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1.
Arch Cardiovasc Dis ; 115(2): 78-86, 2022 Feb.
Article En | MEDLINE | ID: mdl-35115266

BACKGROUND: Myocardial infarction is a major cause of morbidity and mortality. Guidelines have been published to optimize medical care and involve optimization of the care pathway and hospital-city coordination. AIMS: To describe the myocardial infarction care pathway during the year following hospital discharge, and the use of and adherence to secondary prevention drugs. METHODS: A cohort study was conducted using data from the main French health insurance reimbursement database of the ex-Aquitaine region. Information about the medical and pharmaceutical care of hospitalized patients in 2018 was collected for 12 months. Medication adherence was assessed by using the proportion of days covered by the treatment and persistence. RESULTS: A total of 3015 patients were included, and the mean age was 66 years. Almost 76% of the patients had a reimbursement for BAS (combined prescription of beta-blocker/antiplatelet/lipid-lowering drug), BASI (combined prescription of beta-blocker/antiplatelet/lipid-lowering drug/angiotensin-converting enzyme inhibitor) or AS (combined prescription of antiplatelet/lipid-lowering drug) treatment. Medication adherence was around 83% for aspirin and 75% for lipid-lowering drugs for the 1-year persistence. During the same time, the proportion of days covered was suboptimal. Almost 4% of patients died after leaving hospital, 45% went to a cardiac rehabilitation centre and 23% had at least one hospital readmission, whatever the reason. Patients had a mean number of 11 general practitioner consultations during the year. Almost 41% of patients did not have a consultation with a cardiologist, and 38.4% had at least two consultations. Rehabilitation and general practitioner consultations were associated with adherence. CONCLUSIONS: These new results provide clear information on the medical care environment of patients, and help us to improve care transition. Close collaboration between healthcare practitioners is very important in the early stages of outpatient follow-up.


Insurance, Health, Reimbursement , Myocardial Infarction , Aged , Cohort Studies , Critical Pathways , Humans , Medication Adherence , Myocardial Infarction/drug therapy , Prescriptions
2.
Pharmacoepidemiol Drug Saf ; 23(10): 1088-92, 2014 Oct.
Article En | MEDLINE | ID: mdl-24648258

PURPOSE: The aim of this study was to determine whether dosing schedule requirements impair overall cardiovascular drug adherence. METHODS: A cohort study was performed with hospitalized patients at high risk of cardiovascular disease between April and September 2011. Patients were asked whether the prescribed time for taking their statin and antiplatelet drugs created any inconvenience in their daily routine and, if so, were asked to describe the reasons. Patient adherence to treatment was assessed using the Morisky Medication Adherence Scale (MMAS-8). A cohort of physicians was separately studied between June and September 2011. Physicians were interviewed to determine their dosing schedule preference when prescribing statin and anti-platelet drugs, and the rationale for choosing a specific dosing schedule. RESULTS: In the study, 103 patients and 59 physicians were included. Statins were most frequently prescribed in the evening (90%). Thienopyridines were prescribed both at lunch time (41%) and in the morning (35%). Aspirin was most frequently (65.3%) prescribed at lunch time. In total, 24.3% of patients reported being inconvenienced by their drug dosing schedule, and these subjects were less adherent to their drug regimen than those who did not report inconvenience (46.2% versus 16.7%, p = 0.014). Our results also demonstrate that there is no pharmacologic rationale for prescribing a particular drug dosing schedule for statin or anti-platelet drugs. CONCLUSIONS: Physicians should assess patient convenience, when prescribing medication, to optimize treatment adherence.


