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Swallowing function in COVID-19 patients after invasive mechanical
ventilation
Margareta Gonzalez Lindh , Gustav Mattsson , Hirsh Koyi ,
Monica Blom Johansson , Robin Razmi , Andreas Palm
PII: S2590-1095(21)00093-8
DOI: https://doi.org/10.1016/j.arrct.2021.100177
Reference: ARRCT 100177
To appear in: Archives of Rehabilitation Research and Clinical Translation
Please cite this article as: Margareta Gonzalez Lindh , Gustav Mattsson , Hirsh Koyi ,
Monica Blom Johansson , Robin Razmi , Andreas Palm , Swallowing function in COVID-19 patients
after invasive mechanical ventilation, Archives of Rehabilitation Research and Clinical Translation
(2021), doi: https://doi.org/10.1016/j.arrct.2021.100177
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©2021 The Authors. Published by Elsevier Inc. on behalf of American Congress of Rehabilitation
Medicine.
This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
1
Swallowing function in COVID-19 patients after invasive mechanical ventilation
Margareta Gonzalez Lindh1, 2*; Gustav Mattsson2; Hirsh Koyi2, 3; Monica Blom Johansson1;
Robin Razmi2, 4; Andreas Palm2, 5
1. Department of Neuroscience, Speech and Language Pathology, Uppsala University,
Uppsala, Sweden
2. Centre for Research and Development (CFUG), Uppsala University, Region Gävleborg,
Gävle, Sweden.
3. Department of Oncology-Pathology, Karolinska Biomics Center, Karolinska Institutet,
17176 Stockholm, Sweden
4. Section of Infectious Diseases, Department of Medical Sciences, Uppsala Universitet,
Uppsala, Sweden.
5. Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala
Universitet, Uppsala, Sweden.
*Corresponding author:
Margareta Gonzalez Lindh
Phone: +46(0)730-846411
E-mail: margareta.gonzalez.lind@regiongavleborg.se
Running head: Swallowing function in COVID-19 patients
Word count: 2723
Acknowledgements: This study was funded by the Centre for Research and Development
Uppsala University/County Council of Gävleborg. We thank Christian Ehrenborg, MD PhD,
2
Department of infectious diseases in Region Gävleborg, the Speech Pathology Department in
Gävleborg and research assistant Ingrid Olson.
Keywords: COVID-19, dysphagia, intensive care, invasive mechanical ventilation, swallowing
Competing interests: GM has received fees from Alnylam, Internetmedicin, and Merck,
Sharp and Dohme. MGL, HK, MBJ, RR and AP declare no competing interests.
Abstract
Objective: To explore swallowing function and risk factors associated with delayed recovery
of swallowing in COVID-19 patients post invasive mechanical ventilation using the Functional
Oral Intake Scale (FOIS).
Design: Longitudinal cohort study.
Setting: 3 secondary-level hospitals.
Participants: Invasively ventilated patients (n=28), hospitalized with severe COVID-19 who
were referred to the Speech and Language Pathology (SLP) departments post mechanical
ventilation between March 5 and July 5 2020 for an evaluation of swallowing function before
commencing oral diet.
Interventions: SLP assessment, advice and therapy for dysphagia.
Main outcome measures: Oral intake levels at baseline and hospital discharge according to
the Functional Oral Intake Scale (FOIS). Patients were stratified according to FOIS (1-
5=dysphagia, 6-7= functional oral intake). Data regarding comorbidities, frailty, intubation
and tracheostomy, proning and SLP evaluation were collected.
3
Results
Dysphagia was found in 71% of the patients at baseline (in total 79% male, age 61 ±12 years,
BMI 30 ±8 kg/m2). Median FOIS score at baseline was 2 (IQR 1) vs 5 (IQR 2.5) at hospital
discharge. Patients with dysphagia were older (64 ±8.5 vs 53 ±16 years; p= 0.019), had a
higher incidence of hypertension (70% vs 12%; p=0.006) were ventilated invasively longer
(16 ±7 vs 10 ±2 days; p=0.017) or with tracheostomy (9 ±9 vs 1 ±2 days; p=0.03) longer. A
negative association was found between swallowing dysfunction at bedside and days
hospitalized (r=-0.471, p=0.01), and number of days at the Intensive Care Unit (ICU) (r=-0.48,
p=0.01).
Conclusion
Dysphagia is prevalent in COVID-19 patients post invasive mechanical ventilation and is
associated with number of days in hospital and number of days in the ICU. Swallowing
function and tolerance of oral diet improved at discharge (p<0.001).
