Incidence and management of metabolic acidosis with sodium bicarbonate in the ICU: An international observational study.
Intensive care unit
Metabolic acidosis
Mortality
Observational study
Sodium bicarbonate
Vasopressor
Journal
Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902
Informations de publication
Date de publication:
02 02 2021
02 02 2021
Historique:
received:
12
10
2020
accepted:
09
12
2020
entrez:
3
2
2021
pubmed:
4
2
2021
medline:
26
8
2021
Statut:
epublish
Résumé
Metabolic acidosis is a major complication of critical illness. However, its current epidemiology and its treatment with sodium bicarbonate given to correct metabolic acidosis in the ICU are poorly understood. This was an international retrospective observational study in 18 ICUs in Australia, Japan, and Taiwan. Adult patients were consecutively screened, and those with early metabolic acidosis (pH < 7.3 and a Base Excess < -4 mEq/L, within 24-h of ICU admission) were included. Screening continued until 10 patients who received and 10 patients who did not receive sodium bicarbonate in the first 24 h (early bicarbonate therapy) were included at each site. The primary outcome was ICU mortality, and the association between sodium bicarbonate and the clinical outcomes were assessed using regression analysis with generalized linear mixed model. We screened 9437 patients. Of these, 1292 had early metabolic acidosis (14.0%). Early sodium bicarbonate was given to 18.0% (233/1292) of these patients. Dosing, physiological, and clinical outcome data were assessed in 360 patients. The median dose of sodium bicarbonate in the first 24 h was 110 mmol, which was not correlated with bodyweight or the severity of metabolic acidosis. Patients who received early sodium bicarbonate had higher APACHE III scores, lower pH, lower base excess, lower PaCO Early metabolic acidosis is common in critically ill patients. Early sodium bicarbonate is administered by clinicians to more severely ill patients but without correction for weight or acidosis severity. Bicarbonate therapy in acidotic vasopressor-dependent patients may be beneficial and warrants further investigation.
Sections du résumé
BACKGROUND
Metabolic acidosis is a major complication of critical illness. However, its current epidemiology and its treatment with sodium bicarbonate given to correct metabolic acidosis in the ICU are poorly understood.
METHOD
This was an international retrospective observational study in 18 ICUs in Australia, Japan, and Taiwan. Adult patients were consecutively screened, and those with early metabolic acidosis (pH < 7.3 and a Base Excess < -4 mEq/L, within 24-h of ICU admission) were included. Screening continued until 10 patients who received and 10 patients who did not receive sodium bicarbonate in the first 24 h (early bicarbonate therapy) were included at each site. The primary outcome was ICU mortality, and the association between sodium bicarbonate and the clinical outcomes were assessed using regression analysis with generalized linear mixed model.
RESULTS
We screened 9437 patients. Of these, 1292 had early metabolic acidosis (14.0%). Early sodium bicarbonate was given to 18.0% (233/1292) of these patients. Dosing, physiological, and clinical outcome data were assessed in 360 patients. The median dose of sodium bicarbonate in the first 24 h was 110 mmol, which was not correlated with bodyweight or the severity of metabolic acidosis. Patients who received early sodium bicarbonate had higher APACHE III scores, lower pH, lower base excess, lower PaCO
CONCLUSIONS
Early metabolic acidosis is common in critically ill patients. Early sodium bicarbonate is administered by clinicians to more severely ill patients but without correction for weight or acidosis severity. Bicarbonate therapy in acidotic vasopressor-dependent patients may be beneficial and warrants further investigation.
Identifiants
pubmed: 33531020
doi: 10.1186/s13054-020-03431-2
pii: 10.1186/s13054-020-03431-2
pmc: PMC7851901
doi:
Substances chimiques
Sodium Bicarbonate
8MDF5V39QO
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
45Subventions
Organisme : Jikei University School of Medicine
ID : Research Grant
Investigateurs
Tomoko Fujii
(T)
Andrew A Udy
(AA)
Adam M Deane
(AM)
Alistair Nichol
(A)
Rinaldo Bellomo
(R)
Ary Serpa Neto
(AS)
Khaled El-Khawas
(K)
Naorungroj Thummaporn
(N)
Lisa Paxton
(L)
Timothy Fazio
(T)
Robert Short-Burchell
(R)
Allison Bone
(A)
Hannah Bergin
(H)
Sarah Jones
(S)
Jennifer Holmes
(J)
John Santamaria
(J)
Chloe Peppin
(C)
Yahya Shehabi
(Y)
Ravindranath Tiruvoipati
(R)
Victor Ge
(V)
Lee-Anne Clavarino
(LA)
Chelsea Ong
(C)
Owen Roodenburg
(O)
Steven Hirth
(S)
Aiko Tanaka
(A)
Naoya Iguchi
(N)
Shinshu Katayama
(S)
Jun Shima
(J)
Fumie Takatsudo
(F)
Kumie Suzuki
(K)
Shinjiro Saito
(S)
Toshiyuki Karumai
(T)
Yoshiro Hayashi
(Y)
Yu-Chang Yeh
(YC)
Chong-Jen Yu
(CJ)
Shih-Chi Ku
(SC)
Nai-Kuan Chou
(NK)
Ting-Yu Hu
(TY)
Kuang-Hua Cheng
(KH)
Chao-Lun Lai
(CL)
Hsiao-En Tsai
(HE)
Kuo-Ching Yuan
(KC)
An-Yi Wang
(AY)
Shih-Feng Huang
(SF)
Wen-Jinn Liaw
(WJ)
Kuo-Chen Cheng
(KC)
Chin-Ming Chen
(CM)
Bor-Jen Lee
(BJ)
Références
J Crit Care. 2019 Jun;51:184-191
pubmed: 30852347
Clin Exp Nephrol. 2006 Jun;10(2):111-7
pubmed: 16791396
Crit Care Med. 2009 Oct;37(10):2733-9
pubmed: 19885998
J Crit Care. 2012 Apr;27(2):132-7
pubmed: 22033060
Am J Physiol. 1985 Nov;249(5 Pt 2):F630-5
pubmed: 2998202
Am J Physiol. 1968 Jun;214(6):1352-9
pubmed: 5649491
Crit Care. 2011;15(5):R238
pubmed: 21995879
N Engl J Med. 2017 Aug 3;377(5):419-430
pubmed: 28528561
J Crit Care. 2014 Dec;29(6):971-7
pubmed: 25220529
Diabetes Res Clin Pract. 2007 Jul;77(1):113-9
pubmed: 17126447
J Biomed Inform. 2013 Apr;46(2):259-65
pubmed: 23149159
Lancet. 2018 Jul 7;392(10141):31-40
pubmed: 29910040
Ann Thorac Surg. 2016 May;101(5):1644-5
pubmed: 27106412