Cardiovascular Agents/administration & dosage , Drug Prescriptions/statistics & numerical data , Medication Adherence/statistics & numerical data , Practice Patterns, Physicians'/statistics & numerical data , Adult , Aged , Cardiovascular Agents/therapeutic use , Cardiovascular Diseases/drug therapy , Cohort Studies , Drug Administration Schedule , Female , France , Humans , Male , Medication Adherence/psychology , Middle Aged , Practice Patterns, Physicians'/standards , Surveys and Questionnaires , Young Adult
3.
EuroIntervention ; 7(12): 1413-9, 2012 Apr.
Article En | MEDLINE | ID: mdl-22522552

AIMS: Current guidelines recommend the use of dual antiplatelet therapy (DAT) (aspirin+clopidogrel) for patients after acute myocardial infarction (MI). In relation to this, we sought to examine the adherence to this recommended treatment regimen in a population of patients admitted with MI and subsequent percutaneous coronary intervention (PCI). METHODS AND RESULTS: A cohort study was conducted using data from the main health insurance reimbursement database of South West France. Patients hospitalised for MI in 2008 were identified, and then their reimbursement form of DAT for the subsequent 12 months was reviewed. Adherence was assessed by using the proportion of days covered by the treatment and persistence. Among the 634 patients included in the study, 34 had no reimbursement for DAT immediately after discharge. For the remaining patients, the probability of stopping DAT at least for one month was 18.6% (95% CI [15.4;21.8]) during the first three months and 49.1% (95% CI [44.9;53.2]) at 12 months, although the medication availability was 90%. CONCLUSIONS: These results suggest that while this medication is available to patients, the treatment is often stopped before one year. This may account for what has been reported as "resistance" to antiplatelet therapy described in a subset of patients.


Angioplasty, Balloon, Coronary , Aspirin/administration & dosage , Insurance, Health, Reimbursement , Myocardial Infarction/drug therapy , Patient Compliance , Platelet Aggregation Inhibitors/administration & dosage , Ticlopidine/analogs & derivatives , Aged , Clopidogrel , Cohort Studies , Databases, Factual , Drug Therapy, Combination , Female , France , Humans , Male , Myocardial Infarction/therapy , Retrospective Studies , Ticlopidine/administration & dosage
4.
Fundam Clin Pharmacol ; 25(4): 528-33, 2011 Aug.
Article En | MEDLINE | ID: mdl-21729148

The prevalence of statin use is high but adherence low. For public health intervention to be rational, subpopulations of nonadherent subjects must be defined. To categorise statin users with respect to patterns of reimbursement, this study was performed using the main French health reimbursement database for the Aquitaine region of south-western France. The cohort included subjects who submitted a reimbursement for at least one delivery of a statin (index) during the inclusion period (1st of September 2004-31st of December 2004). Indicators of adherence from reimbursement data were considered for principal component analysis. The 119,570 subjects included and analysed had a sex ratio of 1.1, mean (SD) age of 65.9 (11.9), and 13% were considered incident statin users. Principal component analysis found three dimensions that explained 67% of the variance. Using a K-means classification combined with a hierarchical ascendant classification, six groups were characterised. One group was considered nonadherent (10% of study population) and one group least adherent (1%). This novel application of principal component analysis identified groups that may be potential targets for intervention. The least adherent group appears to be one of the most appropriate because of both its relatively small size for case review with prescribing physicians and its very poor adherence.


Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Medication Adherence/statistics & numerical data , Principal Component Analysis , Public Health Practice , Age Factors , Aged , Cardiovascular Diseases/prevention & control , Cohort Studies , Databases, Factual , Drug Prescriptions/statistics & numerical data , Female , France , Humans , Insurance, Health, Reimbursement/statistics & numerical data , Male , Middle Aged , Sex Factors , Time Factors
5.
BMC Cardiovasc Disord ; 11: 46, 2011 Jul 26.
Article En | MEDLINE | ID: mdl-21791073

BACKGROUND: While the factors for poor adherence for treatment with statins have been highlighted, the impact of their combination on adherence is not clear. AIMS: To estimate adherence for statins and whether it differs according to the number of cardiovascular risk factors. METHODS: A cohort study was conducted using data from the main French national health insurance system reimbursement database. Newly treated patients with statins between September 1 and December 31, 2004 were included. Patients were followed up 15 months. The cohort was split into three groups according to their number of additional cardiovascular risk factors that included age and gender, diabetes mellitus and cardiovascular disease (using co-medications as a proxy). Adherence was assessed for each group by using four parameters: (i) proportion of days covered by statins, (ii) regularity of the treatment over time, (iii) persistence, and (iv) the refill delay. RESULTS: 16,397 newly treated patients were identified. Of these statin users, 21.7% did not have additional cardiovascular risk factors. Thirty-one percent had two cardiovascular risk factors and 47% had at least three risk factors. All the parameters showed a sub-optimal adherence whatever the group: days covered ranged from 56% to 72%, regularity ranged from 23% to 33% and persistence ranged from 44% to 59%, but adherence was better for those with a higher number of cardiovascular risk factors. CONCLUSIONS: The results confirm that long-term drug treatments are a difficult challenge, particularly in patients at lower risk and invite to the development of therapeutic education.


