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2 raisons identifiées
Auteur de référence en rhumatologie
21 articles scientifiques publiés — un praticien à la pointe de la recherche
Délais de RDV courts dans la région
124.6 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
CABINET DU DR Aude DIESCE
1 RUE ROBERT DOISNEAU, 86000 POITIERS
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
JAMA · 2024
ImportanceIn 2013, the Trial to Assess Chelation Therapy (TACT) reported that edetate disodium (EDTA)–based chelation significantly reduced cardiovascular disease (CVD) events by 18% in 1708 patients with a prior myocardial infarction (MI).ObjectiveTo replicate the finding of TACT in individuals with diabetes and previous MI.Design, Setting, and ParticipantsA 2 × 2 factorial, double-masked, placebo-controlled, multicenter trial at 88 sites in the US and Canada, involving participants who were 50 years or older, had diabetes, and had experienced an MI at least 6 weeks before recruitment compared the effect of EDTA-based chelation vs placebo infusions on CVD events and compared the effect of high doses of oral multivitamins and minerals with oral placebo. This article reports on the chelation vs placebo infusion comparisons.InterventionsEligible participants were randomly assigned to 40 weekly infusions of an EDTA-based chelation solution or matching placebo and to twice daily oral, high-dose multivitamin and mineral supplements or matching placebo for 60 months. This article addresses the chelation study.Main Outcomes and MeasuresThe primary end point was the composite of all-cause mortality, MI, stroke, coronary revascularization, or hospitalization for unstable angina. Median follow-up was 48 months. Primary comparisons were made from patients who received at least 1 assigned infusion.ResultsOf the 959 participants (median age, 67 years [IQR, 60-72 years]; 27% females; 78% White, 10% Black, and 20% Hispanic), 483 received at least 1 chelation infusion and 476 at least 1 placebo infusion. A primary end point event occurred in 172 participants (35.6%) in the chelation group and in 170 (35.7%) in the placebo group (adjusted hazard ratio [HR], 0.93; 95% CI, 0.76-1.16; P = .53). The 5-year primary event cumulative incidence rates were 45.8% for the chelation group and 46.5% for the placebo group. CV death, MI, or stroke events occurred in 89 participants (18.4%) in the chelation group and in 94 (19.7%) in the placebo group (adjusted HR, 0.89; 95% CI, 0.66-1.19). Death from any cause occurred in 84 participants (17.4%) in the chelation group and in 84 (17.6%) in the placebo group (adjusted HR, 0.96; 95% CI, 0.71-1.30). Chelation reduced median blood lead levels from 9.03 μg/L at baseline to 3.46 μg/L at infusion 40 (P < .001). Corresponding levels in the placebo group were 9.3 μg/L and 8.7 μg/L, respectively.Conclusions and RelevanceDespite effectively reducing blood lead levels, EDTA chelation was not effective in reducing cardiovascular events in stable patients with coronary artery disease who have diabetes and a history of MI.Trial RegistrationClinicalTrials.gov Identifier: NCT02733185
Arthroplasty today · 2024
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Journal of surgical education · 2026 · Journal Article
Kramer P, Jiang K, Weber-Levine C, Soberanis-Mukul RD, et al.
The journal of trauma and acute care surgery · 2026 · Journal Article
Kramer P, Vattipally VN, Menta AK, Jillala RR, et al.
Journal of neurosurgery. Spine · 2025 · Journal Article
Vattipally VN, Aude CA, Ran KR, Jiang K, et al.
Chinese medicine · 2025 · Journal Article
Bian Y, Li F, A X, Xiang Z, et al.
Scientific reports · 2025 · Journal Article
M C S, B K, A U, K C S
Biomacromolecules · 2024 · Journal Article
Kabir A, B M, A N, Selvaraj V, et al.
Arthroplasty today · 2024 · Journal Article
Bass AR, Mehta B, Sculco PK, Zhang Y, et al.
American journal of translational research · 2023 · Journal Article
A R, Mu R, Wu Q, Ga L, et al.
The Journal of rheumatology · 2026 · Letter
Chan KK, Ghosh N, Aude C, DiCarlo E, et al.
Cureus · 2024 · Case Reports
Ravichandran S, Kumar J, Chandrasekaran ND, Irfan S, et al.
Annals of the rheumatic diseases · 2023 · Comparative Study
Bass AR, Abdel-Wahab N, Reid PD, Sparks JA, et al.
Frontiers in pharmacology · 2023 · Journal Article
Ran L, Xu B, Han HH, Wang JY, et al.
Neurosurgery · 2026 · Journal Article
Maroufi SF, Puppalla P, Katkade O, Theodore JN, et al.
JMIR research protocols · 2025 · Journal Article
M A, Ahmad A, A A, Raj LS, et al.
Journal of neurosurgery. Spine · 2026 · Journal Article
Aude CA, Vattipally VN, Jillala R, Khalifeh J, et al.
Journal of neurosurgery. Spine · 2025 · Journal Article
Jillala RR, Aude CA, Vattipally VN, Ran KR, et al.
Clinical rheumatology · 2025 · Journal Article
A K, M EA, M H, H A, et al.
Arthritis & rheumatology (Hoboken, N.J.) · 2026 · Journal Article
Xin P, Li W, A X, Shen J, et al.
JAMA · 2024 · Comparative Study
Lamas GA, Anstrom KJ, Navas-Acien A, Boineau R, et al.
Archives of osteoporosis · 2025 · Journal Article
N BV, A MS, A DR, H SG, et al.
Cureus · 2025 · Journal Article
Muraleedharan A, Chaubey S, A S, Yadav A
Neurosurgery · 2026 · Journal Article
Maroufi SF, Puppalla P, Katkade O, Theodore JN, et al.