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To compare the comfort of oxygen therapy via high-flow nasal cannula (HFNC) versus via conventional face mask in patients with acute respiratory failure. Acute respiratory failure was defined as blood oxygen saturation < 96% while receiving a fraction of inspired oxygen > or = 0.50 via face mask. Oxygen was first humidified with a bubble humidifier and delivered via face mask for 30 min, and then via HFNC with heated humidifier for another 30 min. At the end of each 30-min period we asked the patient to evaluate dyspnea, mouth dryness, and overall comfort, on a visual analog scale of 0 (lowest) to 10 (highest). The results are expressed as median and interquartile range values. We included 20 patients, with a median age of 57 (40-70) years. The total gas flow administered was higher with the HFNC than with the face mask (30 [21.3-38.7] L/min vs 15 [12-20] L/min, P < .001). The HFNC was associated with less dyspnea (3.8 [1.3-5.8] vs 6.8 [4.1-7.9], P = .001) and mouth dryness (5 [2.3-7] vs 9.5 [8-10], P < .001), and was more comfortable (9 [8-10]) versus 5 [2.3-6.8], P < .001). HFNC was associated with higher P(aO(2)) (127 [83-191] mm Hg vs 77 [64-88] mm Hg, P = .002) and lower respiratory rate (21 [18-27] breaths/min vs 28 [25-32] breaths/min, P < .001), but no difference in P(aCO(2)). HFNC was better tolerated and more comfortable than face mask. HFNC was associated with better oxygenation and lower respiratory rate. HFNC could have an important role in the treatment of patients with acute respiratory failure.
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High-Flow Oxygen Therapy in Acute Respiratory Failure
Oriol Roca MD, Jordi Riera MD, Ferran Torres MD PhD, and Joan R Masclans MD PhD
OBJECTIVE: To compare the comfort of oxygen therapy via high-flow nasal cannula (HFNC)
versus via conventional face mask in patients with acute respiratory failure. Acute respiratory
failure was defined as blood oxygen saturation <96% while receiving a fraction of inspired oxygen
>0.50 via face mask. METHODS: Oxygen was first humidified with a bubble humidifier and
delivered via face mask for 30 min, and then via HFNC with heated humidifier for another 30 min.
At the end of each 30-min period we asked the patient to evaluate dyspnea, mouth dryness, and
overall comfort, on a visual analog scale of 0 (lowest) to 10 (highest). The results are expressed as
median and interquartile range values. RESULTS: We included 20 patients, with a median age of
57 (40 –70) years. The total gas flow administered was higher with the HFNC than with the face
mask (30 [21.3–38.7] L/min vs 15 [12–20] L/min, P<.001). The HFNC was associated with less
dyspnea (3.8 [1.3–5.8] vs 6.8 [4.1–7.9], P.001) and mouth dryness (5 [2.3–7] vs 9.5 [8 –10],
P<.001), and was more comfortable (9 [8 –10]) versus 5 [2.3– 6.8], P<.001). HFNC was associated
with higher P
aO
2
(127 [83–191] mm Hg vs 77 [64 88] mm Hg, P.002) and lower respiratory rate
(21 [18 –27] breaths/min vs 28 [25–32] breaths/min, P<.001), but no difference in P
aCO
2
. CON-
CLUSIONS: HFNC was better tolerated and more comfortable than face mask. HFNC was asso-
ciated with better oxygenation and lower respiratory rate. HFNC could have an important role in
the treatment of patients with acute respiratory failure. Key words: acute respiratory failure; respi-
ratory insufficiency; treatment; oxygen therapy; high-flow nasal cannula. [Respir Care 2010;55(4):408
413. © 2010 Daedalus Enterprises]
Introduction
Administration of oxygen is an essential support mea-
sure to maintain proper tissue oxygenation in patients with
acute respiratory failure (ARF). The conventional oxygen
delivery methods have been nasal prongs, nose mask, and
face mask, but the oxygen provided by the conventional
systems may not suffice in patients with ARF.
High-flow oxygen (up to 50 L/min) via nasal cannula,
combined with a heated humidification system, may have
several advantages. High-flow nasal cannula (HFNC) can
decrease oxygen dilution,
1-3
reduce respiratory dead space,
2
and generate some positive airway pressure, because of the
SEE THE RELATED EDITORIAL ON PAGE 485
expiratory resistance generated by the continuous high flow
delivered.
2,3
The heated humidification can facilitate se-
cretion clearance and decrease the development of bron-
chial hyper-response symptoms.
4
HFNC has been evalu-
ated in healthy subjects,
3
patients with stable chronic
obstructive pulmonary disease,
2
and in patients after ab-
dominal surgery.
1
To our knowledge, the experience with
HFNC in patients with ARF is limited to sporadic cases.
5,6
Oriol Roca MD, Jordi Riera MD, and Joan R Masclans MD PhD are
affiliated with the Intensive Care Medicine Department, Hospital Uni-
versitari Vall d’Hebron (A
`rea General), Barcelona, Spain. Oriol Roca
MD is also affiliated with the Respiratory Medicine Department, Hos-
pital Universitari Vall d’Hebron, Barcelona, Spain, and with Centro de
Investigacio´n Biome´dica en Red de Enfermedades Respiratorias
(CIBERES), Instituto de Salud Carlos III, Spain. Ferran Torres MD PhD
is affiliated with Laboratori de Bioestadística i Epidemiologia, Univer-
sitat Auto` noma de Barcelona, and with Servei de Farmacología Clínica,
Institut d’Investigacions Biome` diques August Pi i Sunyer (IDIBAPS),
Hospital Clínic, Barcelona, Spain.
