What Prevents Eligible Patients from Receiving Progesterone Therapy to Prevent Recurrent Preterm Birth ()
1. Introduction
Preterm birth is the leading cause of neonatal mortality, responsible for over 1 million deaths annually. In 2010 approximately 12% of births in the United Stated were preterm. Many studies have shown the value of 17-alpha-hydroxy progesterone caproate (17-OHPC) [1] in significantly reducing the rate of preterm birth in women with a prior preterm delivery. In 2008, ACOG recommended that this therapy be offered to all eligible patients [2] . Our institution adopted a policy to offer progesterone therapy to all eligible women in 2009. Since the use of 17-OHPC has been recommended for patients with a history of prior spontaneous preterm birth by ACOG, and has been adopted as our institutional standard, we set out to evaluate the compliance of our institution with these recommendations as well as to identify barriers contributing to non-compliance.
2. Materials and Methods
This study was a retrospective cohort study of women with a prior preterm delivery being cared for at Advocate Lutheran General Hospital, a suburban tertiary care center. The inclusion criteria consisted of a previous preterm delivery less than 36 weeks between January 1, 2010 and December 31, 2011. Exclusion criteria included primigravida, history of prior preterm birth greater than 36 weeks, history of preterm labor but no preterm delivery, history of an indicated preterm delivery for maternal medical complications such as preeclampsia, or preterm birth associated with maternal or fetal complications such as PPROM or IUGR. This study was approved by the Institutional Review Board at Advocate Lutheran General Hospital.
Descriptive statistics were reported on categorical data as number and (percent) and continuous data as mean ± SD. Independent t-test, Chi-square or Fishers Exact test when necessary was performed to measure statistical differences between 17-OHPC status (given versus not given). A two-tailed p level of 0.05 was considered statistically significant in all analyses. Analyses were performed with SPSS software (release 19.0, International Business Machines, Chicago).
3. Results
Figure 1 is a flow-diagram of patient selection. 318 charts were reviewed, and 66 patients met the eligibility criteria. 21 patients were subsequently excluded for having a history of an indicated preterm delivery or medical complication (15 had PPROM, 1 IUGR, 2 HTN, and 3 had other medical indications for delivery (2 with preterm birth after intrauterine fetal demise, 1 with induction of labor for holoprosencephaly). Two patients were not included as the circumstances of their prior preterm deliveries were unclear from their charts. The demographic data is displayed in Table 1.
Of the 43 eligible patients, 26 patients received 17-OHPC, while 17 did not. There were 10 patients who had preterm deliveries for medical indications (not idiopathic PTL) who were given 17-OHPC; these were counted in the progesterone group (n = 36) in accordance with the intent to treat principle.
Of patients with a prior idiopathic preterm birth, 26 of 43 (60.5%) received 17-OHPC therapy. Of those eligible patients who did not receive progesterone, 8 were not offered the therapy, 3 presented after 28 weeks, 2 declined therapy, and 4 had a prophylactic cerclage as their only form of treatment. The pregnancy and delivery data is compared in Table 2.
Of those patients who were not offered progesterone therapy, it should be noted that one patient had a term delivery following her initial preterm birth, and 5 others had a history of preterm delivery at 34 or 35 weeks. Of these 5 patients, 4 ultimately went on to have full term deliveries (range 37 - 40 wks; mean 38 4/7 wks). For the 5th patient the delivery information was unknown.
4. Discussion
The barrier most commonly identified with progesterone therapy to prevent recurrent preterm birth was the practitioner not offering 17-OHPC therapy. This indicates that continued education regarding the indications and timing for progesterone may be needed. Progesterone therapy to prevent recurrent preterm birth is optimally initiated between 16 and 20 weeks of gestation, and continued through 36 weeks. However, it has been shown to be of benefit when initiated as late as 26 weeks [3] . Thus, initiation of treatment later in pregnancy due to late entry into prenatal care should be considered. In addition, education of patients at the time of a preterm delivery regarding future pregnancies may help improve compliance with progesterone therapy in future pregnancies. A
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Figure 1. Flowchart of patient selection.
*Mean ± SD; †N (%); ‡ Includes the following races: Hispanic, African American, Pacific Islander, Indian, Asian (not Indian), and Unknown.
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Table 2. Pregnancy and delivery results.
*Mean ± SD.
*Corresponding author.
Interestingly, when the first years’ data was analyzed, there was a statistically significant difference between those patients that were offered progesterone compared to those that were not based on their payer status (private insurance versus public assistance). However, this difference was no longer significant when the subsequent years’ data was included, which was coincident with IDPA expanding coverage of 17-OHPC for this indication.
Four of our patients with a previous late preterm birth (34 - 35 weeks) that were not offered progesterone therapy went on to deliver at term. This is in agreement with an earlier study [5] showing that women with their earliest delivery at 20 to 27.9 weeks and at 28 to 33.9 weeks delivered at significantly more advanced gestational ages if treated with 17-OHPC than with placebo and were less likely to deliver at less than 37 weeks. Those with a previous delivery between 34 and 36.9 weeks were not significantly different between 17-OHPC and control.
In addition to studies reporting the success of 17-OHPC in preventing recurrent preterm delivery, there have been smaller reports on the success of vaginal progesterone for this indication [6] . Subsequently, there has been convincing data on the use of vaginal progesterone for a shortened cervix noted in the index pregnancy, without a previous preterm delivery [7] . What still needs to be studied is a direct comparison of 17-OHPC and vaginal progesterone for the prevention of recurrent preterm birth. This is especially timely given the concern of miscarriage and stillbirth associated with 17-OHPC exposure [8] . Although this finding was noted specifically in twin gestations (5 of 164, 3% in exposed versus 0 of 158 in controls, P = 0.06, Fisher exact test) [9] , the increased rate has been noted in singleton pregnancies exposed to 17-OHPC, but the findings were not statistically significant [1] . Additional studies are needed.
NOTES
*Corresponding author.