Keywords: COVID-19, dysphagia, intensive care, invasive mechanical ventilation, swallowing
function, frailty.
List of abbreviations: COVID-19, corona virus disease 2019; FOIS, Functional Oral Intake
Scale; SLP, Speech and Language Pathology, ICU, Intensive Care Unit, IQR, Inter Quartile
Ratio; BMI, Body Mass Index.
Introduction
During the first surge of the corona virus disease 2019 (COVID-19) pandemic, between 7-8%
of patients hospitalized with Covid-19 were admitted to the Intensive Care Unit (ICU)[1]. The
primary reason was respiratory failure. Dysphagia (swallowing dysfunction) is prevalent post
4
prolonged mechanical ventilation (>48 hours) [2]. Invasive ventilation can have a negative
effect on laryngeal competence and swallowing physiology [2, 3] due to oedema, vocal fold
immobility, reduced sensation and muscle disuse [4]. Time intubated is the strongest risk
factor for dysphagia following invasive mechanical ventilation, incidence varying depending
on which cohort is studied and how dysphagia is defined.
A systematic review by Skoretz, Flowers and Martino [5] of 14 studies on a total of 3520
patients (medical, surgical and cardiovascular surgical) following endotracheal intubation
found a reported dysphagia frequency ranging from 3% to 62% where the highest dysphagia
frequencies included patients experiencing prolonged intubation (>24 hours). More than half
of the included studies reported a dysphagia frequency exceeding 20% and dysphagia was
associated with pneumonia, prolonged treatment of antimicrobial therapy, reintubation,
tracheostomy, prolonged hospital and ICU length of stay, and increased short- and long-term
mortality.
Brodsky et al. [6] followed acute respiratory distress syndrome (ARDS) survivors (n=37) with
symptoms of dysphagia after oral intubation prospectively over a 5-year period post
discharge. They found that the median time to recovery was three months (IQR 3-6) with
23% of survivors having symptoms persisting more than six months. All resolved within 5
years after hospital discharge.
Prone positioning has been found to reduce mortality among patients with moderate-to-
severe ARDS [7] and has become standard of care for Covid-19 patients. There is presently
no data on whether or not prone positioning affects swallowing function post mechanical
ventilation in general, nor if COVID-19 patients are particularly vulnerable due to their
frequent need for prolonged ICU-stays.
5
Dysphagia assessment and treatment are in general done by a specialist, often a speech and
language pathologist (SLP), but it can also be performed by other professions (e.g.,
phoniatricians, otolaryngologists, occupational therapists or critical care physicians) [4]. An
instrumental evaluation is often recommended as a complement to a clinical bedside
examination [8] with either a flexible endoscopic evaluation of swallowing (FEES) or with
videofluoroscopy (also called Modified Barium Swallow, MBS). However, both methods are
considered aerosol generating procedures (AGP) and these were restricted during the
COVID-19 pandemic [9].
Dysphagia has been identified as one of the most important sequelae of severe and critical
forms of COVID-19 [10], however the magnitude of short and long term dysphagia in COVID-
19 are not yet known.
The aims of this study were threefold: to determine the incidence and grade of dysphagia in
patients with COVID-19 after mechanical ventilation using level of oral intake, to determine
recovery rate, and to explore risk factors associated with dysphagia.
In this paper, the terms dysphagia and swallowing dysfunction will be used synonymously.
Materials and methods
Participants
This was a longitudinal cohort study of consecutive patients ≥18 years with positive real-time
reverse-transcriptase polymerase chain reaction test (RT-qPCR test) for SARS-CoV-2
admitted to three ICUs in the region (285 452 inhabitants). Patients who contracted COVID-
19 while already in the hospital were excluded. Patients were referred to the SLP
departments post mechanical ventilation between March 5 and July 5 2020 (5 days/week
6
service) for an evaluation of swallowing function before commencing oral diet. This is a
substudy of the Gävleborg COVID-19 cohort study. Data regarding age, clinical frailty
evaluated with the Clinical Frailty Score (CFS) [11] smoking, respiratory and swallowing
parameters, comorbidities, days with tracheostomy, total days with ventilator, total days of
hospitalization, prone position and days between extubation/decannulation and bedside
swallowing evaluation were recorded. Body mass index (BMI) was calculated from body
weight in kilograms divided by height in meters squared (self-reported or from medical
chart), kg/m2.