Dr Roca and Dr Masclans have disclosed relationships with Fisher &
Paykel Healthcare. Dr Riera and Dr Torres have disclosed no conflicts of
interest.
Correspondence: Oriol Roca MD, Servei de Medicina Intensiva (A
`rea
General), Hospital Universitari Vall d’Hebron, Passeig Vall d’Hebron
119-129, 08035 Barcelona, Spain. E-mail: oroca@ir.vhebron.net.
408 RESPIRATORY CARE APRIL 2010 VOL 55 NO4
Thus, the primary aim of this study was to compare the
subjective comfort perceived by ARF patients receiving
oxygen via face mask versus via HFNC, as measured with
a visual analog scale. We previously reported this study in
an abstract.
7
Methods
The manufacturer of the HFNC system we used did not
provide any form of support or consultation in the design,
conduct, or writing of this study.
Study Population
We included 20 patients with ARF, defined as a blood
oxygen saturation (measured via pulse oximetry [S
pO
2
])
96% while receiving humidified oxygen via face mask,
with a fraction of delivered oxygen (F
DO
2
)of0.5. The
exclusion criteria were: unstable clinical status (eg, marked
changes in respiratory variables in the 60 min prior to
inclusion in the study); need for endotracheal intubation;
decreased consciousness (Glasgow coma scale 14); se-
vere hemodynamic instability despite fluid therapy and
vasopressors; severe failure of 2 organs apart from re-
spiratory failure; pregnancy; and lack of patient coopera-
tion.
The study was approved by the ethics committee of our
center, and patients gave their informed consent to partic-
ipate.
Study Design
This was a prospective, comparative study of sequential
interventions. The patients were resting in bed in partial
sitting position, and we recorded baseline respiratory vari-
ables. The oxygen was humidified with a bubble humidi-
fier (Respiflo Water and MN Adapter, Tyco Healthcare,
Gosport, United Kingdom) and administered via standard
face mask (Oxinova, Carburos Medica, Spain) for 30 min,
during which the patient was allowed to use a combination
of face mask and conventional nasal cannula to increase
the total oxygen flow, in which case the total flow deliv-
ered was the sum of the flow from the face mask and
cannula.
We then delivered the oxygen via HFNC (Optiflow,
Fisher & Paykel, Auckland, New Zealand) (Fig. 1) at an
initial flow of 20 –30 L/min, with an F
DO
2
identical to that
with the face mask. The total flow was increased in each
patient according to the criteria of the attending physician.
The same F
DO
2
was maintained over the entire testing
period.
For both face mask and HFNC, F
DO
2
was estimated
following the manufacturer’s specifications.
At the end of each 30-min period we asked the patient
for his or her subjective assessment of the device (see
below) and took a sample of arterial blood. Following the
two 30-min study periods we asked the patient which of
the oxygen systems he or she wanted to continue using.
Variables Measured
We recorded the Sequential Organ Failure Assessment
8
at the time of enrollment, and the Acute Physiology and
Chronic Health Evaluation score
9
at intensive care unit
(ICU) admission. We defined multiple-organ dysfunction
syndrome as failure of 2 organs. We estimated the
degree of radiologic involvement as the number of af-
fected quadrants on the chest radiograph.
10
Throughout the
study periods we monitored electrocardiography variables,
blood pressure, respiratory variables, and adverse events
related to the use of the oxygen therapy systems.
We asked each patient to subjectively evaluate the 2
oxygen therapy methods, after 30 min of use in stable
conditions. With a visual analog scale that ranged from 0
(lowest) to 10 (highest), we asked the patient to rate his or
her dyspnea, mouth dryness, and overall comfort.
11
We also measured arterial blood gas values, acid-base
balance, respiratory rate, and S
pO
2
.
Statistical Analysis
The estimated sample size was 20 patients to achieve a
statistical power of 80% for detecting that an observation
Fig. 1. Diagram of the high-flow nasal cannula. A: Compressed air
source. B: Oxygen source. C: Heated humidifier. D: Nasal cannula.
HIGH-FLOW OXYGEN THERAPY IN ACUTE RESPIRATORY FAILURE
RESPIRATORY CARE APRIL 2010 VOL 55 NO4 409
in one group was lower than in the other, at a probability
of 0.756, with the Mann-Whitney non-parametric test for
independent data, with a protection against type 1 error of
5% bilaterally. Since the study design is actually for de-
pendent data, it was expected that the statistical power
would be higher, according to the correlation found.
12
The results are expressed as the median and interquar-
tile range values, or frequencies (percentage). We com-
pared the results with the Wilcoxon non-parametric test.
The analyses were conducted with statistics software (SPSS
version 13.0, SPSS, Chicago, Illinois). Significance was
set at a 2-tailed Pvalue of .05.
Results
General Characteristics
Twenty patients were included. Fourteen (70%) were
men. The median age was 57 (40 –70) years. Table 1 shows
the cohort’s baseline characteristics. Nineteen patients
(95%) were admitted to the ICU due to hypoxemic ARF.
The median duration of ARF before inclusion in the study
was 4 (3– 8) days.
Subjective Assessment and Respiratory Variables
The results of the subjective assessment show a signif-
icant improvement in the 3 variables analyzed with the use
of HFNC (Table 2). In the evaluation of respiratory vari-
ables, there were no significant differences between the
baseline values and those at the end of 30 min of face
mask use. However, with HFNC there was a significant
increase in P
aO
2
and a reduction in respiratory rate (Fig. 2),
without hypercapnia or acidosis. Arterial blood samples
were not obtained from the 4 patients who did not have
arterial catheters. There was no significant change in mean
arterial pressure or heart rate. Once the testing period had
been completed and the patients were asked to choose
which of the 2 oxygen therapy systems they wanted to
continue using, all chose the HFNC.
