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Antibiotic administration can eradicate intra-amniotic infection or intra-amniotic inflammation in a subset of patients with preterm labor and intact membranes
DC Field | Value | Language |
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dc.contributor.author | 이준호 | - |
dc.date.accessioned | 2020-11-24T05:31:30Z | - |
dc.date.available | 2020-11-24T05:31:30Z | - |
dc.date.issued | 2019-08 | - |
dc.identifier.issn | 0002-9378 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/179884 | - |
dc.description.abstract | Background: Intra-amniotic infection is present in 10% of patients with an episode of preterm labor, and is a risk factor for impending preterm delivery and neonatal morbidity/mortality. Intra-amniotic inflammation is often associated with intra-amniotic infection, but is sometimes present in the absence of detectable microorganisms. Antibiotic treatment of intra-amniotic infection has traditionally been considered to be ineffective. Intra-amniotic inflammation without microorganisms has a prognosis similar to that of intra-amniotic infection. Objective: To determine whether antibiotics can eradicate intra-amniotic infection or intra-amniotic inflammation in a subset of patients with preterm labor and intact membranes. Materials and methods: The study population consisted of women who met the following criteria: 1) singleton gestation between 20 and 34 weeks; 2) preterm labor and intact membranes; 3) transabdominal amniocentesis performed for the evaluation of the microbiologic/inflammatory status of the amniotic cavity; 4) intra-amniotic infection and/or intra-amniotic inflammation; and 5) received antibiotic treatment that consisted of ceftriaxone, clarithromycin, and metronidazole. Follow-up amniocentesis was performed in a subset of patients. Amniotic fluid was cultured for aerobic and anaerobic bacteria and genital mycoplasmas, and polymerase chain reaction was performed for Ureaplasma spp. Intra-amniotic infection was defined as a positive amniotic fluid culture or positive polymerase chain reaction, and intra-amniotic inflammation was suspected when there was an elevated amniotic fluid white blood cell count or a positive result of a rapid test for matrix metalloproteinase-8. For this study, the final diagnosis of intra-amniotic inflammation was made by measuring the interleukin-6 concentration in stored amniotic fluid (>2.6 ng/mL). These results were not available to managing clinicians. Treatment success was defined as eradication of intra-amniotic infection and/or intra-amniotic inflammation or delivery ≥37 weeks. Results: Of 62 patients with intra-amniotic infection and/or intra-amniotic inflammation, 50 received the antibiotic regimen. Of those patients, 29 were undelivered for ≥7 days and 19 underwent a follow-up amniocentesis. Microorganisms were identified by culture or polymerase chain reaction of amniotic fluid obtained at admission in 21% of patients (4/19) who had a follow-up amniocentesis, and were eradicated in 3 of the 4 patients. Resolution of intra-amniotic infection/inflammation was confirmed in 79% of patients (15/19), and 1 other patient delivered at term, although resolution of intra-amniotic inflammation could not be confirmed after a follow-up amniocentesis. Thus, resolution of intra-amniotic inflammation/infection or term delivery (treatment success) occurred in 84% of patients (16/19) who had a follow-up amniocentesis. Treatment success occurred in 32% of patients (16/50) with intra-amniotic infection/inflammation who received antibiotics. The median amniocentesis-to-delivery interval was significantly longer among women who received the combination of antibiotics than among those who did not (11.4 days vs 3.1 days: P = .04). Conclusion: Eradication of intra-amniotic infection/inflammation after treatment with antibiotics was confirmed in 79% of patients with preterm labor, intact membranes, and intra-amniotic infection/inflammation who had a follow-up amniocentesis. Treatment success occurred in 84% of patients who underwent a follow-up amniocentesis and in 32% of women who received the antibiotic regimen. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier | - |
dc.relation.isPartOf | AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Amniocentesis | - |
dc.subject.MESH | Amniotic Fluid / metabolism | - |
dc.subject.MESH | Amniotic Fluid / microbiology | - |
dc.subject.MESH | Anti-Bacterial Agents / therapeutic use* | - |
dc.subject.MESH | Biomarkers / metabolism | - |
dc.subject.MESH | Ceftriaxone / therapeutic use | - |
dc.subject.MESH | Chorioamnionitis / drug therapy* | - |
dc.subject.MESH | Chorioamnionitis / microbiology | - |
dc.subject.MESH | Clarithromycin / therapeutic use | - |
dc.subject.MESH | Delivery, Obstetric | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Interleukin-6 / metabolism | - |
dc.subject.MESH | Leukocyte Count | - |
dc.subject.MESH | Matrix Metalloproteinase 8 / metabolism | - |
dc.subject.MESH | Metronidazole / therapeutic use | - |
dc.subject.MESH | Obstetric Labor, Premature* | - |
dc.subject.MESH | Pregnancy | - |
dc.subject.MESH | Pregnancy Complications, Infectious / drug therapy* | - |
dc.subject.MESH | Pregnancy Complications, Infectious / microbiology | - |
dc.subject.MESH | Retrospective Studies | - |
dc.title | Antibiotic administration can eradicate intra-amniotic infection or intra-amniotic inflammation in a subset of patients with preterm labor and intact membranes | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Obstetrics and Gynecology (산부인과학교실) | - |
dc.contributor.googleauthor | Bo Hyun Yoon | - |
dc.contributor.googleauthor | Roberto Romero | - |
dc.contributor.googleauthor | Jee Yoon Park | - |
dc.contributor.googleauthor | Kyung Joon Oh | - |
dc.contributor.googleauthor | JoonHo Lee | - |
dc.contributor.googleauthor | Agustin Conde-Agudelo | - |
dc.contributor.googleauthor | Joon-Seok Hong | - |
dc.identifier.doi | 10.1016/j.ajog.2019.03.018 | - |
dc.contributor.localId | A04846 | - |
dc.contributor.localId | A00088 | - |
dc.contributor.localId | A05465 | - |
dc.contributor.localId | A02993 | - |
dc.contributor.localId | A04497 | - |
dc.relation.journalcode | J00096 | - |
dc.identifier.eissn | 1097-6868 | - |
dc.identifier.pmid | 30928566 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S000293781930496X | - |
dc.subject.keyword | MMP-8 | - |
dc.subject.keyword | amniotic fluid | - |
dc.subject.keyword | ceftriaxone | - |
dc.subject.keyword | chorioamnionitis | - |
dc.subject.keyword | clarithromycin | - |
dc.subject.keyword | interleukin-6 | - |
dc.subject.keyword | intra-amniotic inflammation | - |
dc.subject.keyword | metronidazole | - |
dc.subject.keyword | pregnancy | - |
dc.subject.keyword | prematurity | - |
dc.subject.keyword | white blood cell | - |
dc.contributor.alternativeName | Lee, Joon Ho | - |
dc.contributor.affiliatedAuthor | 이준호 | - |
dc.citation.volume | 221 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 142.e1 | - |
dc.citation.endPage | 142.e22 | - |
dc.identifier.bibliographicCitation | AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, Vol.221(2) : 142.e1-142.e22, 2019-08 | - |
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