Stetson Raymond C, Smith Brandi N, Sanders Nicole L, Misgen Megan A, Ferrie LaRae J, Schuning Virginia S, Schuh Allison R, Fang Jennifer L, Brumbaugh Jane E
Division of Neonatal Medicine, Mayo Clinic, Rochester, Minn.
Department of Pharmacy Services, Mayo Clinic, Rochester, Minn.
Pediatr Qual Saf. 2020 Jun 26;5(4):e312. doi: 10.1097/pq9.0000000000000312. eCollection 2020 Jul-Aug.
Infants in neonatal intensive care units require painful and noxious stimuli as part of their care. Judicious use of analgesic medications, including opioids, is necessary. However, these medications have long- and short-term side effects, including potential neurotoxicity. This quality improvement project's primary aim was to decrease opioid exposure by 33% in the first 14 days of life for infants less than 1,250 g at birth within 12 months.
A multidisciplinary care team used methodology to identify root causes of the quality gap including: (1) inconsistent reporting of objective pain scales; (2) variable provider prescribing patterns; and (3) variable provider bedside assessment of pain. These root causes were addressed by two interventions: (1) standardized reporting of the premature infant pain profile scores and (2) implementation of an analgesia management pathway.
Mean opioid exposure, measured in morphine equivalents, in infants less than 1,250 g at birth during their first 14 days of life decreased from 0.64 mg/kg/d (95% confidence interval 0.41-0.87) at baseline to 0.08 mg/kg/d (95% confidence interval 0.03-0.13) during the postintervention period ( < 0.001). There was no statistical difference in rates of days to full feedings, unintentional extubations, or central line removals between epochs.
Following the implementation of consistent pain score reporting and an analgesia management pathway, opioid exposure in the first 14 days of life for infants less than 1,250 g was significantly reduced by 88%, exceeding the project aim.
新生儿重症监护病房的婴儿在护理过程中需要接受疼痛性和有害刺激。合理使用包括阿片类药物在内的镇痛药物是必要的。然而,这些药物存在长期和短期副作用,包括潜在的神经毒性。本质量改进项目的主要目标是在12个月内将出生体重小于1250克的婴儿出生后前14天的阿片类药物暴露量降低33%。
一个多学科护理团队采用方法来确定质量差距的根本原因,包括:(1)客观疼痛量表报告不一致;(2)医护人员开处方模式多变;(3)医护人员在床边对疼痛的评估多变。通过两项干预措施解决了这些根本原因:(1)标准化报告早产儿疼痛概况评分;(2)实施镇痛管理路径。
出生体重小于1250克的婴儿在出生后前14天以吗啡当量衡量的平均阿片类药物暴露量从基线时的0.64毫克/千克/天(95%置信区间0.41 - 0.87)降至干预后时期的0.08毫克/千克/天(95%置信区间0.03 - 0.13)(P < 0.001)。各阶段在完全喂养天数、意外拔管或拔除中心静脉导管的发生率方面没有统计学差异。
在实施一致的疼痛评分报告和镇痛管理路径后,出生体重小于1250克的婴儿出生后前14天的阿片类药物暴露量显著降低了88%,超过了项目目标。