Setting
Patients were evaluated by an SLP either at the ICU, or at the High Dependency Unit (HDU)
or COVID-19 ward after being transferred from the ICU. Recommendations were
subsequently given regarding oral intake of medication, liquids, and food. The patients were
monitored until return of safe oral feeding or until discharged to a rehabilitation clinic.
Bedside Swallowing Evaluation (BSE)
A BSE was performed when the patients were deemed medically stable and awake post
mechanical ventilation. It was performed with the patient in an upright position. Assessed
domains included an examination of motor (strength, speed, and range of movement) and
sensory function of intra-oral musculature, cranial nerve examination, respiratory function,
ability to follow single-step verbal commands, dentition, cough quality and dysphonia. Pulse
oximetry was performed, and oxygen support and respiratory rate was recorded. The
patients were observed swallowing different liquids, consistencies and volumes ad modum
the Volume Viscosity Swallowing Test (V-VST)[12] but adding a solid bolus (typically a dry
cracker) and adding a larger volume of water (100 ml) when appropriate [13]. Clinical signs
7
of impaired safety of swallowing (cough, decrease in oxygen saturation or change in voice
quality) and impaired efficacy (bolus retention, posterior bolus leak, multiple re-swallows,
and difficulty initiating a swallow) were analysed and when possible laryngeal palpation. Oral
intake recommendations were based on a patient’s swallowing ability in combination with
other factors such as delirium, postural control, and fatigue.
The Functional Oral Intake Scale, FOIS
The Functional Oral Intake Scale, (FOIS) [14], is the most frequently used scale for evaluation
of oral intake and was used as an outcome measure of swallow function. FOIS is a validated
7-point ordinal scale ranging from level 1 (nothing by mouth), level 2-3 (tube dependent),
level 4 (total oral intake of a single consistency), level 5 (total oral intake of multiple
consistencies requiring special preparation), level 6 (total oral intake with no special
preparations, but minimal restrictions) to a score of 7 (total oral diet with no restrictions).
Patients were stratified according to swallowing function where FOIS level 1-5 was defined
as having dysphagia and level 6-7 as having a functional swallowing. The oral intake
recommendation at hospital discharge was used to determine the secondary outcome
measure.
Follow-up
All patients were invited to answer the 4-point swallowing questionnaire test (4QT) [15] 1-2
months post discharge from hospital or rehabilitation clinic.
Ethical considerations
The study was approved by the Swedish Ethical Authority (Dnr 2020-01746). Informed
consent was obtained from all patients.
8
Statistical analysis
Normally distributed continuous data was presented as mean ± standard deviation and non-
normally distributed data as median with IQR. Categorical data was presented as frequencies
and percentage. The difference between groups was analysed with student t-test for
normally distributed continuous data, with Mann Whitney U- test for non-normally
distributed continuous data and Chi-2-test for categorical variables. The association between
FOIS at ICU discharge (baseline) and number of days in hospital, number of days in the ICU,
age, BMI, number of days intubated, prone position, frailty and tracheostomy were
analysed using Spearman’s rank correlation coefficient. A p-value of < 0.05 was regarded as
significant. Statistical analyses were conducted using the software package Stata, version
16.1 (StataCorp LP; College Station, TX77845 USA).
Results
In total, 28 patients were included in the study (79% male, age 61 ±12 years; range 25-78,
BMI 30 ±8 kg/m2). Baseline characteristics are presented in Table 1. All patients lived at
home and had a median clinical frailty score of 3 (range 1-5) before hospitalization with
COVID-19. No patients had previous dysphagia or neurological diseases. Prone position was
applied in 16 of 28 patients (57%), however length of time prone could not be determined
from the medical records. Median length of ICU stay was 20 days (IQR 17-31) and median
hospital stay was 35 days (IQR 27-52). Delirium was evident in 61% of the patients at BSE.
During hospitalization, one patient died. Out of the surviving 27 patients, 41% (n=11) were
discharged home and the remaining to specialized rehabilitation clinics.
Prevalence of dysphagia
9
Clinical signs of swallowing dysfunction (FOIS 1-5) were found in 20 of 28 patients (71%)
(Table 1), median FOIS was 2 (IQR 1). Feeding tube dependency, complete or partial (FOIS 1-
3) was seen in 57% of the patients (n=15). Three patients were assessed as FOIS 6 which
means that some food or liquid items must be avoided. We chose to categorize them to the
“functional swallowing group” since they were eating food from the regular hospital menu,
only the easy to chew options.
The main presenting dysphagia symptoms were oral and pharyngeal muscle weakness (71%),
cough (50%) and bolus retention (32%) (Table 2).
