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Influence of obesity on mortality, mechanical ventilation time and mobility of critical patients with COVID-19

ABSTRACT

Objective

To identify the influence of obesity on mortality, time to weaning from mechanical ventilation and mobility at intensive care unit discharge in patients with COVID-19.

Methods

This retrospective cohort study was carried out between March and August 2020. All adult patients admitted to the intensive care unit in need of ventilatory support and confirmed to have COVID-19 were included. The outcomes included mortality, time on mechanical ventilation, and mobility at intensive care unit discharge.

Results

Four hundred and twenty-nine patients were included, 36.6% of whom were overweight and 43.8% of whom were obese. Compared with normal body mass index patients, overweight and obese patients had lower mortality (p = 0.002) and longer intensive care unit survival (log-rank p < 0.001). Compared with patients with a normal body mass index, overweight patients had a 36% lower risk of death (p = 0.04), while patients with obesity presented a 23% lower risk (p < 0.001). There was no association between obesity and time on mechanical ventilation. The level of mobility at intensive care unit discharge did not differ between groups and showed a moderate inverse correlation with length of stay in the intensive care unit (r = -0.461; p < 0.001).

Conclusion

Overweight and obese patients had lower mortality and higher intensive care unit survival rates. The duration of mechanical ventilation and mobility level at intensive care unit discharge did not differ between the groups.

Keywords
Obesity; COVID-19; SARS-CoV-2; Coronavirus infections; Mortality; Rehabilitation; Respiration, artificial; Intensive care units

RESUMO

Objetivo

Identificar a influência da obesidade na mortalidade, no tempo de desmame da ventilação mecânica e na mobilidade na alta da unidade de terapia intensiva em pacientes com COVID-19.

Métodos

Trata-se de estudo de coorte retrospectivo realizado entre março e agosto de 2020. Foram incluídos todos os pacientes adultos internados na unidade de terapia intensiva com necessidade de suporte ventilatório e diagnosticados com COVID-19. Os desfechos incluíram mortalidade, duração da ventilação mecânica e mobilidade na alta da unidade de terapia intensiva.

Resultados

Identificamos 429 pacientes, dos quais 36,6% estavam acima do peso e 43,8% eram obesos. Em comparação com os pacientes com índice de massa corporal normal, os pacientes com sobrepeso e obesidade apresentaram menor mortalidade (p = 0,002) e maior sobrevida na unidade de terapia intensiva (log-rank p < 0,001). Em comparação com pacientes com índice de massa corporal normal, aqueles com sobrepeso tiveram risco 36% menor de morte (p = 0,04), enquanto os pacientes com obesidade apresentaram risco 23% menor (p < 0,001). Não houve associação entre obesidade e duração da ventilação mecânica. O nível de mobilidade na alta da unidade de terapia intensiva não diferiu entre os grupos e apresentou correlação inversa moderada com o tempo de internação na unidade de terapia intensiva (r = -0,461; p < 0,001).

Conclusão

Os pacientes com sobrepeso e obesidade tiveram menor mortalidade e maior tempo de sobrevida na unidade de terapia intensiva. A duração da ventilação mecânica e o nível de mobilidade na alta da unidade de terapia intensiva não diferiram entre os grupos.

Obesidade; COVID-19; SARS-CoV-2; Infecções por coronavírus; Mortalidade; Reabilitação; Respiração artificial; Unidades de terapia intensiva

INTRODUCTION

The coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has rapidly evolved into a global pandemic. There are more than 770 million confirmed cases and approximately 6.9 million deaths worldwide.(11. World Health Organization (WHO). Number of COVID-19 cases reported to WHO. Geneve: WHO; 2023 [cited 2023 Sep 4]. Available from: https://covid19.who.int/
https://covid19.who.int/...
) Brazil is the third largest country in terms of the number of confirmed cases (more than 37.7 million) and the second worst in terms of the number of deaths from complications of the disease (exceeding 700 thousand), being identified as the epicenter of the pandemic at several times.(11. World Health Organization (WHO). Number of COVID-19 cases reported to WHO. Geneve: WHO; 2023 [cited 2023 Sep 4]. Available from: https://covid19.who.int/
https://covid19.who.int/...
)

The COVID-19 pandemic overlapped with another well-known global epidemic in our society, that of overweight and obesity. Several meta-analyses have examined the relationship between obesity and adverse outcomes and have revealed an increased risk for hospitalization,(22. Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378

3. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.
-44. Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.)intensive care unit (ICU) admission,(22. Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378

3. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.

4. Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.

5. Ho JS, Fernando DI, Chan MY, Sia CH. Obesity in COVID-19: a systematic review and meta-analysis. Ann Acad Med Singap. 2020;49(12):996-1008.
-66. Földi M, Farkas N, Kiss S, Zádori N, Váncsa S, Szakó L, Dembrovszky F, Solymár M, Bartalis E, Szakács Z, Hartmann P, Pár G, Eross B, Molnár Z, Hegyi P, Szentesi A; KETLAK Study Group. Obesity is a risk factor for developing critical condition in COVID-19 patients: a systematic review and meta-analysis. Obes Rev. 2020;21(10):e13095.)the need for invasive mechanical ventilation (MV),(22. Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378

3. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.
-44. Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.,66. Földi M, Farkas N, Kiss S, Zádori N, Váncsa S, Szakó L, Dembrovszky F, Solymár M, Bartalis E, Szakács Z, Hartmann P, Pár G, Eross B, Molnár Z, Hegyi P, Szentesi A; KETLAK Study Group. Obesity is a risk factor for developing critical condition in COVID-19 patients: a systematic review and meta-analysis. Obes Rev. 2020;21(10):e13095.)and hospital death.(22. Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378

3. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.

4. Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.
-55. Ho JS, Fernando DI, Chan MY, Sia CH. Obesity in COVID-19: a systematic review and meta-analysis. Ann Acad Med Singap. 2020;49(12):996-1008.)However, heterogeneity measures of the death outcome were moderate or substantial, and some authors argue in favor of the existence of an “obesity paradox,” in which overweight individuals have an increased risk of developing the severe form of the disease while mortality is similar or lower than that of patients without obesity.(77. Deng L, Zhang J, Wang M, Chen L. Obesity is associated with severe COVID-19 but not death: a dose-response meta-analysis. Epidemiol Infect. 2021;149:e144.

8. Arbel Y, Fialkoff C, Kerner A, Kerner M. Can reduction in infection and mortality rates from coronavirus be explained by an obesity survival paradox? An analysis at the US statewide level. Int J Obes (Lond). 2020;44(11):2339-42.

9. Auld SC, Caridi-Scheible M, Blum JM, Robichaux C, Kraft C, Jacob JT, Jabaley CS, Carpenter D, Kaplow R, Hernandez-Romieu AC, Adelman MW, Martin GS, Coopersmith CM, Murphy DJ; and the Emory COVID-19 Quality and Clinical Research Collaborative. ICU and ventilator mortality among critically ill adults with coronavirus disease 2019. Crit Care Med. 2020;48(9):e799-804.
-1010. Wolf M, Alladina J, Navarrete-Welton A, Shoults B, Brait K, Ziehr D, et al. Obesity and critical illness in COVID-19: respiratory pathophysiology. Obesity (Silver Spring). 2021;29(5):870-8.)

Studies on COVID-19 have focused on improving the survival of patients in intensive care, with insufficient research on morbidities and functional limitations related to this disease in its critical form resulting from prolonged immobilization in bed, long stays on MV and all ICU support. In different profiles of critically ill patients, mobilization is safe, feasible and beneficial.(1111. Adler J, Malone D. Early mobilization in the intensive care unit: a systematic review. Cardiopulm Phys Ther J. 2012;23(1):5-13.) In non-COVID-19 ICUs, there are potential barriers that make rehabilitation difficult,(1212. Dubb R, Nydahl P, Hermes C, Schwabbauer N, Toonstra A, Parker AM, et al. Barriers and strategies for early mobilization of patients in intensive care units. Ann Am Thorac Soc. 2016;13(5):724-30.) and the pandemic has brought additional challenges, such as the need for strict infection control measures,(1313. Korupolu R, Francisco GE, Levin H, Needham DM. Rehabilitation of critically ill COVID-19 survivors. J Int Soc Phys Rehab Med. 2020;3(2):45-52.) the limitation of physical and human resources to assist in rehabilitation, the high proportion of patients with a high body mass index (BMI),(1414. McWilliams D, Weblin J, Hodson J, Veenith T, Whitehouse T, Snelson C. Rehabilitation levels in patients with COVID-19 admitted to intensive care requiring invasive ventilation. An observational study. Ann Am Thorac Soc. 2021;18(1):122-9.) and the constant need to free up beds to meet an increasing demand for new admissions. Thus, the research focus is placed on stability, survival and early discharge from the ICU and hospital, with rehabilitation, especially in the ICU, potentially being neglected.(1414. McWilliams D, Weblin J, Hodson J, Veenith T, Whitehouse T, Snelson C. Rehabilitation levels in patients with COVID-19 admitted to intensive care requiring invasive ventilation. An observational study. Ann Am Thorac Soc. 2021;18(1):122-9.)

To date, the published data regarding hospital mortality of the obese population admitted to the ICU for COVID-19 are controversial, and there is insufficient evidence regarding the time this population remains on MV and their mobility when they are discharged from the ICU. The fact that obesity is highly prevalent among the population and is a risk factor for the need for hospitalization and MV is a concern. Thus, the objective of this study was to identify the influence of obesity on mortality, time on MV and level of mobility at ICU discharge in patients with COVID-19.

METHODS

Study design

This retrospective cohort study utilized the medical records of patients with confirmed SARS-CoV-2 infection admitted consecutively from March 1 to August 31, 2020, at the COVID-19 ICUs of Hospital de Clínicas de Porto Alegre, a reference for the care of highly complex COVID-19 patients in Rio Grande do Sul, Brazil. The Institutional Research Ethics Committee approved this study (CAAE: 35513220.5.0000.5327), which follows the Declaration of Helsinki. The observational and retrospective nature of the research waived the need for an informed consent form.

Subjects

The sample included patients with a diagnosis of COVID-19 confirmed by reverse transcription polymerase chain reaction (RT‒PCR), of both sexes, aged older than 18 years, admitted to the COVID-19 ICU and in need of ventilatory support (invasive or noninvasive) for more than 24 hours. Patients with incomplete data in their medical records that made it impossible to assess their BMI, with previous functional limitations or who were transferred to another hospital while on MV were excluded from the study. This study was conducted during the first wave of the COVID-19 pandemic when vaccines were still under development, so the patients included were not vaccinated.

Data collection

Data collection was carried out with a thorough reading and review of the patient’s electronic medical records by the researchers, which were extracted to a spreadsheet with access restricted to the study collaborators. Demographic and anthropometric data, previous comorbidities, smoking status and alcohol consumption, and severity scores were collected using the Simplified Acute Physiology Score 3 (SAPS 3). Regarding therapies, data on ventilatory support, hemodialysis, extracorporeal membrane oxygenation (ECMO), nitric oxide (NO), prone position, sedatives, neuromuscular blockers, and corticosteroids were collected. To characterize the clinical evolution in the ICU, we verified the length of stay in the ICU and the hospital, the duration of bed rest (defined as the days elapsed between admission to the ICU and the first time out of bed), mobility scores, MV time, length of hospital stay and ICU mortality.

