th). J Vasc Access. 2020;21(6):NP16–17.
https://doi.org/10.1177%2F1129729820953245
Pittiruti M, Van Boxtel T, Scoppettuolo G et al. European recommendations
on the proper indication and use of peripheral venous access
devices (the ERPIUP consensus): a WoCoVA project. J Vasc Access.
2021:11297298211023274 (epub ahead of print). https://doi.
org/10.1177/11297298211023274.
Pittiruti M, Scoppettuolo G. Raccomandazioni GAVeCeLT 2021 per
l’indicazione, l’impianto e la gestione dei dispositivi per accesso venoso.
GAVeCeLT—Gli Accessi Venosi Centrali a Lungo Termin (ar ticle in Italian).
2021. https://tinyurl.com/y8j7dxth (accessed 31 March 2022)
Prachanpanich N, Morakul S, Kiatmongkolkul N. Eectiveness of securing
central venous catheters with topical tissue adhesive in patients undergoing
cardiac surgery: a randomized controlled pilot study. BMC Anesthesiol.
2021;21(1):70. https://doi.org/10.1186/s12871-021-01282-0
Prince D, Solanki Z, Varughese R, Mastej J, Prince D. Antibacterial eect and
proposed mechanism of action of a topical surgical adhesive. Am J Infect
Control. 2018;46(1):26–29. https://doi.org/10.1016/j.ajic.2017.07.008
Reynolds H, Taraporewalla K, Tower M et al. Novel technologies can provide
eective dressing and securement for peripheral arterial catheters: a pilot
randomised controlled trial in the operating theatre and the intensive care
unit. Aust Crit Care. 2015;28(3):140–148. https://doi.org/10.1016/j.
aucc.2014.12.001
Rickard CM, Edwards M, Spooner AJ et al. A 4-arm randomized controlled
pilot trial of innovative solutions for jugular central venous access device
securement in 221 cardiac surgical patients. J Crit Care. 2016;36:35–42.
https://doi.org/10.1016/j.jcrc.2016.06.006
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prevention of peripheral intravenous catheter failure in adults (SAVE):
a pragmatic, randomised controlled, superiority trial. Lancet. 2018;
392(10145):419–430. https://doi.org/10.1016/S0140-6736(18)31380-1
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2014;15(6):236–239. https://doi.org/10.1177/1757177414551562
Scoppettuolo G, Annetta MG, C Marano, Tanzanella E, Pittiruti MF.
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or PICC placement. Crit Care. 2013;17(Suppl 2):P 174. https://doi.
org/10.1186/cc12112
Scoppettuolo G, Dolcetti L, Emoli A, La Greca A, Biasucci DG, Pittiruti M.
Further benets of cyanoacrylate glue for central venous catheterisation.
Anaesthesia. 2015;70(6):758. https://doi.org/10.1111/anae.13105
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CPD reective questions
Is cyanoacrylate glue (CG) completely safe on the skin at any age?
What evidence is there that CG actually reduces local bleeding at the
exitsite?
Is there evidence that CG may reduce bacterial contamination of the
exitsite?
Which venous access devices may benet from CG being used as a
securement strategy?
... Recently, engineered catheter securement devices and a CSCA have entered practice (1,2,15,(23)(24)(25)(26)(27)(28)(29). Initially, these approaches were limited to central vascular catheter (CVC) securement but are now recommended as an adjunct for peripheral intravenous catheter (PIVC) securement (1,19,28). ...
... The CSCA formulation used in VA has an established safety record, but MARSI remains a risk, particularly if the product is over-applied (16,17,21,24). A characteristic of CSCA is that the adhesive bond forms more efficiently when thin layers are applied, as thicker layers can lead to less effective catheter securement. ...
... They provide effective securement, reduce catheter migration, the risk of accidental removal, and decrease the need for frequent dressing changes (15,23). Furthermore, CSCAs inhibit bacterial and fungal growth, with evidence supporting reductions in the risk of acquiring catheter-associated infection (1,2,5,15,24,(27)(28)(29)(30). ...
