TY - JOUR
T1 - Efficacy of Ascorbic Acid, Thiamine, and Hydrocortisone Combination Therapy
T2 - Meta-analysis of Randomized Controlled Trials
AU - Kato, Takahiro
AU - Mizuno, Tomohiro
AU - Nakanishi, Masanori
AU - Lee, Jeannie K.
AU - Yamada, Shigeki
AU - Tsuboi, Naotake
AU - Takahashi, Kazuo
N1 - Funding Information: This work was supported by JSPS KAKENHI [grant number 21K06696] and the Research Center for Pathogenesis of Intractable Diseases, Research Institute of Meijo University. The Authors thank Yohei Doi for critical review of the manuscript. Publisher Copyright: © 2023 International Institute of Anticancer Research. All rights reserved.
PY - 2023/5
Y1 - 2023/5
N2 - Background/Aim: Sepsis is a life-threatening biological condition that induces systemic tissue and organ dysfunction and confers a high mortality risk. Although the use of hydrocortisone in combination with ascorbic acid and thiamine (HAT therapy) significantly reduced mortality from sepsis or septic shock in a previous study, it did not improve mortality in subsequent randomized controlled trials (RCTs). Therefore, no definitive conclusion has been established on the benefits of HAT therapy for sepsis or septic shock. We performed a meta-analysis to assess the treatment outcomes of HAT therapy in patients with sepsis or septic shock. Patients and Methods: We searched databases (PubMed/MEDLINE, Embase, Scopus and Cochrane Library) for RCTs using the terms “ascorbic acid”, “thiamine”, “sepsis”, “septic shock”, and “RCT”. The primary outcome of this meta-analysis was the mortality rate, and the secondary outcomes were the incidence of new-onset acute renal injury (AKI), intensive care unit (ICU) length of stay (ICU-LOS), change in the Sequential Organ Failure Assessment (SOFA) score within 72 hours, and duration of vasopressor use. Results: Nine RCTs were identified and included in the outcome evaluation. HAT therapy did not improve the 28-day and ICU mortality, new-onset AKI, ICU-LOS, or SOFA scores. However, HAT therapy significantly shortened the duration of vasopressor use. Conclusion: HAT therapy did not improve mortality, the SOFA score, renal injury, or ICU-LOS. Further studies are needed to confirm whether it shortens the duration of vasopressor use.
AB - Background/Aim: Sepsis is a life-threatening biological condition that induces systemic tissue and organ dysfunction and confers a high mortality risk. Although the use of hydrocortisone in combination with ascorbic acid and thiamine (HAT therapy) significantly reduced mortality from sepsis or septic shock in a previous study, it did not improve mortality in subsequent randomized controlled trials (RCTs). Therefore, no definitive conclusion has been established on the benefits of HAT therapy for sepsis or septic shock. We performed a meta-analysis to assess the treatment outcomes of HAT therapy in patients with sepsis or septic shock. Patients and Methods: We searched databases (PubMed/MEDLINE, Embase, Scopus and Cochrane Library) for RCTs using the terms “ascorbic acid”, “thiamine”, “sepsis”, “septic shock”, and “RCT”. The primary outcome of this meta-analysis was the mortality rate, and the secondary outcomes were the incidence of new-onset acute renal injury (AKI), intensive care unit (ICU) length of stay (ICU-LOS), change in the Sequential Organ Failure Assessment (SOFA) score within 72 hours, and duration of vasopressor use. Results: Nine RCTs were identified and included in the outcome evaluation. HAT therapy did not improve the 28-day and ICU mortality, new-onset AKI, ICU-LOS, or SOFA scores. However, HAT therapy significantly shortened the duration of vasopressor use. Conclusion: HAT therapy did not improve mortality, the SOFA score, renal injury, or ICU-LOS. Further studies are needed to confirm whether it shortens the duration of vasopressor use.
KW - HAT therapy
KW - SOFA
KW - Sepsis
KW - mortality
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U2 - 10.21873/invivo.13200
DO - 10.21873/invivo.13200
M3 - Article
C2 - 37103081
SN - 0258-851X
VL - 37
SP - 1236
EP - 1245
JO - In Vivo
JF - In Vivo
IS - 3
ER -