Obesity was defined according to BMI, with weight and height measured in the first 24 hours of ICU admission by the nutritionist in charge. Patients were classified into three groups according to the classification proposed by the World Health Organization (WHO): normal BMI (BMI 18.5 - 24.9kg/m2), overweight (BMI 25 - 29.9kg/m2), and obese (BMI ≥ 30kg/m2).(1515. World Health Organization (WHO). Noncommunicable diseases. Obesity. Geneve: WHO; c2024 [cited 2021 Oct 11]. Available from:)

Outcomes

The primary outcome was ICU mortality. Secondary outcomes included time on MV, defined as the days elapsed between the start and end of invasive ventilatory support, and the level of mobility assessed at the last ICU physical therapy visit, using the following scores:

  • The Perme Intensive Care Unit Mobility Score comprises 15 items grouped into seven categories (mental status, potential mobility barriers, functional strength, mobility in bed, transfers, gait, and resistance). The final score ranges from 0 to 32, with a high score indicating few potential mobility barriers and less need for assistance.(1616. https://www.who.int/health-topics/noncommunicable-diseases/obesity#tab=tab_1
    https://www.who.int/health-topics/noncom...
    )

  • The Intensive Care Unit Mobility Scale is a single domain instrument scored from 0 to 10, with a score of 0 being interpreted as a patient able to perform only passive exercises in bed and a score of 10 meant the patient can walk unaided.(1616. https://www.who.int/health-topics/noncommunicable-diseases/obesity#tab=tab_1
    https://www.who.int/health-topics/noncom...
    )

Statistical analysis

The normality of the data distribution was assessed by visual inspection of histograms and Q-Q plots. Categorical variables are described as frequencies and percentages, while continuous variables are presented as the mean and standard deviation or median and quartiles 1 and 3. Pearson’s chi-square test of independence and Fischer’s exact test were used to compare the categorical variables for demographic data and clinical characteristics between the three BMI groups. To verify the associations of continuous variables between groups, we used one-way ANOVA for normally distributed data and the Kruskal–Wallis test for nonparametric data. When necessary, a post hoc analysis of multiple comparisons with Bonferroni correction was performed. Survival times between BMI groups were compared using Kaplan‒Meier estimates and the log-rank test for the equality of survival curves. Correlations between variables were established using Spearman’s correlation coefficient. To analyze the associations between BMI and ICU mortality, a Poisson regression model with robust variance was used for univariate and multivariate analyses. The results are given as the relative risk and 95% confidence interval (95%CI). The software used was the Statistical Package for Social Sciences (SPSS), version 18, and the significance level adopted was 5%.

RESULTS

During the study period, 536 patients were admitted to the ICU with a diagnosis of COVID-19 and 454 were eligible. Of these, 429 patients were included: 43.8% were obese, 36.6% were overweight, and 19.6% had a normal BMI (Figure 1).

Figure 1
Selection of patients included in the study.

The average overall age was 58 years; overweight and obese patients were younger and presented a lower severity score upon ICU admission through the SAPS 3 than patients with a normal BMI. The sample characterization data, instituted therapies, mobility, and mortality data are presented in table 1.

Table 1
Characteristics of the study population

The mortality rate in the ICU reached 42.4%, and in patients with a normal BMI, it was 61.9%. Compared with patients with a normal BMI, overweight and obese patients had longer ICU survival times (log-rank < 0.001) (Figure 2). According to the Poisson multivariable regression model, overweight and obesity were significant protective factors against mortality in the ICUs of patients who required MV (p = 0.04 and p < 0.001, respectively). Thus, overweight patients had a 36% lower risk of progressing to death than did patients with a normal BMI, while in patients with obesity, the rate was 23%. The SAPS 3 score was presented as an independent risk factor for mortality (p < 0.001), and each additional point in the score represented a 2% risk of death in the ICU for patients who required MV. In the univariate analysis, age and diabetes were risk factors for mortality (p < 0.001 and p = 0.02, respectively), but they lost effect after adjustments of the multivariate analysis. The time on MV did not contribute to ICU mortality (Table 2).

Figure 2
Kaplan–Meier curve for intensive care unit survival time by body mass index group (log-rank p < 0.001).

Table 2
Adjusted relative risks for the association between body mass index category and mortality only for patients on mechanical ventilation

Overall, 83.4% of patients required MV for an overall median time on MV of 15 days (8 - 26), and there was no difference among the three groups (Figure 3). In survivors, the time on MV did not differ between groups (Table 1).

Figure 3
Time on mechanical ventilation in survivors according to body mass index group.

When comparing mobility data, no differences were observed among patients who were obese, overweight or had a normal BMI (Table 1). The median time for the first bed exit in all groups was eight days (3 - 18). At the time of ICU discharge, the average Perme score was 20 ± 8 points, indicating that a higher score corresponds to a lower need for assistance in mobilization. The achieved level of mobility on the ICU Mobility Scale was 5 (4 - 7), meaning that 50% of patients were capable of actively transferring weight from one leg to another up to a chair. There was no association between BMI and mobility at ICU discharge (Perme Score and ICU Mobility Scale) or between BMI and the duration of bed exit. However, the length of ICU stay showed a moderate inverse correlation with the Perme score (r = -0.461, p < 0.001) (Figure 4), and the pattern of this association remained similar when the groups were analyzed separately.

