A Clinical and Physiological Prospective Observational Study on the Management of Pediatric Shock in the Post-Fluid Expansion as Supportive Therapy Trial Era.


Journal

Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies
ISSN: 1529-7535
Titre abrégé: Pediatr Crit Care Med
Pays: United States
ID NLM: 100954653

Informations de publication

Date de publication:
01 07 2022
Historique:
pubmed: 22 4 2022
medline: 12 7 2022
entrez: 21 4 2022
Statut: ppublish

Résumé

Fluid bolus resuscitation in African children is harmful. Little research has evaluated physiologic effects of maintenance-only fluid strategy. We describe the efficacy of fluid-conservative resuscitation of septic shock using case-fatality, hemodynamic, and myocardial function endpoints. Pediatric wards of Mbale Regional Referral Hospital, Uganda, and Kilifi County Hospital, Kenya, conducted between October 2013 and July 2015. Data were analysed from August 2016 to July 2019. Children (≥ 60 d to ≤ 12 yr) with severe febrile illness and clinical signs of impaired perfusion. IV maintenance fluid (4 mL/kg/hr) unless children had World Health Organization (WHO) defined shock (≥ 3 signs) where they received two fluid boluses (20 mL/kg) and transfusion if shock persisted. Clinical, electrocardiographic, echocardiographic, and laboratory data were collected at presentation, during resuscitation and on day 28. Outcome measures were 48-hour mortality, normalization of hemodynamics, and cardiac biomarkers. Thirty children (70% males) were recruited, six had WHO shock, all of whom died (6/6) versus three of 24 deaths in the non-WHO shock. Median fluid volume received by survivors and nonsurvivors were similar (13 [interquartile range (IQR), 9-32] vs 30 mL/kg [28-61 mL/kg], z = 1.62, p = 0.23). By 24 hours, we observed increases in median (IQR) stroke volume index (39 mL/m 2 [32-42 mL/m 2 ] to 47 mL/m 2 [41-49 mL/m 2 ]) and a measure of systolic function: fractional shortening from 30 (27-33) to 34 (31-38) from baseline including children managed with no-bolus. Children with WHO shock had a higher mean level of cardiac troponin ( t = 3.58; 95% CI, 1.24-1.43; p = 0.02) and alpha-atrial natriuretic peptide ( t = 16.5; 95% CI, 2.80-67.5; p < 0.01) at admission compared with non-WHO shock. Elevated troponin (> 0.1 μg/mL) and hyperlactatemia (> 4 mmol/L) were putative makers predicting outcome. Maintenance-only fluid therapy normalized clinical and myocardial perturbations in shock without compromising cardiac or hemodynamic function whereas fluid-bolus management of WHO shock resulted in high fatality. Troponin and lactate biomarkers of cardiac dysfunction could be promising outcome predictors in pediatric septic shock in resource-limited settings.

Identifiants

pubmed: 35446796
doi: 10.1097/PCC.0000000000002968
pii: 00130478-202207000-00004
pmc: PMC7613033
mid: EMS146167
doi:

Substances chimiques

Biomarkers 0
Troponin 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

502-513

Subventions

Organisme : Medical Research Council
ID : MR/R018502/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0601027
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 100693
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0801439
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 203077
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 105603
Pays : United Kingdom
Organisme : EPA
ID : EP-C-15-003
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 by the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Déclaration de conflit d'intérêts

Drs. Obonyo, Olupot-Olupot, and Uyoga are funded and supported through the Wellcome Trust and the Department for International Development funded DELTAS Africa Initiative (DEL-15-003). Dr. Obonyo received funding from Imperial College London (Institutional Strategic Support Funds [105603/Z/14/Z]) and Wellcome Trust Imperial College Centre for Global Health Research [100693/Z/12/Z]) and the Initiative to Develop African Research Leaders/Kenya Medical Research Institute-Wellcome Trust Research Programme. Dr. Chebet received funding from Mbale Clinical Research Institute. Drs. Olupot-Olupot, Nteziyaremye, Muhindo, and Maitland received support for article research from Research Councils UK. Drs. Nteziyaremye, Chebet, Muhindo, and Maitland received support for article research from Wellcome Trust/Charity Open Access Fund. Dr. Maitland received funding from Wellcome East African Overseas Programme Award from the Wellcome Trust (203077/Z/16/Z). The remaining authors have disclosed that they do not have any potential conflicts of interest.

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Auteurs

Nchafatso G Obonyo (NG)

Kenya Medical Research Institute, Clinical Sciences Department, Wellcome Trust Research Programme, Kilifi, Kenya.
Initiative to Develop African Research Leaders, Kilifi, Kenya.
Mbale Clinical Research Institute, Department of Paediatrics, Mbale, Uganda.
Critical Care Research Group, The Prince Charles Hospital, Brisbane, VIC, Australia.

Peter Olupot-Olupot (P)

Initiative to Develop African Research Leaders, Kilifi, Kenya.
Mbale Clinical Research Institute, Department of Paediatrics, Mbale, Uganda.
Busitema University, Faculty of Health sciences, Mbale, Uganda.

Ayub Mpoya (A)

Kenya Medical Research Institute, Clinical Sciences Department, Wellcome Trust Research Programme, Kilifi, Kenya.

Julius Nteziyaremye (J)

Mbale Clinical Research Institute, Department of Paediatrics, Mbale, Uganda.

Martin Chebet (M)

Mbale Clinical Research Institute, Department of Paediatrics, Mbale, Uganda.
Busitema University, Faculty of Health sciences, Mbale, Uganda.

Sophie Uyoga (S)

Kenya Medical Research Institute, Clinical Sciences Department, Wellcome Trust Research Programme, Kilifi, Kenya.
Initiative to Develop African Research Leaders, Kilifi, Kenya.

Rita Muhindo (R)

Mbale Clinical Research Institute, Department of Paediatrics, Mbale, Uganda.

Jonathon P Fanning (JP)

Critical Care Research Group, The Prince Charles Hospital, Brisbane, VIC, Australia.
Faculty of Medicine, University of Queensland, Brisbane, VIC, Australia.

Kenji Shiino (K)

Critical Care Research Group, The Prince Charles Hospital, Brisbane, VIC, Australia.
School of Medicine, Griffith University, Gold Coast, QLD, Australia.

Jonathan Chan (J)

Critical Care Research Group, The Prince Charles Hospital, Brisbane, VIC, Australia.
School of Medicine, Griffith University, Gold Coast, QLD, Australia.

John F Fraser (JF)

Critical Care Research Group, The Prince Charles Hospital, Brisbane, VIC, Australia.
Faculty of Medicine, University of Queensland, Brisbane, VIC, Australia.
School of Medicine, Griffith University, Gold Coast, QLD, Australia.

Kathryn Maitland (K)

Kenya Medical Research Institute, Clinical Sciences Department, Wellcome Trust Research Programme, Kilifi, Kenya.
Department of Infectious Disease and Institute of Global Health and Innovation, Division of Medicine, Imperial College, London, United Kingdom.

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