Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
1.
Am J Perinatol ; 29(7): 489-96, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22399213

ABSTRACT

OBJECTIVE: Examine adherence to treatment guidelines and rates of recurrent spontaneous preterm birth (SPTB) in managed Medicaid patients prescribed 17 α-hydroxyprogesterone caproate (17P). STUDY DESIGN: A retrospective observational study of women receiving 17P between July 2004 and May 2010 through one of Centene's managed Medicaid programs. Included for analysis were singleton pregnancies without cerclage having SPTB history and prescribed 17P by their physician. Compounded 17P was administered through an outpatient program inclusive of patient education, weekly home nurse visits, and 24-7 telephonic nurse access. A health plan-directed pregnancy management program, Start Smart for Your Baby(®), supported the therapy with case management activities. RESULTS: Of the 790 patients studied, 58.6% initiated 17P in the recommended 16- to 20.9-week gestational age window. Elective discontinuation of 17P occurred in 18.6%. Of the 10,583 17P injections administered, 97.5% were administered within the recommended injection interval of 6 to 10 days. Recurrent SPTB occurred in 28.2% of women studied. CONCLUSION: Managed Medicaid patients enrolled in an outpatient 17P administration program supported with maternal case management have high rates of treatment compliance. Their pregnancy outcomes compare favorably to previously published reports that include both Medicaid and commercially insured patients.


Subject(s)
Home Care Services , Hydroxyprogesterones/therapeutic use , Medicaid/statistics & numerical data , Premature Birth/prevention & control , Progestins/therapeutic use , 17 alpha-Hydroxyprogesterone Caproate , Adolescent , Adult , Female , Gestational Age , Guideline Adherence , Humans , Infant, Newborn , Infant, Premature , Medication Adherence , Practice Guidelines as Topic , Pregnancy , Pregnancy Outcome , Retrospective Studies , United States
2.
Manag Care ; 20(4): 39-46, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21553688

ABSTRACT

OBJECTIVE: Examine the effect of a prenatal program on birth outcomes, specifically birth weight, in a managed Medicaid pregnant population, and identify the potential barriers to obtaining the risk screening information required for successful interventions. DESIGN: Retrospective propensity-adjusted cohort comparison. METHODS: Retrospective propensity-adjusted comparison of pregnant women in a managed Medicaid plan enrolled in a prenatal program and pregnant women who were not enrolled. Program enrollment was initiated by receipt of a Notification of Pregnancy (NOP) risk screening assessment. RESULTS: We demonstrate a statistically significant improvement in delivery outcomes in the women who participate in the pregnancy management program (NOP group) compared with those who do not (non-NOP group). The incidence of low-birth-weight infants was lower in the NOP group compared to the non-NOP group. Odds ratio estimates indicate that the NOP participants are likely to have 7.9% lower adverse event frequency for delivery weights <2500 g; 20% lower adverse event frequency for delivery weights <1500 g; and 31.2% lower adverse event frequency for delivery weights <1000 g. All p values are statistically significant. CONCLUSION: Participation in a pregnancy management program improves birth outcomes in women who are at risk of low-birth-weight deliveries. Early identification of pregnant women and their risk factors for the purpose of enrollment in a managed Medicaid prenatal program is an important factor in improving birth outcomes, specifically birth weight. Our results indicate that this is an important area for investment if birth outcomes are to be improved.


Subject(s)
Medicaid , Pregnancy Outcome , Prenatal Care/standards , Adult , Cohort Studies , Female , Humans , Managed Care Programs/standards , Middle Aged , Models, Organizational , Pregnancy , Program Evaluation , Retrospective Studies , United States , Young Adult
3.
Manag Care ; 19(2): 46-52, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20550052

ABSTRACT

OBJECTIVE: To evaluate whether providing 17 alpha-hydroxyprogesterone caproate (17P) to high-risk pregnant women who have a history of preterm delivery in a Medicaid managed care population reduces the rate of recurrent preterm delivery and neonatal intensive care unit (NICU) admissions. STUDY DESIGN: A 2004-2009 longitudinal review of birth outcomes in 193 singleton pregnant women with a history of spontaneous preterm delivery that were treated with 17P versus a control group. METHODOLOGY: Intervention included offering 17P as a benefit to pregnant women who had a history of spontaneous preterm delivery and who were deemed to be appropriate candidates by their doctor. Members for this study were identified by claims review and obstetrical (OB) case managers in the health plans. A process of early identification, using a variety of data sources, was established along with an educational program aimed at physicians, their office staff, and plan members in order to increase 17P utilization in appropriate candidates. RESULTS: Deliveries with a gestational age of less than 35 weeks decreased significantly from 41.67% in the control group to 26.42% in the 17P group when 17P was initiated by 28 weeks of gestation. The NICU admission rate decreased from 45% in the control group to 33.68% in this 17P group, and was nearly significant. CONCLUSION: Offering 17P as a benefit does have a positive effect on reducing the rate of recurrent preterm delivery and rate of NICU admission in a managed Medicaid population. There was no decrease in effectiveness with delay in initiation of 17P as long as it was started by 28 weeks of gestation.


Subject(s)
Hydroxyprogesterones/therapeutic use , Managed Care Programs , Medicaid , National Institute of Child Health and Human Development (U.S.) , Premature Birth/prevention & control , 17 alpha-Hydroxyprogesterone Caproate , Chi-Square Distribution , Female , Gestational Age , Humans , Hydroxyprogesterones/administration & dosage , Infant, Newborn , Infant, Premature , Injections, Intramuscular , Longitudinal Studies , Multicenter Studies as Topic , Patient Compliance , Pregnancy , Premature Birth/economics , Randomized Controlled Trials as Topic , Risk Factors , United States , United States Food and Drug Administration
SELECTION OF CITATIONS
SEARCH DETAIL
...