Patients with dysphagia were older (64 ±8.5 vs 53 ±16 years; p= 0.019), had a higher
incidence of hypertension (70% vs 12%; p=0.006), remained with invasive ventilation (16 ±7
vs 10 ±2 days; p=0.017) or with tracheostomy (9.4 ±9.1 vs 1.1 ±2.2 days; p=0.03) longer.
Median length of ICU stay (28.5, IQR 18.5 vs 15.5, IQR 4.5; p=0.001) and length of
hospitalization (46.5, IQR 24.3 vs 24.0, IQR 10.3; p=0.003) were longer.
Respiratory function post mechanical ventilation
Fifty percent of the patients (n=14) had been tracheotomised (Table 1), but 11 of them were
decannulated at the time of bedside evaluation. Reintubation occurred in seven (25%) of the
patients and three times in one patient. Mean number of days from tracheostomy insertion
to decannulation was 7 (SD 8.6). See Table 2 for respiratory vitals at BSE.
Recovery Rate
At discharge from hospital, all patients had been decannulated and 47% (n=9) of the patients
with a FOIS of 1-5 at BSE had recovered a functional oral intake (FOIS 7). Of the 11 patients
discharged home, one remained with restrictions in oral intake (FOIS 5). In the group going
10
to the rehabilitation clinic, 56% (nine of 16) remained with diet restrictions (FOIS 1-5) with
four patients (15%) having complete or partial tube dependency (FOIS 1-3). Figure 1 shows
the distribution of FOIS score at BSE and hospital discharge.
Follow-up
In total 79% (n=22) attended a follow-up visit 8 weeks (IQR 3.75) post discharge from the
hospital. Of the six patients lost to follow-up one patient cancelled the appointment. The
remaining five were lost due to death (n=1), patient returning to his home country (n=1),
patient belonging to another region (n= 2) or patient being followed at the local clinic (n=1).
Dysphagia had resolved in 13 of the 14 patients (93%) with the remaining patient reporting
mild dysphagia symptoms. One of the patients in the “no dysphagia group” at discharge
reported mild dysphagia symptoms at follow-up. The reported symptoms were: “it takes
longer to eat meals than it used to” and “swallowing is effortful”. Information on taste,
smell, nutrition and voice complaints are reported in Table 3. If the patient had skipped a
question and did not comment on it as being a problem in the conversation with the
physician, it was scored as having no problem.
Associated risk factors
A moderate negative association was found between swallowing function at BSE and
number of days in hospital (r=-0.471, p=0.01) Figure 2a, and number of days in the ICU (r=-
0.48, p=0.01) Figure 2b, and also needing nutritional support at discharge (r=-0.445, p=0.02).
There was a moderate association between FOIS at baseline and whether you were
discharged home or to rehabilitation clinic (r-0.541, p=0.004). No significant associations
were found between FOIS level at baseline and age, BMI, number of days intubated, prone
position, CFS or having had a tracheostomy (p>0.05).
11
Discussion
This longitudinal cohort study found that dysphagia frequency post invasive mechanical
ventilation in patients with COVID-19 was high, with an incidence of 71% requiring
significant nutritional and swallowing interventions. This is in accordance with emerging data
on this patient group [16]. Patients presented most frequently with signs of oral and
pharyngeal muscle weakness at the BSE but also with significant fatigue and delirium,
indicating that the dysphagia was multi-factorial.
Despite the average length of intubation far exceeding the time known to increase the risk of
swallowing dysfunction [5] there was a rapid trajectory of improvement with the majority of
patients (85%) having a full oral intake on one or multiple consistencies at discharge from
hospital to the rehabilitation clinic (Figure 2). This is in accordance with results presented by
Lima et al. [17] where 101 ICU patients diagnosed with COVID-19 were compared to 150
critical ICU patients with prolonged orotracheal intubation (≥ 48 hours) from the same
institution. Dysphagia after prolonged intubation was common in both groups of their study.
However, despite patients with COVID-19 remaining intubated longer than the other group
they had less sustained dysphagia at discharge [17]. Dysphagia post mechanical ventilation
can be multifactorial. It can be the direct result of the underlying problem requiring ICU
admission (medical and/or surgical), but may also be acquired as a result of ICU care [18].
Further studies on the underlying causes of variations in dysphagia resolution are needed.
