Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points

Background: Although single daily 24 hours preparation of hydrocortisone solution infusion is widely used in intensive care clinical practice, most manufacturers limit its infusion time to only four hours. The data on efficacy of this practice are scarce. Objective: To determine the physical and che...

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Main Authors: Jiraporn Leanpolchareanchai, Pitchaya Dilokpattanamongkol, Tospon Lertwattanachai, Auranee Trisataya, Amaraporn Wongrakpanich, Thanist Pravitharangul
Other Authors: Ramathibodi Hospital
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Published: 2022
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/74633
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spelling th-mahidol.746332022-08-04T11:25:17Z Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points Jiraporn Leanpolchareanchai Pitchaya Dilokpattanamongkol Tospon Lertwattanachai Auranee Trisataya Amaraporn Wongrakpanich Thanist Pravitharangul Ramathibodi Hospital Vajira Hospital Mahidol University Medicine Background: Although single daily 24 hours preparation of hydrocortisone solution infusion is widely used in intensive care clinical practice, most manufacturers limit its infusion time to only four hours. The data on efficacy of this practice are scarce. Objective: To determine the physical and chemical stability of hydrocortisone solution used in intensive care units (ICU). Materials and Methods: Powder form of 100 mg hydrocortisone was reconstituted first with sterile water for injection (SWI) and then added to normal saline solution (NSS) to obtain 1 and 2 mg/mL solutions, or first reconstituted with NSS then added to bag of NSS to obtain 1 mg/mL solution. The solutions were then stored in three different conditions, refrigerator (4±2?), ICU (25±3°), and hospital room (30±2°) temperatures for 48 hours. The physical and chemical stabilities were assessed at an initial time, 4, 8, 12, 24, and 48 hours. Results: Hydrocortisone reconstituted in SWI showed an acceptable labeled amount range (100.28±3.83%), similar to reconstitution in NSS (96.05±1.00%). Hydrocortisone solutions of 1 and 2 mg/mL stored at 4±2?, 25±3°, and 30±2° showed similar percent label amount, and the statistical tests were not significantly different among the three ranges of temperatures (p>0.05). Conclusion: Hydrocortisone reconstituted using SWI followed by NSS to obtain final concentrations of 1 to 2 mg/mL or using only NSS to obtain a final concentration of 1 mg/mL, provided an acceptable range of % hydrocortisone remaining up to 48 hours when stored at 4±2?, 25±3?, and 30±2?. 2022-08-04T04:25:17Z 2022-08-04T04:25:17Z 2022-04-01 Article Journal of the Medical Association of Thailand. Vol.105, No.4 (2022) 10.35755/jmedassocthai.2022.04.13293 01252208 2-s2.0-85128484137 https://repository.li.mahidol.ac.th/handle/123456789/74633 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85128484137&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Jiraporn Leanpolchareanchai
Pitchaya Dilokpattanamongkol
Tospon Lertwattanachai
Auranee Trisataya
Amaraporn Wongrakpanich
Thanist Pravitharangul
Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
description Background: Although single daily 24 hours preparation of hydrocortisone solution infusion is widely used in intensive care clinical practice, most manufacturers limit its infusion time to only four hours. The data on efficacy of this practice are scarce. Objective: To determine the physical and chemical stability of hydrocortisone solution used in intensive care units (ICU). Materials and Methods: Powder form of 100 mg hydrocortisone was reconstituted first with sterile water for injection (SWI) and then added to normal saline solution (NSS) to obtain 1 and 2 mg/mL solutions, or first reconstituted with NSS then added to bag of NSS to obtain 1 mg/mL solution. The solutions were then stored in three different conditions, refrigerator (4±2?), ICU (25±3°), and hospital room (30±2°) temperatures for 48 hours. The physical and chemical stabilities were assessed at an initial time, 4, 8, 12, 24, and 48 hours. Results: Hydrocortisone reconstituted in SWI showed an acceptable labeled amount range (100.28±3.83%), similar to reconstitution in NSS (96.05±1.00%). Hydrocortisone solutions of 1 and 2 mg/mL stored at 4±2?, 25±3°, and 30±2° showed similar percent label amount, and the statistical tests were not significantly different among the three ranges of temperatures (p>0.05). Conclusion: Hydrocortisone reconstituted using SWI followed by NSS to obtain final concentrations of 1 to 2 mg/mL or using only NSS to obtain a final concentration of 1 mg/mL, provided an acceptable range of % hydrocortisone remaining up to 48 hours when stored at 4±2?, 25±3?, and 30±2?.
author2 Ramathibodi Hospital
author_facet Ramathibodi Hospital
Jiraporn Leanpolchareanchai
Pitchaya Dilokpattanamongkol
Tospon Lertwattanachai
Auranee Trisataya
Amaraporn Wongrakpanich
Thanist Pravitharangul
format Article
author Jiraporn Leanpolchareanchai
Pitchaya Dilokpattanamongkol
Tospon Lertwattanachai
Auranee Trisataya
Amaraporn Wongrakpanich
Thanist Pravitharangul
author_sort Jiraporn Leanpolchareanchai
title Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
title_short Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
title_full Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
title_fullStr Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
title_full_unstemmed Stability of Hydrocortisone Sodium Succinate in Intensive Care Units: Focus on Practical Points
title_sort stability of hydrocortisone sodium succinate in intensive care units: focus on practical points
publishDate 2022
url https://repository.li.mahidol.ac.th/handle/123456789/74633
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