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1.
Transplant Proc ; 50(3): 943-946, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29458999

RESUMO

We report a case of successful combined heart liver transplant in a patient with a congenital solitary kidney. The patient had normal renal function before combined heart-liver transplantation and developed acute kidney injury requiring slow continuous dialysis and subsequent intermittent dialysis for almost 8 weeks post transplantation. Her renal function recovered and she remains off dialysis now 7 months post transplantation. She only currently has mild chronic renal insufficiency. We believe this is the first reported case of successful heart liver transplant in a patient with a congenital solitary kidney.


Assuntos
Transplante de Coração/métodos , Transplante de Fígado/métodos , Rim Único/congênito , Injúria Renal Aguda/etiologia , Adulto , Terapia Combinada/efeitos adversos , Terapia Combinada/métodos , Feminino , Transplante de Coração/efeitos adversos , Humanos , Transplante de Fígado/efeitos adversos , Complicações Pós-Operatórias/etiologia , Diálise Renal , Insuficiência Renal Crônica/etiologia
2.
Pediatr Hematol Oncol ; 24(7): 469-79, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17786783

RESUMO

The authors investigated the prevalence of low bone mass in patients from Tehran, Iran, with beta-thalassemia major (n = 203), aged 10-20 years, and the potential risk factors for osteoporosis in this patient population. Prevalence of osteoporosis was 50.7% in lumbar spine, 10.8% in femur, and 7.9% in both regions with no significant difference between the two genders. The following factors were associated with low BMD: height for age and weight for age below 3rd percentile, delayed puberty or hypogonadism, age when Desferal (for iron chelation) was started, duration of Desferal therapy, and serum zinc. Low serum copper and 25(OH)D were not associated with low BMD.


Assuntos
Densidade Óssea , Doenças Ósseas Metabólicas/etiologia , Osteoporose/etiologia , Talassemia beta/complicações , Adolescente , Doenças Ósseas Metabólicas/epidemiologia , Criança , Feminino , Fraturas Ósseas/epidemiologia , Humanos , Irã (Geográfico)/epidemiologia , Masculino , Osteoporose/epidemiologia , Osteoporose/fisiopatologia , Prevalência , Talassemia beta/fisiopatologia
3.
Kidney Int ; 69(10): 1899-903, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16598198

RESUMO

Progression of renal disease and cardiovascular complications in type II diabetes mellitus have been shown to correlate with control of blood glucose, lipids, blood pressure, and smoking. These factors, however, do not appear to totally explain these diabetic complications. Renal disease and cardiovascular complications in type II diabetes are associated with vascular abnormalities and fibrosis, both of which may occur with impaired fibrinolysis. A cross-sectional study was therefore performed in 107 type II diabetic patients recruited from the Denver Metropolitan Area to examine the effect of impaired fibrinolysis, as assessed by the ratio of plasminogen activator inhibitor (PAI-1) to tissue-type plasminogen activator (t-PA). With urinary albumin excretion (UAE) as a risk factor for both renal disease progression and cardiovascular complications, the patients were analyzed with respect to UAE less than and greater than 1 gm/day. The age, blood glucose, hemoglobin A1C, duration of diabetes, lipids, body mass index, and smoking were no different between the groups. As expected, the group with greater UAE had worse renal function, the serum creatinine (1.98 +/- 0.24 vs 1.21 +/- 0.05 mg/dl, P < 0.001) and creatinine clearance (55.5 +/- 6.0 vs 76.8 +/- 2.7 ml/min, P < 0.001) were significantly different. The type II diabetic patients with greater UAE exhibited significantly higher PAI-1/t-PA (2.43 +/- 0.26 vs 1.85 +/- 0.07, P < 0.03). The past history of cardiac complications was also higher (87.5 vs 72.3%, P < 0.07) in the diabetic patients with more impaired fibrinolysis and greater UAE. Thus a prospective, randomized clinical trial in type II diabetes with PAI-1 inhibitors is needed.


Assuntos
Albuminúria/fisiopatologia , Diabetes Mellitus Tipo 2/fisiopatologia , Nefropatias Diabéticas/fisiopatologia , Fibrinólise , Idoso , Anti-Hipertensivos/uso terapêutico , Atenolol/uso terapêutico , Doenças Cardiovasculares/complicações , Estudos de Coortes , Creatinina/sangue , Estudos Transversais , Diabetes Mellitus Tipo 2/diagnóstico , Progressão da Doença , Enalapril/uso terapêutico , Seguimentos , Humanos , Hidroclorotiazida/uso terapêutico , Hipertensão/complicações , Hipertensão/tratamento farmacológico , Inibidor 1 de Ativador de Plasminogênio/sangue , Fatores de Risco , Fatores de Tempo , Ativador de Plasminogênio Tecidual/sangue
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