Figure 4
Correlation of the Perme score at intensive care unit discharge with length of stay in the intensive care unit (r = -0.461, p < 0.001).

DISCUSSION

This single-center study evaluated the influence of obesity on mortality, time on MV, and level of mobility at ICU discharge in critically ill patients diagnosed with COVID-19. In addition to having lower mortality rates, overweight and obese patients also had longer ICU survival times than did patients with a normal BMI. Overweight and obesity were found to be protective factors for predicting ICU mortality after adjustment for confounders. There was no association between obesity and time on MV. The level of mobility at ICU discharge did not differ between the groups and showed a moderate inverse correlation with the length of stay in the ICU.

The prevalence of obese patients admitted to the ICU for COVID-19 was high in the present study (43.8%), as also described in previous publications.(1717. Kawaguchi YM, Nawa RK, Figueiredo TB, Martins L, Pires-Neto RC. Perme Intensive Care Unit Mobility Score and ICU Mobility Scale: translation into Portuguese and cross-cultural adaptation for use in Brazil. J Bras Pneumol. 2016;42(6):429-34.

18. Nakeshbandi M, Maini R, Daniel P, Rosengarten S, Parmar P, Wilson C, et al. The impact of obesity on COVID-19 complications: a retrospective cohort study. Int J Obes (Lond). 2020;44(9):1832-7.

19. Simonnet A, Chetboun M, Poissy J, Raverdy V, Noulette J, Duhamel A, Labreuche J, Mathieu D, Pattou F, Jourdain M; LICORN and the Lille COVID-19 and Obesity study group. High prevalence of obesity in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) requiring invasive mechanical ventilation. Obesity (Silver Spring). 2020;28(7):1195-9.
-2020. Dana R, Bannay A, Bourst P, Ziegler C, Losser MR, Gibot S, et al. Obesity and mortality in critically ill COVID-19 patients with respiratory failure. Int J Obes (Lond). 2021;45(9):2028-37.)Obesity is an independent factor associated with an increased risk of ICU admission for COVID-19.(2020. Dana R, Bannay A, Bourst P, Ziegler C, Losser MR, Gibot S, et al. Obesity and mortality in critically ill COVID-19 patients with respiratory failure. Int J Obes (Lond). 2021;45(9):2028-37.) In a retrospective cohort, approximately half of the individuals admitted to the ICU with SARS-CoV-2 had a BMI ≥ 30kg/m2, which is different from the distribution observed in previous years of hospitalization for pulmonary causes, in which the prevalence of obesity was only 25.8%.(1818. Nakeshbandi M, Maini R, Daniel P, Rosengarten S, Parmar P, Wilson C, et al. The impact of obesity on COVID-19 complications: a retrospective cohort study. Int J Obes (Lond). 2020;44(9):1832-7.) In the study by van der Voort (2020), 90% of patients infected with SARS-CoV-2 with respiratory failure had a BMI greater than 25kg/m2 and the severity of the disease increased significantly with a high BMI.(2121. Suresh S, Siddiqui M, Abu Ghanimeh M, Jou J, Simmer S, Mendiratta V, et al. Association of obesity with illness severity in hospitalized patients with COVID-19: a retrospective cohort study. Obes Res Clin Pract. 2021;15(2):172-6.) In a pair-matched 1:2 case-control study, patients with obesity were more likely to develop severe SARS‒CoV‒2 disease and require intensive treatment after confounding factors were excluded.(2222. van der Voort PH, Moser J, Zandstra DF, Muller Kobold AC, Knoester M, Calkhoven CF, et al. Leptin levels in SARS-CoV-2 infection related respiratory failure: A cross-sectional study and a pathophysiological framework on the role of fat tissue. Heliyon. 2020;6(8):e04696.)

Obesity can increase the severity of the disease and potentially predispose younger individuals to the need for hospitalization and ICU admission.(1818. Nakeshbandi M, Maini R, Daniel P, Rosengarten S, Parmar P, Wilson C, et al. The impact of obesity on COVID-19 complications: a retrospective cohort study. Int J Obes (Lond). 2020;44(9):1832-7.,2323. Russo A, Pisaturo M, Zollo V, Martini S, Maggi P, Numis FG, et al. Obesity as a risk factor of severe outcome of COVID-19: a pair-matched 1:2 case-control study. J Clin Med. 2023;12(12):4055.)Although we did not assess the risk of ICU admission, in addition to the high prevalence of obesity, overweight patients were younger than patients with a normal BMI. Kass et al. reported an inverse correlation between age and BMI in a population of 265 patients admitted to the ICU with COVID-19, in which younger individuals admitted to the hospital were more likely to be obese.(2424. Lighter J, Phillips M, Hochman S, Sterling S, Johnson D, Francois F, et al. Obesity in patients younger than 60 years is a risk factor for COVID-19 hospital admission. Clin Infect Dis. 2020;71(15):896-7.)

The association between obesity and a greater risk of death is controversial. Some studies argue for the existence of an “obesity paradox,” in which patients with obesity have an increased risk of critical illness but similar mortality compared to patients without obesity.(77. Deng L, Zhang J, Wang M, Chen L. Obesity is associated with severe COVID-19 but not death: a dose-response meta-analysis. Epidemiol Infect. 2021;149:e144.

8. Arbel Y, Fialkoff C, Kerner A, Kerner M. Can reduction in infection and mortality rates from coronavirus be explained by an obesity survival paradox? An analysis at the US statewide level. Int J Obes (Lond). 2020;44(11):2339-42.

