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1.
Transplant Proc ; 48(6): 1927-33, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27569924

RESUMO

Posttransplantation lymphoproliferative disorder (PTLD) after solid organ transplantation may carry a poorer prognosis than lymphoma in immunocompetent individuals, but comparative data are lacking. In a retrospective, single-center, case-control study, 21 cases of PTLD were identified in patients undergoing kidney transplantation since 2000, and compared to 42 nontransplanted controls cared for in the same institution and matched for age, prognostic index, and cerebral localization. Two-year and 5-year overall survival was 57% and 44%, respectively, in PTLD patients and 71% and 58% in controls (log-rank test P = .20). On multivariable analysis, overall survival was similar for PTLD and control patients (hazard ratio 1.71, 95% confidence interval 0.81 to 3.61, P = .16). Response rate to first-line chemotherapy was similar between the 2 groups. Death was due to progression of the disease in 46% vs 94% of PTLD and control patients, respectively (P < .01), or sepsis in 31% vs 0% (P = .03). Treatment-related mortality was significantly higher in PTLD (19%) than in controls (0%, P = .03). In conclusion, response to first-line chemotherapy and overall survival are similar in PTLD and control patients, whereas causes of death were significantly different. Better prevention and management of infectious complications could improve the results in PTLD patients.


Assuntos
Transplante de Rim/efeitos adversos , Transtornos Linfoproliferativos/etiologia , Adulto , Idoso , Estudos de Casos e Controles , Feminino , Humanos , Linfoma/mortalidade , Transtornos Linfoproliferativos/mortalidade , Masculino , Pessoa de Meia-Idade , Prognóstico , Modelos de Riscos Proporcionais , Estudos Retrospectivos
2.
Pediatrics ; 78(1): 10-4, 1986 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-3725477

RESUMO

Patent ductus arteriosus is common among premature neonates, especially those with birth weights less than 1,500 g. In vitro, room light inhibits the contraction of immature piglet's ductal rings. Because phototherapy is used frequently from the first days of life to treat jaundice in preterm neonates, we compared the occurrence of patent ductus arteriosus among premature infants exposed to this intense light source with those whose chests were shielded. Seventy-four babies with respiratory distress syndrome were randomly assigned to either a treatment group (chest shielded with aluminum foil while on phototherapy, 36 babies) or control group (no shield, 38 babies). All were on radiant warmers, received mechanical ventilation for respiratory distress syndrome, and phototherapy (Air Shields model PTU 78-1) from day 1 of life. Irradiance was maintained at greater than 4.0 microW/cm2/nm in all cases. Although both groups had similar birth weights, gestational ages, severity of respiratory distress syndrome, intravenous fluid intake, and duration of phototherapy, the incidence of patent ductus arteriosus was significantly less in the shield group (shield 11/36 v No shield 23/38; P = .009). Patent ductus arteriosus murmurs developed in shielded patients at a later date, they required less vigorous treatment (ie, indomethacin), and they had shorter hospitalizations (74 v 85 days; P less than .05). The significant reduction of patent ductus arteriosus with shielding suggests that phototherapy may play a role in the occurrence of patent ductus arteriosus in premature infants. Shielding may be a practical method to decrease this common complication should this initial observation be confirmed.


Assuntos
Permeabilidade do Canal Arterial/etiologia , Icterícia Neonatal/terapia , Fototerapia/efeitos adversos , Proteção Radiológica/métodos , Síndrome do Desconforto Respiratório do Recém-Nascido/terapia , Permeabilidade do Canal Arterial/mortalidade , Permeabilidade do Canal Arterial/prevenção & controle , Feminino , Humanos , Recém-Nascido , Icterícia Neonatal/complicações , Masculino , Síndrome do Desconforto Respiratório do Recém-Nascido/complicações
3.
Transplant Proc ; 44(9): 2818-20, 2012 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-23146531

RESUMO

Although only 2 cases of Pneumocystis jiroveci pneumonia were observed in our center between 2004 and 2009, we diagnosed 9 cases in 2010. Each patient had been in contact in the hospital with at least 1 other patient suffering P jiroveci pneumonia. Genotyping of P jiroveci pneumonia strains demonstrates a total homogeneity of the DNA sequences in the 7 patients already analyzed. CD4+ lymphocyte count was significantly lower at M3 in P jiroveci pneumonia patients than in controls. Our clinical and molecular data confirm that interhuman transmission of P jiroveci is possible, particularly to lymphopenic transplant recipients.


Assuntos
Infecção Hospitalar/epidemiologia , Epidemias , Transplante de Rim/imunologia , Linfopenia/imunologia , Pneumocystis carinii/patogenicidade , Pneumonia por Pneumocystis/epidemiologia , Linfócitos T/imunologia , Contagem de Linfócito CD4 , Distribuição de Qui-Quadrado , Infecção Hospitalar/imunologia , Infecção Hospitalar/microbiologia , Infecção Hospitalar/terapia , Infecção Hospitalar/transmissão , França/epidemiologia , Genótipo , Humanos , Transplante de Rim/efeitos adversos , Pneumocystis carinii/genética , Pneumonia por Pneumocystis/imunologia , Pneumonia por Pneumocystis/microbiologia , Pneumonia por Pneumocystis/terapia , Pneumonia por Pneumocystis/transmissão , Estudos Retrospectivos , Fatores de Risco , Fatores de Tempo
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