Shaina A. Bird Pharm.D., Michael R. Thuyns Pharm.D.
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Thuyns Pharm.D.","doi":"10.1002/jac5.2069","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>Few validated approaches exist for the transition from intravenous (IV) insulin infusion to subcutaneous (SQ) insulin post-operatively in cardiothoracic surgery patients.</p>\n </section>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>This study aimed to assess whether a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only SQ insulin is safe and efficacious for post-operative glycemic control following 24 h of IV insulin administration.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>A retrospective, single-center, observational study investigating outcomes associated with a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only insulin from May 2023 through July 2023 when compared with a historical nursing-driven protocol observed from May 2021 through July 2021. Adult cardiac intensive care unit patients who received an insulin infusion within 24 h of cardiothoracic surgery and subsequently transitioned to SQ insulin were observed. The primary outcome was percentage of blood glucose (BG) readings at goal (140–180 mg/dL). Secondary outcomes included percentage of BG readings in a clinically acceptable range (110–180 mg/dL), hypoglycemia (<70 mg/dL), severe hypoglycemia (<40 mg/dL), administration of rescue dextrose, reinitiation of insulin infusion following transition, and surgical site infection.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Use of a pharmacist-driven protocol improved the percentage of BG readings in goal range when compared with a nursing driven protocol (24.4% vs. 12.4%, <i>p</i> = 0.001). More BG readings were in the clinically acceptable range in the pharmacist-driven group: 69.6% of readings versus 58.5% in the nursing-driven group (<i>p</i> = 0.011). There were fewer hypoglycemic events in the pharmacist-driven group. There were no reports of severe hypoglycemia, further IV insulin requirements, or surgical site infections in either group. Pharmacist compliance to the protocol was high at 92.4%.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>A pharmacist-driven protocolized approach to the transition to SQ insulin post-operatively in cardiothoracic patients is both safe and efficacious. The pharmacist-driven protocol resulted in an improved percentage of BG readings in goal range and fewer hypoglycemic events when compared with the historical nursing-driven protocol.</p>\n </section>\n </div>","PeriodicalId":73966,"journal":{"name":"Journal of the American College of Clinical Pharmacy : JACCP","volume":"8 2","pages":"123-128"},"PeriodicalIF":1.3000,"publicationDate":"2025-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jac5.2069","citationCount":"0","resultStr":"{\"title\":\"Safety and efficacy of a pharmacist-driven protocolized transition from insulin infusion to subcutaneous insulin in patients undergoing cardiothoracic surgery\",\"authors\":\"Shaina A. Bird Pharm.D., Michael R. 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Adult cardiac intensive care unit patients who received an insulin infusion within 24 h of cardiothoracic surgery and subsequently transitioned to SQ insulin were observed. The primary outcome was percentage of blood glucose (BG) readings at goal (140–180 mg/dL). Secondary outcomes included percentage of BG readings in a clinically acceptable range (110–180 mg/dL), hypoglycemia (<70 mg/dL), severe hypoglycemia (<40 mg/dL), administration of rescue dextrose, reinitiation of insulin infusion following transition, and surgical site infection.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Use of a pharmacist-driven protocol improved the percentage of BG readings in goal range when compared with a nursing driven protocol (24.4% vs. 12.4%, <i>p</i> = 0.001). More BG readings were in the clinically acceptable range in the pharmacist-driven group: 69.6% of readings versus 58.5% in the nursing-driven group (<i>p</i> = 0.011). There were fewer hypoglycemic events in the pharmacist-driven group. There were no reports of severe hypoglycemia, further IV insulin requirements, or surgical site infections in either group. Pharmacist compliance to the protocol was high at 92.4%.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>A pharmacist-driven protocolized approach to the transition to SQ insulin post-operatively in cardiothoracic patients is both safe and efficacious. 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引用次数: 0
摘要
对于心胸外科患者术后从静脉(IV)胰岛素输注到皮下(SQ)胰岛素输注的过渡,目前很少有经过验证的方法。目的:本研究旨在评估药师驱动的方案使用基础、膳食、纠正或仅纠正的SQ胰岛素在静脉注射胰岛素24小时后对术后血糖控制是否安全有效。方法回顾性、单中心、观察性研究调查了2023年5月至2023年7月期间使用基础、膳食、矫正或仅矫正胰岛素的药剂师驱动方案的相关结果,并与2021年5月至2021年7月期间观察到的历史护理驱动方案进行了比较。观察了在心胸外科手术后24小时内接受胰岛素输注并随后过渡到SQ胰岛素的成人心脏重症监护病房患者。主要终点是血糖(BG)读数达到目标(140-180 mg/dL)的百分比。次要结果包括BG读数在临床可接受范围内的百分比(110-180 mg/dL),低血糖(70 mg/dL),严重低血糖(40 mg/dL),给予援救葡萄糖,转移后重新开始胰岛素输注,手术部位感染。结果与护理驱动方案相比,药剂师驱动方案的使用提高了BG读数在目标范围内的百分比(24.4% vs 12.4%, p = 0.001)。在药剂师驱动组中,更多的BG读数在临床可接受范围内:69.6%的读数高于护理驱动组的58.5% (p = 0.011)。药剂师驱动组的低血糖事件较少。两组均无严重低血糖、进一步静脉注射胰岛素或手术部位感染的报告。药师对方案的依从性高达92.4%。结论药师驱动的协议化方法在心胸外科患者术后过渡到SQ胰岛素是安全有效的。与以往的护理驱动方案相比,药剂师驱动方案提高了BG读数在目标范围内的百分比,并减少了低血糖事件。
Safety and efficacy of a pharmacist-driven protocolized transition from insulin infusion to subcutaneous insulin in patients undergoing cardiothoracic surgery
Introduction
Few validated approaches exist for the transition from intravenous (IV) insulin infusion to subcutaneous (SQ) insulin post-operatively in cardiothoracic surgery patients.
Objective
This study aimed to assess whether a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only SQ insulin is safe and efficacious for post-operative glycemic control following 24 h of IV insulin administration.
Methods
A retrospective, single-center, observational study investigating outcomes associated with a pharmacist-driven protocol utilizing basal, prandial, correctional, or correctional-only insulin from May 2023 through July 2023 when compared with a historical nursing-driven protocol observed from May 2021 through July 2021. Adult cardiac intensive care unit patients who received an insulin infusion within 24 h of cardiothoracic surgery and subsequently transitioned to SQ insulin were observed. The primary outcome was percentage of blood glucose (BG) readings at goal (140–180 mg/dL). Secondary outcomes included percentage of BG readings in a clinically acceptable range (110–180 mg/dL), hypoglycemia (<70 mg/dL), severe hypoglycemia (<40 mg/dL), administration of rescue dextrose, reinitiation of insulin infusion following transition, and surgical site infection.
Results
Use of a pharmacist-driven protocol improved the percentage of BG readings in goal range when compared with a nursing driven protocol (24.4% vs. 12.4%, p = 0.001). More BG readings were in the clinically acceptable range in the pharmacist-driven group: 69.6% of readings versus 58.5% in the nursing-driven group (p = 0.011). There were fewer hypoglycemic events in the pharmacist-driven group. There were no reports of severe hypoglycemia, further IV insulin requirements, or surgical site infections in either group. Pharmacist compliance to the protocol was high at 92.4%.
Conclusions
A pharmacist-driven protocolized approach to the transition to SQ insulin post-operatively in cardiothoracic patients is both safe and efficacious. The pharmacist-driven protocol resulted in an improved percentage of BG readings in goal range and fewer hypoglycemic events when compared with the historical nursing-driven protocol.