Frailty was screened on admission using the Clinical Frailty Scale (CFS) [11, 19], validated as a
predictor of outcomes in older people. The CFS is now increasingly being used as a triage
tool to make clinical decisions in the management of COVID-19 patients [19]. A CFS score of
5 is the most widely used cut off point to define frailty (1-3= fit, 4-5= pre-frail and ≥6 frail). In
12
this cohort 25/28 patients were categorized as fit and this might partly explain the rapid
improvement and that no association was found between swallowing dysfunction and age or
number of days invasively ventilated.
In total, 15 patients (57.1%) were completely or in part feeding tube dependent (FOIS 1-3) at
the BSE but at hospital discharge this number had decreased to 4 patients (15%) and the rest
(n=11) were discharged on an oral diet without feeding tube dependency either home or to
specialized rehab. This demonstrates a rapid and progressive improvement in the cohort but
does not provide detailed information regarding swallowing physiology since no
instrumental evaluations were performed.
Emerging data suggests that prone positioning might not have the negative effect on
swallowing that has been hypothesized [20]. If and how it influenced on swallowing function
on this cohort cannot be established due to missing data in the medical charts.
Tracheostomy was performed in 50% of the patients. There was a good success of weaning,
with the majority decannulated before the BSE and all patients decannulated at discharge.
This is in accordance with the case series presented by Cardasis et al [21] where 74% of their
24 patients were decannulated at discharge from hospital. Like theirs, our cohort had a high
baseline level of health with a median Clinical Frailty Score of 3 pre COVID-19.
Although dysphagia was common at bedside evaluation, the prognosis for resolution of
dysphagic concerns seems good and recovery of swallowing function in COVID-19 patients
after invasive mechanical ventilation was high. Only two patients reported some element of
dysphagia at follow up. Contrastingly, 54% (n=12) reported dysphonia and were referred for
SLP evaluation. This is consistent with emerging data from other countries [17, 20].
13
The factors most strongly associated with dysphagia in this cohort: prolonged hospital length
of stay and ICU length of stay, did not differ from the review by Skoretz, Flowers and
Martino or Brodsky et al. [5, 18] However, restrictions in oral intake seemed to resolve faster
in this group of COVID-19 patients.
Strengths and weaknesses
The strengths of this study were the longitudinal design and that patient-related outcome
measures (the 4QT) were collected at follow-up, which is valuable when determining
patients’ perception of their outcome. The study also had several limitations: it is a small
sample size and only patients referred to SLP were included. Swallowing function was only
measured by FOIS and although it is a validated way of estimating the functional eating
ability of a patient, it does not analyse the biomechanical aspects of swallowing which is
important when designing interventions for improving swallowing function. Nor does it take
patients’ subjective perception of swallowing in to consideration. However, oral intake is
probably a more patient-centered and meaningful outcome compared to physiological
swallow measures from the patient perspective, as argued by Regan et al [22]. When using a
clinical judgement in (any) assessment of an impairment, there is always a risk of bias. In this
study we used validated scales such as FOIS and the clinical frailty scale in an effort to
control for inter-rater bias. Finally, follow-up data were based on patient-reported outcome
measures, not a clinician rated scale, which means that there were some inconsistencies in
how swallowing symptoms were expressed.
Conclusion:
In this study, the majority of COVID-19 patients needed precautionary measures to ascertain
a safe oral intake post mechanical ventilation. We therefore recommend that screening of
14
swallowing function is added to the local ICU policies. In circumstances such as these, where
the aerosol generating aspects are uncertain, best practice for assessing swallowing function
in COVID-19 patients is a carefully executed BSE, to avoid further potential stressors on a
reduced lung function.
Significance
The results provide new knowledge regarding prevalence, assessment and outcome for this
new patient group, both to medicine in general and to speech pathology in Sweden. We
have also gained new knowledge about factors associated with swallowing dysfunction.
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15
15. Tsang, K., et al., A New Simple Screening Tool-4QT: Can It Identify Those with Swallowing
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Figure legends
Figure 1. Number of patients with each Functional Oral Intake Scale (FOIS) score at Bedside
Swallowing Evaluation and at hospital discharge.
Figure 2. Scatterplot with regression line depicting the relationship between Functional Oral
Intake Scale (FOIS) level and: a) number of days in hospital and b) number of days in the
Intensive Care Unit (ICU).
16
17
18
Table 1. Demographic and clinical characteristics stratified according to swallowing function at the
Bedside Swallowing Evaluation.
