Skip to main content

Efficacy of extracorporeal membrane oxygenation for acute respiratory failure with interstitial lung disease: a case control nationwide dataset study in Japan

Abstract

Background

Whether acute respiratory failure in patients with interstitial lung disease is reversible remains uncertain. Consequently, indications for extracorporeal membrane oxygenation in these patients are still controversial, except as a bridge to lung transplantation. The objective of this study was to clarify in-hospital mortality and prognostic factors in interstitial lung disease patients undergoing extracorporeal membrane oxygenation.

Methods

In this case–control study using the Japanese Diagnosis Procedure Combination database, hospitalized interstitial lung disease patients receiving invasive mechanical ventilation and extracorporeal membrane oxygenation from 2010 to 2017 were reviewed. Patients’ characteristics and treatment regimens were compared between survivors and non-survivors to identify prognostic factors. To avoid selection biases, patients treated with extracorporeal membrane oxygenation as a bridge to lung transplantation were excluded.

Results

A total of 164 interstitial lung disease patients receiving extracorporeal membrane oxygenation were included. Their in-hospital mortality was 74.4% (122/164). Compared with survivors, non-survivors were older and received high-dose cyclophosphamide, protease inhibitors, and antifungal drugs more frequently, but macrolides and anti-influenza drugs less frequently. On multivariate analysis, the following factors were associated with in-hospital mortality: advanced age (odds ratio [OR] 1.043; 95% confidence interval [CI] 1.009–1.078), non-use of macrolides (OR 0.305; 95% CI 0.134–0.698), and use of antifungal drugs (OR 2.416; 95% CI 1.025–5.696).

Conclusions

Approximately three-quarters of interstitial lung disease patients undergoing extracorporeal membrane oxygenation died in hospital. Moreover, advanced age, non-use of macrolides, and use of antifungal drugs were found to correlate with a poor prognosis.

Background

Regardless of the type of interstitial lung disease (ILD), the associated acute respiratory failure (ARF) leads to a poor prognosis, especially in patients requiring invasive mechanical ventilation (IMV) [1,2,3]. Extracorporeal membrane oxygenation (ECMO), also known as extracorporeal life support, is a life-saving procedure established for severe respiratory failure, cardiac shock, and cardiac arrest. Veno-venous ECMO serves as an artificial lung that provides oxygenation and removes carbon dioxide by draining and reinfusing the blood through cannulas located in central veins. ECMO enables lung-protective ventilation and reduces complications such as ventilator-induced lung injury and oxygen toxicity [4]. Ever since ECMO therapy proved successful in influenza A (H1N1)-induced severe acute respiratory distress syndrome (ARDS) [5], as well as severe adult respiratory failure (CESAR trial) [6] in 2009, the use of ECMO for respiratory failure in adults has expanded rapidly.

ECMO therapy is indicated in patients with potentially reversible causes of respiratory failure or those awaiting lung transplantation [7, 8]. Due to difficulties in predicting the reversibility of respiratory failure, which arise from its heterogeneous causes, the indications for ECMO in ILD patients with ARF need to be discussed. Moreover, even in-hospital mortality and prognostic factors in ILD patients receiving ECMO have not been clarified. The aim of this study was to elucidate the mortality rate and identify prognostic factors in these patients by using nationwide data from the Japanese Diagnosis Procedure Combination (DPC) database.

Methods

Study design and data source

This was a retrospective, case–control study using a nationwide inpatient database of acute care hospitals in Japan (i.e., the DPC database) to assess the efficacy of ECMO therapy for ARF in ILD patients treated between 2010 and 2017. The DPC is a case-mix classification system that is linked with a lump-sum payment system for inpatient care reimbursement. The Japanese DPC database includes data on the following characteristics: age, sex, weight, admission and discharge status, main diagnosis, admission-precipitating diagnosis, resource-consuming diagnosis, comorbidities, complications, surgery, and procedures performed and medications administered during hospitalization. Diagnoses are recorded using International Classification of Diseases, 10th revision, codes by attending physicians. Surgery and procedures performed during hospitalization are recorded according to the Japanese fee schedule for reimbursement.