Adverse Effects
Five patients (25%) reported some mild adverse effects
that may have been related to the HFNC. The most com-
mon (3 patients) was a sensation of cervical-thoracic dis-
comfort that appeared during the initial period of increas-
ing flow, and immediately disappeared when flow was
decreased. Another patient said that the gas temperature
was too high. In all the latter cases the effects appeared in
the initial few minutes of the testing period and had com-
pletely disappeared by the end of the testing period. The
other patient who reported an adverse effect had nonspecific
nasal discomfort, and nasal mucosal lesions were detected
during HFNC use. On the other hand, mucosal lesions were
seen before HFNC in another patient, probably related to the
previous use of conventional nasal cannula.
Discussion
This study presents the first results of applying humid-
ified HFNC in patients with ARF. HFNC was associated
with less dyspnea and mouth dryness, and greater overall
comfort.
The dyspnea decrease may be due to several factors.
With HFNC the higher flow delivered, the correction of
hypoxemia, and the reduction in the respiratory rate may
play an important role. Second, although there was signif-
icantly less mouth dryness, this variable was likely to have
continued improving after the 30 min of the study, because
30 min may have been too short to determine the true
effects of the heated humidification system on mouth dry-
ness. Third, the patients found HFNC significantly more
comfortable, and there may be several reasons for this.
The above-mentioned benefits surely played a part. Under-
humidified oxygen therapy is also associated with discom-
fort in critically ill patients.
13
That HFNC does not affect
speaking and allows food ingestion could also play a role.
This increased comfort is consistent with the fact that all
the patients chose to continue with HFNC after having
tried it.
Table 1. Baseline Characteristics
Patients (n)20
Age (median and IQR y) 57 (40–70)
Male (n, %) 14 (70)
APACHE II score (median and IQR) 14.0 (10.5–17.5)
SOFA score (median and IQR) 4.0 (3.2–6.0)
Multiple organ dysfunction syndrome (n, %) 4 (20)
Intrapulmonary ARF (n, %) 17 (85)
Extrapulmonary ARF (n, %) 3 (15)
Etiology of ARF (n,%)
Pneumonia 13 (65)
Extrapulmonary ALI 3 (15)
Acute lung-graft rejection 1 (5)
Severe asthma exacerbation 1 (5)
COPD exacerbation 1 (5)
Cardiogenic lung edema 1 (5)
Duration of ARF before inclusion
(median and IQR)
4 (3–8)
Number of affected quadrants on chest
radiograph (median and IQR)
3 (2–4)
APACHE II Acute Physiology and Chronic Health Evaluation II
SOFA Sequential Organ Failure Assessment
ARF acute respiratory failure
ALI acute lung injury
COPD chronic obstructive pulmonary disease
HIGH-FLOW OXYGEN THERAPY IN ACUTE RESPIRATORY FAILURE
410 RESPIRATORY CARE APRIL 2010 VOL 55 NO4
We assessed the variables studied with visual analog
scales. These scales are solid, well recognized systems
for measuring patients’ perceptions of variables such as
dyspnea.
14-18
In fact, the visual analog scale is consid-
ered the most appropriate instrument for repeated mea-
surement of a subjective variable in a given patient, as
it is sufficiently sensitive to detect changes occurring
minute by minute.
19
The effect of HFNC on oxygenation is equally im-
portant. As compared to the conventional oxygen mask,
we found improvement in oxygenation after 30 min of
HFNC. We did not measure fraction of inspired oxygen
(F
IO
2
) because that would have required placing a pha-
ryngeal catheter, which might have generated artifacts
in the subjective evaluations. However, the oxygenation
improvement with HFNC might have been due to a
higher F
IO
2
achieved with the higher flow with HFNC.
At low flow the oxygen is diluted with ambient air
because the oxygen flow is lower than the patient’s
inspiratory flow demand. Wettstein et al
20
measured the
F
IO
2
in the pharynx during nasal cannula at low flow
(1– 6 L/min) and high flow (6 –15 L/min). There was a
progressive increase in pharyngeal F
IO
2
with each in-
crease of oxygen flow. That study analyzed only flows
up to 15 L/min, but the present study shows how this
effect may persist and possibly increase with higher
flow in patients with ARF.
Nevertheless, with a given F
IO
2
, other factors may
contribute to improved oxygenation with HFNC. First,
continuous high flow can wash-out exhaled air from the
upper airway and thus reduce dead space.
2
Second, na-
sal cannula seems to be better tolerated than face mask,
which has been reported to improve patient adherence
to therapy and oxygenation.
21
Third, the high flow ex-
erts a continuous positive airway pressure in both healthy
Table 2. Subjective Evaluation and Respiratory, Hemodynamic, and Gas-Exchange Data*
Face Mask HFNC P
Subjective Evaluation
Dyspnea 6.8 (4.1–7.9) 3.8 (1.3–5.8) .001
Mouth dryness 9.5 (8.0–10.0) 5 (2.3–7.0) .001
Overall comfort 5.0 (2.3–6.8) 9.0 (8.0–10.0) .001
Respiratory and Gas-Exchange Variables
Total oxygen flow (L/min) 15.0 (12.0–20.0) 30.0 (21.3–38.7) .001
Fraction of delivered oxygen 1.0 (0.8–1.0) 1.0 (0.8–1.0) .32
Respiratory rate (breaths/min) 28 (25–32) 21 (18–27) .001
pH
7.42 7.38–7.47 7.44 (7.38–7.50) .06
P
aO
2(mm Hg)
77 (64–88) 127 (83–191) .002
P
aCO
2(mm Hg)
37 (33–45) 37 (32–43) .51
HCO
3
(mmol/L)
25.0 (22.1–28.5) 24.5 (22.2–29.1) .09
Base excess (mmol/L)
1.0 (2.3–4.8) –1.0 (–2.3 to 5.3) .055
S
pO
2(%) 95 (91–97) 98 (96–99) .002
Hemodynamic Variables
Mean arterial pressure (mm Hg) 87 (76–94) 86 (71–93) .36
Heart rate (beats/min) 94 (77–112) 85 (73–108) .99
* All values are median and interquartile range.