9. Auld SC, Caridi-Scheible M, Blum JM, Robichaux C, Kraft C, Jacob JT, Jabaley CS, Carpenter D, Kaplow R, Hernandez-Romieu AC, Adelman MW, Martin GS, Coopersmith CM, Murphy DJ; and the Emory COVID-19 Quality and Clinical Research Collaborative. ICU and ventilator mortality among critically ill adults with coronavirus disease 2019. Crit Care Med. 2020;48(9):e799-804.
-1010. Wolf M, Alladina J, Navarrete-Welton A, Shoults B, Brait K, Ziehr D, et al. Obesity and critical illness in COVID-19: respiratory pathophysiology. Obesity (Silver Spring). 2021;29(5):870-8.,2020. Dana R, Bannay A, Bourst P, Ziegler C, Losser MR, Gibot S, et al. Obesity and mortality in critically ill COVID-19 patients with respiratory failure. Int J Obes (Lond). 2021;45(9):2028-37.)Before our study, some retrospective cohorts analyzed the mortality of obese patients in the ICU and, similar to our data, found that the percentage of survivors was greater(99. Auld SC, Caridi-Scheible M, Blum JM, Robichaux C, Kraft C, Jacob JT, Jabaley CS, Carpenter D, Kaplow R, Hernandez-Romieu AC, Adelman MW, Martin GS, Coopersmith CM, Murphy DJ; and the Emory COVID-19 Quality and Clinical Research Collaborative. ICU and ventilator mortality among critically ill adults with coronavirus disease 2019. Crit Care Med. 2020;48(9):e799-804.) or similar(1010. Wolf M, Alladina J, Navarrete-Welton A, Shoults B, Brait K, Ziehr D, et al. Obesity and critical illness in COVID-19: respiratory pathophysiology. Obesity (Silver Spring). 2021;29(5):870-8.,2525. Kass DA, Duggal P, Cingolani O. Obesity could shift severe COVID-19 disease to younger ages. Lancet. 2020;395(10236):1544-5.

26. Pouwels S, Ramnarain D, Aupers E, Rutjes-Weurding L, van Oers J. Obesity may not be associated with 28-day mortality, duration of invasive mechanical ventilation and length of intensive care unit and hospital stay in critically ill patients with severe acute respiratory syndrome coronavirus-2: a retrospective cohort study. Medicina (Kaunas). 2021;57(7):674.
-2727. Kooistra EJ, de Nooijer AH, Claassen WJ, Grondman I, Janssen NA, Netea MG, van de Veerdonk FL, van der Hoeven JG, Kox M, Pickkers P; RCI-COVID-19 study group l. A higher BMI is not associated with a different immune response and disease course in critically ill COVID-19 patients. Int J Obes (Lond). 2021;45(3):687-94.)for obese patients. This lower mortality rate in obese patients in the ICU may be related to the obesity paradox as a protective effect or to the selection bias of less severely obese patients admitted to the ICU and limitations inherent to observational research. The ICUs of the present study are part of the reference hospital for high-complexity care for patients with COVID-19 in Rio Grande do Sul, Brazil. Thus, patients with greater severity and/or patients believed to have greater potential for complications were referred for highly complex treatment, as were patients with greater potential for recovery.

Several meta-analyses have examined the relationship between obesity and an increased risk of in-hospital death,(22. Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378

3. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.

4. Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.

5. Ho JS, Fernando DI, Chan MY, Sia CH. Obesity in COVID-19: a systematic review and meta-analysis. Ann Acad Med Singap. 2020;49(12):996-1008.
-66. Földi M, Farkas N, Kiss S, Zádori N, Váncsa S, Szakó L, Dembrovszky F, Solymár M, Bartalis E, Szakács Z, Hartmann P, Pár G, Eross B, Molnár Z, Hegyi P, Szentesi A; KETLAK Study Group. Obesity is a risk factor for developing critical condition in COVID-19 patients: a systematic review and meta-analysis. Obes Rev. 2020;21(10):e13095.,2828. Sprockel Díaz JJ, Coral Zuñiga VE, Angarita Gonzalez E, Tabares Rodríguez SC, Carrillo Ayerbe MP, Acuña Cortes IS, et al. Obesity and the obesity paradox in patients with severe COVID-19. Med Intensiva (Engl Ed). 2023;47(10):565-74.)however, measures of death outcome heterogeneity are moderate or substantial. The most recent systematic review that addressed the effect of obesity on mortality revealed high-certainty evidence that class III obesity is associated with an increased risk of death in patients with COVID-19, but in mild cases of obesity (classes I and II), this factor may not be independently associated.(2828. Sprockel Díaz JJ, Coral Zuñiga VE, Angarita Gonzalez E, Tabares Rodríguez SC, Carrillo Ayerbe MP, Acuña Cortes IS, et al. Obesity and the obesity paradox in patients with severe COVID-19. Med Intensiva (Engl Ed). 2023;47(10):565-74.)

Regarding the time on MV, we observed, as in other studies, the need for prolonged time in patients with COVID-19.(2929. Tadayon Najafabadi B, Rayner DG, Shokraee K, Shokraie K, Panahi P, Rastgou P, et al. Obesity as an independent risk factor for COVID-19 severity and mortality. Cochrane Database Syst Rev. 2023;5(5):CD015201.) However, this demand for longer MV time was not associated with obesity, as in the study by Pouwels et al., which even reported duration of MV similar to our data: 14 (8 - 23) days.(2525. Kass DA, Duggal P, Cingolani O. Obesity could shift severe COVID-19 disease to younger ages. Lancet. 2020;395(10236):1544-5.) Kooistra et al., despite finding no difference in time on MV between patients with and without obesity, reported a median MV duration of 22 (16 - 40) days.(2626. Pouwels S, Ramnarain D, Aupers E, Rutjes-Weurding L, van Oers J. Obesity may not be associated with 28-day mortality, duration of invasive mechanical ventilation and length of intensive care unit and hospital stay in critically ill patients with severe acute respiratory syndrome coronavirus-2: a retrospective cohort study. Medicina (Kaunas). 2021;57(7):674.)