In April 2020, this system included 1,757 hospitals with a total of 483,180 beds, which covers nearly all acute inpatients in Japan [9]. The specificity and sensitivity of diagnoses and procedures recorded in the DPC database have already been validated by Yamana et al. [10]. Since all patient data were obtained in an anonymous manner, the requirement for individual informed consent was waived. This study was approved by the institutional review board of the General Clinical Research Center, Oita University Hospital, on May 20, 2019 (approval no. 1613).

Patient selection and data extraction

Adult patients with both ILD codes (ICD-10: J670, J671, J672, J673, J674, J675, J676, J677, J678, J679, J700, J701, J702, J703, J704, J708, J82, J840, J841, J849, M0510, M313, M321, M330, M331, M332, M348, M351) and IMV codes were drawn from the 2010–2017 DPC database. After 388 cases with an ECMO code were found, ILD patients on ECMO for cardiac and temporary perioperative reasons were excluded to confine the study to those receiving ECMO for ARF. That is, patients with diagnostic or surgical codes pertaining to cardiovascular diseases such as coronary artery bypass grafting, intra-aortic balloon pumping, aortic dissection, cardiac arrest, and cardiogenic shock, as well as those with codes related to lung cancer surgery, lung transplantation, and pulmonary alveolar proteinosis, were excluded from this analysis (Fig. 1).

Fig. 1
figure1

Patient selection diagram

Statistical analysis

Statistical analyses were performed using IBM SPSS statistical software (version 22; IBM SPSS, Tokyo, Japan). Continuous variables are described as medians with interquartile range (IQR), and categorical variables as frequencies and percentages. The confidence interval in two-sided analyses was set at 95%. The odds ratio of in-hospital mortality for each variable was estimated using a logistic regression model. Variables that were found to be significantly different (p < 0.05) between survivors and non-survivors on univariate analysis were entered into the multivariate analysis in a stepwise manner, with body mass index (BMI) forced into the model because of its clinical importance in recovery. Significance was defined as a p-value < 0.05 for all analyses.

Results

This study examined 164 ILD patients undergoing ECMO for ARF in 88 hospitals, of whom 122 (74.4%) died during hospitalization. The median age was 65 years (IQR, 57–71 years), with patients over 70 years old constituting 31% of the study population. Survivors were found to be significantly younger than non-survivors; however, no significant differences were observed in sex and BMI between the two groups (Table 1).

Table 1 Comparison of clinical characteristics between the non-survivors group and the survivors group on univariate analysis

As shown in Table 2, most of the patients received broad-spectrum antibiotics, high-dose systemic steroids defined as the equivalent of methylprednisolone ≥ 500 mg/day, and low-dose systemic steroids defined as the equivalent of methylprednisolone < 500 mg/day.

Table 2 Comparison of drugs and procedures between non-survivors and survivors on univariate analysis

Patients who were treated with macrolides were concurrently administered other antibiotics in 65 of 66 cases: azithromycin in 57/66 patients (86.4%); erythromycin in 7/66 (10.6%); and clarithromycin in 6/66 (9.1%) (overlap permitted).

Survivors were treated more frequently with macrolides and anti-influenza drugs and less frequently with anti-fungal drugs, high-dose cyclophosphamide, and protease inhibitors. ECMO duration was significantly longer in non-survivors than in survivors, whereas duration of intubation was not significantly different between the two groups. Kaplan–Meier cumulative survival curve analysis showed that successful weaning from ECMO occurred mostly during the early days after its initiation (Fig. 2).

Fig. 2
figure2

Kaplan–Meier curve plotted for cumulative survival in relation to the duration of extracorporeal membrane oxygenation for acute respiratory failure among interstitial lung disease patients

Multivariate analysis, which involved constructing multiple models adjusted for significant variables on univariate analysis and BMI in a stepwise manner, showed that advanced age, absence of macrolide use, and use of antifungal drugs were associated with significantly higher in-hospital mortality (Table 3).

Table 3 Multivariate logistic regression analysis used to identify variables associated with in-hospital death

Discussion

This study showed that in-hospital mortality of ILD patients receiving ECMO for ARF was approximately 75%. It also demonstrated that advanced age, absence of macrolide use, and use of antifungal drugs were associated with significantly higher in-hospital mortality among these patients.

