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Practice of Placenta Submission for Histopathological Examination, Experience of a Teaching/Tertiary Care Hospital in Saudi Arabia

Authors
  • Aljhdali, Hessa M1
  • Abdullah, Layla S1
  • Alhazmi, Dalia A2
  • Almosallam, Ahmed M3
  • Bondagji, Nabeel S4
  • 1 Anatomic Pathology, King Abdulaziz University Faculty of Medicine, Jeddah, SAU
  • 2 Anatomic Pathology, King Abdulaziz University Hospital, Jeddah, SAU
  • 3 Anatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU
  • 4 Obstetrics and Gynecology, Fetomaternal Medicine, King Abdulaziz University Faculty of Medicine, Jeddah, SAU
Type
Published Article
Journal
Cureus
Publisher
Cureus, Inc.
Publication Date
Aug 22, 2021
Volume
13
Issue
8
Identifiers
DOI: 10.7759/cureus.17364
PMID: 34567903
PMCID: PMC8454601
Source
PubMed Central
Keywords
Disciplines
  • Pathology
License
Unknown
External links

Abstract

Objectives The aim of this study is to determine the appropriateness of histopathologic examination of the placenta at King Abdulaziz University Hospital (KAUH), Jeddah, based on the guidelines of the College of American Pathologists (CAP). Methods It is a retrospective review of obstetric and pathologic records for all deliveries at KAUH, between January 1, 2017, and April 30, 2019. The placentae were assessed for eligibility to undergo pathologic examination. Furthermore, examined and non-examined placentae meeting the CAP criteria were compared based on their actual indications. Results There were 8,929 deliveries, of which 1,444 (16.2%) placentae met the CAP guidelines. A total of 583/1,444 placentae (40.4%; 95% confidence interval [CI] = 37.8-43) were sent for pathologic examination. Of the 7,485 placentae that did not require submission for pathological examination, as determined by the pathologist, 7,456 (99.6%; 95% CI = 99.4-99.7) were not submitted appropriately. The labor and delivery staff were more likely to submit placentae with fetal/neonatal indications rather than those with maternal indications for examination, which was statistically significant (odds ratio = 6.5; 95% CI = 5.08-8.30). Conclusion While most of the examined placentae at KAUH met the CAP guidelines, there was a substantial under-submission of eligible placentae. Further studies are advised to reveal the reasons behind this underestimation so that correctional measures may be adopted, as placenta examination is a valuable tool to understand the risk factors and pathogenesis of deleterious maternal, neonatal, and fetal events.

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