† Only in patients with an arterial catheter.
HFNC high-flow nasal cannula
SpO2blood oxygen saturation measured via pulse oximetry
Fig. 2. Change in respiratory rate with change from face mask to
high-flow nasal cannula (HFNC).
HIGH-FLOW OXYGEN THERAPY IN ACUTE RESPIRATORY FAILURE
RESPIRATORY CARE APRIL 2010 VOL 55 NO4 411
volunteers and patients with chronic obstructive pulmo-
nary disease,
3
who additionally showed an increase in
exercise capacity. The airway pressure generated is di-
rectly related to the flow administered; tracheal pressure
of up to 5 cm H
2
O has been recorded with a flow of
50 L/min.
3
In the present study, however, airway pres-
sure was not measured. Moreover, the reported effect
was observed with higher flows than we used in the
majority of patients in this study. Thus, it is unlikely
that a continuous positive airway pressure effect would
have contributed to improved oxygenation in our pa-
tients.
Also, the heated humidifier system may indirectly
affect oxygenation. Active humidification improves
mucociliary function, facilitates secretion clearance,
and decreases atelectasis formation, which improves
ventilation-perfusion ratio and oxygenation. However,
in the present study it is unlikely that those factors
could have affected oxygenation after only 30 min. On
the other hand, heated humidification systems may at-
tenuate the development of bronchial hyper-response
symptoms,
4
so humidified HFNC may be particularly
beneficial in patients with respiratory infection, chronic
obstructive pulmonary disease, or bronchial asthma.
The pronounced reduction in respiratory rate in the
present study is also important, particularly because it
was not associated with changes in the P
aCO
2
or pH. This
finding is consistent with other reported data
1,2
and may
have contributed to the improvement in dyspnea and
comfort.
There were some adverse effects with HFNC, but
several points should be taken into account when inter-
preting these results. First, all the adverse effects from
HFNC were mild. Second, the sensation of cervical-
thoracic discomfort disappeared when the flow was de-
creased. In addition, outside the testing period we found
that higher flows could be achieved with HFNC with no
cervical-thoracic discomfort. Similarly, the feeling of
excessive gas temperature, reported by one patient, also
disappeared during the testing period. Third, some of
the patients received oxygen at the beginning of the
study with a combination of face mask and conventional
nasal cannula. Therefore, the nasal mucosal lesion dis-
covered during HFNC could have been the result of an
additive effect of both systems, as suggested by the fact
that such a lesion was observed in one patient before
HFNC. Therefore, we believe that HFNC could be con-
sidered comfortable, especially given that after the test-
ing period all the patients chose to continue with HFNC.
Limitations
First, we did not use a randomized design; instead, pa-
tients were allowed to choose which of the 2 oxygen ther-
apy systems they wanted to continue with. Second, we
could not quantify the relative contribution of each factor
involved in the HFNC system (nasal cannula, high flow,
warm gas, humidification) to the results obtained. Third, in
an attempt to avoid generating artifacts in the subjective
evaluation, we did not measure the F
IO
2
. Fourth, the pa-
tients could not be blinded to the systems being tested.
Nevertheless, these limitations do not detract from the
favorable results obtained with HFNC in patients with
ARF in a study whose main objective was to compare the
comfort of the 2 oxygen systems.
Conclusions
HFNC can improve the clinical tolerance of oxygen
therapy in patients with ARF. In addition to the subjective
benefit, our patients showed improved oxygenation and a
reduced respiratory rate. Thus, we consider this HFNC
system useful for integrated treatment of ARF, although
further investigation is needed to determine the clinical
scenarios in which its benefits will have the greatest im-
pact.
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... facial total é semelhante à das máscaras oronasais, não comprometendo sua escolha e aplicação (6) . pacientes bem avaliados (26) . ...
... (13,31) . (26) . Em face de comprometimento da ventilação e perfusão pulmonar, desde a era moderna, tem sido administrado para aumentar a pressão parcial alveolar de oxigênio (PaO2) (32) . ...
... A cânula nasal de alto fluxo foi primeiramente e tem sido extensamente descrita em população pediátrica e neonatal, mas apenas nos últimos anos grandes trabalhos randomizados foram realizados em adultos, demonstrando que os principais benefícios de seu uso durante a insuficiência respiratória aguda hipoxêmica são a diminuição da frequência respiratória, taxa de reintubação e da mortalidade em 90 dias (26) . (29,30) . ...