A systematic review of ILD patients treated in intensive care units without ECMO showed that mortality was 65% in patients with idiopathic pulmonary fibrosis during the period 2005–2017 and 48% in mixed ILD patients between 2010 and 2017 [2]. In the present study, the rate of in-hospital mortality (74.4%) in mixed ILD patients treated with ECMO was higher than previously reported mortality rates among patients receiving conventional treatments without ECMO. A possible reason for the higher mortality in ECMO cases is that patients treated with ECMO were generally refractory to conventional IMV, indicating the greater severity of their condition compared to the patients treated without ECMO.

The decision regarding the time of ECMO weaning in successful cases or ECMO withdrawal in refractory cases needs to be discussed carefully. In the present study, survivors were successfully weaned from ECMO after a median period of 8 days (IQR, 4–14 days) whereas ECMO was withdrawn in non-survivors at a median of 14 days (IQR, 8–27 days). Indeed, Kaplan–Meier survival curve analysis showed that successful weaning from ECMO was more frequent in the early days after its initiation. On the other hand, 67.2% of non-survivors died on the day of withdrawal, which implies that they relied entirely on ECMO as a life-sustaining procedure at the end of their lives. The present results suggest that continuation of ECMO over 14 days is less likely to produce a good outcome.

Survivors had a shorter, but not significantly, duration of ventilation than non-survivors. This variable is subject to lead-time bias. The DPC dataset was obtained from a single hospitalization at each hospital. Bias may be introduced, for example, if a previously ventilated patient was transferred to another hospital to receive ECMO therapy. The start of ventilation is considered to begin on the date of admission at the receiving hospital. In such a case, duration of ventilation would be underestimated by an unknown length of time. It is unknown how this bias may have affected the statistical comparison.

In the present study, advanced age was significantly associated with high in-hospital mortality. The Respiratory EMO Survival Prediction score [11] and Predicting Death for Severe ARDS on Veno-venous ECMO (PRESERVE) score [12] include young age as an indication for ECMO, regardless of the type of respiratory failure. In addition, the Extracorporeal Life Support Organization Guidelines for Adult Respiratory Failure published in 2017 have suggested a higher risk of a poor prognosis with increasing age [13]. Furthermore, the Extracorporeal Life Support Organization Coronavirus Disease 2019 Interim Guidelines have referred to age ≥ 65 years as contraindication for ECMO [14]. The present results in ILD patients are consistent with these guidelines. ECMO therapy consumes a considerable amount of medical resources, so the cost–benefit balance needs to be considered on a case-by-case basis, especially in elderly patients.

There was no significant difference in BMI between survivors and non-survivors, which contradicts the PRESERVE scoring system stating that a BMI value > 30 kg/m2 is related to a good prognosis [12]. This disparity in results could be attributed to the low number of obese patients in the present study (n = 9), which may have prevented meaningful statistical analyses. Further research is needed to determine how obesity affects the prognosis of ILD patients undergoing ECMO.

Use of macrolides was found to correlate significantly with a good prognosis in the present study. Macrolides have immunomodulatory effects [15,16,17], and their combined administration is capable of diminishing mortality in critically ill patients with community-acquired pneumonia [18]. In fact, an official clinical practice guideline of the American Thoracic Society and Infectious Diseases Society of America recommended macrolide-containing regimens for the treatment of hospitalized patients with severe pneumonia [19]. Furthermore, an investigation of the effectiveness of azithromycin for the treatment of acute exacerbations of idiopathic pulmonary fibrosis reported that mortality was significantly lower in patients treated with azithromycin than in those treated with fluoroquinolones [20]. Therefore, antibiotic therapy with macrolide-containing regimens might prove effective not only in patients with severe community-acquired pneumonia, but also in ILD patients receiving ECMO.

The present study also demonstrated an association between use of antifungal drugs and increased in-hospital mortality. Since observational studies are unable to determine causal relationships, whether antifungal drug use or fungal infections could have impacted the results remains unclear. Antifungal drugs are generally administered when patients are thought to develop fungal infections during immunosuppressive therapy. Thus, a diagnosis of fungal infections, rather than antifungal drug use per se, might affect a patient’s prognosis.

Use of anti-influenza virus drugs was significantly associated with survival to discharge on univariate analysis in the present study, but it was not included in the multivariate analysis. The efficacy of ECMO in H1N1-related ARDS has been reported [5]. In this regard, whereas ECMO might be beneficial for influenza-related respiratory disorder itself, its efficacy could be limited when this disease is accompanied by ILD.

