Background Post-Intensive Care Syndrome (PICS) includes cognitive, psychological, and physical impairments following critical illness. The long-term impact of COVID-19-related ARDS on PICS domains remains under-explored, particularly in resource-limited settings.
Objective To assess the prevalence and trajectory of cognitive, mental, and physical impairments among COVID-19 ARDS survivors at ICU discharge and at 6 months, and to explore associated risk factors.
Methods This was an observational cohort study of 30 mechanically ventilated COVID-19 patients admitted to a tertiary ICU in South India during the second wave (Delta variant). Patients were assessed at ICU discharge (or first follow-up) and at 6 months using the Montreal Cognitive Assessment (MoCA), SF-36 health survey, modified MRC dyspnea scale, 6-minute walk test (6MWT), and physical examination. Risk factors were analyzed using multivariable linear regression.
Results At discharge, mild cognitive impairment was prevalent (MoCA: 25.17±3.63), with significant improvement at 6 months (27.07±2.72, p<0.001). SF-36 domains showed persistent deficits in emotional well-being (36.31→50.83), fatigue (33.28→45.91), and pain (51.38→71.47) (all p<0.01). Functional capacity improved on 6MWT, with >350m walked increasing from 23% to 53%. Risk factors included steroid duration, SOFA score, antifungal exposure, and fasting hypoglycemia. Other parameters like Muscle wasting, dyspnea, and gastrointestinal symptoms also showed partial recovery.
Conclusion COVID-19 ARDS survivors experience significant but partially reversible PICS across multiple domains. Structured post-ICU rehabilitation and early identification of modifiable risk factors may improve recovery trajectories. Findings highlight the need for integrated post-ICU care pathways in similar settings.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Kovai Medical Center and Hospital (KMCH), KMCH Ethics committee, approval granted. Ref: EC/AP/885/03/2022
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Footnotes↵# Co- Authors
Email id: parvathynarayanan82gmail.com, Phone Number: 9500753889, Email id: docgopi79gmail.com, Phone number: 9790832509, Email id: vijayss87pmgmail.com, Phone number: 807295265
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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