Worz Chad, Postolski Josh, Williams Kevin
Consult Pharm. 2017 Apr 1;32(4):222-227. doi: 10.4140/TCP.n.2017.222.
It is the current practice in most long-term care facilities to use manual logs when documenting refrigerator temperatures. This process is commonly associated with poor or fabricated compliance, little oversight, and documentation errors, both because of overt omissions and unsubstantiated values. It is also well-established that medication storage requirements are mandated by the Centers for Medicare & Medicaid Services (CMS). This analysis demonstrates the potential risk of poor cold-chain management of medications and establishes the possible utility of digitally recorded continuous temperature monitoring over manual logs. This small case-oriented review of a large nursing facility's storage process attempts to expose the risk associated with improper medication storage.
The primary outcome of the study was to determine if a difference existed between temperature logs completed manually compared with those done with a continuous monitor.
American Thermal Instruments (ATI) thermometers were placed into each of the existing refrigerators in a 147-bed nursing facility. Through a mobile app, the data recorded in each refrigerator were compiled into daily reports. Data were collected from a total of 12 refrigerators, 3 of which were medication refrigerators. Logging intervals were done over a 263-minute period and compiled the lowest recorded temperature, highest recorded temperature, and the average temperature for each refrigerator. In addition, reports showing the real-time results were compiled using the ATI DataNow service.
All of the refrigerators analyzed had highest temperature recorded readings exceeding the maximum allowable temperature (50°F for refrigerator). All of the refrigerators had lowest temperature recorded readings below the minimum allowable temperature (32°F for refrigerators). All of the refrigerators also reported average temperatures outside of the allowable temperature range. The results necessitated the replacement of a refrigerator and the evaluation of a dairy refrigerator in the food service area. This resulted in consistent measurements within the allowable range.
Following this analysis, it can be concluded that the common assumptions about the effectiveness of manual temperature logs should be verified. It can also be concluded that continuous temperature monitoring improves temperature-reporting accuracy. Proper medication storage is mandated by CMS; risk does exist that an improperly stored vaccine, biologic, or medication could lose effectiveness. While it has not been proven, improved medication storage offered from continuous monitoring could result in improved medication viability and hence improved patient outcomes associated with those medications.
在大多数长期护理机构中,目前记录冰箱温度时使用的是手工日志。这个过程通常与合规性差或数据造假、监督不足以及记录错误有关,原因包括明显的遗漏和未经证实的数据。众所周知,药物储存要求是由医疗保险和医疗补助服务中心(CMS)规定的。本分析展示了药物冷链管理不善的潜在风险,并确立了数字记录的连续温度监测相对于手工日志可能具有的效用。这个针对大型护理机构储存过程的小型案例回顾试图揭示与药物储存不当相关的风险。
该研究的主要结果是确定手动完成的温度日志与连续监测完成的温度日志之间是否存在差异。
将美国热仪器公司(ATI)的温度计放置在一家拥有147张床位的护理机构的每台现有冰箱中。通过移动应用程序,将每台冰箱记录的数据汇编成每日报告。总共从12台冰箱收集数据,其中3台是药物冰箱。记录间隔为263分钟,汇总每台冰箱记录的最低温度、最高温度和平均温度。此外,使用ATI DataNow服务编制显示实时结果的报告。
所有分析的冰箱记录的最高温度读数均超过了允许的最高温度(冰箱为50°F)。所有冰箱记录的最低温度读数均低于允许的最低温度(冰箱为32°F)。所有冰箱报告的平均温度也超出了允许的温度范围。这些结果导致一台冰箱被更换,并对食品服务区域的一台冷藏冰箱进行了评估。这使得温度测量结果在允许范围内保持一致。
经过此分析,可以得出结论,关于手工温度日志有效性的常见假设应该得到验证。还可以得出结论,连续温度监测提高了温度报告的准确性。CMS规定了正确的药物储存;确实存在疫苗、生物制品或药物储存不当可能失去效力的风险。虽然尚未得到证实,但连续监测带来的更好的药物储存可能会提高药物的活力,从而改善与这些药物相关的患者治疗效果。