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A cirurgia cardíaca é um dos procedimentos cirúrgicos mais realizados em todo o mundo, sendo registrados em torno de 6 milhões de casos anualmente. Suas complicações pulmonares são frequentes, resultando em aumento do tempo de internação hospitalar, dos custos e da morbidade perioperatória. A interrupção completa da ventilação artificial invasiva deve ser feita assim que possível, evoluindo para extubação orotraqueal. Entretanto, sinais e sintomas de agravo do quadro respiratório podem aparecer, recomendando o emprego de VNI como forma terapêutica. Atualmente, a diversidade de interfaces para o uso de VNI, além de recursos, tais como, CNAF e a oferta de CPAP por capacetes, precisam de mais estudos em indivíduos submetidos a cirurgia cardíaca. Através da metodologia de revisão da literatura em bases de dados validadas, identificou-se os principais recursos utilizados para a terapia em questão, compreendendo seus potenciais e limitações. A escolha mais frequente da máscara facial e da máscara facial total foi evidente. A primeira, pelo baixo custo e tempo de uso em práticas clínicas com fortes evidencias. E a segunda, pela capacidade de gerar mais conforto e consequentemente maior adesão. A CNAF mostra-se eficiente em quadros de hipoxemia, que é uma das complicações mais frequentes desta cirurgia, podendo manter uma PEEP variável pelo fluxo. Quanto ao capacete, possui características únicas, proporcionando uma CPAP contínua através do fluxo elevado. Seu conforto é questionável e os resultados em pós-operatório são animadores. Conclui-se que, os efeitos conhecidos da pressão positiva elevam o grau de recomendação da terapia. A escolha criteriosa do recurso é vital, devendo-se considerar os efeitos fisiológicos e a capacidade de adaptação do paciente. Capacetes e CNAF podem ser indicados, porém, são escassos os estudos para este grupo.
... Thus, they require an additional management approach to improve their daily functions. Recently, the efficacy of a high-flow nasal cannula (HFNC) has been found in patients with acute exacerbations of respiratory failure, and it became available for home use in Japan in April 2022 [4][5][6]. However, there are few studies demonstrating the efficacy of home visit rehabilitation for patients who use HFNC at home. ...
... The initial goal was to increase sitting time during home oxygenation while partially discontinuing HFNC. It had a risk of increased carbon dioxide retention and dyspnea caused by hypoxemia [4][5][6]. In addition, the patient had chronic heart failure, which exacerbated dyspnea. ...
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A high-flow nasal cannula is used as the primary therapy for patients with respiratory failure. Its effectiveness, however, is contingent upon proper patient monitoring by trained healthcare professionals. The case report highlights the benefits of home nursing and rehabilitation in an 81-year-old woman with rheumatoid-related interstitial pneumonia (complicated by drug-induced interstitial pneumonia) who developed respiratory failure. She lived at home with her family while undergoing high-flow therapy. At the outset of the home visit care, she was bedridden, had an indwelling urinary catheter, ate with assistance, and had to wipe her entire body because she could not bathe. Five months after receiving home visit care, she was able to use a portable toilet. However, she was unable to walk because of dyspnea and muscle weakness. She then went through five months of home visit rehabilitation before being able to move around her home with a walker. In addition, she was able to ride out in the back seat of her husband's car. Her quality of life improved as her daily activities improved, and she was able to participate in leisure activities. This experience suggests that home visit rehabilitation may be beneficial in promoting outdoor activities in patients with interstitial pneumonia caused by severe respiratory failure.
... Optimising the management of ARF to improve survival is a key priority for clinicians. Non-invasive respiratory support therapy (NIRS) such as conventional oxygen therapy (COT), high-flow nasal oxygen (HFNO), and non-invasive ventilation (NIV) are important respiratory supports that may be delivered in medical wards to adults with ARF outside of intensive care units and emergency departments [3,4]. Of these supports, conventional oxygen therapy (COT) is the cornerstone of management for hypoxaemia associated with ARF. ...
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Background/Objectives: Conventional oxygen therapy (COT) is the cornerstone of management for hypoxaemia associated with acute respiratory failure (ARF) in wards. COT implementation guidance is provided in local health guidance documents (LHGDs). This study aimed to identify ward-delivered adult COT implementation LHGDs in Australian health services and assess their content and accuracy. Methods: A scoping review was conducted on 1 May 2022 and updated on 19 December 2023 to identify public health services COT LHGDs. Data were extracted and analysed regarding COT initiation, monitoring, maintenance and weaning, and management of clinical deterioration. Results: Thirty-seven included LHGDs, and eleven referenced the Australian COT guidelines. A definition in the LHGDs for hypoxaemia is that any oxygen saturation (SpO2) or arterial blood gas (ABG) is rare. None required ABG prior to COT initiation. Twenty-nine provided target SpO2 aims for initiation and maintenance. Fifteen did not specify the criteria for clinical review. Nine LHGDs provided guidance on weaning. Conclusions: There was considerable variation in the structure and content of COT LHGDs in Australian health services. Variations and limited guideline concordance of LHGDs may impact the quality and safety of health care. Considerations for future research include the development and implementation of standardised core LHGD recommendations for COT, as well as conducting a national oxygen audit to better measure and benchmark the safety and quality of care.
... We have observed a statistically significant HR within 2 hours of application of HFNC therapy. Roca et al. 20 examined IVC collapse during inspiratory pause by echocardiography in subjects with NYHA class III hear failure. HFNC decreased the inspiratory collapse of IVC, and it suggested that HFNC was supportive for subjects with severe heart failure. ...
