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Situation Analysis of Intravenous Admixture in Thai Hospitals and Their Readiness for Introducing Automated Intravenous Admixture Solutions

ศิตาพร ยังคง; Sitaporn Youngkong; สมหญิง พุ่มทอง; Somying Pumtong; จิรพงศ์ สุขสิริวรพงศ์; Jiraphong Suksiriworapong; อุกฤษฏ์ สิทธิบุศย์; Ukrit Sitthiboot; ปราการเกียรติ ยังคง; Prakrankiat Youngkong;
Date: 2567-06
Abstract
Intravenous admixture (IV admixture) preparation is one of the most important pharmaceutical services provided for patients in hospitals. Currently, the increasing and varying demand for IV admixture items according to the medical prescriptions are observed. Automated solutions for IV admixture preparations in hospitals have been introduced to improve medication safety and workflow efficiency. However, there has been no study on situation of IV admixture in Thai hospitals. This resulted in the difficulties in determining the workflow problems and identifying the readiness for hospitals in introducing the automated solutions. Thus, this study aims to study the most recent situation of IV admixture preparations in the Thai hospitals and to preliminarily consider their readiness for introducing automated intravenous admixture solutions. The cross-sectional survey with self-administered questionnaire developed by the research team (COA.No.MU-DT/PY-IRB 2022/031.3006 approved on 30 June 2022) was conducted during August-December 2022. The questionnaires were distributed to 210 government hospitals in Thailand via post-mails. One hundred and twelve forms were returned (53.3% response rate). However, 13 hospitals (6.2%) could not fill the form due to the requirement of the hospital ethical committee approval, so this group was omitted from the survey. The other 96 hospitals completed the forms (response rate was 45.7% when considered the response from this group). Of these, 66 hospitals (68.8%) had IV admixture preparations in their hospitals and completed the forms, while the remaining 30 hospitals (31.2%) stated that they did not prepare IV admixture in their hospitals. From the total 66 hospitals with IV admixture preparations, cytotoxic drugs were the most common IV admixture items prepared in the hospitals (90.9%), followed by Total Parenteral Nutrition (TPN) (72.7%), extemporaneous IV admixture preparations (40%), and IV admixture prepared in large scale (14%), respectively. Average number of items prepared in the hospitals was 30 items per day for cytotoxic drugs, and 17 items per day for TPN. These number depends on the size of the hospitals (the more hospital-beds, the greater number of items prepared). More than half of the 66 hospitals reported that they prepared cytotoxic drugs more than a round per day. The workforce in the sterile production department (including the 4 categories of IV admixture preparations) of each hospital was around 2-3 full-time equivalent. All of them were trained prior to work in this department. For the IV admixture preparation working space, the largest area was for preparing cytotoxic drugs (27.9±23.7 m2), and this was around 29±28.4% of the total production area. From their reported IV admixture preparations, the top 5 cytotoxic preparations in hospital were 5-Fluorouracil, Cyclophosphamide, Doxorubicin, Oxaliplatin and Paclitaxel. The top extemporaneous IV admixture preparations were antibiotic group (e.g., Cefotaxime, Ceftazidime and Gentamicin) and high alert drugs (e.g., Heparin and Morphine). In addition, high alert drug group was reported as the top IV admixture prepared in large scale. According to the medication errors, inappropriate preparation, including wrong concentration and wrong dose, was the most commonly reported errors. However, the error incidents were reported less than 1% of the total IV admixture preparations. Almost all hospitals indicated their destruction protocols for the IV admixture prepared by their hospitals. During the survey, there has been one hospital using a robot for cytotoxic preparation and the other hospital was during the trial of using a robot for cytotoxic preparation in a closed system. There were a number of limitations of this study’s findings due to the scope of this study (the survey did not include the large community hospitals or M2-leveled hospitals, and did not include IV admixture preparation in the hospital in-patient wards), the misunderstanding nature of self-administered questionnaire used in this study, and the differences in the record, monitoring, and reporting systems of those hospitals.
Copyright ผลงานวิชาการเหล่านี้เป็นลิขสิทธิ์ของสถาบันวิจัยระบบสาธารณสุข หากมีการนำไปใช้อ้างอิง โปรดอ้างถึงสถาบันวิจัยระบบสาธารณสุข ในฐานะเจ้าของลิขสิทธิ์ตามพระราชบัญญัติสงวนลิขสิทธิ์สำหรับการนำงานวิจัยไปใช้ประโยชน์ในเชิงพาณิชย์
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