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1.
Hypertens Pregnancy ; 31(1): 79-90, 2012.
Article in English | MEDLINE | ID: mdl-21219123

ABSTRACT

OBJECTIVE: To evaluate the effectiveness of the Mississippi Protocol (MP) to treat HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome. METHODS: Uniform early initiation of MP (corticosteroids, magnesium sulfate, systolic blood pressure control) was studied prospectively in patients admitted with severe preeclampsia/class 1 or class 2 HELLP syndrome. RESULTS: One hundred and ninety patients between 2000 and 2007 received MP without suffering maternal death, stroke, or liver rupture. Only 39 of 163 patients (24%) not class 1 when MP began progressed to class 1 disease; only 18.2% of class 1 and 2.4% of class 2 subsequently developed major maternal morbidity. CONCLUSION: Early initiation of MP inhibits HELLP syndrome disease progression and severity.


Subject(s)
HELLP Syndrome/therapy , Academic Medical Centers/statistics & numerical data , Adult , Clinical Protocols , Disease Progression , Female , Humans , Pregnancy , Prospective Studies , Treatment Outcome , Young Adult
2.
J Miss State Med Assoc ; 52(3): 72-5, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21476464

ABSTRACT

OBJECTIVE: Bacterial vaginosis (BV) is associated with preterm labor and may be positive in 15% of asymptomatic high-risk women. Fetal fibronectin (fFN) has been shown in symptomatic women to predict infection-related preterm birth. The purpose of this study was to quantitate the relationship between BV/fFN and preterm delivery in high-risk asymptomatic women. METHODS: Women at high-risk for spontaneous preterm delivery were tested for BV/fFN between 20-28 weeks gestation. Women positive for BV were treated with metronidazole, and fFN results were not used by physicians in treatment. After delivery, test results and pregnancy outcomes were entered in a deidentified database and analyzed. RESULTS: Of 232 women tested for BV/fFN over a 24-month epoch, results divided participants into 4 groups: Group A (N = 12; +BV/+fFN); Group B (N = 22; -BV/+fFN); Group C (N = 68; +BV/-fFN); and Group D (N = 130; -BV/-fFN). Demographics were the same between the 4 groups (P = NS) as was the gestational age at delivery (36.41 +/- 3.96 to 37.18 +/- 3.03 weeks). The incidence ofpreterm labor (P = .075), spontaneous early delivery (P = .936) and infants < 2500 gm (P = .664) was also similar. CONCLUSIONS: In asymptomatic high-risk women, testing for fFN/BV during mid-pregnancy does not appear warranted.


Subject(s)
Anti-Infective Agents/therapeutic use , Fetal Proteins/analysis , Fibronectins/analysis , Metronidazole/therapeutic use , Pregnancy Complications, Infectious/drug therapy , Premature Birth/prevention & control , Vaginosis, Bacterial , Adult , Anti-Infective Agents/administration & dosage , Apgar Score , Birth Weight , Chi-Square Distribution , Enzyme-Linked Immunosorbent Assay , Female , Gestational Age , Humans , Hydrogen-Ion Concentration , Infant, Newborn , Maternal Age , Metronidazole/administration & dosage , Parity , Pregnancy , Pregnancy Outcome , Randomized Controlled Trials as Topic , Statistics, Nonparametric , Time Factors , Vaginosis, Bacterial/drug therapy
3.
Am J Perinatol ; 28(3): 187-94, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20827656

ABSTRACT

We assessed pregnancy outcomes for patients with HELLP syndrome (hemolysis; elevated liver enzymes; low platelet count) with and without concurrent eclampsia. We performed a retrospective investigation of data spanning three decades of patients with class 1 or 2 HELLP syndrome with concurrent eclampsia (HELLP + E) and patients with HELLP syndrome without eclampsia. Data were analyzed by appropriate tests for continuous or categorical outcomes with differences considered significant if P < 0.05. During 1981 to 1996 and 2000 to 2006, there were 693 patients with class 1 or 2 HELLP syndrome; altogether, 70 patients had HELLP + E. The only demographic difference was greater nulliparity in HELLP + E patients. Otherwise, inconsistent and clinically insignificant differences were observed between groups. Despite the relatively large size of the study groups, we were unable to detect a significant worsening of maternal or perinatal outcome in HELLP + E patients compared with HELLP patients. In our experience, eclampsia does not appear to contribute a significant adverse impact upon the course or outcome of HELLP syndrome pregnancies.


Subject(s)
Eclampsia/epidemiology , HELLP Syndrome , Pregnancy Outcome , Adolescent , Adult , Apgar Score , Birth Weight , Blood Pressure , Comorbidity , Female , HELLP Syndrome/physiopathology , Humans , Incidence , Infant Mortality , Infant, Newborn , Parity , Pregnancy , Retrospective Studies , Risk Assessment , Young Adult
4.
Am J Obstet Gynecol ; 190(6): 1582-7; discussion 1587-9, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15284741

ABSTRACT

OBJECTIVE: The purpose of this study was to codify the relationship between bacterial vaginosis/fetal fibronectin and preterm labor/birth. STUDY DESIGN: In this prospective study, 185 women who were symptomatic for preterm labor were assessed for bacterial vaginosis and fetal fibronectin. RESULTS: These women comprised 4 groups: group A (n=23 women; +bacterial vaginosis/+fetal fibronectin); group B (n=31 women; -bacterial vaginosis/+fetal fibronectin); group C (n=47 women; +bacterial vaginosis/-fetal fibronectin); and group D (n=84 women; -bacterial vaginosis/-fetal fibronectin). The time interval from gestational age at testing until delivery was significantly shorter for groups A and B versus groups C and D (P < or =.05 and P <.001, respectively). Similarly, delivery at <32 weeks of gestation was increased in group B (26%) compared with groups A (9%), C (2%), and D (5%; P <.009; odds ratio, 165.90; 95% CI, 30.02, 916.08). CONCLUSION: Women who are symptomatic for preterm labor should be considered for fetal fibronectin and bacterial vaginosis testing.


Subject(s)
Fibronectins , Glycoproteins/metabolism , Obstetric Labor, Premature/epidemiology , Pregnancy Complications, Infectious/epidemiology , Pregnancy Outcome , Vaginosis, Bacterial/epidemiology , Adult , Biomarkers/analysis , Cohort Studies , Female , Gestational Age , Glycoproteins/analysis , Humans , Incidence , Infant, Newborn , Infant, Premature , Pregnancy , Probability , Prospective Studies , Risk Assessment , Sensitivity and Specificity , Severity of Illness Index , Statistics, Nonparametric , Vaginosis, Bacterial/diagnosis
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