key: cord-0875854-9j2yx0mu
authors: Funakoshi, Kenji; Morita, Takayoshi; Kumanogoh, Atsushi
title: Longer Prehospitalization and Preintubation Periods in Intubated Non-survivors and ECMO Patients With COVID-19: A Systematic Review and Meta-Analysis
date: 2021-10-15
journal: Front Med (Lausanne)
DOI: 10.3389/fmed.2021.727101
sha: 13698483f6ede2148747fe6f84de395fa6f4488f
doc_id: 875854
cord_uid: 9j2yx0mu

Purpose: There is no clear consensus on the clinical course of critical COVID-19 patients. We examined the clinical course among intubated survivors, non-survivors, and extracorporeal membrane oxygenation (ECMO) patients to reveal the standard clinical course and the difference among critical COVID-19 patients. Methods: In this systematic review and meta-analysis, we searched PubMed, Web of Science, and Scopus for original studies published until December 11, 2020, including case accumulation and clinical course reporting. Pregnant patients and children were excluded. We followed PRISMA guidelines and registered them with PROSPERO (CRD42021235534). Results: Of the 11,716 studies identified, 94 met the selection criteria, and 2,549 cases were included in this meta-analysis. The times from intubation to extubation and death were 12.07 days (95% confidence interval 9.80–14.33 days) and 10.14 days (8.18–12.10 days), respectively, and the ECMO duration was 14.72 days (10.57–18.87 days). The time from symptom onset to hospitalization (prehospitalization period) of intubated survivors, non-survivors, and ECMO patients was 6.15 (4.61–7.69 days), 6.45 (4.55–8.34 days), and 7.15 days (6.48–7.81 days), and that from symptom onset to intubation (preintubation period) was 8.58 (7.36–9.80 days), 9.14 (7.26–11.01 days), and 10.54 days (9.18–11.90 days), respectively. Sensitivity analysis showed that the time from intubation to extubation and death was longer in the US and Europe than in East Asia. Conclusion: For COVID-19, we hypothesize that prehospitalization and preintubation periods are longer in intubated non-survivors and ECMO patients than in intubated survivors. These periods may serve as a predictor of disease severity or death and support therapeutic strategy determination.

Coronavirus disease 2019 (COVID-19) is a pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and was first reported in Wuhan, China, in December 2019 (1) . As of August 2021, COVID-19 had spread to 223 countries, areas, or territories, and the global cumulative case numbers have reached 197 million. Over 4.2 million COVID-19 patients have died since the start of the pandemic (2), even though every government has taken aggressive preventive measures such as lockdown (3), universal masking (4) , and social distancing (4) . The hospitalization rate of COVID-19 is reportedly 14% (almost 10 times higher than influenza) (5) (6) (7) . Moreover, up to 26.1% of hospitalized COVID-19 patients are admitted to the intensive care unit (ICU) (8) . Therefore, COVID-19 has placed an unprecedented burden on the ICU, and in some regions, ICU capacity exceeds 100% with only COVID-19 patients because of the astonishing number, high rate of ICU admission, and long clinical course (9) . Furthermore, 71-88% of COVID-19 patients in the ICU need intubation (2.45-4.01 times higher than influenza) (10) (11) (12) (13) (14) , and 3-27.2% of intubated COVID-19 patients require ECMO (10, 15) . Overall, the high occupancy rate of hospital beds and ICUs by COVID-19 patients is a serious problem worldwide.

The clinical course of patients with severe COVID-19 from symptom onset to clinical events is highly informative when considering prognosis, therapeutic strategy, ICU bed management, and medical economy. Nevertheless, comparing each patient's clinical course with the standard clinical course of COVID-19 is difficult because there is no consensus to date regarding the standard clinical course. For example, the duration of intubation has been reported to be 10-16 days (16, 17) , yet both the patients' backgrounds and regions where the studies were conducted differed in these reports. Moreover, known risk factors for COVID-19 mortality include age (18) , sex (19) , comorbidities (19) , and blood counts (absolute lymphocyte number and CRP) (20) ; however, few articles have assessed differences in the clinical course between intubated survivors, non-survivors, and ECMO patients.