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Neonatal vascular access continues to pose challenges. Recent times have seen considerable innovations in practice and the design and manufacture of materials used to provide infusion-based therapies with the intent of reducing the incidence and severity of vascular access-related complications. However, despite these efforts, vascular access-related complication rates remain high in this patient group and research evidence remains incomplete. In neonates, a medical-grade formulation of cyanoacrylate adhesive is widely used to secure percutaneously inserted central venous catheters and is beginning to establish a role in supporting the effective securement of other devices, such as umbilical and peripheral intravenous catheters. This Perspective article considers issues specific to the removal of cyanoacrylate used to secure vascular access devices from neonatal skin before its bonding releases due to natural skin exfoliation processes. The aim of this information is to ensure the safe and effective removal of octyl-cyanoacrylate adhesive-secured vascular access catheters from neonatal skin and stimulate professional discussion.
... Protection of the exit site with glue [38,39] and semipermeable transparent membrane [40] Catheters included in the present study are only those secured with a subcutaneous anchoring system (SAS) (SecurAcath™, Interrad Medical, Inc. Plymouth, MN). Fully implantable catheters and central venous catheters stabilized only with tissue adhesive and other sutureless securement were excluded from the study. ...
... Cyanoacrylate glue. The use of Cyanoacrylate glue during CVC insertion is nowadays part of several insertion bundles [25,39]. The glue has three important roles, since it secures the catheter, stops bleeding and has antimicrobial activities. ...
... However, the preliminary results of the present paper might represent the basis for a larger randomized study aimed at evaluating the safety and efficacy of the dialkylcarbamoylchloride dressing compared to current, already standardized exit-site dressing techniques, such as cyanoacrylate glue [39,51] and/or chlorhexidine felt pads [55]. ...
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Unlabelled: Dialkylcarbamoylchloride dressing is a fatty acid derivative that has been shown in vitro to bind a number of pathogenic microorganisms. The purpose of this prospective study was to evaluate the safety and the efficacy of this technology in the care of the exit site of central venous catheter in a paediatric and neonatal population. Methods: The study was conducted from September 2020 to December 2022 at the Infermi Hospital in Rimini. Central venous catheters were placed using the SIC bundle for insertion. Dialkylcarbamoylchloride dressing was placed below the subcutaneous anchoring at the time of CVC placement and at each dressing change. Data about the catheters and the exit site were recorded and then compared with an historical cohort. Results: 118 catheters were placed during the studied period. The dialkylcarbamoylchloride dressing was well-tolerated. No case of systemic or local infection was recorded. The comparison with the historical cohort showed a reduction in the rate of exit site infection (p value 0.03). Conclusion: Dialkylcarbamoylchloride dressing is well-tolerated in paediatric and neonatal population. It represents a promising tool as a strategy for infection prevention.
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In pediatric patients, the choice of the venous access device currently relies upon the operator's experience and preference and on the local availability of specific resources and technologies. Though, considering the limited options for venous access in children if compared to adults, such clinical choice has a great critical relevance and should preferably be based on the best available evidence. Though some algorithms have been published over the last 5 years, none of them seems fully satisfactory and useful in clinical practice. Thus, the GAVePed-which is the pediatric interest group of the most important Italian group on venous access, GAVeCeLT-has developed a national consensus about the choice of the venous access device in children. After a systematic review of the available evidence, the panel of the consensus (which included Italian experts with documented competence in this area) has provided structured recommendations answering 10 key questions regarding the choice of venous access both in emergency and in elective situations, both in the hospitalized and in the non-hospitalized child. Only statements reaching a complete agreement were included in the final recommendations. All recommendations were also structured as a simple visual algorithm, so as to be easily translated into clinical practice.