Cardiovascular Diseases/drug therapy , Cardiovascular Diseases/psychology , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Hypercholesterolemia/psychology , Age Factors , Aged , Cardiovascular Diseases/enzymology , Cohort Studies , Female , Humans , Hypercholesterolemia/drug therapy , Hypercholesterolemia/enzymology , Male , Medication Adherence/psychology , Middle Aged , Risk Factors , Sex Factors
6.
Therapie ; 65(4): 379-85, 2010.
Article Fr | MEDLINE | ID: mdl-20854762

The reimbursement databases of the French health insurance systems are greatly used for pharmaceoepidemiological research. However, the terminology used to describe them in subsequent articles and abstracts vary greatly and thus lead to a problem of identification during bibliograhic research or during the process of indexation in medline. In this article we have fixed the terminology used and proposed both a terminology and appropriate MeSH terms for indexation for the futur. Fifty-six published studies were included. At least six different root terms were found to define the French health insurance system, 64.3% of the publications mentioned the term "database", and 30.4% mentioned the term "reimbursement". We propose that abstracts of future articles contain the three terms: database, reimbursement, and health insurance. We also propose to include in the keywords of an article the MeSH terms that are most appropriate to define these three concepts: Insurance, Health, Reimbursement and Databases, Factual.


Insurance, Health, Reimbursement/statistics & numerical data , Insurance, Health, Reimbursement/standards , Pharmacoepidemiology/standards , Terminology as Topic , Databases, Factual , France , MEDLINE , Research
7.
Eur J Clin Pharmacol ; 66(7): 743-8, 2010 Jul.
Article En | MEDLINE | ID: mdl-20429000

INTRODUCTION: Reimbursement databases are potentially invaluable tools to develop and conduct pharmacoepidemiological studies on drug use. However, two types of factors that may influence the performance of a database can be distinguished: firstly, factors related to the constitution of the database, and secondly, factors related to the data. For the latter, we think that two are important: the presence of the drug in the database and the capacity to capture real-life use, both of which are influenced by the marketing status (e.g., OTC) and whether reimbursement is possible. OBJECTIVES: To illustrate and discuss to what extent reimbursement databases are relevant tools to conduct drug utilization studies with regard to the data on drugs. METHODS: In order to illustrate the reliability of data in reimbursement databases, data from the main French national health insurance database (55 million individuals) were compared to national drug sales in France (units) during the same year. RESULTS: Depending on the ATC class, the capture in the database of drugs actually sold ranged from 32 to 81%. DISCUSSION: Capture of classes of drugs in the database may be explained by the specific characteristics of the French health insurance system (reimbursable drugs, OTC market share). These characteristics influence the studies that can be performed both in terms of the topic but also the methodology. This problem probably exists for the other reimbursement databases used worldwide. CONCLUSION: Studies should be designed according to the strengths and weaknesses of reimbursement databases that were not originally developed for pharmacoepidemiology.


Databases, Factual , Drug Utilization/statistics & numerical data , Insurance, Health, Reimbursement , Pharmacoepidemiology/methods , Drug Utilization/economics , France , Humans , National Health Programs , Pharmaceutical Preparations/economics
8.
Pharmacoepidemiol Drug Saf ; 19(3): 256-65, 2010 Mar.
Article En | MEDLINE | ID: mdl-20128015