Data on mobility immediately after critical illness in patients with COVID-19 are limited, probably reflecting the nature of the pandemic, when the priority is stabilization and survival of these patients. The study by Medrinal et al. revealed that the mobility levels at ICU discharge were similar to ours and concluded, using the Medical Research Council score, that 69% of COVID-19 ICU survivors developed acquired muscle weakness in the ICU.(3030. Bain W, Yang H, Shah FA, Suber T, Drohan C, Al-Yousif N, et al. COVID-19 versus non-COVID-19 acute respiratory distress syndrome: comparison of demographics, physiologic parameters, inflammatory biomarkers, and clinical outcomes. Ann Am Thorac Soc. 2021;18(7):1202-10.) A survey conducted at the same hospital as the present study revealed that critically ill patients with COVID-19 who developed acquired muscle weakness in the ICU showed compromised strength and mobility at hospital discharge and increased functional dependency six months after ICU discharge.(3131. Medrinal C, Prieur G, Bonnevie T, Gravier FE, Mayard D, Desmalles E, et al. Muscle weakness, functional capacities and recovery for COVID-19 ICU survivors. BMC Anesthesiol. 2021;21(1):64.,3232. Schmidt D, Piva TC, Glaeser SS, Piekala DM, Berto PP, Friedman G, et al. Intensive care unit-acquired weakness in patients with COVID-19: occurrence and associated factors. Phys Ther. 2022;102(5):pzac028.) A retrospective study in Italy highlighted significant functional impairment in this patient profile, with substantial improvement at hospital discharge through an early rehabilitation program.(3333. Schmidt D, Margarites AG, Alvarenga LP, Paesi PM, Friedman G, Sbruzzi G. Post-COVID-19 intensive care unit-acquired weakness compromises long-term functional status. Phys Ther. 2023;103(12):pzad117.)

Obese patients represent an additional challenge for rehabilitation within the ICU. The prospective study by McWillians et al. described the rehabilitation of 110 COVID-19 survivors who required MV and observed a significant impact of BMI on time before first mobilization: patients with a BMI > 40kg/m2 took an average of 8 days longer to sit at the bedside for the first time, compared with those with a BMI < 25kg/m2.(1414. McWilliams D, Weblin J, Hodson J, Veenith T, Whitehouse T, Snelson C. Rehabilitation levels in patients with COVID-19 admitted to intensive care requiring invasive ventilation. An observational study. Ann Am Thorac Soc. 2021;18(1):122-9.)This delay was not observed in our study; there was no difference in the median number of days of bed rest between different BMI groups, even with the severity evidenced by the higher prevalence of neuromuscular blocker use and prone position in patients with a BMI > 25kg/m2. It should be noted that rehabilitation started early, with patients still intubated, as the median bed rest time was eight days and the median duration of mechanical ventilation among survivors was 14 days.

At the time of ICU discharge, 50% of our patients reached the level of mobility to transfer from the bed to the chair, similar to the findings of studies by McWilliams et al. and Medrinal et al.(1414. McWilliams D, Weblin J, Hodson J, Veenith T, Whitehouse T, Snelson C. Rehabilitation levels in patients with COVID-19 admitted to intensive care requiring invasive ventilation. An observational study. Ann Am Thorac Soc. 2021;18(1):122-9.,3030. Bain W, Yang H, Shah FA, Suber T, Drohan C, Al-Yousif N, et al. COVID-19 versus non-COVID-19 acute respiratory distress syndrome: comparison of demographics, physiologic parameters, inflammatory biomarkers, and clinical outcomes. Ann Am Thorac Soc. 2021;18(7):1202-10.)Mobility levels with high dependence at ICU discharge even at the start of early rehabilitation may reflect the severity of the disease with the need for prolonged MV, sedatives, and neuromuscular blockers. Another factor to be considered is that the MV and ICU length of stay is very close, with medians of 14 and 15 days, respectively, suggesting that ICU discharge occurs early post-extubation to release critical beds due to the unprecedented burden on the health system. Mobility in our study was inversely associated with the length of ICU stay. In a study by Timenetsky et al., patients in the group that showed improved mobility at ICU discharge had shorter ICU stays and a shorter duration of mechanical ventilation.(3434. Ricotti S, Petrucci L, Carenzio G, Carlisi E, Di Natali G, de Silvestri A, Lisi C; Covid Rehabilitation Group. Functional assessment and rehabilitation protocol in acute patients affected by SARS-CoV-2 infection hospitalized in the intensive care unit and in the medical care unit. Eur J Phys Rehabil Med. 2022;58(2):316-23.)

Our study has limitations. First, there is the potential for residual confounding due to the observational design. Mortality can be influenced by many other factors potentiated by the pandemic, such as socioeconomic disparities, advance directives and health decisions, difficulty accessing the health system and overcrowding. Second, we did not measure the severity of pulmonary involvement using the oxygenation index or other tests. Third, data on mobility levels were collected only at ICU discharge, limiting any conclusions about overall physical recovery. In addition, the study was carried out at a single hospital and may not be representative of other populations. Fourth, the study was conducted during the first wave of the pandemic, when SARS-CoV-2 vaccines were under development. Although this was a single-center study, the institution was the reference center for intensive care of patients with COVID-19.