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Epicutaneo-cava catheters are the most widely used central venous catheters in the neonate, but their insertion and management are potentially associated with several complications, both during placement (failure to proceed with the catheter, primary malposition, etc.) and during maintenance (infection, venous thrombosis, catheter dislocation, secondary malposition, etc.). Recent studies have identified methods and techniques that may be effective in minimizing the risk of most of these complications. This paper proposes a structured, sequential insertion bundle—nicknamed “the SIECC protocol” (SIECC = Safe Insertion of Epicutaneo-Cava Catheters)—which includes seven evidence-based strategies which have been proven to increase the safety, effectiveness, and cost-effectiveness of the procedure.
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Implantation of centrally inserted central venous catheter (CICC) may be complicated by bleedings particularly in patients with severe coagulopathy or taking antithrombotic drugs. It has been shown that the application of the Italian Group for Venous Access Devices (GAVeCeLT) bundle reduces the incidence of bleeding in patients admitted to intensive care units (ICU), but its effectiveness has never been demonstrated in different contexts. In this study we evaluated the incidence of bleeding after urgent internal jugular CICC (J-CICC) implantation in patients with increased or no risk of bleeding complications when recommended preventive strategies are applied systematically. We included 185 patients admitted to Internal Medicine Units who underwent urgent J-CICC implantation from April 2016 to December 2018. The incidence of major and minor bleeding immediately after the procedure and in the following 30 days was recorded. None of the enrolled patients showed major bleeding. The incidence of minor bleedings was 2.1% (95% IC: 0.03–4.2) with two patients requiring line removal and repositioning (1.1%; 95% IC: −0.45 to 2.6). Bleeds were not correlated with age or sex, although they all occurred in female subjects. The incidence of bleeds was not increased in patients with increased risk of bleeding compared with those without (5.0% vs 1.3%; p = 0.16). The use of anti-thrombotic medications was significantly associated with increased risk of minor bleedings ( p = 0.03). In this study we demonstrated that the application of the GAVeCeLT suggested bundle can minimize the number of bleeding complications even in patients hospitalized in Internal Medicine Units. Further data are needed in patients taking antithrombotic drugs who appear to be more prone to minor bleeding, however the benefit of completing the procedure appears to significantly outweigh the risk of mechanical complications.
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Background Treatment via a peripherally inserted central venous catheter is important for anticancer treatment, perioperative management, and nutritional management. In this study, we aimed to investigate the usefulness of cyanoacrylate glue (CG) in managing peripherally inserted central venous catheters in adults. Methods This retrospective cohort study enrolled 411 adults requiring a central venous catheter for treatment in the Chiba University Esophageal‐Gastro‐Intestinal Surgery department between January 2021 and October 2022. The preventive effect of CG in reducing adverse events, including infection, tip migration, and thrombus formation, was evaluated by reviewing electronic medical records, chest radiographs, and contrast‐enhanced computed tomography scans. Results CG and other dressings were used in 158 (CG group) and 253 (control group) patients, respectively. The incidence of catheter infection based on the clinical course was lower in the CG group (3.2%) than in the control group (9.1%; p =0.03). However, cases of infection confirmed by blood or catheter culture did not differ between the CG (1.3%) and control (1.9%) groups ( p =1.0). Chest radiographs revealed that catheter tip migration was lesser in the CG group (8.2±6.7 mm) than in the control group (15.0±15.8 mm; p <0.01). There were two cases of venous thrombus formation in the control group. Conclusion In a population dominated by esophago‐gastroenterological malignancy, peripherally inserted central catheter securement via CG was associated with decreased catheter removal due to suspected catheter infection. Further research on larger cohorts is needed to determine if other adverse events decrease following peripherally inserted central catheter securement via CG. This article is protected by copyright. All rights reserved.