PURPOSE: To describe the reimbursement databases available in France for pharmacoepidemiological research and their use. METHODS: France has a publicly funded health system that systematically covers the population. Within this system, three main insurance schemes provide health services to citizens in France and each have their own reimbursement database. Together these three databases cover almost 97% of the French population (respectively for 54.5, 3.6, and 3.3 million individuals, and a total of 61.4 million individuals). Data in these concern patients, prescribers, all the medical acts reimbursed, prescription and undertaking of laboratory tests (but without results), private hospital data, partial public hospital data and vital status. Their use is regulated but access is free and the data are anonymous. PubMed and Scopus were searched for relevant studies published from January 1988 to June 2009. RESULTS: 110 published studies were included. The topics and the study characteristics were extremely wide-ranging. The studies assessed patterns of drug use, have tested interventions, supported or improved prescribing practices, tested compliance with the French governmental Health guidelines, assessed physicians' prescribing practices and performed economic and cost-effectiveness assessments. The number of articles published increased greatly between 2002 and 2003. CONCLUSIONS: The French reimbursement databases were greatly used over the last 20 years. They can provide data on exposure to drugs and can be used to study patterns of drug utilization although their limitations must be considered.


Databases, Factual/statistics & numerical data , Insurance, Health, Reimbursement/statistics & numerical data , Pharmacoepidemiology/methods , Economics, Pharmaceutical , France , Guideline Adherence , Humans , Pharmaceutical Preparations/administration & dosage , Pharmaceutical Preparations/economics , Practice Patterns, Physicians'
9.
Am J Geriatr Psychiatry ; 17(12): 1059-67, 2009 Dec.
Article En | MEDLINE | ID: mdl-20104062

OBJECTIVE: The authors investigated the association between death of older people and use of psychotropic drugs before and during the Western European August 2003 heatwave. METHOD: A retrospective population-based case-control study was conducted using the French social security insurance national database. Exposure to psychotropic drugs in cases aged 70-100 years who died before (N = 2,093) and during (N = 9,531) the August 2003 heatwave was compared with those of survivors matched for age, gender, and presence of chronic illness, by using conditional logistic regressions. RESULTS: The association between death and psychotropic drug use was modified by level of external temperature (Wald chi(2) = 13.1, degree of freedom = 1, p <0.001). Use of any psychotropic drug was associated with a 30% increased risk of death during the heatwave, with a significant dose-response relationship between the number of psychotropic drugs and the risk of death (adjusted odds ratio [aOR] for linear trend 1.25, 95% confidence interval [95% CI]: 1.21-1.29). During the heatwave, therapeutic classes independently associated with an increased risk of death were antidepressants (aOR 1.71, 95% CI: 1.57-1.86) and antipsychotics (aOR 2.09, 95% CI: 1.89-2.35), whereas exposure to anxiolytics/hypnotics use (aOR 0.85, 0.79-0.91) was associated with a decreased risk. Findings remained unchanged after adjustment on cardiotropic, antidementia, or anti-parkinsonian drug use. CONCLUSION: Our findings suggest that a causal relationship may exist between psychotropic drug use during a heatwave and increased risk of death in older people. The risk/benefit ratio of antidepressant and antipsychotic drugs should be carefully assessed in older people during a heatwave.


Heat Stress Disorders/chemically induced , Heat Stress Disorders/mortality , Hot Temperature/adverse effects , Psychotropic Drugs/adverse effects , Aged , Aged, 80 and over , Antidepressive Agents/adverse effects , Antipsychotic Agents/adverse effects , Case-Control Studies , Dose-Response Relationship, Drug , Europe/epidemiology , Female , France/epidemiology , Geriatric Assessment/methods , Geriatric Assessment/statistics & numerical data , Humans , Male , Odds Ratio , Retrospective Studies , Risk Factors
10.
Clin Ther ; 30 Spec No: 1058-68, 2008.
Article En | MEDLINE | ID: mdl-18640480