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The aim of our study was to determine whether high flow oxygen therapy reduced the rate of endotracheal intubation and improve pulmonary outcome score. A total of 300 consecutive patients were enrolled in the study. The etiologies of acute respiratory failure were classified into trauma, lung diseases, fluid overload states and undifferentiated. Patients were randomized by block randomization method into two groups. First group received HFNC while the second received conventional oxygen therapy. Patients in both the groups were escalated to either NIV or invasive mechanical ventilator support if there were any signs of respiratory distress noted. Pulmonary outcome scoring done at 2 hours was designed to see if there was any improvement in patient’s condition in both the groups. SPSS (version 21.0, Illinois, Chicago) was used for the statistical analysis. The partial pressures of oxygen improved significantly in the HFNC group as compared to the COT group irrespective of the etiology. The partial pressures of CO2 on ABG were similar in both the groups until 12 hrs. However, pCO2 was earlier reduced in the HFNC group as compared to the COT group. Steady decrease in serum lactate levels were observed in HFNC group. The base deficit was corrected between 6-12 hours in patients of HFNC group which could not be seen in patients of COT group. There was a statistically significant difference noted at 12 and 24 hours between the two groups. The mean length of stay in HFNC group was around 4 days which was less compared to the length of hospital stay in COT which was an average of 7 days. The mortality in HFNC group was 4% and in COT group was 7.33% in our study. The study demonstrated that the use of HFNC in ED patients presenting with AHRF was associated with a greater reduction in need for escalation of ventilation requirements and improves pulmonary outcomes compared with standard oxygen therapy.
... This results in dryness of nasal mucosa and interfere with mucociliary clearance which cause discomfort to patient, increases chance of infection, might increase respiratory effort, and increases the chance for intubation. 8,9 Thus, a prospective observational study was designed to evaluate the outcome of improvised bCPAP for the treatment for RDS and to identify the factors associated with its failure. By analyzing the outcomes and potential factors contributing to success or failure, the study aimed to shed light on the use of this low-cost and easily accessible alternative in managing RDS in resource-limited settings. ...
... HFNT is an oxygen therapy which can deliver warmed, humidified oxygen with a fraction of inspiratory oxygen (FiO 2 ) up to 1, and a maximum flow of 60 L/min. HFNC has several physiological advantages: lung alveolar recruitment due to the generation of positive end-expiratory pressure (3-5 cmH 2 O), CO 2 washout from the upper airway with a reduction in anatomic dead space [50], enhanced secretion clearance and expectoration [51], flow-dependent unloading of respiratory muscles based in part on the match between patient's inspiratory needs, and the amount of the flow rate provided by the system. ...
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The management of patients with life-threatening respiratory disease in the ICU and at home has become increasingly of interest over the past decades. Growing knowledge supports the use of NRS, aimed at improving patient comfort and improving quality of life. However, its role during palliative care is not well defined, and evidence of support remains limited. The aim of this narrative review is to examine the recent evidence relating to the use of non-invasive respiratory support at the end of life, in order to clarify who benefits and when. The literature research was conducted on PubMed, using MeSH words. A review of the relevant literature showed that non-invasive respiratory support techniques for patients with life-limiting respiratory disease vary (from high-flow oxygen therapy to conventional oxygen therapy, from CPAP to NPPV) and each has precise indications. To date, from the hospital to the home setting, the monitoring and application of these respiratory support techniques have varied widely. In conclusion, the choice of respiratory support in this category of patients should be based on the technique that will optimize the comfort of the patient and improve the quality of their life. On the other hand, regarding monitoring, both telemedicine and ultrasound diagnostics help to satisfy the patient’s wish to spend the last period of his life in the home environment, to avoid inappropriately aggressive diagnostic interventions, and to reduce the high costs of hospitalized procedures in this category of patients.
... With the outbreak of COVID-19, concerns were raised about choosing the appropriate approach to manage patients' hypoxia. Among oxygen delivery methods, HFNC is more tolerable for patients with severe respiratory failure [11]. The alveolar membrane is a structure that optimizes respiratory conditions through the isotherm of body heat (37° C) and breathing air [12]. ...
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Background: The effect of using high flow oxygen delivery through the nasal cannula (HFNC) in COVID-19 patients has been associated with different results. This study aimed to evaluate the effect of different HFNC temperatures in COVID-19 patients. Methods: Patients were randomly divided into three groups under high current oxygenation with temperatures of 31, 34, and 37. Except for the temperature, other device settings were set equally. After 24 hours, clinical conditions were on the agenda and compared with the conditions before the intervention. Results: Fever, sore throat, malaise, diarrhea in patients of 31 degree group and indicators of nausea, cough, body pain, headache have changed the most in 37 degree group. Abdominal pain has shown the greatest change in the 34 degree group. PR, DBP, and SpO2 indices changed the most at 31 degrees and RR and SBP at 37 degrees. PR, RR, SBP and SPO2 indices showed significant values in intra-group comparison, and in inter-group comparison, only PR, RR indices had significant differences. In intra-group analysis, PaCO2, WBC, CRP, ESR and ferritin had significant changes, and in inter-group comparison, none of the indicators had significant differences. Conclusion: Based on the results of the present study, reducing the temperature in the use of HFNC can improve the clinical conditions of patients with COVID-19.
... In the intensive care setting, HFNCs are the standard of care in patients with severe hypoxemia [5]. ...
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Background: While high-flow nasal cannulas (HFNCs) represent the standard of care in the intensive care unit for patients with severe hypoxemia, its use in homecare settings is uncommon despite its potential. The potential benefits and challenges of the high-flow nasal cannula (HFNC) in homecare settings compared to standard long-term oxygen via nasal low-flow therapy are unclear. Methods: We conducted a prospective monocentric feasibility study at the Department of Respiratory Medicine, University Hospital, Goethe University Frankfurt, Germany. Patients with interstitial lung disease or severe bronchiectasis (including cystic fibrosis) were enrolled into the study. The HFNC was introduced during hospitalization. The patients’ compliance with home use advice and arterial blood gas results were evaluated at a 4–6-week follow-up. Results: A total of 12 patients were analyzed. HFNC initiation did not result in a significant improvement of the pO2/fiO2 (p/f) ratio. Only 8 out of 12 (66.6%) patients used the HFNC at home after the initial in-hospital initiation. Only 7 of the total 12 patients were using the therapy at a follow-up 3–6 weeks after HFNC onset. Two patients died during the observation, resulting in a surveillance mortality rate of 16.7%. Conclusions: The feasibility data showed low adherence to the HFNC at home. The lack of any positive effect on the p/f ratio may be due to low airflow rates and overall mild hypoxemia compared to patients with severe respiratory failure in the ICU.
