Antidepressant Use and Suicidality: Comparative Safety in Children and Adults
Antidepressant Use and Suicidality: Comparative Safety in Children and Adults
批准号:
7290379
负责人:
Sebastian G. Schneeweiss
金额:
$37.05万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-26 至 2010-07-31
关键词:
Accident and Emergency departmentAdmission activityAdolescentAdultAgeAlgorithmsAntideAntidepressive AgentsArtsBehaviorBritish ColumbiaChildClassClinicalCodeCohort StudiesDataDatabasesDemographic FactorsDiagnosisDoseEmergency SituationFaceFeeling suicidalFrequenciesFutureGeneral PractitionersGesturesHospitalsIndividualInterventionLinkMedicaidMedicareMedicare/MedicaidMental DepressionMeta-AnalysisMethodsMonitorMorbidity - disease rateObservational StudyOutcomePatient MonitoringPatientsPatternPharmaceutical PreparationsPhysiciansPlacebosPolicy MakerPopulationPredictive ValuePrevalenceProvincePublicationsRandomizedRandomized Controlled Clinical TrialsRateRelative (related person)ReportingResearchResearch PersonnelRiskRisk ManagementRunningSafetyScoring MethodSelf-Injurious BehaviorSerotoninSpecialistSuicideSuicide attemptTreatment FactorTreatment ProtocolsUnited States Food and Drug AdministrationVisitaccomplished suicideage groupbasecohortcomparativedesigndosageexperiencehealth care service utilizationimprovedinnovationmanprogramsreuptakesuicidalsuicide ratetime usetrend
中文摘要
描述(由申请人提供):2004年10月,美国食品和药物管理局(FDA)发布了一项咨询意见,即抗抑郁药可能与儿童和青少年自杀想法和行为的风险增加有关。这些警告是由其对该年龄组所有可用的抗抑郁药随机试验的荟萃分析引起的,在这些试验中,随机接受抗抑郁药的患者的自杀意念或行为率几乎是安慰剂组的两倍。然而,在警告之后,临床医生,政策制定者和患者仍然需要在重要的治疗问题上提供指导。我们建议汇集3大队列的患者谁开始抗抑郁药治疗(医疗补助<65;医疗保险65+,和全省人口为基础的队列在不列颠哥伦比亚省),并链接到他们的医疗保健利用的数据。我们将采用几种创新的分析方法来产生有助于指导治疗选择的数据。具体来说,我们将回答以下研究问题:1)根据类别、特定药剂、剂量和使用持续时间确定抗抑郁药使用者的自杀率。2)确定可能改变抗抑郁药使用和自杀倾向之间关系的社会人口统计学、临床和伴随治疗因素。3)确定FDA行动对抗抑郁药使用和临床结局的影响。4)确定治疗开始后患者监测的模式和潜在可修改的决定因素,以帮助设计和确定未来的风险管理干预措施。5)评估和提高医院和急诊室入院时自杀未遂编码的准确性。这项由经验丰富的跨学科团队使用多种分析方法进行的大型药物流行病学研究将评估围绕抗抑郁药治疗安全性的最关键问题,并将为制定和制定更好的处方和风险管理策略提供指导。
英文摘要
DESCRIPTION (provided by applicant): In October 2004, the U.S. Food and Drug Administration (FDA) issued an advisory that antidepressants may be associated with an increased risk of suicidal thoughts and behaviors in children and adolescents. These warnings were prompted by its meta-analysis of all available randomized trials of antidepressants in this age group, in which patients randomized to antidepressants had nearly twice the rate of suicidal ideation or behavior relative to those given placebo. However, following the warnings clinicians, policymakers, and patients still need guidance on important treatment questions. We propose pooling 3 large cohorts of patients who initiated antidepressant therapy (Medicaid <65; Medicare 65+, and a province-wide population-based cohort in British Columbia) and link that use to data on their health care utilization. We will employ several innovative analytic methods to produce data that will help guide treatment choices. Specifically, we will answer the following research questions: 1) Identify the rates of suicidality in users of antidepressants in terms of class, specific agents, dosages, and durations of use. 2) Identify sociodemographic, clinical, and concomitant treatment factors that may modify the relationship between antidepressant use and suicidality. 3) Identify the impact of FDA actions on antidepressant utilization and clinical outcomes. 4) Identify patterns and potentially modifiable determinants of patient monitoring after initiation of therapy to help design and target future risk management interventions. 5) Assess and improve the accuracy of coding attempted suicide in hospital and emergency room admissions. This large pharmacoepidemiologic study by an experienced interdisciplinary team using multiple analytic methods will assess the most critical issues surrounding the safety of antidepressant therapy, and will provide guidance to develop and target better prescribing and risk management strategies.
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