In this study, we conducted a systematic review and metaanalysis of the clinical course, i.e., time (days) from symptom onset, hospitalization, intubation, and ECMO initiation to each Abbreviations: CIs, confidence intervals; COVID-19, Coronavirus disease 2019; ECMO, extracorporeal membrane oxygenation; ECMO-death period, duration from ECMO initiation to death; ECMO period, duration from ECMO initiation to decannulation; hospitalization-death period, duration from hospitalization to death; hospitalization-discharge period, duration from hospitalization to discharge; hospitalization-ECMO period, duration from hospitalization to ECMO initiation; hospitalization-intubation period, duration from hospitalization to intubation; ICU, intensive care unit; intubation-death period, duration from intubation to death; intubation-ECMO period, duration from intubation to ECMO initiation; intubation period, duration from intubation to extubation; IQR, interquartile range; preECMO period, duration from symptom onset to ECMO initiation; prehospitalization period, duration from symptom onset to hospitalization; preintubation period, duration from symptom onset to intubation; SARS-CoV-1, severe acute respiratory syndrome coronavirus 1; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; SD, standard deviation; symptom-death period, duration from symptom onset to death. clinical event in critical COVID-19 patients. We also assessed the difference in the clinical course between intubated survivors, non-survivors, and ECMO patients with COVID-19 to reveal whether the clinical course is a prognostic factor. Finally, we conducted sensitivity analysis to assess factors (patient background and region) that may influence the time from intubation to extubation or death.

This meta-analysis was performed following the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement (Supplementary Table 1 ) (21) . This study searched for articles documenting the clinical course in critical COVID-19 patients: the time (days) from symptom onset to hospitalization (prehospitalization period) to intubation (preintubation period) and to ECMO initiation (pre-ECMO period); the time from hospitalization to intubation (hospitalization-intubation period) and to ECMO initiation (hospitalization-ECMO period), discharge (hospitalizationdischarge period), and death (hospitalization-death period); the time from hospitalization to death (hospitalization-death period); the time from intubation to extubation (intubation period), to ECMO (intubation-ECMO period), and to death (intubation-death period); and the time from ECMO initiation to decannulation (ECMO period) and to death (ECMO-death period). Three sources, namely, PubMed, Web of Science, and Scopus, were searched [(COVID-19) OR (SARS-CoV-2) AND (intensive care unit) OR (acute respiratory distress syndrome) OR (mechanical ventilation) OR (extracorporeal membrane oxygenation)], with no language restriction. The searches were performed to identify articles published until December 11th, 2020, when the SARS-CoV-2 vaccine was first approved in the world, including "online first" articles, published until December 11, 2020, when the SARS-CoV-2 vaccine was first approved. The last searches were performed on June 26, 2021.

The inclusion criteria were studies of human subjects, case accumulations, a title or abstract consisting of the clinical course of intubated survivors, non-survivors, and/or ECMO patients with COVID-19, and a link from the search site to the full text (PDF or website) of the article. In this study, "survivors" referred to extubated patients who had not died during the study period. This study excluded studies involving children (under 18 years old) and pregnant women and non-English articles; a case report was also excluded because properly calculating the average value and standard deviation (SD) was difficult. Redundancies between the search sites were eliminated, i.e., individual studies were counted only once in this analysis.

Data were extracted from all studies included in this analysis (author, year of publication, country where the study was conducted, number of patients, age, percentage of males, comorbidities, and treatment); the details are provided in Table 1 . The average number of days and SD showing each clinical course or the median number of days and interquartile range (IQR) and/or range were extracted. The average number of days and SD were calculated from the median and IQR or range data using the reported methods if only the median and IQR or range were given in the study (22) . Two authors (K.F. and T.M.) independently assessed and selected references. In cases of inconsistent results, a third author (A.K.) provided an opinion to resolve the issue. The quality of the selected studies was evaluated according to the study quality assessment tools (Quality Assessment Tool for Case Series Studies) from the National Heart, Lung, and Blood Institute (NHLBI) (23) . The evidence level was assessed based on the Oxford Centre for Evidence-Based Medicine 2011 (24) . Asymmetry in a funnel plot was employed to determine publication bias.

