Using existing data to understand and ameliorate risk in opioid agonist therapy
Using existing data to understand and ameliorate risk in opioid agonist therapy
批准号:
9904242
负责人:
Louisa Degenhardt
金额:
$4.86万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-15 至 2021-07-31
关键词:
Adverse eventAftercareBuprenorphineCessation of lifeClinicClinicalComorbidityCriminal JusticeDataData SetDevelopmentDrug abuseEpidemicEventGoalsHealthHospitalizationKnowledgeLinkLogisticsMachine LearningMethadoneMethodsModelingNeoadjuvant TherapyNew South WalesOutcomeOverdosePatient riskPatientsPersonsPharmaceutical PreparationsPopulationPrisonsProbabilityProviderRecording of previous eventsResearchRiskRisk AssessmentRisk FactorsSafetySpecialistSpecific qualifier valueTechniquesTimeTrainingUnited StatesWithholding Treatmentadverse event riskadverse outcomebaseeffective therapyexperienceindividualized medicineinnovationlearning strategymortalitymortality risknovelopioid agonist therapyopioid epidemicopioid useopioid use disorderoverdose deathpoint of carepopulation basedpopulation healthprediction algorithmprescription opioidprotective factorsrandom forestresponserisk minimizationrisk prediction modelscale uptreatment durationtreatment planning
中文摘要
项目摘要/摘要
美国正处于阿片类药物流行之中,导致前所未有的过量死亡
以及其他伤害。阿片类激动剂疗法是治疗阿片类药物使用障碍的有效方法。
(燕麦)加美沙酮或丁丙诺啡。然而,存在关于不良反应风险的重大问题。
临床结果,包括治疗期间和治疗后的死亡率和住院率,以及计划外治疗
停止。这些风险的大小是什么,患者、治疗环境和提供者因素可能是什么
是促成风险还是防范风险?此外,越来越明显的是,更复杂的方法
需要比目前使用的更好的患者评估和治疗计划,以将风险降至最低。我们的目标是:1.
确定特定不良临床结果(例如死亡率、住院时间和ED)的风险大小
出现症状和计划外停药)在使用美沙酮和丁丙诺啡的燕麦中和之后;
确定与不良临床结果相关的患者、治疗环境和提供者风险因素
以及美沙酮和丁丙诺啡燕麦后;以及3.开发风险预测模型来识别患者
在燕麦片治疗期间和之后出现不良临床结果的风险最大。为了实现这些目标,本项目将使用
现有基于人口的澳大利亚OAT数据,链接到几个卫生和刑事司法数据集,以
提供对治疗暴露和结果的丰富了解。这些数据将被用于通知
指导在美国提供高质量阿片类药物使用障碍治疗的战略。
具体地说,该项目将提供有关不良临床结果风险大小的数据。
具体的治疗和治疗后时期,并确定患者、治疗环境和提供者因素
影响风险。此外,它还将使用创新的机器学习技术来展示
常规收集的数据用于在护理点评估患者风险,从而允许制定
量身定制的治疗计划,最大限度地减少风险和最大限度地保留治疗。
英文摘要
PROJECT SUMMARY/ABSTRACT
The United States is in the midst of an opioid epidemic, leading to unprecedented levels of overdose deaths
and other harms. Effective treatment for opioid use disorders is available, in the form of opioid agonist therapy
(OAT) with methadone or buprenorphine. However, there are significant questions about the risk of adverse
clinical outcomes, including mortality and hospitalization during and after treatment, and unplanned treatment
cessation. What is the magnitude of these risks, and what patient, treatment setting, and provider factors may
contribute to or protect against risk? Additionally, it is increasingly clear that more sophisticated approaches to
patient assessment and treatment planning than are currently used are needed to minimise risk. We aim to: 1.
Determine the magnitude of risk for specific adverse clinical outcomes (e.g. mortality, hospitalization and ED
presentation, and unplanned treatment cessation) during and after OAT with methadone and buprenorphine; 2.
Identify patient, treatment setting, and provider risk factors associated with adverse clinical outcomes during
and after OAT with methadone and buprenorphine; and 3. Develop a risk prediction model to identify patients
at greatest risk of adverse clinical outcomes during and after OAT. To achieve these aims, this project will use
existing population-based Australian data on OAT, linked to several health and criminal justice datasets to
provide a rich understanding of treatment exposures and outcomes. These data will be used to inform
strategies to guide the delivery of high-quality treatment for opioid use disorder in the United States.
Specifically, the project will provide data about the magnitude of risk of adverse clinical outcomes during
specific treatment and post-treatment periods, and identify patient, treatment setting and provider factors that
influence risk. Additionally, it will use innovative machine learning techniques to demonstrate the potential for
routinely collected data to be used to assess patient risk at point-of-care, allowing for the development of
tailored treatment plans that minimize risk and maximize treatment retention.
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Correlates of indicators of potential extra-medical opioid use in people prescribed opioids for chronic non-cancer pain.
服用阿片类药物治疗慢性非癌性疼痛的患者中潜在的非医疗阿片类药物使用指标的相关性。
DOI:
10.1111/dar.13021
发表时间:
2020
期刊:
Drug and alcohol review
影响因子:
3.8
作者:
[SantoJr,Thomas, Larance,Briony, Bruno,Raimondo, Gisev,Natasa, Nielsen,Suzanne, Degenhardt,Louisa, Campbell,Gabrielle]
通讯作者:
Campbell,Gabrielle
Risks of harm with cannabinoids, cannabis, and cannabis-based medicine for pain management relevant to patients receiving pain treatment: protocol for an overview of systematic reviews.
大麻素、大麻和以大麻为基础的药物用于与接受疼痛治疗的患者相关的疼痛管理的危害风险:系统评价概述的方案。
DOI:
10.1097/pr9.0000000000000742
发表时间:
2019
期刊:
Pain reports
影响因子:
4.8
作者:
[Gilron,Ian, Blyth,FionaM, Degenhardt,Louisa, DiForti,Marta, Eccleston,Christopher, Haroutounian,Simon, Moore,Andrew, Rice,AndrewSC, Wallace,Mark]
通讯作者:
Wallace,Mark
DOI:
10.1016/s2215-0366(18)30337-7
发表时间:
2018-12
期刊:
The lancet. Psychiatry
影响因子:
--
作者:
[GBD 2016 Alcohol and Drug Use Collaborators]
通讯作者:
GBD 2016 Alcohol and Drug Use Collaborators
DOI:
10.1016/s2468-2667(18)30110-5
发表时间:
2018-07
期刊:
The Lancet. Public health
影响因子:
--
作者:
[Campbell G, Hall WD, Peacock A, Lintzeris N, Bruno R, Larance B, Nielsen S, Cohen M, Chan G, Mattick RP, Blyth F, Shanahan M, Dobbins T, Farrell M, Degenhardt L]
通讯作者:
Degenhardt L
Cannabis use and non-cancer chronic pain - Authors' reply.
大麻的使用和非癌症慢性疼痛 - 作者的答复。
DOI:
10.1016/s2468-2667(18)30182-8
发表时间:
2018
期刊:
The Lancet. Public health
影响因子:
--
作者:
[Campbell,Gabrielle, Hall,Wayne, Degenhardt,Louisa, Dobbins,Timothy, Farrell,Michael]
通讯作者:
Farrell,Michael
共 15 条
海外基金