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In the past 5 years, non-dialysis femoral venous access has changed in terms of indications, techniques of insertion, and expected incidence of complications. To the traditional non-emergency indication for femoral catheters—obstruction of the superior vena cava—many other indications have been added, both in intensive and non-intensive care. The insertion technique has evolved, thanks to ultrasound guided venipuncture, tunneling, and ultrasound based intraprocedural tip location. Insertion of femorally inserted central catheters may be today regarded as a procedure with an extremely low intraprocedural and post-procedural risk. The risk of infection is reduced by the possibility of the exit site at mid-thigh, by the use of cyanoacrylate glue for sealing the exit site, and by appropriate intraprocedural strategies of infection prevention. The risk of catheter-related thrombosis is low, due to several concomitant strategies: a proper match between vein diameter and catheter caliber; an accurate intraprocedural assessment of tip location by ultrasound and/or intracavitary ECG; the consistent use of ultrasound guided venipuncture and micro-introducer kits; an adequate stabilization of the catheter at the exit site. The risk of mechanical complications and the risk of lumen occlusion are minimized when using polyurethane, power injectable catheters. All these novelties have brought a revolution in the field of femoral venous access, so that this route may be considered as safe and effective as other approaches to central venous catheterization.
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In the neonatal intensive care units (NICU), epicutaneo-caval catheters (ECCs) are common alternative vascular routes. Pericardial effusion (PCE) and cardiac tamponade (CT) are rare but serious complications in infants with ECCs. It may be asymptomatic or present with a variety of significant clinical signs, including dyspnea, bradycardia, sudden asystole, and hypotension. If untreated, PCE can be fatal. This report presents, three cases of ECC-associated PCE/CT during NICU stay. All three patients were born before 30 weeks of gestation and weighed less than 1500 g. Echocardiography was used for diagnosis all patients. PCE/CT was detected incidentally in one patient and after hemodynamic deterioration in the other two. In one patient, CT was developed due to catheter malposition, and the other two patient, the catheter tip was found in the right atrium. PCE did not recur in any of the patients after pericardial fluid was drained and the catheters were removed. No PCE/CT-related deaths were observed. In all three patients, X-ray was used to evaluate the location of the catheter tips. However, after clinical deterioration, echocardiography showed that in the first two cases the tips were actually in the right atrium. Real-time ultrasound was suggested with strong evidence to evaluate the location of the catheter tip and to detect secondary malapposition. PCE/CT should be considered in the presence of unexplained and refractory respiratory distress, abnormal heart rate and blood pressure, and metabolic acidosis in a neonate with ECC. Early diagnosis and prompt pericardiocentesis are essential to reduce mortality and improve prognosis. Prospective studies with educational interventions should be designed to demonstrate that the use of point-of-care ultrasound (POCUS) can be easily acquired and may reduce complications.
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Background: Calcium gluconate is widely used to treat neonatal hypocalcemia, severe hyperkalemia, and convulsions. However, extravasation of calcium gluconate can lead to iatrogenic calcinosis, causing symptoms such as local redness and swelling, cutaneous plaque, soft tissue calcification, and cutaneous tissue necrosis. Therefore, this study retrospectively analyzed the conservative treatment results of neonatal iatrogenic calcinosis. Methods: Data of neonates diagnosed with iatrogenic calcinosis cutis caused by calcium gluconate exudation between December 2012 and June 2021 were analyzed retrospectively. The clinical data included medical history, physical examination, laboratory findings, and radiographs. All the patients were conservatively treated, and the curative effect and prognosis were followed up by evaluating radiographs and limb function. Patients with complications, such as recurrence or limb dysfunction, were further followed up. Results: Overall, 16 neonates (sex: 10 male and 6 female infants; age: 17.5 ± 7.8 days) were included. Iatrogenic calcinosis cutis was located around the left wrist, right wrist, left ankle, and right ankle in four, one, six, and five patients, respectively. Calcification healed within 1-3 months (mean: 1.6 ± 0.6 months). After a follow-up of 0.5-8.5 years (mean: 3.5 ± 2.8 years), the appearance, joint function, local growth, and development of the lesion of the neonates with iatrogenic calcinosis cutis were consistent with those of the healthy ones. Conclusion: For neonatal iatrogenic calcinosis cutis without cutaneous and subcutaneous tissue necrosis, symptomatic support treatment is effective and does not affect the limbs' appearance and function.Level of evidence: IV.