A meta-analysis was performed to estimate the clinical course of intubated survivors, non-survivors, and ECMO patients with COVID-19. Clinical data were analyzed using the metamean package. Outcomes are described as the mean number of days at each event, such as admission, intubation, or death from the onset of COVID-19 (baseline) and 95% confidence intervals (CIs) for each clinical course. For all outcomes, mean differences were calculated using the random-effects model (DerSimonian and Laird method) (25) . I 2 values of 25, 50, and 75% were defined as low, moderate, and high, respectively (26) . All analyses were conducted using R version 4.0.3 (R Project for Statistical Computing) (27) . Sensitivity analyses were carried out with regard to the intubation period and intubation-death period based on region (East Asia, the US, and Europe), age, sex, and comorbidities (hypertension and diabetes mellitus). Spearman's correlation coefficient was calculated in R version 4.0.3. P values ≤ 0.05 were considered statistically significant. This study was registered with PROSPERO (CRD42021235534).

We identified 17,259 articles and excluded 5,543 due to duplication. We also screened 11,716 publications and identified 94 articles (15) (16) (17) , with 2,549 cases, from among 1,559 articles that underwent full-text assessment (Figure 1) . Each article is summarized in Supplementary Table 1. The mean age ranged from 38 to 75 years, and the rate of male patients ranged from 0% to 100%. COVID-19 patients were reportedly treated with glucocorticoids, tocilizumab/sarilumab, remdesivir, and hydroxychloroquine; however, treatment was not described in more than 70% of the articles. There were 36 articles from the US, 19 from China, ten from France, seven from Italy, five from Japan, and a few from other countries. Despite several cohort studies, there were few intubated survivors and non-survivors, and most were case accumulations. Therefore, the risk of bias was calculated based on case accumulation. The risk of bias was more than 5 points, with 6.71 points as the average, i.e., moderate risk (Supplementary Table 2) .

Moreover, we conducted a meta-analysis on the clinical course of intubated survivors, non-survivors, and ECMO patients with COVID-19. First, we analyzed the intubation period and the intubation-death period of intubated survivors and non-survivors. Thirty-three reports with 325 survivors and 24 reports with 1,225 non-survivors were identified and analyzed (Figure 2) . The average intubation period among intubated survivors was 12.07 days (95% CIs 9.80-14.33 days), and the average intubation-death period was 10.14 days (8.18-12.10 days). The prehospitalization periods for intubated survivors and non-survivors were 6.15 (4.61-7.69 days) and 6.45 (4.55-8.34 days) days, respectively, and the preintubation periods were 8.58 days (7.36-9.80 days) and 9.64 days (7.75-11.53 days), respectively. A symptom-death period of 17.86 days (13.02-22.69 days) was calculated (Figure 3) . Additionally, the hospitalizationintubation period among intubated survivors and non-survivors was 2. The results provided above are summarized in Figure 5 . The prehospitalization and preintubation periods of intubated nonsurvivors and ECMO patients appeared to be longer than those of intubated survivors (no direct comparison).

Finally, sensitivity analysis focusing on regional differences and patient backgrounds was performed. The regions where the studies were conducted were classified into three groups: Europe, the US, and East Asia. The intubation period was 14. Figure 3) , and the intubation-death period was 13.05 days (9.53-16.58 days), 11.34 days (8.06-14.61 days), and 5.39 days (-1.14-11.91 days), respectively. Both the intubation period and intubation-death period tended to be longer in the US and Europe than in East Asia. Nevertheless, the mean age of intubated survivors did not differ much among Europe [ China was 65 (±4)]. We also analyzed age, sex, and comorbidities (diabetes mellitus and hypertension) but found no significant differences (data not shown).

This study demonstrated the clinical course and differences among the clinical courses of intubated survivors, non-survivors, and ECMO patients with COVID-19. In this meta-analysis, intubation, intubation-death, and ECMO periods were 12.07 days (9.80-14.33 days), 10.14 days (8.18-12.10 days), and 14.72 days (10.57-18.87 days), respectively. The prehospitalization periods of intubated survivors, non-survivors, and ECMO patients were 6.15 days (4.61-7.69 days), 6.45 days (4.55-8.34 days), and 7.15 days (6.48-7.81 days), respectively, and the preintubation periods were 8.58 days (7.36-9.80 days), 9.14 days (7.26-11.01 days), and 10.54 days (9.18-11.90 days), respectively. According to sensitivity analysis, the intubation period in survivors and the intubation-death period were longer in the US and Europe than in East Asia.

