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1.
Circulation ; 127(11): 1177-83, 2013 Mar 19.
Artículo en Inglés | MEDLINE | ID: mdl-23426104

RESUMEN

BACKGROUND: In developing economies, there are patients in whom pacemaker implantation is delayed because they cannot afford one. Reused devices have been a solution. To address concerns about safety, a cohort of consecutive patients implanted with a reused pacemaker was compared with a control group. METHODS AND RESULTS: A cohort of 603 consecutive patients from 2000 to 2010 was studied in an ambispective noninferiority study. The study group patients (n=307) received resterilized pacemakers, and the control group patients (n=296) received a new pacemaker. A combined end point of 3 major outcomes-unexpected battery depletion, infection, and device dysfunction-was analyzed. A total of 85 pacemakers had to be explanted, 31 in the control group (10.5%) and 54 in the study group (17.6%; relative risk, 1.68; 95% confidence interval, 1.1-2.5; P=0.02). Forty-three reached the primary end point, 16 in the control group (5.5%) and 27 in the study group (7.2%; relative risk, 1.3; 95% confidence interval, 0.70-2.45; P=0.794). In terms of individual outcomes, 5 new pacemakers (1.7%) and 11 resterilized pacemakers (3.6%) had unexpected battery depletion (relative risk, 2.12; 95% confidence interval, 0.75-6; P=0.116); 3.7% new pacemakers and 3.2% reused pacemakers had a procedure-related infection (relative risk, 0.87; 95% confidence interval, 0.38-2.03; P=0.46); and 1 pacemaker in the study group malfunctioned. CONCLUSIONS: Pacemaker reuse is feasible and safe and is a viable option for patient with bradyarrhythmias. Other than the expected shorter battery life, reuse of pacemaker generators is not inferior to the use of new devices.


Asunto(s)
Bradicardia/terapia , Falla de Equipo/estadística & datos numéricos , Marcapaso Artificial/efectos adversos , Marcapaso Artificial/estadística & datos numéricos , Adulto , Anciano , Estudios de Cohortes , Suministros de Energía Eléctrica/estadística & datos numéricos , Equipo Reutilizado , Estudios de Factibilidad , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Infección de la Herida Quirúrgica/epidemiología , Factores de Tiempo
2.
Amyloid ; 19(4): 171-6, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22928869

RESUMEN

BACKGROUND: The phenotypic heterogeneity of transthyretin amyloidosis (ATTR) familial polyneuropathy may be linked to the type of mutation and to the environmental factors. A gender difference in relation to the severity of the disease has been suspected. More than 100 different pathogenic variants of hereditary transthyretin (TTR) mutations have been reported. OBJECTIVE: To describe 32 patients with confirmed TTR Ser50Arg mutation from the same geographical origin. METHODS: Seven families with up to four affected generations underwent genetic testing and prospective clinical and laboratory evaluations. RESULTS: The mutation was confirmed in seven patients from different families with clinical symptoms compatible with ATTR amyloidosis, and in 25 (62%) of the 40 direct relatives tested. Of the 32 patients with positive test results, 18 (56%) were men. Only 5 (16%) subjects were disease-free at the time of the genetic test (mean age: 20, range: 18-30-year-old). The rest developed symptoms at a young age, between ages 36 and 41. Symptomatic, histologically positive patients were older than carriers and symptomatic patients without a confirmatory biopsy. The later generation displayed symptoms at a younger age. Initial manifestations in the 27 symptomatic patients were neuropathic in 19 (70%), gastrointestinal in 6 (22%) and autonomic in 1 (4%). Significant differences were demonstrated among genders, where men had a considerably worse outcome. CONCLUSION: ATTR Ser50Arg mutation was associated with an early onset, an unbalanced male to female ratio, a more aggressive course in males and possibly displayed anticipation.


Asunto(s)
Amiloide/genética , Amiloidosis Familiar/epidemiología , Amiloidosis Familiar/genética , Mutación , Polineuropatías/epidemiología , Polineuropatías/genética , Prealbúmina/genética , Adolescente , Adulto , Edad de Inicio , Amiloidosis Familiar/complicaciones , Biopsia , Análisis Mutacional de ADN , Femenino , Humanos , Masculino , México/epidemiología , Persona de Mediana Edad , Linaje , Polineuropatías/complicaciones , Factores Sexuales
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