ABSTRACT

Background: To reveal the potential efficiency of high-flow oxygen therapy in acute pancreatitis complicated with acute respiratory dysfunction compared with conventional oxygen therapy.

Materials and Methods: We retrospectively analyzed 69 patients treated with high- flow oxygen or conventional oxygen therapy, then compared the difference of prime and second outcomes between the two groups.

Results: The High-flow oxygen group had lower intubation rate (25.6% vs 56.7%, P= 0.013) and longer median time to intubation (64.25h vs 7.75h, P<0.001) compared with the conventional oxygen group. High flow oxygen had a stronger effect on improving dyspnea (87.2% vs 56.7%, P=0.006) and regression of respiratory failure (66.7% vs 26.7%, P=0.001). In the univariate and multivariate analyses, high-flow oxygen and APACHE II score were independent predict factors to respiratory failure regression (OR =20.381, P=0.038; OR=36.827, P=0.026). Patients treated with highflow oxygen had shorter intensive care unit stay length (19.5±13.4 vs 7.8±4.7, P=0.009) and early mortality tended to be significantly lower (17.9% vs 40.0%, P= 0.058).

Conclusion: High-flow oxygen is a more effective method for acute pancreatitis complicated with acute respiratory dysfunction than conventional oxygen therapy.

Introduction

Pulmonary complications of acute pancreatitis (AP) characterized by increased permeability of the pulmonary microvasculature and alveolar spaces filled with leaked proteinrich exudate were frequent with morbidity about 75%, [1,2] including acute lung injury (ALI) or ARDS, atelectasis, pleural effusion, alteration in diaphragmatic function, i.e. [3-5]. It usually resulted in a need of endotracheal intubation and mechanical ventilation, in addition, the mechanisms were complex and still to be discovered [6]. It was reported that 30%-60% of death was related to pancreatitis- associated ALI and ARDS [7-9]. Furthermore, nearly one-third of death of acute pancreatitis prior to admission to hospital were associated with ALI [10]. Studies have revealed that acute respiratory dysfunction (ARD) was an independent prognostic factors for hospital mortality in severe acute pancreatitis (SAP) along with the age, chronic health situation, and organ failures, which was associated with 60% of death within first week [11,12]. Therefore, more attention have been paid on treatment of pancreatitis-associated respiratory complications for reducing early death.

HFNC, which is increasingly used in intensive care unit (ICU) and non-ICU wards was considered as an alternative to Noninvasive Positive Pressure Ventilation (NPPV) and conventional oxygen therapy (COT) with better tolerated and decreasing work of breathing [13,14]. It could provide heated and humidified air and reduce airway secretion and atelectasis with high-flow rates of up to 60 L/min as well as high FiO2 from 0.21 to 1.0 [15,16]. Previous studies have revealed that HFNC has the capability of generating low levels of positive end-expiratory pressure and decreasing physiological dead space through flushing expired carbon dioxide into the upper airway [17]. It has been applied to various diseases, including various respiratory failure, cardiogenic pulmonary edema, postextubation, postoperative patients, and infants [15,16,18-20]. However, the efficiency of HFNC in acute pancreatitis is unclear. Our research is intended to illustrate the value of HFNC in acute pancreatitis complicated with acute respiratory failure.

Material and Methods

Trial Design

All acute pancreatitis complicated with ARD admitted to ICU were included in this retrospective study from January 2014 to June 2019. This trial was approved by the ethical committee of our hospital (approval number:KY030-01) and was registered on the Chinese Clinical Trial Registry (www.chictr.org.cn/, registration number: ChiCTR2000029202) and written informed consent was obtained from patients or their families before HFNC treatment.

Patients

Computed tomography (CT) combined with supportive specific laboratory data were used in the diagnosis of AP. All AP were enrolled if they followed one of the following criteria: PaO2/FiO2 < 300 mmHg; respiratory rate > 25/min; dyspnea or accessory muscle use; asynchronous or paradoxical breathing; required >5 L/min O2 to maintain SpO2 >92%.Exclusion criteria: need for immediate intubation, central nervous system disorder, cannot answer questions, contraindications for the use of the mask (noncooperative patient).Patients were asked to grade their dyspnea score [21] (improvement; no change; deterioration) and comfort score [22] (poor; acceptable; good) 1 hour after intervention.

