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Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in France.
Prot-Bertoye, Caroline; Lebbah, Saïd; Daudon, Michel; Tostivint, Isabelle; Jais, Jean-Philippe; Lillo-Le Louët, Agnés; Pontoizeau, Clément; Cochat, Pierre; Bataille, Pierre; Bridoux, Franck; Brignon, Pierre; Choquenet, Christian; Combe, Christian; Conort, Pierre; Decramer, Stéphane; Doré, Bertrand; Dussol, Bertrand; Essig, Marie; Frimat, Marie; Gaunez, Nicolas; Joly, Dominique; Le Toquin-Bernard, Sophie; Méjean, Arnaud; Meria, Paul; Morin, Denis; N'Guyen, Hung V; Normand, Michel; Pietak, Michel; Ronco, Pierre; Saussine, Christian; Tsimaratos, Michel; Friedlander, Gérard; Traxer, Olivier; Knebelmann, Bertrand; Courbebaisse, Marie.
Afiliación
  • Prot-Bertoye C; Department of Physiology, Functional Renal Explorations Department, AP-HP (Public Assistance Hospitals of Paris), Georges Pompidou European Hospital, Paris Descartes University, Paris, France.
  • Lebbah S; INSERM UMRS 1138, Paris, France.
  • Daudon M; Department of Biostatistics, AP-HP, Necker Hospital for Sick Children, Paris Descartes University, Medicine, Paris, France.
  • Tostivint I; Department of Physiology, Functional Renal Explorations Department, AP-HP, Tenon Hospital Pierre and Marie Curie University, INSERM UMR S 1155, Paris, France.
  • Jais JP; Department of Nephrology, AP-HP, Pitié-Salpétrière Hospital, Paris, France.
  • Lillo-Le Louët A; Department of Biostatistics, AP-HP, Necker Hospital for Sick Children, Paris Descartes University, Paris, France.
  • Pontoizeau C; Inserm UMRS 1138 team 22, Paris, France.
  • Cochat P; Department of Pharmacovigilance, AP-HP, Georges Pompidou European Hospital, Paris, France.
  • Bataille P; Functional Unit of Metabolomics, Functional Explorations Department, APHP, Necker Hospital for Sick Children, Paris Descartes University, Paris, France.
  • Bridoux F; Department of Pediatrics, Hospices Civils de Lyon, Centre de Référence des Maladies Rénales Rares Néphrogones, Lyon, France.
  • Brignon P; Department of Nephrology, Boulogne-sur-Mer Hospital, Boulogne sur Mer, France.
  • Choquenet C; Department of Neprhology, Poitiers University Hospital, Poitiers University, Poitiers, France.
  • Combe C; Department of Nephrology, Pasteur Hospital, Colmar, France.
  • Conort P; Department of Urology, Princesse Grace Hospital, Monaco, France.
  • Decramer S; Department of Nephrology, Bordeaux University Hospital, Bordeaux University, Bordeaux, France.
  • Doré B; Department of Urology, AP-HP, Pitié-Salpétrière Hospital, Paris, France.
  • Dussol B; Department of Nephrology and Internal Medicine, Toulouse University Children Hospital, Toulouse, France.
  • Essig M; INSERM U1048, Toulouse, France.
  • Frimat M; Department of Urology, Poitiers University Hospital, Poitiers University, Poitiers, France.
  • Gaunez N; Department of Nephrology, AP-HM (Public Assistance Hospitals of Marseille), Conception Hospital, Aix-Marseille University, Marseille, France.
  • Joly D; Department of Nephrology, Dialysis and Transplantation, Limoges University Hospital, Limoges University, Limoges, France.
  • Le Toquin-Bernard S; INSERM UMR-S850, Limoges, France.
  • Méjean A; Department of Nephrology, Claude Huriez University Hospital, Lille, France.
  • Meria P; Department of Urology, Niort Hospital, Niort, France.
  • Morin D; Department of Nephrology, AP-HP, Necker Hospital for Sick Children, Paris Descartes University, Medicine, Paris, France.
  • N'Guyen HV; Department of Urology, Private Saint-Martin Hospital, Caen, France.
  • Normand M; Department of Urology, AP-HP, Georges Pompidou European Hospital, Paris Descartes University, Medicine, Paris, France.
  • Pietak M; Department of Urology, AP-HP, Saint-Louis Hospital, Paris, France.
  • Ronco P; Department of Pediatrics (Pediatric Nephrology and Diabetology), Montpellier University Hospital, Montpellier, France.
  • Saussine C; CNRS, UMR 5203-INSERM U661, Montpellier, France.
  • Tsimaratos M; Department of Urology, AP-HP, Saint-Louis Hospital, Paris, France.
  • Friedlander G; Department of Nephrology, Private Saint-Martin Hospital, Pessac, France.
  • Traxer O; Department of Urology, AP-HP, Georges Pompidou European Hospital, Paris, France.
  • Knebelmann B; Department of Nephrology and Dialysis, AP-HP, Tenon Hospital, Pierre and Marie Curie University, Paris, France.
  • Courbebaisse M; INSERM Unit 702, Paris, France.
BJU Int ; 124(5): 849-861, 2019 11.
Article en En | MEDLINE | ID: mdl-30801923
ABSTRACT

OBJECTIVE:

To evaluate medical treatments, in terms of adverse events (AEs) and therapeutic goals, in a large series of patients with cystinuria. PATIENTS AND

METHODS:

Data from 442 patients with cystinuria were recorded retrospectively. Crystalluria was studied in 89 patients. A mixed-effects logistic regression model was used to estimate how urine pH, specific gravity and cysteine-binding thiols (CBT) correlate with risk of cystine crystalluria.

RESULTS:

Alkalizing agents and CBT agents were given to 88.8% (n = 381) and 55.3% (n = 238) of patients, respectively. Gastrointestinal AEs were reported in 12.3%, 10.4% and 2.6% of patients treated with potassium bicarbonate, potassium citrate and sodium bicarbonate, respectively (P = 0.008). The percentages of patients who experienced at least one AE with tiopronin (24.6%) and with D-penicillamine (29.5%) were similar (P = 0.45). Increasing urine pH and decreasing urine specific gravity significantly reduced the risk of cystine crystalluria, whereas D-penicillamine and tiopronin treatments did not reduce this risk (odds ratio [OR] 1 for pH ≤6.5; OR 0.52 [95% confidence interval {95% CI} 0.28-0.95] for 7.0 <pH ≤7.5, P = 0.03; OR 0.26 [95% CI 0.13-0.53] for 7.5 < pH ≤8.0, P <0.001; OR 1 for specific gravity ≤1.005 OR 5.76 [95% CI 1.45-22.85] for 1.006 ≤ specific gravity ≤1.010, P = 0.01; and OR 11.06 [95% CI 2.76-44.26] for 1.011 ≤ specific gravity ≤ 1.014, P < 0.001). Increased urine pH significantly increased the risk of calcium phosphate crystalluria (OR 1 for pH≤ 6.5; OR 6.09 [95% CI 2.15-17.25] for pH >8.0, P <0.001).

CONCLUSION:

Adverse events were frequent with D-penicillamine and tiopronin. Alkaline hyperdiuresis was well tolerated and reduced cystine crystalluria. Urine specific gravity ≤1.005 and urine pH >7.5, while warning about calcium-phosphate crystallization, should be the goals of medical therapy.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Cistinuria Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: BJU Int Asunto de la revista: UROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Asunto principal: Cistinuria Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: BJU Int Asunto de la revista: UROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Francia