RESUMO
Objective: The aim of this retrospective review is to evaluate trends in the management of maternal and congenital syphilis (CS) in a tertiary care center in New Orleans, LA. Study Design: All cases of maternal and neonatal syphilis over a five year period at Touro Infirmary, New Orleans, LA, were identified using ICD-9/10 codes. Charts were reviewed for demographic and obstetrical variables, stage of syphilis at diagnosis, lab values, and treatment regimen. Newborn treatment and other outcomes were recorded. Results: During the study period 106 infected mother-baby pairs were identified. Of these, 73 charts are available for review. 41% (n = 30) of women received inadequate therapy according to their stage of disease. 9% of newborns (n = 6) were found to be symptomatic for CS; however, only 83.3% of these were admitted to the neonatal intensive care unit. Only 20% (n = 6) of infants were adequately treated with an extended penicillin regimen if the mother was not adequately treated. Furthermore, only 63.0% of newborns had a nontreponemal titer performed. Conclusion: With rising rates of CS, strict adherence to the 2015 CDC guidelines for treatment of syphilis must be maintained.
Assuntos
Antibacterianos/uso terapêutico , Penicilinas/uso terapêutico , Complicações Infecciosas na Gravidez/tratamento farmacológico , Sífilis Congênita/tratamento farmacológico , Sífilis/tratamento farmacológico , Adolescente , Adulto , Feminino , Humanos , Recém-Nascido , Masculino , Nova Orleans/epidemiologia , Gravidez , Complicações Infecciosas na Gravidez/epidemiologia , Estudos Retrospectivos , Sífilis/epidemiologia , Sífilis Congênita/epidemiologia , Adulto JovemRESUMO
BACKGROUND: Necrotizing enterocolitis (NEC) is a leading cause of newborn gastrointestinal emergencies, affecting 1-3 per 1000 live births. Although NEC has been linked to a microbial etiology, associations with maternal intrapartum and resultant newborn early-onset invasive Group B streptococcus (EO-GBS) have been weakly defined. OBJECTIVE: The study aim was to determine the relationship between EO-GBS and NEC. STUDY DESIGN: Data from 2008 to 2015 were collected from pediatric records with ICD diagnosis codes consistent with all stages of NEC, with the exception of neonatal EO-GBS data (only available 2011-2015). RESULTS: For the 131 newborns meeting inclusion criteria, the mean gestational age (GA) and birthweight at delivery was 30.2 weeks and 1449â¯g. Maternal comorbidities were not associated with a more advanced stage of NEC, however male gender (OR 3.2, pâ¯<â¯.001), lower mean 1 (ORâ¯=â¯0.89, pâ¯=â¯.045) and 5â¯min Apgar scores (ORâ¯=â¯0.84, pâ¯=â¯.009) were significantly associated with higher NEC stage, after controlling for GA. Infectious morbidities including chorioamnionitis (ORâ¯=â¯1.5, pâ¯=â¯.553) and intrapartum antibiotic administration (ORâ¯=â¯1.3, pâ¯=â¯.524) were not significantly associated with higher NEC stage. Neither neonatal sepsis workup (ORâ¯=â¯0.27, pâ¯=â¯.060) nor positive blood culture (ORâ¯=â¯0.97, pâ¯=â¯.942) prior to NEC diagnosis were statistically significant. Type of feed prior to diagnosis (pâ¯=â¯.530) was not significantly associated with NEC stage, however, expressed breast milk tended to be protective against higher stage of NEC (ORâ¯=â¯0.49, pâ¯=â¯.055). Type of feed included total parenteral nutrition, mother's or donor expressed breast milk, trophic, full and high calorie feeds. Of the 579 newborns admitted from 2011 to 2015, 13 (2%) were diagnosed with EO-GBS and 64 met diagnostic criteria for NEC. GBS positive newborns had significantly higher odds of NEC (ORâ¯=â¯5.37, pâ¯=â¯.009). NEC stage was not significantly different for patients with GBS positive vs. GBS negative mothers (pâ¯=â¯.732), nor was there a significant difference in GA (pâ¯=â¯.161). CONCLUSION: Our study is the first to describe a strong correlation between neonatal EO- GBS disease and NEC, with more than a five-fold increase in the odds of developing NEC in newborns of GBS positive mothers. PURPOSE: To investigate a possible relationship between EO-GBS disease and the neonatal diagnosis of NEC. Secondary analysis will determine if maternal antepartum and intrapartum factors along with neonatal variables contribute to a more advanced stage of NEC by retrospective chart review of patient data collected at Children's Hospital: New Orleans.