Impact of a Pharmacist-Driven Medication Diluent Volume Optimization Protocol on Fluid Balance and Outcomes in Critically Ill Patients

IF 0.8 Q4 PHARMACOLOGY & PHARMACY
Michael L. Behal, Breanne M. Mefford, Chris Donaldson, Melanie E. Laine, Emily G. Cox, Kathryn M. Ruf, Aric Schadler, Kat M. Spezzano, B. Bissell
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Abstract

Background: Volume overload (VO) is common in the intensive care unit (ICU) and associated with negative outcomes. Approaches have been investigated to curtail VO; however, none specifically focused on medication diluent volume optimization. Objective: Investigate the impact of a pharmacist-driven medication diluent volume optimization protocol on fluid balance in critically ill patients. Methods: A prospective, pilot study was conducted in a medical ICU during October 2021 to December 2021 (pre) and February 2022 to April 2022 (post). A pharmacist-driven medication diluent volume optimization protocol focusing on vasopressor and antimicrobial diluent volumes was implemented. Demographics and clinical data were collected during ICU admission up to 7 days. The primary outcome was net fluid balance on day 3. Secondary outcomes were medication volumes administered, net fluid balance, ICU length of stay, and mortality. Results: Supply chain shortages caused the study to stop at the end of February 2022. Overall, 152 patients were included (123 pre group, 29 post group). The most common admission diagnosis was acute respiratory failure (35%). Vasopressors and antimicrobials were utilized in 47% and 66% of patients, respectively. Net fluid balance on day 3 was greater but not significant in the post group (227.1 mL [−1840.3 to 3483.7] vs 2012.3 mL [−2686.0 to 4846.0]; P = .584). Antimicrobial diluent volumes were significantly less in the post group. No differences were seen in other secondary outcomes. Protocol group assignment was not associated with net fluid balance on day 3. Conclusion: Despite decreasing antimicrobial volume contributions, optimizing diluent volumes alone did not significantly impact overall volume status. Future studies should focus on comprehensive approaches to medication diluent optimization and fluid stewardship.
药剂师驱动的稀释剂量优化方案对重症患者体液平衡和预后的影响
背景:容量超负荷(VO)是重症监护病房(ICU)的常见病,并与不良预后有关。目前已研究出多种方法来减轻容量超负荷,但没有一种方法专门针对药物稀释剂容量的优化。目标:调查药剂师驱动的药物稀释剂量优化方案对重症患者体液平衡的影响。方法:在 2021 年 10 月至 2021 年 12 月(前期)和 2022 年 2 月至 2022 年 4 月(后期)期间,在内科重症监护病房开展了一项前瞻性试点研究。实施了药剂师驱动的药物稀释剂量优化方案,重点关注血管加压药和抗菌药的稀释剂量。在重症监护室入院 7 天内收集人口统计学和临床数据。主要结果是第 3 天的净液体平衡。次要结果是用药量、净液体平衡、重症监护室住院时间和死亡率。研究结果由于供应链短缺,研究于 2022 年 2 月底停止。总共纳入了 152 名患者(123 名组前患者,29 名组后患者)。最常见的入院诊断是急性呼吸衰竭(35%)。分别有 47% 和 66% 的患者使用了血管加压药和抗菌药。术后组患者第 3 天的净液体平衡量更大,但无显著性差异(227.1 mL [-1840.3 to 3483.7] vs 2012.3 mL [-2686.0 to 4846.0];P = .584)。术后组的抗菌稀释剂用量明显减少。其他次要结果无差异。方案组分配与第 3 天的净体液平衡无关。结论尽管抗菌药物的用量有所减少,但仅靠优化稀释剂用量并不会对总体容量状况产生明显影响。未来的研究应重点关注药物稀释剂优化和液体管理的综合方法。
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来源期刊
Hospital Pharmacy
Hospital Pharmacy PHARMACOLOGY & PHARMACY-
CiteScore
1.70
自引率
0.00%
发文量
63
期刊介绍: Hospital Pharmacy is a monthly peer-reviewed journal that is read by pharmacists and other providers practicing in the inpatient and outpatient setting within hospitals, long-term care facilities, home care, and other health-system settings The Hospital Pharmacy Assistant Editor, Michael R. Cohen, RPh, MS, DSc, FASHP, is author of a Medication Error Report Analysis and founder of The Institute for Safe Medication Practices (ISMP), a nonprofit organization that provides education about adverse drug events and their prevention.
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