Evidence map›Paper›PMID 38983762›Full record

ArticleWorld journal of nephrology2024

Physico-chemical characterization of acid base disorders in patients with COVID-19: A cohort study.

Sergio Pinto de Souza, Juliana R Caldas, Marcelo Barreto Lopes, Marcelo Augusto Duarte Silveira, Fernanda Oliveira Coelho, Igor Oliveira Queiroz, Pedro Domingues Cury, Rogério da Hora Passos

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Article in World journal of nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Sergio Pinto de SouzaDepartment of Nephrology, Hospital São Rafael, Salvador, BA 41253190, Brazil.
Juliana R CaldasDepartment of Intensive Care, D'Or Institute for Research and Education (IDOR), Salvador, BA 41253190, Brazil.
Marcelo Barreto LopesDepartment of Nephrology, Hospital São Rafael, Salvador, BA 41253190, Brazil.
Marcelo Augusto Duarte SilveiraDepartment of Nephrology, Hospital São Rafael, Salvador, BA 41253190, Brazil.
Fernanda Oliveira CoelhoDepartment of Nephrology, Hospital São Rafael, Salvador, BA 41253190, Brazil.
Igor Oliveira QueirozHospital São Rafael, D'Or Institute for Research and Education (IDOR), Salvador, BA 41253190, Brazil.
Pedro Domingues CuryHospital São Rafael, D'Or Institute for Research and Education (IDOR), Salvador, BA 41253190, Brazil.
Rogério da Hora PassosDepartment of Intensive Care Unit, Hospital Israelita Albert Einstein, Sao Paulo, SP 05652900, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcid-base imbalance has been poorly described in patients with coronavirus disease 2019 (COVID-19). Study by the quantitative acid-base approach may be able to account for minor changes in ion distribution that may have been overlooked using traditional acid-base analysis techniques. In a cohort of critically ill COVID-19 patients, we looked for an association between metabolic acidosis surrogates and worse clinical outcomes, such as mortality, renal dialysis, and length of hospital stay.

aimTo describe the acid-base disorders of critically ill COVID-19 patients using Stewart's approach, associating its variables with poor outcomes.

methodsThis study pertained to a retrospective cohort comprised of adult patients who experienced an intensive care unit stay exceeding 4 days and who were diagnosed with severe acute respiratory syndrome coronavirus 2 infection through a positive polymerase chain reaction analysis of a nasal swab and typical pulmonary involvement observed in chest computed tomography scan. Laboratory and clinical data were obtained from electronic records. Categorical variables were compared using Fisher's exact test. Continuous data were presented as median and interquartile range. The Mann-Whitney

resultsIn total, 211 patients were analyzed. The mortality rate was 13.7%. Overall, 149 patients (70.6%) presented with alkalosis, 28 patients (13.3%) had acidosis, and the remaining 34 patients (16.2%) had a normal arterial pondus hydrogenii. Of those presenting with acidosis, most had a low apparent strong ion difference (SID) (20 patients, 9.5%). Within the group with alkalosis, 128 patients (61.0%) had respiratory origin. The non-survivors were older, had more comorbidities, and had higher Charlson's and simplified acute physiology score 3. We did not find severe acid-base imbalance in this population. The analyzed Stewart's variables (effective SID, apparent SID, and strong ion gap and the effect of albumin, lactate, phosphorus, and chloride) were not different between the groups.

conclusionAlkalemia is prevalent in COVID-19 patients. Although we did not find an association between acid-base variables and mortality, the use of Stewart's methodology may provide insights into this severe disease.

Indexed as

Acid-base statusAcute respiratory syndromeCOVID-19Critically ill patientsPhysicochemical approach

Identifiers

PMID38983762
PMCPMC11229835

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