Obesity paradox seen in cardiogenic shock with overweight and obesity having the lowest, whereas cachexia has the highest mortality using the large Nationwide Inpatient Sample (NIS) database

Abstract

Introduction The obesity paradox has been observed in patients with cardiovascular disease. The goal of this study was to evaluate if obesity has a protective effect in patients presenting with cardiogenic shock.

Method Using a large Nationwide Inpatient sample (NIS) database, we evaluated mortality in patients with cardiogenic shock based on weight categories in adults.

Results A total of 843,020 patients had a diagnosis of cardiogenic shock in the database over age 18. We found that overweight and obesity had the lowest mortality using univariate or multivariate analysis (overweight mortality of 20.66% vs obesity mortality of 26.6 % vs 34,3% of normal weights). In contrast, cachexia was associated with the highest mortality in univariate analysis (cachexia 40.4%). Using multivariate analysis adjusting for baseline characteristics and comorbidities, these relations remained unchanged (cachexia MVOR; 1.13, CI: 1.21-1.13, p <0.001, overweight MVOR: 0.52, CI; 0.43-0.65, p<0.001, obesity MVOR: 0.76, CI: 0.73-0.79, p<0.001). After multivariate adjustment, morbid obesity had similar mortality to patients with normal weight (morbid obesity MVOR: 0.99, CI 0.95-01.03, p=0.6)

Conclusion We observe a partial obesity paradox in patients with cardiogenic shock, showing that overweight followed by obesity has the lowest mortality whereas cachexia has the highest mortality despite multivariate adjustment.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

No founding

Author Declarations

I 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:

This database is publicaly available without any patients identifier exempt from IRB

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the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

Data Availability

it is nis data base pulicaly available

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