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Original Article

Sterile intra-amniotic inflammation in asymptomatic patients with a sonographic short cervix: prevalence and clinical significance

, , , , , , , , , , , & show all
Pages 1343-1359 | Received 21 Jul 2014, Accepted 10 Aug 2014, Published online: 24 Sep 2014

Figures & data

Table 1. Demographic and clinical characteristics of the study population.

Table 2. Inflammatory markers in amniotic fluid, pregnancy outcomes and placental pathology results of patients in whom microorganisms were detected in amniotic fluid using standard cultivation techniques vs. PCR/ESI-MS.

Table 3. Frequency of intra-amniotic inflammation and clinical outcome in asymptomatic patients with a sonographic short cervix before 24 weeks of gestation according to the results of PCR/ESI-MS, AF cultures and AF interleukin-6 concentrations.

Figure 1. Kaplan–Meier survival curves of amniocentesis-to-delivery interval (days) among asymptomatic patients diagnosed with a CL ≤25 mm, according to the presence of microbial-associated or sterile intra-amniotic inflammation. Patients in whom labor was induced were censored and are represented by crosses. The amniocentesis-to-delivery interval among women with sterile intra-amniotic inflammation was significantly shorter than that of: (1) women without intra-amniotic inflammation; and (2) women with MIAC [median 35, (IQR: 10–70) versus median 71, (IQR: 47–98) days, and median 79, (IQR: 51–99) days (p < 0.001 and p = 0.02), respectively]. There was no significant difference in the amniocentesis-to-delivery interval between patients with sterile intra-amniotic inflammation and those with microbial-associated intra-amniotic inflammation (p > 5).

Figure 1. Kaplan–Meier survival curves of amniocentesis-to-delivery interval (days) among asymptomatic patients diagnosed with a CL ≤25 mm, according to the presence of microbial-associated or sterile intra-amniotic inflammation. Patients in whom labor was induced were censored and are represented by crosses. The amniocentesis-to-delivery interval among women with sterile intra-amniotic inflammation was significantly shorter than that of: (1) women without intra-amniotic inflammation; and (2) women with MIAC [median 35, (IQR: 10–70) versus median 71, (IQR: 47–98) days, and median 79, (IQR: 51–99) days (p < 0.001 and p = 0.02), respectively]. There was no significant difference in the amniocentesis-to-delivery interval between patients with sterile intra-amniotic inflammation and those with microbial-associated intra-amniotic inflammation (p > 5).

Table 4. Magnitude of association between type of intra-amniotic inflammation and risk of spontaneous preterm delivery at <34 weeks of gestation both unrestricted and restricted to patients whose diagnosis of a sonographic short cervix was performed <24 weeks of gestation.

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