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Objective The objective of the study was to assess the efficacy of the use of cyanoacrylate glue (CAG) as a means of securing midline catheters and peripherally inserted central catheters with the modified micro-Seldinger technique in adult hospitalised patients. Methods Randomised clinical trial with two groups (1:1): control and intervention. The control group received a securement method with a sutureless device plus transparent dressing and the intervention group received the same securement method plus the CAG. The study was approved by the Drug Research Ethics Committee of the Lleida Health Region. Results A total of 216 patients were assessed. The two groups of the trial were homogenously distributed in terms of sociodemographic and clinical variables. The intervention group had a statistically significant lower incidence of peri-catheter bleeding and/or oozing during the 7-day study period (odds ratio (OR), 0.6; 95% confidence level (CI), 0.44–0.81; p < 0.001) and a statistically significant lower incidence of catheter dislodgements during the first 24 h (OR, 0.2; 95% CI, 0.04–0.91; p = 0.03). There were no statistically significant differences in the incidence of phlebitis (OR, 1.30; 95% CI, 0.60–2.83; p = 0.56) or catheter-related pain (OR, 0.88; 95% CI, 0.40–1.94; p = 0.84). Conclusion Midline catheters and peripherally inserted central catheters secured with CAG had fewer complications than catheters not secured with this adhesive.
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Background: Within every neonatal clinical setting, vascular access devices are considered essential for administration of fluids, nutrition, and medications. However, use of vascular access devices is not without danger of failure. Catheter securement adhesives are being evaluated among adult populations, but to date, studies in neonatal settings are scant. Purpose: This research describes the prevalence of peripherally inserted central catheter failure related to catheter securement before and after the introduction of tissue adhesive for catheter securement. The identified modifiable risks might be used to evaluate efficacy, to innovate neonatal practice and support future policy developments. Method and setting: This was a retrospective observational analysis of routinely collected anonymized intravenous therapy-related data. The study was carried out at the tertiary neonatal intensive care unit (112 beds) of the Women's Wellness and Research Center of Hamad Medical Corporation, Doha, Qatar. Results: The results showed that the use of an approved medical grade adhesive for catheter securement resulted in significantly less therapy failures, compared with the control group. This remains significant after adjusting for day of insertion, gestational age, birth weight, and catheter type. Implications for practice and research: In parallel with currently published international literature, this study's findings support catheter securement with an octyl-based tissue adhesive in use with central venous catheters. When device stabilization is most pertinent, securement with tissue adhesive is a safe and effective method for long-term vascular access among the neonatal population.
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Background Continuous peripheral nerve catheters (CPNCs) have been used for postoperative pain relief. A common problem encountered with CPNCs is pericatheter leakage, which can lead to dressing adhesive failure. Frequent dressing changes increase the risk of catheter dislodgement and infections. Adhesive glue is effective in securing the peripheral nerve catheter and decreasing leakage around the catheter insertion site. This study aimed to evaluate the incidence of pericatheter leakage with fixation using 2-octyl cyanoacrylate glue (Dermabond ® ) as compared to sterile strips. Methods Thirty patients undergoing unilateral total knee arthroplasty (TKA) with continuous femoral nerve catheter for postoperative analgesia were randomized into the catheter fixation with 2-octyl cyanoacrylate glue (Dermabond ® ) group or the sterile strip group. The primary outcome was the incidence of pericatheter leakage. Secondary outcomes included the frequent of catheter displacement, the difficulty of catheter removal, pain score and patient satisfaction. Results The incidence of pericatheter leakage at 24 and 48 h was 0% versus 93 and 0% versus 100% in the Dermabond ® and sterile strip groups, respectively ( P < 0.001). The incidence of displacement at 24 and 48 h was 6.7% versus 93.3 and 6.7% versus 100% in the Dermabond® and sterile strip, respectively ( P < 0.001). There was no difference in numeric rating scale, difficulty of catheter removal, or satisfaction scores between groups. Conclusions Catheter fixation with 2-octyl cyanoacrylate glue (Dermabond ® ) decreased the incidence of pericatheter leakage, as well as catheter displacement, over 48 h as compared to sterile strip fixation. Trial registration This trial was registered on Thai clinical trial registry: TCTR20200228002 , registered 24 February 2020- Retrospectively registered.
