Ascertainment and validation of major bleeding events in a primary care database.
Adolescent
Adult
Aged
Aged, 80 and over
Anticoagulants
/ adverse effects
Child
Child, Preschool
Emergency Service, Hospital
/ statistics & numerical data
Female
Female Urogenital Diseases
/ chemically induced
Gastrointestinal Hemorrhage
/ chemically induced
Hospitalization
/ statistics & numerical data
Humans
Incidence
Intracranial Hemorrhages
/ chemically induced
Male
Male Urogenital Diseases
/ chemically induced
Middle Aged
Predictive Value of Tests
Primary Health Care
/ statistics & numerical data
Registries
/ statistics & numerical data
Risk Assessment
/ methods
Risk Factors
Rivaroxaban
/ adverse effects
Validation Studies as Topic
Warfarin
/ adverse effects
Young Adult
anticoagulants
bleeding
databases
pharmacoepidemiology
primary care
rivaroxaban
validation studies
Journal
Pharmacoepidemiology and drug safety
ISSN: 1099-1557
Titre abrégé: Pharmacoepidemiol Drug Saf
Pays: England
ID NLM: 9208369
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
21
12
2017
revised:
09
05
2018
accepted:
28
05
2018
pubmed:
28
6
2018
medline:
24
3
2020
entrez:
28
6
2018
Statut:
ppublish
Résumé
The purpose of the study is to evaluate the impact of validation on the identification of major bleeding events in The Health Improvement Network (THIN) database in patients receiving anticoagulant therapy. Patients aged 2 to 89 years with a first prescription for an anticoagulant (rivaroxaban or warfarin) between 2012 and 2015 were identified in THIN. Major bleeding events, defined as bleeding events necessitating hospitalization or referral to accident and emergency services or a specialist clinic, were identified using a 2-step ascertainment process based on read codes only, and then validated using a 2-step process requiring manual review of patients' records. The positive predictive value for the ascertainment of major intracranial (IC) bleeds using only read codes was 96.9%, compared with 70.4% for gastrointestinal (GI) bleeds and 64.1% for urogenital (UG) bleeds. The incidence rate of major IC bleeding events was therefore similar when it was calculated before and after validation (0.32 per 100 person-years and 0.31 per 100 person-years, respectively). The incidence rate of major GI bleeds identified using read codes alone was reduced following validation from 2.05 to 0.94 per 100 person-years, and that of major UG bleeds decreased from 2.45 to 1.11 per 100 person-years. Major GI and UG bleeding events ascertained from THIN using read codes require validation using additional information to prevent outcome misclassification. The absence of validation may lead to overestimated incidence rates of major bleeding for GI and UG bleeds.
Substances chimiques
Anticoagulants
0
Warfarin
5Q7ZVV76EI
Rivaroxaban
9NDF7JZ4M3
Types de publication
Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
148-155Informations de copyright
© 2018 John Wiley & Sons, Ltd.