Abstract

Chronic histiocytic intervillositis (CHI) is a rare, but highly recurrent inflammatory placental lesion wherein maternal macrophages infiltrate the intervillous space. Pregnancies with CHI are at high risk of fetal growth restriction, miscarriage or stillbirth. Presently, the diagnosis can only be made after histopathological examination of the placenta. Given its proposed immunological etiology, current treatments include aspirin, heparin, and immunomodulatory agents. However, the rationale for these medications is largely based upon small case series and reports as there is a lack of larger studies investigating treatment efficacy. Therefore, this study sought to determine whether inclusion of immunomodulatory medications was effective at reducing the severity of lesions and improving pregnancy outcomes in subsequent pregnancies. Thirty-three women with a history of CHI in at least one pregnancy (index case) were identified retrospectively through medical records. Twenty-eight participants presented with a first subsequent pregnancy and a further 11 with a second subsequent pregnancy at a specialist clinic for pregnancy after loss. Data on maternal demographics, medical history, medication, pregnancy outcome, and placental pathology was collected and compared between pregnancies. Twenty-seven (69%) subsequent pregnancies were treated with at least one or both of prednisolone and hydroxychloroquine. Inclusion of at least one immunomodulatory agent in treatment regimen resulted in an almost 25% increase in overall livebirth rate (61.5 vs. 86.2%). In women treated with immunomodulatory medication a greater proportion of placentas had reduced severity of lesions compared to those treated without (86.7 vs. 33.3%, respectively). A reduction in CHI severity was associated with a 62.3% improvement in livebirth rate compared to those where severity remained unchanged in relation to the index case. These data provide preliminary evidence that the use of immunomodulatory medication in the management of CHI improves histopathological lesions and the chance of livebirth in subsequent pregnancies. Due to CHI's rarity and ethical and feasibility issues, randomized controlled trials in affected women are challenging to conduct. As a result, collaboration between centers is required in future to increase study sample sizes and elucidate the mechanisms of hydroxychloroquine and prednisolone in reducing pathology.

Highlights

  • Chronic histiocytic intervillositis (CHI), known as chronic intervillositis or chronic intervillositis of unknown etiology [1], is a pregnancy disorder strongly associated with fetal growth restriction, miscarriage, stillbirth and neonatal death [2,3,4,5]

  • By retrospectively identifying women with a previous diagnosis of CHI, we aimed to investigate pregnancy outcomes and placental pathology in subsequent pregnancies referred to a specialist service following poor perinatal outcome, stillbirth or neonatal death

  • Decreased severity of CHI in subsequent pregnancies was associated with a 62.3% increase in livebirth rate compared to pregnancies where severity was unchanged [20/22 (90.9%) vs. 2/7 (28.6%), respectively] (p = 0.003; Figure 4B). These data suggest that the use of one or both of prednisolone and hydroxychloroquine in the treatment of CHI resulted in a reduction of disease severity and a trend toward an increase in livebirth rate

Read more

Summary

Introduction

Chronic histiocytic intervillositis (CHI), known as chronic intervillositis or chronic intervillositis of unknown etiology [1], is a pregnancy disorder strongly associated with fetal growth restriction, miscarriage, stillbirth and neonatal death [2,3,4,5]. Owing to the presence of maternal macrophages and the reported increased incidence in women with autoimmune disease, CHI has been hypothesized to be a disorder of failed maternal-fetal tolerance and excessive inflammation [9]. On this basis and due to the presence of intervillous and perivillous fibrin, current treatments include thromboprophylactic agents such as aspirin and low-molecular-weight heparin (LMWH) as well as those aimed at suppressing inflammation e.g., corticosteroids and hydroxychloroquine [9]. Due to the high rate of recurrence of CHI and severe consequences of the disorder, studies are urgently needed to determine effective therapies

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call