Article
Introduction The primary clinical presentation of the COVID-19 pandemic is severe acute respiratory illness. The primary management strategy for COVID-19 patients is supportive care. In the early times of the pandemic, there was uncertainty regarding the use of high-flow nasal cannula (HFNC) among COVID-19 patients in the Western communities, thus increasing early intubation rates and potentially associated harms such as sedation complications and prolonged intensive care unit stay. In June 2020, HFNC was introduced in Johns Hopkins Aramco Healthcare as the primary supportive therapy to manage hypoxemic COVID-19 patients and to minimize the risks associated with endotracheal intubation. Methods We have performed a retrospective study design for subjects treated for acute hypoxemic respiratory failure secondary to COVID-19 and managed with HFNC. Patients included in the study if they were 14-year-old or older, had a laboratory-confirmed diagnosis of COVID-19 by polymerase chain reaction testing, and were treated with HFNC for at least 6 h. Patients were excluded if endotracheal intubation was performed before initiation of HFNC, required elective intubation or patient on do-not-resuscitate status. Patients on alternation modality between HFNC and noninvasive ventilation (NIV) were subgrouped in data analysis. Results During the study period between May 31, 2020, and November 31, 2020, our search identified 122 subjects with respiratory failure secondary to COVID-19 who required the use of HFNC, 18 patients were excluded due to the exclusion criteria, 50 patients were started on, improved and weaned off HFNC, 30 patients were on alternation modality between HFNC and NIV, improved and weaned off and 24 patients failed HFNC and got intubated. Conclusions In this retrospective study, utilizing HFNC in subjects with hypoxemic respiratory failure related to COVID-19 was found to be effective to reduce the intubation risk by 76.9%.
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Introduction Acute respiratory failure is a life-threatening condition frequently found in the emergency department. High-flow nasal oxygen (HFNO) is increasingly used in emergency departments for patients with hypoxaemic acute respiratory failure. However, despite the increasing number of studies, its potential advantages regarding the need for therapeutic escalation and mortality have not been precisely evaluated. Our objective is to compare conventional oxygen therapy to HFNO when they are initiated during the first hour following the patient’s arrival at the emergency department, with the hypothesis that HFNO would reduce the need for ventilatory therapy escalation. Methods and analysis This is a multicentric, prospective, open and randomised superiority study. 500 inpatients will be randomised (1:1) to receive conventional oxygen therapy or HNFO. The primary outcome is a failure in the oxygen therapy defined as the need for a therapeutic escalation within 4 hours after therapy initiation. Ethics and dissemination The study has been submitted and approved by the Comité de Protection des Personnes Nord Ouest IV (20 October 2020). As required, a notification was sent to the Agence nationale de sécurité du médicament et des produits de santé (22 October 2020). The research results will be published in peer-reviewed publications and presented at international conferences. Trial registration number NCT04607967 .
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This paper presents the form and validation results of APACHE II, a severity of disease classification system. APACHE II uses a point score based upon initial values of 12 routine physiologic measurements, age, and previous health status to provide a general measure of severity of disease. An increasing score (range 0 to 71) was closely correlated with the subsequent risk of hospital death for 5815 intensive care admissions from 13 hospitals. This relationship was also found for many common diseases.When APACHE II scores are combined with an accurate description of disease, they can prognostically stratify acutely ill patients and assist investigators comparing the success of new or differing forms of therapy. This scoring index can be used to evaluate the use of hospital resources and compare the efficacy of intensive care in different hospitals or over time.
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We used a high-flow nasal cannula with a patient who required a high fraction of inspired oxygen but could not tolerate a nasal or facial mask. We saw a 92-year-old woman with delirium and dementia in the intensive care unit for multi-lobar pneumonia with severe hypoxemia. Attempts to oxygenate the patient failed because she was unable to tolerate various facial and nasal masks. We then tried a high-flow nasal cannula (Vapotherm 2000i), which she tolerated well, and she had marked improvement in gas exchange and quality of life. The patient had severe health-care-associated pneumonia, accompanied by delirium and hypoxemia. It became apparent that the patient's death was imminent, and the goal of therapy was palliative. She had previously clearly expressed a desire not to undergo intubation and mechanical ventilation. In a situation where the patient was agitated and unable to tolerate a mask, the high-flow cannula reduced her agitation and improved her dyspnea, oxygenation, tolerance of oxygen therapy, and comfort at the end of life. Oxygen via high-flow cannula may enhance quality of life by reducing hypoxemia in patients who are unable to tolerate a mask but need a high oxygen concentration.
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We report the first case of a patient with severe acute respiratory failure who underwent fibrobronchoscopy with oxygen administration provided by high-flow nasal cannula. We present the case of a patient with severe myasthenia gravis who was admitted to the Department of Intensive Care Medicine of our hospital with severe acute respiratory failure. The muscle weakness inherent to the patient's underlying condition made expectoration of respiratory secretions difficult and led to the development of bilateral atelectasis. Non-invasive mechanical ventilation sessions were established, but there was no significant clinical improvement; hence, oxygen administration by humidified high-flow nasal cannula (Optiflow™, Fisher & Paykel, New Zealand) was decided. The patient experienced a subjective improvement, a decrease in respiratory rate, and an improvement in oxygenation, which, following appropriate premedication, allowed diagnostic–therapeutic bronchoscopy to be performed at bedside, without requiring endotracheal intubation or mechanical ventilation for the procedure. The improvement experienced by the patient with high-flow nasal cannula, following appropriate premedication, allowed diagnostic–therapeutic bronchoscopy to be performed.