Despite these limitations, this study also has notable strengths: it has a considerable sample size; it uses relative risks as opposed to odds ratios, which are often calculated in other studies and may exaggerate the risk ratio; it is one of the few to assess the relationship between obesity and mobility in patients with COVID-19; and the main outcome considerations refer exclusively to patients who have completed their stay in the ICU, which allows conviction in the conclusions. Future research should systematically assess strength and functionality for better conclusions about overall physical recovery, further aiding health decisions. Additionally, studies should better assess the impact of overweight/obesity, particularly on health outcomes such as mortality, as most of the evidence encompasses this category in individuals with a normal BMI.

CONCLUSION

The results suggest that overweight and obese patients have lower mortality and longer survival times in the intensive care unit than patients with a normal body mass index, although they are more often in need of “aggressive” therapies during SARS-CoV-2 infection. Patients with COVID-19 who required mechanical ventilation for a prolonged period, regardless of the high body mass index range, were inversely associated with the length of intensive care unit stay, but overweight and obesity did not influence the level of mobility or assistance. In conclusion, it is recommended that obese patients be monitored to prevent unfavorable clinical and functional outcomes through the implementation of supportive therapies and early initiation of rehabilitation programs.

REFERENCES

  • 1
    World Health Organization (WHO). Number of COVID-19 cases reported to WHO. Geneve: WHO; 2023 [cited 2023 Sep 4]. Available from: https://covid19.who.int/
    » https://covid19.who.int/
  • 2
    Huang Y, Lu Y, Huang YM, Wang M, Ling W, Sui Y, et al. Obesity in patients with COVID-19: a systematic review and meta-analysis. Metabolism. 2020;113:154378
  • 3
    Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. Obesity aggravates COVID-19: an updated systematic review and meta-analysis. J Med Virol. 2021;93(5):2662-74.
  • 4
    Cai Z, Yang Y, Zhang J. Obesity is associated with severe disease and mortality in patients with coronavirus disease 2019 (COVID-19): a meta-analysis. BMC Public Health. 2021;21(1):1505.
  • 5
    Ho JS, Fernando DI, Chan MY, Sia CH. Obesity in COVID-19: a systematic review and meta-analysis. Ann Acad Med Singap. 2020;49(12):996-1008.
  • 6
    Földi M, Farkas N, Kiss S, Zádori N, Váncsa S, Szakó L, Dembrovszky F, Solymár M, Bartalis E, Szakács Z, Hartmann P, Pár G, Eross B, Molnár Z, Hegyi P, Szentesi A; KETLAK Study Group. Obesity is a risk factor for developing critical condition in COVID-19 patients: a systematic review and meta-analysis. Obes Rev. 2020;21(10):e13095.
  • 7
    Deng L, Zhang J, Wang M, Chen L. Obesity is associated with severe COVID-19 but not death: a dose-response meta-analysis. Epidemiol Infect. 2021;149:e144.
  • 8
    Arbel Y, Fialkoff C, Kerner A, Kerner M. Can reduction in infection and mortality rates from coronavirus be explained by an obesity survival paradox? An analysis at the US statewide level. Int J Obes (Lond). 2020;44(11):2339-42.
  • 9
    Auld SC, Caridi-Scheible M, Blum JM, Robichaux C, Kraft C, Jacob JT, Jabaley CS, Carpenter D, Kaplow R, Hernandez-Romieu AC, Adelman MW, Martin GS, Coopersmith CM, Murphy DJ; and the Emory COVID-19 Quality and Clinical Research Collaborative. ICU and ventilator mortality among critically ill adults with coronavirus disease 2019. Crit Care Med. 2020;48(9):e799-804.
  • 10
    Wolf M, Alladina J, Navarrete-Welton A, Shoults B, Brait K, Ziehr D, et al. Obesity and critical illness in COVID-19: respiratory pathophysiology. Obesity (Silver Spring). 2021;29(5):870-8.
  • 11
    Adler J, Malone D. Early mobilization in the intensive care unit: a systematic review. Cardiopulm Phys Ther J. 2012;23(1):5-13.
  • 12
    Dubb R, Nydahl P, Hermes C, Schwabbauer N, Toonstra A, Parker AM, et al. Barriers and strategies for early mobilization of patients in intensive care units. Ann Am Thorac Soc. 2016;13(5):724-30.
  • 13
    Korupolu R, Francisco GE, Levin H, Needham DM. Rehabilitation of critically ill COVID-19 survivors. J Int Soc Phys Rehab Med. 2020;3(2):45-52.
  • 14
    McWilliams D, Weblin J, Hodson J, Veenith T, Whitehouse T, Snelson C. Rehabilitation levels in patients with COVID-19 admitted to intensive care requiring invasive ventilation. An observational study. Ann Am Thorac Soc. 2021;18(1):122-9.
  • 15
    World Health Organization (WHO). Noncommunicable diseases. Obesity. Geneve: WHO; c2024 [cited 2021 Oct 11]. Available from:
  • 16
    https://www.who.int/health-topics/noncommunicable-diseases/obesity#tab=tab_1
    » https://www.who.int/health-topics/noncommunicable-diseases/obesity#tab=tab_1
  • 17