For COVID-19, the intubation period in survivors and the intubation-death period appear to be more prolonged than those in patients intubated for other diseases or reasons. In addition, the intubation periods in survivors and nonsurvivors were 12.1 days and 10 days, respectively. In contrast, previously reported intubation periods in ICU patients, including postoperative patients, chronic obstructive pulmonary disease (COPD) patients, pneumocystis pneumonia survivors, acute respiratory distress syndrome (ARDS) patients, communityacquired pneumonia patients, and SARS-CoV-1 pneumonia survivors, were 3.3 ± 3 days (mortality 24.3%) (119), 6.8 ± 4.9 days (mortality 13%) (120), 7.7 ± 8.2 days (121), 8.8 (± 6) days (122), 10-11 days (123), 12.1 ± 6.1 days (124), and 7.3-15 days (mean days are calculated from each original datum) (125) (126) (127) , respectively. One study comparing COVID-19 with influenza found that the intubation period in COVID-19 patients was longer than that in influenza patients (16.2 vs. 7.3 days) (127) . Thus, the intubation period in COVID-19 survivors is prolonged compared with that in patients intubated due to COPD, HIV-PCP, and influenza. However, approximately the same duration has been observed for patients intubated due to communityacquired pneumonia and SARS-CoV-1 or COVID-19.

Moreover, the ECMO period in COVID-19 patients was not longer than that in patients with ARDS for other reasons. Although ECMO is commonly used during cardiac surgery, severe ARDS patients (aPaO 2 :FiO 2 of <80 mmHg, a Murray score >3.0 and pH<7.20) have been treated with ECMO, improving the survival rate to more than 50% (128, 129) . Accordingly, critical COVID-19 patients also receive ECMO. In our meta-analysis, the ECMO period with COVID-19 was 14.72 days (10.57-18.87 days); in previous reports, the ECMO period in severe ARDS patients was 10.3 ± 7.5 (mean days were calculated from the data) days (128) and 15 ± 13 days (129) , and that in severe ARDS patients with influenza was 10 days (130) . These data indicate that the ECMO period in COVID-19 patients is not as long as we expected. We presume that time is needed to improve both ARDS caused by COVID-19 and ARDS caused by other reasons, as recovery in patients with critical ARDS is difficult.

In this study, the preintubation period was longer in intubated survivors than in intubated non-survivors or ECMO patients. This tendency was also observed when assessing data for the prehospitalization and hospitalization-intubation periods, despite no direct comparison. Indeed, the time from symptom onset to pneumonia was longer in COVID-19 patients with severe disease than in those without severe disease (131), the time from symptom onset to dyspnea and hospitalization in ICU COVID-19 patients was longer than that in non-ICU COVID-19 patients, and the time from symptom onset to ICU admission tended to be longer in COVID-19 non-survivors than in COVID-19 survivors (10) .

There are two possibilities for these findings. First, hospitalization delay and lack of medical resources may contribute to the result. COVID-19 pandemic forces people to self-restraint, and it leads to hospitalization delay. Moreover, a shortage of ventilators also leads to intubation delay and poor prognosis (132) (133) (134) . In fact, the hospitalization-intubation period among non-survivors, and ECMO patients tended to be longer than that among intubated survivors; the hospitalizationintubation period among intubated survivors, non-survivors, and ECMO patients with COVID-19 was 2.62 days (1.66-3.58 days), 3.28 days (2.15-4.41 days), and 3.39 (2.08-4.69 days), respectively. Second, a critical condition itself leads to a long prehospitalization period. Although the mechanism has yet to be elucidated, some of the COVID-19 patients experience asymptomatic hypoxia, which is also called "silent hypoxia." In COVID-19 patients, 28.1% of hospitalized patients are estimated to have "silent hypoxia;" 33% of hospitalized patients with "silent hypoxia" are admitted to the ICU, and 25.9% of hospitalized patients with "silent hypoxia" die (135) . Hence, "silent hypoxia" itself is a critical condition that leads to a long prehospitalization period. In this situation, monitoring blood oxygen, early hospitalization with oxygen supplementation, and systemic management arguably lead to a better prognosis.