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Since several innovations have recently changed the criteria of choice and management of peripheral venous access (new devices, new techniques of insertion, new recommendations for maintenance), the WoCoVA Foundation (WoCoVA = World Conference on Vascular Access) has developed an international Consensus with the following objectives: to propose a clear and useful classification of the currently available peripheral venous access devices; to clarify the proper indication of central versus peripheral venous access; discuss the indications of the different peripheral venous access devices (short peripheral cannulas vs long peripheral cannulas vs midline catheters); to define the proper techniques of insertion and maintenance that should be recommended today. To achieve these purposes, WoCoVA have decided to adopt a European point of view, considering some relevant differences of terminology between North America and Europe in this area of venous access and the need for a common basis of understanding among the experts recruited for this project. The ERPIUP Consensus (ERPIUP = European Recommendations for Proper Indication and Use of Peripheral venous access) was designed to offer systematic recommendations for clinical practice, covering every aspect of management of peripheral venous access devices in the adult patient: indication, insertion, maintenance, prevention and treatment of complications, removal. Also, our purpose was to improve the standardization of the terminology, bringing clarity of definition, and classification.
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Background Central venous catheters (CVCs) play an important role during cardiac surgery. Topical tissue adhesives form a thin film of coating that becomes bound to keratin in the epidermis. The advantage of this “super glue” lies in its antimicrobial activity. This study aimed to evaluate fixation of CVCs with topical tissue adhesive in patients (prone to bleed) undergoing cardiac surgery regarding its ability to reduce the incidence of pericatheter leakage. Methods This randomized controlled trial included 150 patients > 15 years of age who were (1) scheduled to undergo elective cardiac surgery, (2) required CVC insertion at the internal jugular vein, and (3) scheduled for transfer postoperatively to the cardiac intensive care unit. We randomly assigned patients to a topical tissue adhesive group (TA) or a standard control group (SC). The primary outcome was a change in dressing immediately postoperatively due to pericatheter blood oozing. Secondary outcomes were the number of dressings, total dressings per catheter day, and composite outcome of catheter failure within 3 days. Both intention-to-treat and per-protocol analyses were performed. Seven patients violated the protocol (three TA patients and four SC patients). Results Regarding the primary outcome, the SC group exhibited a significantly increased incidence of dressing change immediately postoperatively due to pericatheter leakage compared with the TA group in both the intention-to-treat analysis (5.33% vs 18.67%, RR 0.25 [95% CI 0.08 to 0.79], P = 0.012) and the per-protocol analysis (5.56% vs 16.90%, RR 0.289 [95% CI 0.09 to 0.95], P = 0.031). No significant differences were noted in the number of dressings, total dressings per catheter day, or composite outcome of catheter failure within 3 days between the two groups. Multiple logistic regression analysis was performed to adjust baseline characteristics that were different in the per-protocol analysis. The results showed that the risk ratio of immediate postoperative dressing change in TA patients was 0.25 compared to the SC group ([95% CI 0.07 to 0.87], P = 0.029) in the per-protocol analysis. Conclusion The use of a topical tissue adhesive can reduce the incidence of immediate postoperative pericatheter blood oozing. Trial registration TCTR20180608004 , retrospectively registered on June 06, 2018.