Study Intervention

All patients were treated with COT though face mask or nasal cannula before enrolled. In the COT group, oxygen therapy was applied continuously through face mask or nasal cannula at a flow rate up to 10 liters per minute. The rate was adjusted to obtain SpO2>92% until patients recovered or were intubated. High flow humidified oxygen (37°C and 44mgH2O/L) was delivered continuously through a nasal cannula with Optiflow (Fisher and Paykel Healthcare) with a primal flow rate of 50L/min, a primal FIO2 of 50%, and dynamic adjustments to obtain SpO2>92%. HFNC was switched to COT if SpO2 was ≥95% at ≤5 L/min O2 or the PaO2:FIO2 was at least 300. Intubation and mechanical ventilation decisions were made by the physicians with the criteria: respiratory arrest; respiratory pauses with loss of consciousness or gasping respiration; encephalopathy; cardiovascular instability; unmanageable secretions; respiratory fatigue; refractory hypoxemia (HFNC:SpO2≤ 88% with FIO2 = 100%; COT: SpO2≤88% with at least 10L/min), or respiratory acidosis (pH<7.30 and PaCO2 ≥50mmHg).

Primary and Second Outcomes

The primary outcomes are the early intubation rate, defined as percentage of intubation and mechanical ventilation in 10 days and the median time to intubation from patients enrolled. The second outcome includes changes in physiological parameters as well as arterial blood gases and grade of dyspnea, comfort score, regression of respiratory failure after 1 hour intervention, adverse events (atelectasis, pleural effusion and abdominal distension), early mortality defined as mortality in 10 days and ICU stay length.

Statistical Analysis

The Chi-square test or Fisher test was used in the comparisons for categorical variables while the unpaired Student’s t test or Mann-Whitney U test were performed for continuous variables. The analysis of the data obtained before and after intervention from each patient was made with the paired Wilcoxon test. Variables associated with respiratory failure regression were assessed by univariate and multivariate logistic- regression analyses. Variables suspected to be associated with regression of respiratory failure with a P<0.10 after univariate analysis were accounted into the multivariate analysis. All statistical analyses were performed using IBM SPSS, Version 19.0 (IBM Corp., Armonk, NY, USA) or GraphPad Prism version 6.0 (GraphPad Software Inc., San Diego, CA, USA). A p value (two-tailed) <0.05 was considered statistically significant.

Results

Patients

A total of eighty-one patients with AP were admitted to ICU. Seven were intubated immediately at admission and five did not meet the classification criteria at last. Ultimately, sixty-nine patients were included in this retrospective study. 30 out of 69 were treated with conventional oxygen through nasal cannula or face mask, while 39 were treated with HFNC. Baseline characteristics of patients, including demographic data, severity of illness (APACHE II), etiology, severity of AP (Ranson score and Balthazar score) and associated comorbidities were recorded in Table 1. Vital signs and arterial blood gases before and after enrollment (1h) were collected in Table 2. We also evaluated the incidence of atelectasis and pleural effusion in the two groups by CT.

Primary Outcome

The early intubation rate was 25.6% (10 of 39 patients) in the HFNC group, 56.7% (17 of 30) in the COT group (P=0.013) Table 3, Figure 1. The median time to intubation was 64.25h in the HFNC group, 7.75h in the COT group (P<0.001) Table 3. Meanwhile, we compared the intraabdominal pressure (cm H2O) before intubation of intubated patients in the two groups (HFNC 21.7 vs COT 19.1; P=0.103; not shown).