The reasons why the intubation period was shorter in East Asia than in the US and Europe may include selection bias, information bias, differences in treatment, ventilator and ICU bed availability, race, and genetics. We detected bias concerning the East Asia data, which showed minor variations in regions and faculties compared to those from the US and Europe because East Asia's data were mainly from China, especially Wuhan. The shortage of ventilators and ICU beds has been highlighted in the US and Europe (132, 136) , and it arguably contributed to a delay of intubation and a prolonged clinical course. Race and genetic background are also possible reasons for the observed clinical differences among regions. For example, data from the US show that Asians were hospitalized less but that Black and Hispanics were hospitalized more (137, 138) . Sixteen percent of the genes were derived from Neanderthals, one of the prognostic factors maintained in Europe (almost 0% in East Asia) (139) . GWASs have revealed that SNPs and blood type, the percentages of which differ among races and regions, are also prognostic factors. Thus, an international cohort study is needed to reveal the difference in clinical course between race and region.

There were also some limitations in this meta-analysis. Although many studies were included, more studies and patients are needed. Furthermore, heterogeneity was high because it was difficult to standardize the patients' backgrounds. This study revealed the clinical course of survivors and non-survivors, but a direct comparison with survivors and non-survivors is still needed. Clinical information, for example, age, BMI, cardiac disease, kidney disease, and chronic obstructive disease, was not sufficiently described in the cases we included, and articles in some of the countries reporting were limited. Social information was also not described in the cases we included; however, whether social information, such as patient or national income level, affects the clinical course is of great interest. Moreover, differences in viral strain and treatment including anti-inflammatory treatment, because of the study period. In general, comparing clinical data with our data will reveal more knowledge about COVID-19.

Our data indicate that prehospitalization and intubation periods were longer in intubated non-survivors and ECMO patients than in intubated survivors with COVID-19. These periods might serve as predictors of disease severity or death and support therapeutic strategy determination. In the near future, viral strains and treatments should be taken into account when evaluating the clinical course of COVID-19.

The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.

KF and TM designed the study, carried out the literature search, independently acquired the data, screened the records, extracted the data, assessed the risk of bias, and performed the statistical analyses. All authors contributed to the article and approved the submitted version.

This work was supported by research grants from the Center of Innovation program (COISTREAM) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) (to AK), the Japan Society for the Promotion of Science (JSPS) KAKENHI (JP18H05282 to AK), the Japan Agency for Medical Research and Development (AMED) (J200705023, J200705710, J200705049, JP18cm016335, JP18cm059042, and J210705582 to AK), a grant from the Kansai Economic Federation (KANKEIREN), and Grants from Mitsubishi Foundation (to AK). This work was also supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI (JP21K16287 to TM).

We thank our colleagues from Osaka University Center of Medical Data Science and Advanced Clinical Epidemiology Investigator's Research Project for their providing insight and expertise for our research.

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed. 2021.727101/full#supplementary-material

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Clinical outcomes and characteristics of patients hospitalized for Influenza or COVID-19 in Germany

Efficacy and economic assessment of conventional ventilatory support versus extracorporeal membrane oxygenation for severe adult respiratory failure (CESAR): a multicentre randomised controlled trial

Extracorporeal membrane oxygenation for severe acute respiratory distress syndrome

Extracorporeal membrane oxygenation in severe influenza infection with respiratory failure: a systematic review and meta-analysis

Clinical characteristics of coronavirus disease 2019 in China

Critical supply shortages -the need for ventilators and personal protective equipment during the Covid-19 pandemic

Non-invasive ventilation in communityacquired pneumonia and severe acute respiratory failure

Failure of high-flow nasal cannula therapy may delay intubation and increase mortality

Asymptomatic hypoxia in COVID-19 is associated with poor outcome

A national strategy for ventilator and ICU resource allocation during the coronavirus disease 2019 pandemic

Clinical outcomes in young US adults hospitalized with COVID-19

Assessment of COVID-19 hospitalizations by race/ethnicity in 12 States

The major genetic risk factor for severe COVID-19 is inherited from Neanderthals

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.