Venebio Group, LLC, Richmond, Virginia.
Department of Public Health Sciences, University of North Carolina at Charlotte, Charlotte, North Carolina, USA.
Pain Med. 2018 Jan 1;19(1):68-78. doi: 10.1093/pm/pnx009.
To validate a risk index that estimates the likelihood of overdose or serious opioid-induced respiratory depression (OIRD) among medical users of prescription opioids.
A case-control analysis of 18,365,497 patients with an opioid prescription from 2009 to 2013 in the IMS PharMetrics Plus commercially insured health plan claims database (CIP). An OIRD event occurred in 7,234 cases. Four controls were selected per case. Validity of the Risk Index for Overdose or Serious Opioid-induced Respiratory Depression (RIOSORD), developed previously using Veterans Health Administration (VHA) patient data, was assessed. Multivariable logistic regression was used within the CIP study population to develop a slightly refined RIOSORD. The composition and performance of the CIP-based RIOSORD was evaluated and compared with VHA-based RIOSORD.
VHA-RIOSORD performed well in discriminating OIRD events in CIP (C-statistic = 0.85). Additionally, re-estimation of logistic model coefficients in CIP yielded a 0.90 C-statistic. The resulting comorbidity and pharmacotherapy variables most highly associated with OIRD and retained in the CIP-RIOSORD were largely concordant with VHA-RIOSORD. These variables included neuropsychiatric and cardiopulmonary disorders, impaired drug excretion, opioid characteristics, and concurrent psychoactive medications. The average predicted probability of OIRD ranged from 2% to 83%, with excellent agreement between predicted and observed incidence across risk classes.
RIOSORD had excellent predictive accuracy in a large population of US medical users of prescription opioids, similar to its performance in VHA. This practical risk index is designed to support clinical decision-making for safer opioid prescribing, and its clinical utility should be evaluated prospectively.
验证一种风险指数,用于估计处方类阿片药物医学使用者发生过量或严重阿片类药物引起的呼吸抑制(OIRD)的可能性。
采用病例对照分析,对 2009 年至 2013 年 IMS PharMetrics Plus 商业保险健康计划理赔数据库(CIP)中 18365497 名接受阿片类药物处方的患者进行分析。7234 例患者发生 OIRD 事件。每例病例选择 4 名对照。评估先前使用退伍军人健康管理局(VA)患者数据开发的《过量或严重阿片类药物引起的呼吸抑制风险指数(RIOSORD)》的有效性。在 CIP 研究人群中采用多变量逻辑回归建立稍作改进的 RIOSORD。评估和比较基于 CIP 和基于 VHA 的 RIOSORD 的组成和性能。
VHA-RIOSORD 在 CIP 中区分 OIRD 事件的表现良好(C 统计量=0.85)。此外,在 CIP 中重新估计逻辑模型系数得出的 C 统计量为 0.90。与 OIRD 最密切相关并保留在 CIP-RIOSORD 中的共病和药物治疗变量在很大程度上与 VHA-RIOSORD 一致。这些变量包括神经精神和心肺疾病、药物排泄受损、阿片类药物特征和同时使用的精神活性药物。OIRD 的平均预测概率范围为 2%至 83%,风险类别之间的预测和观察发生率具有极好的一致性。
RIOSORD 在大量美国处方类阿片药物医学使用者中具有出色的预测准确性,与在 VA 中的表现相似。该实用风险指数旨在支持更安全地开具阿片类药物处方的临床决策,其临床实用性应前瞻性评估。