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Association between Type of Fluid Received Prior to Enrollment, Type of Admission, and Effect of Balanced Crystalloid in Critically Ill Adults: A Secondary Exploratory Analysis of the BaSICS Clinical Trial.
Zampieri, Fernando G; Machado, Flávia R; Biondi, Rodrigo S; Freitas, Flávio G R; Veiga, Viviane C; Figueiredo, Rodrigo C; Lovato, Wilson J; Amêndola, Cristina P; Serpa-Neto, Ary; Paranhos, Jorge L R; Lúcio, Eraldo A; Oliveira-Júnior, Lúcio C; Lisboa, Thiago C; Lacerda, Fábio H; Maia, Israel S; Grion, Cintia M C; Assunção, Murillo S C; Manoel, Airton L O; Corrêa, Thiago D; Guedes, Marco Antonio V A; Azevedo, Luciano C P; Miranda, Tamiris A; Damiani, Lucas P; Brandão da Silva, Nilton; Cavalcanti, Alexandre B.
Afiliação
  • Zampieri FG; HCor Research Institute, São Paulo, Brazil.
  • Machado FR; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Biondi RS; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Freitas FGR; Departamento de Anestesiologia, Dor e Terapia Intensiva, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Veiga VC; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Figueiredo RC; Instituto de Cardiologia do Distrito Federal, Brasília, Brazil.
  • Lovato WJ; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Amêndola CP; Hospital SEPACO, São Paulo, Brazil.
  • Serpa-Neto A; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Paranhos JLR; BP - A Beneficência Portuguesa de São Paulo, São Paulo, Brazil.
  • Lúcio EA; Hospital Maternidade São José, Centro Universitário do Espírito Santo, Colatina, Brazil.
  • Oliveira-Júnior LC; Hospital das Clínicas, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil.
  • Lisboa TC; Fundação Pio XII, Hospital de Câncer de Barretos, Barretos, Brazil.
  • Lacerda FH; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Maia IS; Hospital Israelita Albert Einstein, São Paulo, Brazil.
  • Grion CMC; Santa Casa de Misericórdia de São João Del Rei, São João Del Rei, Brazil.
  • Assunção MSC; Hospital São Francisco, Santa Casa de Porto Alegre, Porto Alegre, Brazil.
  • Manoel ALO; Hospital Geral Clériston Andrade, Feira de Santana, Brazil.
  • Corrêa TD; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Guedes MAVA; Hospital Santa Rita, Santa Casa de Porto Alegre, Porto Alegre, Brazil.
  • Azevedo LCP; Hospital da Luz, São Paulo, Brazil.
  • Miranda TA; HCor Research Institute, São Paulo, Brazil.
  • Damiani LP; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
  • Brandão da Silva N; Hospital Nereu Ramos, Florianópolis, Brazil.
  • Cavalcanti AB; Brazilian Research in Intensive Care Network, São Paulo, Brazil.
Am J Respir Crit Care Med ; 205(12): 1419-1428, 2022 06 15.
Article em En | MEDLINE | ID: mdl-35349397
ABSTRACT
Rationale The effects of balanced crystalloid versus saline on clinical outcomes for ICU patients may be modified by the type of fluid that patients received for initial resuscitation and by the type of admission.

Objectives:

To assess whether the results of a randomized controlled trial could be affected by fluid use before enrollment and admission type.

Methods:

Secondary post hoc analysis of the BaSICS (Balanced Solution in Intensive Care Study) trial, which compared a balanced solution (Plasma-Lyte 148) with 0.9% saline in the ICU. Patients were categorized according to fluid use in the 24 hours before enrollment in four groups (balanced solutions only, 0.9% saline only, a mix of both, and no fluid before enrollment) and according to admission type (planned, unplanned with sepsis, and unplanned without sepsis). The association between 90-day mortality and the randomization group was assessed using a hierarchical logistic Bayesian model. Measurements and Main

Results:

A total of 10,520 patients were included. There was a low probability that the balanced solution was associated with improved 90-day mortality in the whole trial population (odds ratio [OR], 0.95; 89% credible interval [CrI], 0.66-10.51; probability of benefit, 0.58); however, probability of benefit was high for patients who received only balanced solutions before enrollment (regardless of admission type, OR, 0.78; 89% CrI, 0.56-1.03; probability of benefit, 0.92), mostly because of a benefit in unplanned admissions due to sepsis (OR, 0.70; 89% CrI, 0.50-0.97; probability of benefit, 0.96) and planned admissions (OR, 0.79; 89% CrI, 0.65-0.97; probability of benefit, 0.97).

Conclusions:

There is a high probability that balanced solution use in the ICU reduces 90-day mortality in patients who exclusively received balanced fluids before trial enrollment. Clinical trial registered with www.clinicaltrials.gov (NCT02875873).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article