Changes in Physiological Parameters and Arterial Blood Gases

After 1 hour of intervention, patients treated with HFNC had decreased respiratory rate (breaths/min), heart rate (beats/min) (27 vs 21, P<0.001; 121 vs 104, P=0.008) and increased PaO2 (mmHg) (64 vs 110; P< 0.001), while PaCO2 (mmHg) and PaO2/ FiO2 (mmHg) had no changes (37 vs 42, P=0.087; 189 vs 210, P=0.539) compared with baseline. However, in the COT group, after 1 hour of intervention, respiratory rate, heart rate, and PaO2/FiO2 were similar (30 vs 26, P=0.166; 114 vs 109, P=0.486; 192 vs 201, P=0.142) with baseline, whereas PaCO2 and PaO2 were higher (38 vs 50; P< 0.001; 64 vs 83; P<0.001) Table 2. There was no difference in physiological parameters and arterial blood gases at baseline between the HFNC group and the COT group. Compared with the COT group, patients treated with HFNC had decreased respiratory rates, PaCO2 (21 vs 26, P=0.020: 42 vs 50, P<0.001) and increased PaO2 (110 vs 83, P=0.003) 1 hour after intervention. Patients showed greater improvement in PaO2 in the HFNC group than that in the COT group. (P<0.001) Table 2.

Dyspnea Grade, Comfort Score, and Respiratory Dysfunction Regression

The comfort score was similar between the two groups (P=0.596, Table 2). There was a higher proportion of patients felling improvement in dyspnea in the HFNC group (87.2% vs 56.7%, P=0.006) Figure 2. Improved in respiratory dysfunction was defined as respiratory rate <25/min and improvement in breathing effort, including accessory breathing muscle activity and/or paradoxical breathing. Finally, 34 out of 69 patients (26 in the HFNC group vs 8 in the COT group; P=0.001; Figure 3) got respiratory failure regression 1 h after intervention. In the univariate analysis the following parameters were associated with respiratory failure improvement: APACHE II score, PaO2 at baseline and Oxygen strategies. Higher APACHE II score, lower PaO2 at baseline and conventional oxygen therapy exhibited an increased risk for poorer regression of respiratory failure (OR =12.250, 95% CI 1.268-118.361, P=0.030; OR=8.000, 95% CI 1.252-51.137, P= 0.028; OR=6.429, 95% CI 1.026-40.261, P=0.047). In multivariate logistic-regression analyses, HFNC and APACHE II score were independent predict factors to regression of respiratory failure (OR =20.381, 95% CI 1.177-351.911, P=0.038; OR=36.827, 95% CI 1.529-887.083, P=0.026) Table 4.

Adverse Events and Clinical Outcomes

No significant differences were found for adverse events between the two groups. Early mortality in the HFNC group had trend to be significantly lower than that in the COT group (17.9% vs 40.0%, P= 0.058). Patients treated with COT had much longer ICU stay length (19.5±13.4 vs 7.8±4.7, P=0.009) Table 5.

Discussion

Accumulating research have revealed some advantages of HFNC application in pneumonia-associated respiratory dysfunction, including decreased intubation rate, lower 90-day mortality, and increased ventilator-free days compared with NPPV and/or COT [23-26]. Despite this, COT with a face mask or nasal cannula is still the first-line treatment for those lacking studies about HFNC application in AP associated respiratory dysfunction. However, COT is not able to satisfy some patients with severe hypoxemia. Therefore, to our knowledge, this study illustrated the efficiency of HFNC in acute pancreatitis complicated with acute respiratory dysfunction for the first time. In this study, eliminating the effect of secondary infection on intubation, we compared the early intubation rate and the median time to intubation of the two groups in combination with the pathophysiological characteristics of pancreatitis. Severe acute pancreatitis has two representative phases. The first stage is in the first ten days, with characteristics of the systemic inflammatory response syndrome (SIRS). The second usually comes up during the second week and is marked by infectious manifestations [27]. In the end, we found patients in the HFNC group had a lower early intubation rate and a longer median time to intubation.