The strength of this study is that a large number of patients from a nationwide database were included in the analysis. However, some limitations are derived from the retrospective nature of the study. First, the subtype of ILD was uncertain because its input was not required in the DPC database. However, antifibrotic agents covered by Japanese health insurance only for patients with idiopathic pulmonary fibrosis were used in just 12 cases during the study period. Presumably, the number of idiopathic pulmonary fibrosis cases would be limited. Second, no standardized ECMO initiation and management protocol exists among hospitals, giving rise to selection and intervention biases. Third, the level of mechanical ventilation could not be reported because the DPC database does not include this information. Finally, long-term outcomes could not be clarified owing to the lack of post-discharge information.

Conclusions

In-hospital mortality of ILD patients receiving ECMO for ARF was found to be nearly 75%. The indications for ECMO in ILD patients who are not lung transplantation candidates should be carefully considered. Advanced age, non-use of macrolides, and use of anti-fungal drugs may be associated with a poor prognosis in ILD patients undergoing ECMO therapy.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ARF:

Acute respiratory failure

BMI:

Body mass index

DPC:

The Japanese Diagnosis Procedure Combination

ECMO:

Extracorporeal membrane oxygenation

ILD:

Interstitial lung disease

IMV:

Invasive mechanical ventilation

IQR:

Interquartile range

References

  1. 1.

    Gaudry S, Vincent F, Rabbat A, Nunes H, Crestani B, Naccache JM, Wolff M, Thabut G, Valeyre D, Cohen Y, Mal H. Invasive mechanical ventilation in patients with fibrosing interstitial pneumonia. J Thorac Cardiovasc Surg. 2014;147:47–53.

    Article  Google Scholar 

  2. 2.

    Huapaya JA, Wilfong EM, Harden CT, Brower RG, Danoff SK. Risk factors for mortality and mortality rates in interstitial lung disease patients in the intensive care unit. Eur Respir Rev. 2018;27:1.

    Article  Google Scholar 

  3. 3.

    Gannon WD, Lederer DJ, Biscotti M, Javaid A, Patel NM, Brodie D, Bacchetta M, Baldwin MR. Outcomes and mortality prediction model of critically ill adults with acute respiratory failure and interstitial lung disease. Chest. 2018;153:1387–95.

    Article  Google Scholar 

  4. 4.

    Abrams D, Brodie D. Extracorporeal membrane oxygenation for adult respiratory failure: 2017 update. Chest. 2017;152:639–49.

    Article  Google Scholar 

  5. 5.

    Davies A, Jones D, Bailey M, Beca J, Bellomo R, Blackwell N, Forrest P, Gattas D, Granger E, Herkes R, et al. Extracorporeal membrane oxygenation for 2009 influenza A(H1N1) acute respiratory distress syndrome. JAMA. 2009;302:1888–95.

    CAS  Article  Google Scholar 

  6. 6.

    Peek GJ, Mugford M, Tiruvoipati R, Wilson A, Allen E, Thalanany MM, Hibbert CL, Truesdale A, Clemens F, Cooper N, et al. Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial. Lancet. 2009;374:1351–63.

    Article  Google Scholar 

  7. 7.

    Faverio P, De Giacomi F, Sardella L, Fiorentino G, Carone M, Salerno F, Ora J, Rogliani P, Pellegrino G, Sferrazza Papa GF, et al. Management of acute respiratory failure in interstitial lung diseases: overview and clinical insights. BMC Pulm Med. 2018;18:70.

    Article  Google Scholar 

  8. 8.

    Trudzinski FC, Kaestner F, Schäfers HJ, Fähndrich S, Seiler F, Böhmer P, Linn O, Kaiser R, Haake H, Langer F, et al. Outcome of patients with interstitial lung disease treated with extracorporeal membrane oxygenation for acute respiratory failure. Am J Respir Crit Care Med. 2016;193:527–33.

    CAS  Article  Google Scholar 

  9. 9.

    Hayashida K, Murakami G, Matsuda S, Fushimi K. History and profile of Diagnosis Procedure Combination (DPC): development of real data collection system for acute inpatient care in Japan. J Epidemiol. 2020;31(1):1–1.

    Article  Google Scholar 

  10. 10.

    Yamana H, Moriwaki M, Horiguchi H, Kodan M, Fushimi K, Yasunaga H. Validity of diagnoses, procedures, and laboratory data in Japanese administrative data. J Epidemiol. 2017;27:476–82.