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Abstract Background Extracorporeal membrane oxygenation (ECMO), an invasive mechanical therapy, provides cardio-respiratory support to critically ill patients when maximal conventional support has failed. ECMO is delivered via large-bore cannulae which must be effectively secured to avoid complications including cannula migration, dislodgement and accidental decannulation. Growing evidence suggests tissue adhesive (TA) may be a practical and safe method to secure vascular access devices, but little evidence exists pertaining to securement of ECMO cannulae. The aim of this study was to determine the safety and efficacy of two TA formulations (2-octyl cyanoacrylate and n-butyl-2-octyl cyanoacrylate) for use in peripherally inserted ECMO cannula securement, and compare TA securement to ‘standard’ securement methods. Methods This in vitro project assessed: (1) the tensile strength and flexibility of TA formulations compared to ‘standard’ ECMO cannula securement using a porcine skin model, and (2) the chemical resistance of the polyurethane ECMO cannulae to TA. An Instron 5567 Universal Testing System was used for strength testing in both experiments. Results Securement with sutures and n-butyl-2-octyl cyanoacrylate both significantly increased the force required to dislodge the cannula compared to a transparent polyurethane dressing (p = 0.006 and p = 0.003, respectively) and 2-octyl cyanoacrylate (p = 0.023 and p = 0.013, respectively). Suture securement provided increased flexibility compared to TA securement (p
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Aim Evaluate the feasibility of an efficacy randomised control trial (RCT) of paediatric peripheral intravenous catheter (PIVC) securement to prevent failure without resultant skin damage. Methods A 3-arm, pilot RCT in an XX paediatric hospital. Random assignment of 330 children to receive (i) bordered polyurethane dressing (BPU) + non-sterile foam (NSF), (ii) integrated securement dressing (ISD) + sterile foam (SF), or (iii) tissue adhesive (TA)+ NSF. Primary outcomes were feasibility and PIVC failure. Secondary outcomes included: skin/bloodstream infection; occlusion; infiltration; dislodgement; phlebitis; dwell; serious adverse events; acceptability and microbial colonisation of catheter tips, wound site, and foam. Results Most feasibility outcomes were confirmed; 98% of eligible patients consented, 96% received their allocated dressing and no patients were lost to follow up. Eligilbility feasibility (58%) was not met. 11 randomised patients did not require a PIVC. Of 319 patients receiving a PIVC (20,716 PIVC-hours), a significant reduction in PIVC failure was demonstrated with ISD, 31/107 (29%, p = 0.017) compared to BPU, 47/105 (45%). Although not statistically significant, compared to BPU, TA 34/107 (32%, p = 0.052) was associated with less PIVC failure. On Cox regression, no securement intervention significantly reduced PIVC failure. Older age (HR 0.92; 95% confidence interval [CI] 0.88–0.96; p = <0.01), no infection at baseline (HR 0.51; 95% CI 0.34–0.78) and insertion by vascular access specialist (HR 0.40; 95% CI 0.26–0.64) were significantly associated with reduced failure (p < 0.05). Conclusion ISD and TA had reduced PIVC failure compared to BPU. A large efficacy trial to test statistical differences is feasible and needed.