OBJECTIVES: This study evaluated adherence to anti-inflammatory controller medication for asthma in a French population. METHODS: This was an observational cohort study that employed data from the health insurance database for the Aquitaine region of France. Eligible subjects were aged between 15 and 45 years and had > or = 1 reimbursement claim for anti-inflammatory controller medication between December 1, 2003, and December 31, 2003. Data were collected from June 1, 2003, to May 28, 2005. New users were defined as those having no reimbursement claim for any asthma controller medication in the 6 months preceding the index date; all others were considered previous users. All subjects were followed for 17 months. Continuous multiple-interval measures of medication availability and medication gaps, treatment persistence, and time to first renewal were calculated for users of inhaled corticosteroids (ICS) alone, users of ICS combined with a long-acting beta2-agonist (LABA) in a single inhaler (ICS/LABA) or in separate inhalers (ICS + LABA), and users of oral leukotriene antagonists. RESULTS: The study population contained 12,502 new and previous users of anti-inflammatory controller medication for asthma. Their mean (SD) age was 32.0 (8.9) years and 58.3% were female. Previous users had better adherence to treatment than new users with respect to all measures. Adherence was best in previous users of leukotriene antagonists. However, only 40.2% of previous users of leukotriene antagonists had sufficient medication (95% CI, 37.6-42.9), compared with 56.8% of previous users of ICS + LABA (95% CI, 50.7-62.8), 65.5% of previous users of ICS only (95% CI, 63.1-67.9), and 69.8% of previous users of ICS/LABA (95% CI, 68.2-71.4). The rate of persistence over a 1-year period was 44.3% for previous users of leukotriene antagonists (95% CI, 41.7-46.8), compared with 27.1% for previous users of ICS only (95% CI, 25.1-29.1), 32.1% for previous users of ICS/LABA (95% CI, 30.5-33.6), and 44.1% for previous users of ICS + LABA (95% CI, 38.2-50.0). CONCLUSION: Adherence to treatment was poor (< or = 44%) in these users of anti-inflammatory controller medications for asthma.


Glucocorticoids/therapeutic use , Patient Compliance , Administration, Inhalation , Adolescent , Adrenergic beta-Agonists/therapeutic use , Adult , Asthma , Drug Therapy, Combination , Drug Utilization , Female , France , Glucocorticoids/administration & dosage , Humans , Insurance Claim Review , Leukotriene Antagonists/therapeutic use , Male , Middle Aged
12.
Eur Psychiatry ; 22(6): 335-8, 2007 Sep.
Article En | MEDLINE | ID: mdl-17513091

OBJECTIVE: To assess if use of psychotropic drugs is associated with an increased risk of admission for heat-related pathologies during a heat wave period. METHOD: We conducted a matched case-control study. Cases were defined as subjects admitted to an emergency department for heat-related pathology (hyperthermia or heat stroke) over the August 2003 heat wave. Controls were defined as subjects living in the same area but not hospitalised over the same period and who had at least one prescription form submitted for refunding by the social security insurance in July 2003. Multivariate analyses were used to identify psychotropic drugs independently associated with hospital referral during the heat wave period. RESULTS: Out of the 1405 patients admitted to the emergency department, 56 (4%) presented with heat-related pathology. The mean age of cases was 83 years. Multivariate analyses showed that cases were more likely than controls to be treated with anticholinergic drugs (OR 6.0, 95% CI 1.8-19.6), antipsychotics (OR 4.6, 95% CI 1.9-11.2) or anxiolytics (OR 2.4, 95% CI 1.3-4.4). CONCLUSION: In special risk situations such as heat waves, the risk/benefit ratio of psychotropic drugs which could interfere with body temperature regulation has to be carefully assessed, particularly in the elderly.


Emergency Service, Hospital/statistics & numerical data , Heat Stress Disorders/chemically induced , Hospitalization/statistics & numerical data , Hot Temperature/adverse effects , Psychotropic Drugs/adverse effects , Age Factors , Aged , Aged, 80 and over , Anti-Anxiety Agents/adverse effects , Anti-Anxiety Agents/therapeutic use , Antipsychotic Agents/adverse effects , Antipsychotic Agents/therapeutic use , Case-Control Studies , Cholinergic Antagonists/adverse effects , Cholinergic Antagonists/therapeutic use , Cross-Sectional Studies , Female , France , Heat Stress Disorders/epidemiology , Humans , Male , Middle Aged , Psychotropic Drugs/therapeutic use , Retrospective Studies , Risk , Sex Factors , Sweating/drug effects , Utilization Review/statistics & numerical data
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