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1.
J Clin Endocrinol Metab ; 106(1): e192-e203, 2021 01 01.
Article de Anglais | MEDLINE | ID: mdl-32995889

RÉSUMÉ

BACKGROUND: Although congenital adrenal hyperplasia (CAH) is known to be associated with adrenal crises (AC), its association with patient- or clinician-reported sick day episodes (SDE) is less clear. METHODS: Data on children with classic 21-hydroxylase deficiency CAH from 34 centers in 18 countries, of which 7 were Low or Middle Income Countries (LMIC) and 11 were High Income (HIC), were collected from the International CAH Registry and analyzed to examine the clinical factors associated with SDE and AC. RESULTS: A total of 518 children-with a median of 11 children (range 1, 53) per center-had 5388 visits evaluated over a total of 2300 patient-years. The median number of AC and SDE per patient-year per center was 0 (0, 3) and 0.4 (0.0, 13.3), respectively. Of the 1544 SDE, an AC was reported in 62 (4%), with no fatalities. Infectious illness was the most frequent precipitating event, reported in 1105 (72%) and 29 (47%) of SDE and AC, respectively. On comparing cases from LMIC and HIC, the median SDE per patient-year was 0.75 (0, 13.3) vs 0.11 (0, 12.0) (P < 0.001), respectively, and the median AC per patient-year was 0 (0, 2.2) vs 0 (0, 3.0) (P = 0.43), respectively. CONCLUSIONS: The real-world data that are collected within the I-CAH Registry show wide variability in the reported occurrence of adrenal insufficiency-related adverse events. As these data become increasingly used as a clinical benchmark in CAH care, there is a need for further research to improve and standardize the definition of SDE.


Sujet(s)
Hyperplasie congénitale des surrénales/épidémiologie , Insuffisance surrénale/complications , Insuffisance surrénale/épidémiologie , Maladie aigüe , Adolescent , Hyperplasie congénitale des surrénales/complications , Soins ambulatoires/statistiques et données numériques , Enfant , Enfant d'âge préscolaire , Femelle , Géographie , Hospitalisation/statistiques et données numériques , Humains , Nourrisson , Nouveau-né , Mâle , Enregistrements
2.
Article de Anglais | MEDLINE | ID: mdl-33255540

RÉSUMÉ

Rare disease (RD) registries are important platforms that facilitate communication between health care professionals, patients and other members of the multidisciplinary team. RD registries enable data sharing and promotion of research and audits, often in an international setting, with the overall aim of improving patient care. RD registries also have a fundamental role in supporting the work of clinical networks such as the European Reference Networks (ERNs) for rare diseases. With the recent expansion of RD registries, it has become even more essential to outline standards of good practice in relation to governance, infrastructure, documentation, training, audits and adopting the Findable, Accessible, Interoperable and Reusable (FAIR) data principles to maintain registries of high quality. For the purpose of this paper, we highlight vital aspects of data access and data governance policies for RD registries, using the European Registries for Rare Endocrine Conditions (EuRRECa) as an example of a project that aims to promote good standards of practice for improving the quality of utilization of RD registries.


Sujet(s)
Politique (principe) , Maladies rares , Enregistrements , Europe/épidémiologie , Union européenne/statistiques et données numériques , Humains , Diffusion de l'information , Maladies rares/épidémiologie , Enregistrements/normes
4.
Hypertension ; 74(4): 767-775, 2019 10.
Article de Anglais | MEDLINE | ID: mdl-31422693

RÉSUMÉ

Concerns exist regarding the potential increased cardiovascular risk from lowering diastolic blood pressure (DBP) in hypertensive patients. We analyzed 30-year follow-up data of 10 355 hypertensive patients attending the Glasgow Blood Pressure Clinic. The association between blood pressure during the first 5 years of treatment and cause-specific hospital admissions or mortality was analyzed using multivariable adjusted Cox proportional hazard models. The primary outcome was a composite of cardiovascular admissions and deaths. DBP showed a U-shaped association (nadir, 92 mm Hg) for the primary cardiovascular outcome hazard and a reverse J-shaped association with all-cause mortality (nadir, 86 mm Hg) and noncardiovascular mortality (nadir, 92 mm Hg). The hazard ratio for the primary cardiovascular outcome after adjustment for systolic blood pressure was 1.38 (95% CI, 1.18-1.62) for DBP <80 compared with DBP of 80 to 89.9 mm Hg (referrant), and the subdistribution hazard ratio after accounting for competing risk was 1.33 (1.17-1.51) compared with DBP ≥80 mm Hg. Cause-specific nonfatal outcome analyses showed a reverse J-shaped relationship for myocardial infarction, ischemic heart disease, and heart failure admissions but a U-shaped relationship for stroke admissions. Age-stratified analyses showed DBP had no independent effect on stroke admissions among the older patient subgroup (≥60 years of age), but the younger subgroup showed a clear U-shaped relationship. Intensive blood pressure reduction may lead to unintended consequences of higher healthcare utilization because of increased cardiovascular morbidity, and this merits future prospective studies. Low on-treatment DBP is associated with increased risk of noncardiovascular mortality, the reasons for which are unclear.


Sujet(s)
Pression sanguine/physiologie , Diastole/physiologie , Hypertension artérielle/physiopathologie , Infarctus du myocarde/physiopathologie , Adulte , Sujet âgé , Antihypertenseurs/usage thérapeutique , Mesure de la pression artérielle , Femelle , Humains , Hypertension artérielle/traitement médicamenteux , Hypertension artérielle/mortalité , Mâle , Adulte d'âge moyen , Infarctus du myocarde/mortalité , Facteurs de risque , Taux de survie , Soins de santé tertiaires
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