    Article  Google Scholar 

  11. 11.

    Schmidt M, Bailey M, Sheldrake J, Hodgson C, Aubron C, Rycus PT, Scheinkestel C, Cooper DJ, Brodie D, Pellegrino V, et al. Predicting survival after extracorporeal membrane oxygenation for severe acute respiratory failure. The Respiratory Extracorporeal Membrane Oxygenation Survival Prediction (RESP) score. Am J Respir Crit Care Med. 2014;189:1374–82.

    Article  Google Scholar 

  12. 12.

    Schmidt M, Zogheib E, Rozé H, Repesse X, Lebreton G, Luyt CE, Trouillet JL, Bréchot N, Nieszkowska A, Dupont H, et al. The PRESERVE mortality risk score and analysis of long-term outcomes after extracorporeal membrane oxygenation for severe acute respiratory distress syndrome. Intensive Care Med. 2013;39:1704–13.

    CAS  Article  Google Scholar 

  13. 13.

    Extracorporeal Life Support Organization (ELSO) Guidelines for Adult Respiratory Failure August, 2017. http://www.elso.org.

  14. 14.

    Shekar K, Badulak J, Peek G, Boeken U, Dalton HJ, Arora L, Zakhary B, Ramanathan K, Starr J, Akkanti B, et al. Extracorporeal life support organization coronavirus disease 2019 interim guidelines: a consensus document from an international group of interdisciplinary extracorporeal membrane oxygenation providers. Asaio J. 2020;66:707–21.

    CAS  Article  Google Scholar 

  15. 15.

    Zimmermann P, Ziesenitz VC, Curtis N, Ritz N. The immunomodulatory effects of macrolides-a systematic review of the underlying mechanisms. Front Immunol. 2018;9:302.

    Article  Google Scholar 

  16. 16.

    Friedlander AL, Albert RK. Chronic macrolide therapy in inflammatory airways diseases. Chest. 2010;138:1202–12.

    CAS  Article  Google Scholar 

  17. 17.

    Kanoh S, Rubin BK. Mechanisms of action and clinical application of macrolides as immunomodulatory medications. Clin Microbiol Rev. 2010;23:590–615.

    CAS  Article  Google Scholar 

  18. 18.

    Sligl WI, Asadi L, Eurich DT, Tjosvold L, Marrie TJ, Majumdar SR. Macrolides and mortality in critically ill patients with community-acquired pneumonia: a systematic review and meta-analysis. Crit Care Med. 2014;42:420–32.

    CAS  Article  Google Scholar 

  19. 19.

    Metlay JP, Waterer GW, Long AC, Anzueto A, Brozek J, Crothers K, Cooley LA, Dean NC, Fine MJ, Flanders SA, et al. Diagnosis and treatment of adults with community-acquired pneumonia. An Official Clinical Practice Guideline of the American Thoracic Society and Infectious Diseases Society of America. Am J Respir Crit Care Med. 2019;200:e45–67.

    Article  Google Scholar 

  20. 20.

    Kawamura K, Ichikado K, Yasuda Y, Anan K, Suga M. Azithromycin for idiopathic acute exacerbation of idiopathic pulmonary fibrosis: a retrospective single-center study. BMC Pulm Med. 2017;17:94.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author information

Affiliations

Authors

Contributions

YU, KK, KF, KH, and JK designed this study and drafted the manuscript. YU, KK MY, and KF contributed to data collection, data analysis, and manuscript preparation. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kosaku Komiya.

Ethics declarations

Ethics approval and consent for participate

The study protocol was approved by the institutional ethics committee of Oita University (approval no. 1613; approval date: May 20, 2019).

Consent for publication

Since all patient data were obtained in an anonymous manner, the requirement for individual informed consent was waived.

Competing interests

All authors have stated that there are no competing interests in connection with this article.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Usagawa, Y., Komiya, K., Yamasue, M. et al. Efficacy of extracorporeal membrane oxygenation for acute respiratory failure with interstitial lung disease: a case control nationwide dataset study in Japan. Respir Res 22, 211 (2021). https://doi.org/10.1186/s12931-021-01805-w

Download citation

Keywords

  • Extracorporeal membrane oxygenation
  • Interstitial lung disease
  • Macrolides
  • Mortality
  • Respiratory failure