Characteristics
Total
Functional
swallow
FOIS 6-7
Dysphagia,
FOIS 1-5
p-value
N=28
N=8
N=20
Age, years, mean (SD)
61.0 (11.9)
52.9 (15.6)
64.2 (8.5)
0.019
Sex, male. % (n)
79% (22)
88% (7)
75% (15)
0.47
BMI (kg/m2), mean (SD)
30.1 (7.9)
30.7 (10.8)
29.9 (6.7)
0.79
CFS, range 1-5. % (n)
0.44
1
4% (1)
12% (1)
0% (0)
2
21% (6)
25% (2)
20% (4)
3
64% (18)
50% (4)
70% (14)
4
7% (2)
12% (1)
5% (1)
5
4% (1)
0% (0)
5% (1)
Smoking, % (n)
Ex-smoker
35% (9)
38% (3)
33% (6)
Never smoker
58% (15)
62% (5)
56% (10)
Smoker
8% (2)
0% (0)
11% (2)
Prone position, % (n)
57% (16)
38% (3)
65% (13)
0.18
Chronic cardiac disease, % (n)
14% (4)
0% (0)
20% (4)
0.17
Hypertension, % (n)
54% (15)
12% (1)
70% (14)
0.006
Diabetes, % (n)
21% (6)
12% (1)
25% (5)
0.47
Duration of orotracheal intubation, mean (SD)
14.1 (6.5)
9.6 (2.1)
15.9 (6.8)
0.017
Number of days in ICU, median (IQR)
20.0 (14.5)
15.5 (4.5)
28.5 (18.5)
<0.001
Tracheostomy, % (n)
50% (14)
25% (2)
60% (12)
0.094
Days with tracheostomy, mean (SD)
7 (8.6)
1.1 (2.2)
9.4 (9.1)
0.03
Number of days in hospital, median (IQR)
35.0 (25.3)
24.0 (10.3)
46.5 (24.3)
0.003
Number of days from extubation/decannulation to SLP evaluation,
mean (SD)
3.4 (2.6)
4.6 (3.1)
3.0 (2.3)
0.12
Discharged home, % (n)
41% (11)
100% (8)
16% (3)
<0.001
Discharged to rehab, % (n)
59% (16)
0% (0)
84% (16)
<0.001
Diseased, % (n)
5% (1)
0% (0)
8% (1)
0.42
Data are presented as mean (standard deviation, SD), percentage (number) or median (Inter Quartile
Range, IQR). FOIS= Functional Oral Intake Scale. CFS= Clinical Frailty Scale. SLP= Speech Language
Pathologist. Significant p-values are reported in bold.
19
Table 2. Respiratory vitals and swallowing symptoms at SLP evaluation
Parameters
Total
Functional
swallowing
FOIS 6-7
Swallowing
dysfunction
FOIS 1-5
p-value
N=28
N=8
N=20
Respiratory vitals
Breaths per minute
22.6 (4.0)
20.4 (2.2)
23.6 (4.2)
0.053
Oxygen saturation % (SD)
91.8 (17.8)
95.4 (2.2)
90.2 (21.4)
0.50
Oxygen by nasal cannula (n)
64% (18)
11% (3)
54% (15)
0.64
High Flow Nasal Cannula (n)
18% (5)
12% (1)
20% (4)
0.64
Swallowing and voice symptoms
Posterior leak
25% (7)
12% (1)
30% (6)
0.26
Bolus retention
32% (9)
38% (3)
30% (6)
0.28
Multiple reswallows
21% (6)
38% (3)
15% (3)
0.26
Oral muscle weakness
71% (20)
25% (2)
90% (18)
<0.001
Weak mastication
29% (8)
38% (3)
25% (5)
<0.001
Cough
50% (14)
12% (1)
65% (13)
0.035
Wet voice
14% (4)
0% (0)
20% (4)
0.17
Drop in O2 saturation
7% (2)
12% (1)
5% (1)
0.15
Pharyngeal muscle weakness
71% (20)
25% (2)
90% (18)
<0.001
Fatigue
93% (26)
75% (6)
100% (20)
0.020
Dysphonia bedside
96% (27)
100% (8)
95% (19)
0.52
Data are presented as mean (standard deviation, SD) or percentage (number). FOIS=
Functional Oral Intake Scale. SLP= Speech Language Pathologist.
Table 3. Patient-reported symptoms at follow up visit
n=22
None
Mild
Moderate
Dysgeusia (taste)
% (n)
59% (13)
41% (9)
Anosmia
(Smell) % (n)
64% (14)
36% (8)
*Nutritional
problems % (n)
96% (21)
4% (1)
Dysphonia
% (n)
45% (10)
45% (10)
9% (2)
*Difficulty eating and drinking enough, weight loss.