We also compared other outcomes, including changes in physiological parameters and arterial blood gases, comfort score, regression of dyspnea and respiratory dysfunction, adverse events, early mortality, and ICU stay length between the two groups and found that first, HFNC was superior to COT in improving dyspnea, decreasing respiratory rate and heart rate, preventing carbon dioxide retention, and had a stronger effect on improving PaO2. However, we did not find a difference in PO2/FiO2 between the two groups, indicating that HFNC could improve PO2 with higher FiO2, but it could not improve physiopathologic changes. Second, HFNC was independently associated with the regression of respiratory dysfunction. Third, the comfort score of HFNC was similar to that of COT. At last, patients treated with HFNC had shorter ICU stay length and lower early mortality. We hypothesize that the reason why the early mortality between the two groups did not reach statistical significance would be due to the limited number of patients in our study. Above all, we would come to the conclusion that HFNC is prior to COT in acute pancreatitis complicated with acute respiratory dysfunction. There are some limitations to our reach. First, this study is a single center with a small number of patients. Second, we did not compare HFNC and NPPV. Hence, in the future, we should compare HFNC, NPPV and COT in multicenter studies with large samples.

Conclusion

HFNC is a more efficient option in acute pancreatitis complicated with acute respiratory failure and may be an alternative treatment to COT.

Declaration of Conflicting Interests

The authors declare that they have no competing interests.

Acknowledgement

So many thanks to Qi HE, PHD, a statistician, for statistical aid.

References

1. Imrie CW, Ferguson JC, Murphy D, Blumgart LH (1977) Arterial hypoxia in acute pancreatitis. Br J Surg 64(3): 185-188.
2. Steinberg W, Tenner S (1994) Acute pancreatitis. N Engl J Med 330(17): 1198-1210.
3. Baron TH, Morgan DE (1999) Acute necrotizing pancreatitis. N Engl J Med 340(18): 1412-1417.
4. Wyncoll DL (1999) The management of severe acute necrotising pancreatitis: an evidence-based review of the literature. Intensive Care Med 25(2): 146-156.
5. Shields CJ, Winter DC, Redmond HP (2002) Lung injury in acute pancreatitis: mechanisms, prevention, and therapy. Curr Opin Crit Care 8(2): 158-163.
6. Pastor CM, Matthay MA, Frossard JL (2003) Pancreatitis-associated acute lung injury: new insights. Chest 124(6): 2341-2351.
7. Andersson R, Andersson B, Haraldsen P, Drewsen G, Eckerwall G (2004) Incidence, management and recurrence rate of acute pancreatitis. Scand J Gastroenterol 39(9): 891-894.
8. McKay CJ, Evans S, Sinclair M, Carter CR, Imrie CW (1999) High early mortality rate from acute pancreatitis in Scotland, 1984-1995. Br J Surg 86(10): 1302-1305.
9. Blum T, Maisonneuve P, Lowenfels AB, Lankisch PG (2001) Fatal outcome in acute pancreatitis: its occurrence and early prediction. Pancreatology 1(3): 237-241.
10. Andersson R, Andren-Sandberg A (2003) Fatal acute pancreatitis. Characteristics of patients never reaching hospital. Pancreatology 3(1): 64-66.
11. Halonen KI, Leppaniemi AK, Puolakkainen PA, Lundin JE, Kemppainen EA, et al. (2000) Severe acute pancreatitis: prognostic factors in 270 consecutive patients. Pancreas 21(3): 266-271.
12. Jaber S, Chanques G, Sebbane M, Salhi F, Delay JM, et al. (2006) Noninvasive positive pressure ventilation in patients with respiratory failure due to severe acute pancreatitis. Respiration 73(2): 166-172.
13. Besnier E, Hobeika S, S NS, Lambiotte F, Du Cheyron D, et al. (2019) High-flow nasal cannula therapy: clinical practice in intensive care units. Ann Intensive Care 9(1): 98.
14. Zemach S, Helviz Y, Shitrit M, Friedman R, Levin PD (2019) The Use of High-Flow Nasal Cannula Oxygen Outside the ICU. Respir Care 64(11): 1333-1342.
15. Roca O, Riera J, Torres F, Masclans JR (2010) High-flow oxygen therapy in acute respiratory failure. Respir Care 55(4): 408-413.