    Kawaguchi YM, Nawa RK, Figueiredo TB, Martins L, Pires-Neto RC. Perme Intensive Care Unit Mobility Score and ICU Mobility Scale: translation into Portuguese and cross-cultural adaptation for use in Brazil. J Bras Pneumol. 2016;42(6):429-34.
  • 18
    Nakeshbandi M, Maini R, Daniel P, Rosengarten S, Parmar P, Wilson C, et al. The impact of obesity on COVID-19 complications: a retrospective cohort study. Int J Obes (Lond). 2020;44(9):1832-7.
  • 19
    Simonnet A, Chetboun M, Poissy J, Raverdy V, Noulette J, Duhamel A, Labreuche J, Mathieu D, Pattou F, Jourdain M; LICORN and the Lille COVID-19 and Obesity study group. High prevalence of obesity in severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) requiring invasive mechanical ventilation. Obesity (Silver Spring). 2020;28(7):1195-9.
  • 20
    Dana R, Bannay A, Bourst P, Ziegler C, Losser MR, Gibot S, et al. Obesity and mortality in critically ill COVID-19 patients with respiratory failure. Int J Obes (Lond). 2021;45(9):2028-37.
  • 21
    Suresh S, Siddiqui M, Abu Ghanimeh M, Jou J, Simmer S, Mendiratta V, et al. Association of obesity with illness severity in hospitalized patients with COVID-19: a retrospective cohort study. Obes Res Clin Pract. 2021;15(2):172-6.
  • 22
    van der Voort PH, Moser J, Zandstra DF, Muller Kobold AC, Knoester M, Calkhoven CF, et al. Leptin levels in SARS-CoV-2 infection related respiratory failure: A cross-sectional study and a pathophysiological framework on the role of fat tissue. Heliyon. 2020;6(8):e04696.
  • 23
    Russo A, Pisaturo M, Zollo V, Martini S, Maggi P, Numis FG, et al. Obesity as a risk factor of severe outcome of COVID-19: a pair-matched 1:2 case-control study. J Clin Med. 2023;12(12):4055.
  • 24
    Lighter J, Phillips M, Hochman S, Sterling S, Johnson D, Francois F, et al. Obesity in patients younger than 60 years is a risk factor for COVID-19 hospital admission. Clin Infect Dis. 2020;71(15):896-7.
  • 25
    Kass DA, Duggal P, Cingolani O. Obesity could shift severe COVID-19 disease to younger ages. Lancet. 2020;395(10236):1544-5.
  • 26
    Pouwels S, Ramnarain D, Aupers E, Rutjes-Weurding L, van Oers J. Obesity may not be associated with 28-day mortality, duration of invasive mechanical ventilation and length of intensive care unit and hospital stay in critically ill patients with severe acute respiratory syndrome coronavirus-2: a retrospective cohort study. Medicina (Kaunas). 2021;57(7):674.
  • 27
    Kooistra EJ, de Nooijer AH, Claassen WJ, Grondman I, Janssen NA, Netea MG, van de Veerdonk FL, van der Hoeven JG, Kox M, Pickkers P; RCI-COVID-19 study group l. A higher BMI is not associated with a different immune response and disease course in critically ill COVID-19 patients. Int J Obes (Lond). 2021;45(3):687-94.
  • 28
    Sprockel Díaz JJ, Coral Zuñiga VE, Angarita Gonzalez E, Tabares Rodríguez SC, Carrillo Ayerbe MP, Acuña Cortes IS, et al. Obesity and the obesity paradox in patients with severe COVID-19. Med Intensiva (Engl Ed). 2023;47(10):565-74.
  • 29
    Tadayon Najafabadi B, Rayner DG, Shokraee K, Shokraie K, Panahi P, Rastgou P, et al. Obesity as an independent risk factor for COVID-19 severity and mortality. Cochrane Database Syst Rev. 2023;5(5):CD015201.
  • 30
    Bain W, Yang H, Shah FA, Suber T, Drohan C, Al-Yousif N, et al. COVID-19 versus non-COVID-19 acute respiratory distress syndrome: comparison of demographics, physiologic parameters, inflammatory biomarkers, and clinical outcomes. Ann Am Thorac Soc. 2021;18(7):1202-10.
  • 31
    Medrinal C, Prieur G, Bonnevie T, Gravier FE, Mayard D, Desmalles E, et al. Muscle weakness, functional capacities and recovery for COVID-19 ICU survivors. BMC Anesthesiol. 2021;21(1):64.
  • 32
    Schmidt D, Piva TC, Glaeser SS, Piekala DM, Berto PP, Friedman G, et al. Intensive care unit-acquired weakness in patients with COVID-19: occurrence and associated factors. Phys Ther. 2022;102(5):pzac028.
  • 33
    Schmidt D, Margarites AG, Alvarenga LP, Paesi PM, Friedman G, Sbruzzi G. Post-COVID-19 intensive care unit-acquired weakness compromises long-term functional status. Phys Ther. 2023;103(12):pzad117.
  • 34
    Ricotti S, Petrucci L, Carenzio G, Carlisi E, Di Natali G, de Silvestri A, Lisi C; Covid Rehabilitation Group. Functional assessment and rehabilitation protocol in acute patients affected by SARS-CoV-2 infection hospitalized in the intensive care unit and in the medical care unit. Eur J Phys Rehabil Med. 2022;58(2):316-23.
  • 35
    Timenetsky KT, Serpa Neto A, Lazarin AC, Pardini A, Moreira CR, Corrêa TD, et al. The Perme Mobility Index: a new concept to assess mobility level in patients with coronavirus (COVID-19) infection. PloS One. 2021;16(4):e0250180.

Edited by

Responsible editor: Thiago Costa Lisboa https://orcid.org/0000-0003-4306-2212

Publication Dates

  • Publication in this collection
    08 July 2024
  • Date of issue
    2024

History

  • Received
    23 Oct 2023
  • Accepted
    14 Mar 2024
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