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1.
Medicina (Kaunas) ; 58(8)2022 Jul 23.
Artículo en Inglés | MEDLINE | ID: mdl-35893099

RESUMEN

Pulmonary Alveolar Proteinosis (PAP) is a rare, usually autoimmune, disease, where surfactant accumulates within alveoli due to decreased clearance, causing dyspnea and hypoxemia. The disease is even more rare in pregnancy; nevertheless, it has been reported in pregnant women and can even appear for the first time during pregnancy as an asthma-like illness. Therefore, awareness is important. Similarly to many autoimmune diseases, it can worsen during pregnancy and postpartum, causing maternal and fetal/neonatal complications. This paper offers a narrative literature review of PAP and pregnancy, while illustrating a case of a pregnant patient with known PAP who developed preeclampsia in the third trimester but had an overall fortunate maternal and neonatal outcome.


Asunto(s)
Enfermedades Autoinmunes , Proteinosis Alveolar Pulmonar , Surfactantes Pulmonares , Enfermedades Autoinmunes/complicaciones , Disnea/etiología , Femenino , Humanos , Recién Nacido , Pulmón , Embarazo , Proteinosis Alveolar Pulmonar/complicaciones , Proteinosis Alveolar Pulmonar/diagnóstico , Proteinosis Alveolar Pulmonar/terapia
2.
Pediatrics ; 120(6): e1476-80, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-18055665

RESUMEN

OBJECTIVES: The purpose of this work was to investigate the effect of institutionalization on death and CD4 decline in a cohort of 325 HIV-infected Romanian children. METHODS: A retrospective database analysis was conducted. Data from a nearly 3-year period were examined with Kaplan-Meier survival analysis and Cox regression analysis models. Subjects all received primary and HIV specialty care and treatment at the Romanian American Children's Center in Constanta, Romania. Children in one group resided with their biological families and the other children resided in "family home"-style institutions. RESULTS: There was no difference between groups for death during the follow-up period, although there was a trend for survival advantage for children in institutional care. There was no statistically significant difference between the study groups in terms of CD4 decline, although there was a trend toward greater decline among children who resided with their biological families. Children with their biological families were more likely to experience disease progression through either death or CD4 decline than were children in institutions. CONCLUSIONS: The family home-style institution may prove to be a replicable model for the safe and appropriate care of HIV-infected orphaned and abandoned children and teens.


Asunto(s)
Infecciones por VIH/mortalidad , Institucionalización/estadística & datos numéricos , Adolescente , Niño , Progresión de la Enfermedad , Femenino , Infecciones por VIH/terapia , Humanos , Masculino , Rumanía
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