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1.
Eur J Epidemiol ; 17(8): 715-20, 2001.
Article in English | MEDLINE | ID: mdl-12086088

ABSTRACT

BACKGROUND: Bloodstream infection represents a major threat among neonates under intensive care with considerable impact on morbidity and mortality. This study evaluated extra stay, attributable mortality and the risk factors associated with late-onset bloodstream infection (LO-BSI) among neonates admitted to a neonatal intensive care unit during a 4-year period. METHODS: A retrospective matched cohort study was conducted. For each case, there was one control patient without LO-BSI matched for sex, birth weight, gestational age, duration of hospitalization prior to the date of LO-BSI in the respective cases, underlying illness and birth date. A novel test, sequential plan, was employed for attributable mortality analysis in addition to standard tests. Multiple logistic regression was employed for risk factor analysis. RESULTS: Fifty pairs of cases and controls were compared. LO-BSI prolonged hospital stay of 25.1 days in pairs where both subjects survived. Overall attributable mortality was 24% (95% CI: 9-39% p < 0.01) and specific attributable mortality due to Staphylococcus epidermidis was 26.7% (95% CI: 23-30.4%; p = 0.01). Blood and/or blood components transfusion was independently associated with neonatal LO-BSI (OR: 21.2; 95% CI: 1.1-423). CONCLUSIONS: LO-BSI infection prolongs hospital stay and is associated with increased mortality among neonates. In the present series, blood transfusion was a significant risk factor for LO-BSI.


Subject(s)
Length of Stay/statistics & numerical data , Sepsis/mortality , Brazil/epidemiology , Case-Control Studies , Female , Humans , Infant, Newborn , Intensive Care Units, Neonatal , Logistic Models , Male , Retrospective Studies , Risk Factors , Sepsis/microbiology , Staphylococcus epidermidis/isolation & purification , Statistics, Nonparametric
2.
Am Heart J ; 124(2): 413-7, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1636585

ABSTRACT

Maternal and fetal complications in a consecutive series of 60 pregnancies in 49 patients with prosthetic heart valves were prospectively evaluated. Group 1 consisted of 40 pregnancies in 31 patients who were taking oral anticoagulants. No oral anticoagulation was used in 20 pregnancies in 19 patients (group 2). In group 1 there were three instances of acute valvular thrombosis during the 35 pregnancies in patients with mechanical prostheses, with two maternal deaths. There were two episodes of cerebral embolism, one in group 1 and one in group 2. Patients with isolated aortic valve replacement had fewer maternal complications (2 of 13) than patients with isolated mitral valve replacement (15 of 42) without statistical significance. Severe bioprosthesis dysfunction occurred in 4 of 25 pregnancies (one rupture and three stenosis) with two maternal deaths, one in the puerperium and the other in the postoperative period of cardiac surgery during pregnancy. When analyzing obstetric events we observed seven spontaneous abortions and one hydatidiform mole. All spontaneous abortions occurred in group 1. The incidences of prematurity and low birth weight were significantly higher in group 1 than in group 2 (46.6% vs 10.5%, p less than 0.05, and 50% vs 10.5%, p less than 0.05, respectively). Moreover, there was a significant association between prematurity and the mother's New York Heart Association functional class (61.5% in classes III and IV vs 22.2% in classes I and II, p less than 0.05). There were five neonatal deaths, all in group 1 (p = NS vs group 2). Three infants had warfarin-related congenital defects.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Abnormalities, Drug-Induced/epidemiology , Abortion, Spontaneous/epidemiology , Anticoagulants/adverse effects , Heart Valve Prosthesis , Obstetric Labor, Premature/epidemiology , Pregnancy Complications, Cardiovascular/drug therapy , Abortion, Spontaneous/chemically induced , Adult , Anticoagulants/therapeutic use , Female , Humans , Infant, Low Birth Weight , Infant, Newborn , Obstetric Labor, Premature/chemically induced , Pregnancy , Pregnancy Complications, Cardiovascular/epidemiology , Prospective Studies , Risk Factors
3.
Bull World Health Organ ; 70(1): 85-91, 1992.
Article in English | MEDLINE | ID: mdl-1314711

ABSTRACT

Described is the evaluation in Brazil of the immune response of early immunization with trivalent oral poliovirus vaccine (TOPV). A total of 85 normal neonates from São Paulo were assigned one of the following immunization schedules: group A--one dose of TOPV at birth and subsequent doses at 2, 4, and 9 months of age; or group B--one dose of TOPV at 2, 4 and 6 months of age. Blood samples were collected sequentially from the mother at delivery, from the umbilical cord, and from the child at 2, 4, 6, 9 and 12 months of age for assay of poliovirus neutralizing antibodies. Administration of TOPV at birth, in addition to establishing immunity against poliomyelitis at an earlier stage, produced a superior immune response to poliovirus type 3. At the end of the first year, the proportion of susceptible individuals was 3.7% in group A and 25.9% in group B. When immunization against poliomyelitis is started at birth, excellent seroconversion rates are obtained from the third dose onward.


Subject(s)
Antibody Formation , Poliovirus Vaccine, Oral/immunology , Poliovirus/immunology , Age Factors , Antibodies, Viral/isolation & purification , Humans , Immunization Schedule , Infant , Infant, Newborn , Poliovirus Vaccine, Oral/administration & dosage
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