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Background: Short peripheral intravenous catheters (PIVCs) fail prior to completion of therapy in up to 63% of hospitalizations. This unacceptably high rate of failure has become the norm for the most common invasive procedure in all of medicine. Securement strategies may improve PIVC survival. Methods: We conducted a prospective, single-site, parallel, two-arm randomized controlled investigation with a primary outcome of catheter failure comparing securement with standard semi-permeable dressing and clear tape (SPD) to standard semipermeable dressing and clear tape with cyanoacrylate glue (SPD + CG). Adult emergency department patients with a short PIVC and anticipated hospital duration ⩾ 48 h were enrolled and followed until IV failure or completion of therapy for up to 7 days. Secondary outcomes included complications and cost comparisons between groups. Primary outcome was assessed by intention to treat and per protocol analyses. Findings: 350 patients were enrolled between November 2019 and October 2020. PIVC survival for SPD + CG was similar to SPD group with the absolute risk difference of IV failure in the intention-to-treat (−5.8%, p = 0.065) population and improved in the per protocol (−8.1%, p = 0.04) population, respectively. Kaplan-Meier survival analysis indicated there was a significant benefit of the SPD + CG at greater than 2 days of hospitalization (p = 0.04). Prior to 48 h, there was no survival enhancement to either group (p = 0.98) in the intention to treat population. In a multivariable analysis with piecewise Cox regression, when the IV was functional greater than 48 h, the risk of IV failure in the SPD + CG was 43% less than the SPD group (adjusted hazard ratio [HR] 0.57, 95% confidence interval [CI] 0.34 to 0.97; p = 0.04). Cumulative cost related to IV during hospitalization was similar between groups with a lower incremental rescue cost in the SPD + CG group. Interpretation: SPD combined with cyanoacrylate glue provides similar benefit to patients compared to SPD alone and potentially improves short PIVC survival when the IV was inserted >48 h. As this strategy is cost neutral, it could be considered in admitted patients, particularly those with longer anticipated hospital durations.
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Introduction Epicutaneo-caval catheters (ECC) are pivotal for drug and fluid infusion in neonates. Given the intrinsic importance of the catheter for the patients’ health and the need to avoid stressful and painful procedures on premature or critically ill newborns with fragile and poor vein asset, it is clearly necessary an accurate bundle for ECC insertion and management to avoid complications that may lead to non-elective ECC removal. Among others, dislodgment is an acknowledged complication, and conventionally adopted fixing devices seem alone unsatisfying in relation to ECC securement. Object To evaluate the usefulness of medical Cyanoacrylate Glue (CG) as a solution to strengthen conventional ECC securement. Methods Since the use of CG has become part of our ECC insertion bundle in 2018, the present study compares all term and preterm neonates admitted in our NICU in 2018 who required an ECC for any cause (92 cases) with an historical cohort formed by all neonates who required an ECC in 2017 (80 patients). Results CG added to usual securement devices is effective in reducing ECC accidental dislodgment. Moreover, it is easy and safe to apply and remove, limits bleeding and oozing at the puncture site, and may also be an effective antimicrobial mechanical barrier.
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Introduction: A serious complication associated with Central Venous Access Device (CVAD) is infection because of bacterial contamination, either by the extra-luminal or by the intra-luminal route.We evaluated the efficacy, the safety, and the cost-effectiveness of two strategies for non-inferiority in controlling bacterial colonization of the exit-site of Peripherally-Inserted Central Catheters (PICC). Methods: After PICC placement, a skin swab of the exit site was taken and cultured. In group A the exit site was sealed with N-butyl-cyanoacrylate glue, while in group B a chlorhexidine-releasing sponge dressing was applied. A second skin culture was taken at day 7. Results: A total of 51 patients were enrolled in each group. In 42 patients the second skin culture was not performed because of 20 patients were lost at follow-up or deceased and in 22 patients the dressing needed to be changed early, because of local bleeding (13 cases, in group B) or because of dressing detachment (four in group A and five in group B). The microbiological study was completed in 36 patients in group A and 24 in group B. No microorganisms were isolated in any patient. Conclusions: Both strategies were effective in controlling bacterial colonization. Glue was effective in reducing local bleeding, and it was more cost-effective than sponge dressing. During the first week, when local bleeding and bacterial colonization must be prevented, glue might be more appropriate than chlorhexidine-releasing dressing; after the first week chlorhexidine-releasing dressing might be preferable, considering that the safety of glue application on the skin for prolonged periods is still questionable.