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Home infusion program with enzyme replacement therapy for Fabry disease: The experience of a large Italian collaborative group.
Concolino, D; Amico, L; Cappellini, M D; Cassinerio, E; Conti, M; Donati, M A; Falvo, F; Fiumara, A; Maccarone, M; Manna, R; Matucci, A; Musumeci, M B; Nicoletti, A; Nisticò, R; Papadia, F; Parini, R; Peluso, D; Pensabene, L; Pisani, A; Pistone, G; Rigoldi, M; Romani, I; Tenuta, M; Torti, G; Veroux, M; Zachara, E.
Affiliation
  • Concolino D; Department of Medical and Surgical Science, Pediatric Unit, University "Magna Graecia", Catanzaro, Italy.
  • Amico L; Nephrology Unit, Ospedali Riuniti Villa Sofia, Cervello, Palermo, Italy.
  • Cappellini MD; Rare Diseases Centre, Department of Medicine and Medical Specialities, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan, Italy.
  • Cassinerio E; Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
  • Conti M; Rare Diseases Centre, Department of Medicine and Medical Specialities, Fondazione IRCCS Ca' Granda - Ospedale Maggiore Policlinico, Milan, Italy.
  • Donati MA; Nephrology Unit, Azienda Ospedaliera Brotzu, Cagliari, Italy.
  • Falvo F; Metabolic and Neuromuscular Unit, AOU Meyer Hospital, Florence, Italy.
  • Fiumara A; Department of Medical and Surgical Science, Pediatric Unit, University "Magna Graecia", Catanzaro, Italy.
  • Maccarone M; Regional Referral Center for Inborn Errors Metabolism, Pediatric Clinic, Department of Clinical and Experimental Medicine, University of Catania, Via Santa Sofia 78, Catania, Italy.
  • Manna R; Nephrology and Dialysis Unit, Ospedale di Lanciano, Chieti, Italy.
  • Matucci A; Periodic Fevers Research and Rare Diseases Centre, Internal Medicine Department, Policlinico Gemelli, Largo A. Gemelli, 8, 00168 Rome, Italy.
  • Musumeci MB; SOD Immunoallergologia, AOU Careggi, Firenze, Italy.
  • Nicoletti A; Sapienza University, Department of Molecular and Clinical Medicine, Cardiology, Sant'Andrea Hospital, Rome, Italy.
  • Nisticò R; Department of Medical and Surgical Science, Pediatric Unit, University "Magna Graecia", Catanzaro, Italy.
  • Papadia F; Neuroimaging Research Unit, Institute of Bioimaging and Molecular Physiology, National Research Council, Germaneto, Catanzaro, Italy.
  • Parini R; U.O.C. Malattie Metaboliche Genetica Medica, PO Giovanni XXIII, A.O.U. Policlinico Consorziale, Bari, Italy.
  • Peluso D; UOS Malattie Metaboliche Rare, Clinica Pediatrica, Ospedale San Gerardo, Via Pergolesi 33, Monza, Italy.
  • Pensabene L; Neurology Unit, Azienda Ospedaliera S. Carlo, Potenza, Italy.
  • Pisani A; Department of Medical and Surgical Science, Pediatric Unit, University "Magna Graecia", Catanzaro, Italy.
  • Pistone G; Renal Unit, Department of Public Health, "Federico II" University, Naples, Italy.
  • Rigoldi M; UOC Dermatologia e MTS Dipartimento DIBIMIS AOUP "Paolo Giaccone" Palermo, Italy.
  • Romani I; Dept. of Internal Medicine, San Gerardo Hospital, Monza, Italy.
  • Tenuta M; NEUROFARBA Department, University of Florence, V.le Pieraccini 6, 50139 Florence, Italy.
  • Torti G; Neurology Unit, Azienda Ospedaliera Universitaria S. G. di Dio e Ruggi D'Aragona, Salerno, Italy.
  • Veroux M; Clinica Nefrologica, Ospedale San Gerardo, Monza, Italy.
  • Zachara E; Vascular Surgery and Organ Transplant Unit, Department of Medical, Surgery Sciences and Advanced Technologies "GF Ingrassia", University of Catania, 95123 Catania, Italy.
Mol Genet Metab Rep ; 12: 85-91, 2017 Sep.
Article in En | MEDLINE | ID: mdl-28702361
ABSTRACT
Fabry disease (FD) [OMIM 301500] is an X-linked lysosomal storage disorder caused by a deficiency of the lysosomal enzyme alpha-galactosidase A, resulting in progressive multisystem accumulation of globotriaosylceramide (Gb3). Although the introduction of Enzyme Replacement Therapy (ERT) resulted in a variety of clinical benefits, life-long intravenous (IV) treatment with ERT with an every other week schedule, may interfere with daily life activities and impact on QoL. We report here a multicentric, observational, longitudinal data analysis on a large cohort of 85 Italian FD patients (45 males, 40 females) from 11 out of 20 Italian regions, who received a cumulative number of 4269 home infusions of agalsidase alfa. For the whole cohort, the average duration of home therapy was 1 year and 11 months (range 3 months-4 years and 6 months), and during this period, compliance to treatment (number of infusions performed vs scheduled) reached 100%. The EQ-5 VAS scale was administered to patients to evaluate the self-reported QoL, 58% of patients showing an increase of EQ-5 VAS score at follow up compared to baseline (home treatment start) or remaining stable. A mild increase of average disease severity, measured through Mainz Severity Score Index (MSSI), was found during hospital treatment (p < 0,007), while it remained stable between the first home therapy infusion and last follow up. Interestingly, 4 out of 7 (57%) patients, showing an improvement in FD-related clinical status after starting home therapy, had previously a sub-optimal compliance to treatment during the period of hospital treatment management. Only 4 adverse non serious reactions (0,093%) were reported totally in 2 patients during home treatment. We conclude that home infusions in eligible patients with FD are safe, contribute to improve treatment compliance and therapeutic clinical outcomes, and may have a positive impact on self-perceived QoL.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Genet Metab Rep Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Genet Metab Rep Year: 2017 Document type: Article