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The article discusses the problem of determining the number of observations required by some common nonparametric tests, so that the tests have power at least 1 – β against alternatives that differ sufficiently from the hypothesis being tested. It is shown that the number of observations depends on certain simple probabilities. A method is suggested for fixing the value of the appropriate probability when determining sample size.
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To measure (1) the discomfort in non-intubated patients under high-flow oxygen therapy (HFOT) humidified with bubble (BH) or heated humidifiers (HH), and (2) the hygrometric properties of oxygen with a BH and an HH. This was a randomized cross-over study in critically ill patients during a 3-day period. The humidification device used at days 1 and 3 was changed for the other at day 2. (2) It was also an experimental bench study using the psychrometric method with five randomized flows (3, 6, 9, 12 and 15 l/min) and different humidification techniques. Discomfort, particularly dryness of the mouth and throat, was measured for two humidification conditions (BH and HH) using a 0-10 numerical rating scale (NRS) by patients requiring HFOT with a face mask at a flow >/=5 l/min, in a double-blinded condition. (1) In this clinical study, 30 patients treated by HFOT at a median flow of 7.8 l/min (5.1-10.9) were included. The global incidence of moderate (NRS = 4-6) and severe discomfort (NRS = 7-10) was 25 and 29%, respectively. The median intensities of both mouth and throat dryness were significantly lower with the HH than with the BH [7.8 (5.0-9.4) vs. 5.0 (3.1-7.0), P = 0.001 and 5.8 (2.3-8.5) vs. 4.3 (2.0-5.0), P = 0.005, respectively]. (2) In the bench study, the mean absolute humidity measured at an ambient temperature of 26 degrees C with the HH was two times greater than with the BH (30 +/- 1 vs. 16 +/- 2 mg/l, P < 0.05) regardless of the flow rate. Compared to bubble humidifiers, the use of a heated-humidifier in patients with high-flow oxygen therapy is associated with a decrease of dryness symptoms mediated by increased humidity delivered to the patient.
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The measurement of dyspnea during an exercise task provides an opportunity to simulate daily physical activities that lead to breathing difficulty in patients with lung disease. Although the exact stimulus for the sensation of breathlessness is unknown, it is possible to measure dyspnea during exercise by applying the principles of psychophysics to the analysis of various stimulus-response relationships. It is logical to consider that the exercise task, te, work or power production, causes both physiologic and perceptual responses. A 0 to 10 category scale with ratio properties developed by Borg and a visual analogue scale are the most commonly used instruments for rating the severity of dyspnea during exercise. The ratings of breathlessness are generally reliable over time and are sensitive to evaluate an acute intervention in patients with stable respiratory disease. The exercise intensity-dyspnea relationship appears to be the most appropriate stimulus-response relationship for quantifying dyspnea during exercise. Measure what can be measured, make measurable what cannot be measured. Galileo Galilei (1564-1642)
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The purpose of this study was to evaluate the reproducibility of visual analog scale ratings of the effort to breathe (VASe) and the degree of discomfort evoked by breathing (VASd) in patients with chronic obstructive pulmonary disease (COPD) during exercise. Six subjects with moderately severe COPD (FEV1 = 1.12 +/- 0.29 L, FEV1/FVC = 44 +/- 4%) underwent progressive incremental exercise testing to a symptom-limited maximum every week for 8 wk. VASe and VASd were highly correlated in each subject (r = 0.99 +/- 0.01). The slope of the VASd/VASe relationship for all trials in all subjects was not significantly different from 1, indicating that our subjects were rating a common sensation with the two scales. VASe at maximal exercise was reproducible in every subject; the within-subject coefficient of variation (CV) was 6% (range, 2 to 10%) and compared favorably with physiologic indices: 7% (range, 3 to 12%) for oxygen consumption and 10% (range, 5 to 16%) for minute ventilation (VI). In contrast, submaximal VAS ratings were highly variable. At 66% of the maximal work load, the within-subject CV for VASe was 21% (range, 11 to 28%) compared with 6% (range, 4 to 7%) for VO2 (p less than 0.003) and 10% (range, 5 to 16%) for VI (p less than 0.01). VASe correlated linearly with VI and VO2 in all subjects in all trials. However, within an individual subject the slope and position of these relationships varied widely between trials.(ABSTRACT TRUNCATED AT 250 WORDS)
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The purpose of this study was to validate a vertical visual analogue scale (VVAS) as a measure of clinical dyspnea. Concurrent validity was demonstrated by having asthmatics score their dyspnea intensity on both a VVAS and a horizontal visual analogue scale (HVAS), and then measuring their peak expiratory flow rate (PEFR). Correlation between the VVAS and HVAS was r = .97; between the VVAS and the PEFR, correlation was r = -.85, demonstrating the concurrent validity of the VVAS as a measure of dyspnea. Construct validity then was established, using the contrasted-groups approach with repeated measures. Both asthmatics and those with chronic obstructive lung disease (COPD) rated their dyspnea on the VVAS during times of severe and little airway obstruction. The dyspnea ratings at times of severe versus low obstruction were found to be different for both the asthmatic and COPD subjects. The VVAS was shown to have both concurrent and construct validity as a measure of dyspnea.