16. Frat JP, Brugiere B, Ragot S, Chatellier D, Veinstein A, et al. (2015) Sequential application of oxygen therapy via high-flow nasal cannula and noninvasive ventilation in acute respiratory failure: an observational pilot study. Respir Care 60(2): 170-178.
17. Dysart K, Miller TL, Wolfson MR, Shaffer TH (2009) Research in high flow therapy: mechanisms of action. Respir Med 103(10): 1400-1405.
18. Rochwerg B, Granton D, Wang DX, Helviz Y, Einav S, et al. (2019) High flow nasal cannula compared with conventional oxygen therapy for acute hypoxemic respiratory failure: a systematic review and meta-analysis. Intensive Care Med 45(5): 563-572.
19. Zhu Y, Yin H, Zhang R, Ye X, Wei J (2019) High-flow nasal cannula oxygen therapy versus conventional oxygen therapy in patients after planned extubation: a systematic review and meta-analysis. Crit Care 23(1): 180.
20. Milesi C, Essouri S, Pouyau R, Liet JM, Afanetti M, et al. (2017) High flow nasal cannula (HFNC) versus nasal continuous positive airway pressure (nCPAP) for the initial respiratory management of acute viral bronchiolitis in young infants: a multicenter randomized controlled trial (TRAMONTANE study). Intensive Care Med 43(2): 209-216.
21. Delclaux C, L'Her E, Alberti C, Mancebo J, Abroug F, et al. (2000) Treatment of acute hypoxemic nonhypercapnic respiratory insufficiency with continuous positive airway pressure delivered by a face mask: A randomized controlled trial. JAMA 284(18): 2352-2360.
22. Gregoretti C, Confalonieri M, Navalesi P, Squadrone V, Frigerio P, et al. (2002) Evaluation of patient skin breakdown and comfort with a new face mask for non- invasive ventilation: a multi-center study. Intensive Care Med 28(3): 278-284.
23. Frat JP, Thille AW, Mercat A, Girault C, Ragot S, et al. (2015) High-flow oxygen through nasal cannula in acute hypoxemic respiratory failure. N Engl J Med 372(23): 2185-2196.
24. Frat JP, Ragot S, Girault C, Perbet S, Prat G, et al. (2016) Effect of non-invasive oxygenation strategies in immunocompromised patients with severe acute respiratory failure: a post-hoc analysis of a randomised trial. Lancet Respir Med 4(8): 646- 652.
25. Coudroy R, Jamet A, Petua P, Robert R, Frat JP, et al. (2016) High-flow nasal cannula oxygen therapy versus noninvasive ventilation in immunocompromised patients with acute respiratory failure: an observational cohort study. Ann Intensive Care 6(1): 45.
26. Sklar MC, Mohammed A, Orchanian-Cheff A, Del Sorbo L, Mehta S, et al. (2018) The Impact of High-Flow Nasal Oxygen in the Immunocompromised Critically Ill: A Systematic Review and Meta-Analysis. Respir Care 63(12): 1555-1566.
27. Werner J, Feuerbach S, Uhl W, Buchler MW (2005) Management of acute pancreatitis: from surgery to interventional intensive care. Gut 54(3): 426-436.

ABSTRACT

Background: To reveal the potential efficiency of high-flow oxygen therapy in acute pancreatitis complicated with acute respiratory dysfunction compared with conventional oxygen therapy.

Materials and Methods: We retrospectively analyzed 69 patients treated with high- flow oxygen or conventional oxygen therapy, then compared the difference of prime and second outcomes between the two groups.

Results: The High-flow oxygen group had lower intubation rate (25.6% vs 56.7%, P= 0.013) and longer median time to intubation (64.25h vs 7.75h, P<0.001) compared with the conventional oxygen group. High flow oxygen had a stronger effect on improving dyspnea (87.2% vs 56.7%, P=0.006) and regression of respiratory failure (66.7% vs 26.7%, P=0.001). In the univariate and multivariate analyses, high-flow oxygen and APACHE II score were independent predict factors to respiratory failure regression (OR =20.381, P=0.038; OR=36.827, P=0.026). Patients treated with highflow oxygen had shorter intensive care unit stay length (19.5±13.4 vs 7.8±4.7, P=0.009) and early mortality tended to be significantly lower (17.9% vs 40.0%, P= 0.058).

Conclusion: High-flow oxygen is a more effective method for acute pancreatitis complicated with acute respiratory dysfunction than conventional oxygen therapy.