Ileosigmoid knotting: A review of 923 cases

Atamanalp, Sabri Selcuk and Disci, Esra and Peksoz, Rifat and Atamanalp, Refik Selim and Tatar Atamanalp, Cansu (2022) Ileosigmoid knotting: A review of 923 cases. Pakistan Journal of Medical Sciences, 38 (3). ISSN 1682-024X

[thumbnail of 5320-Article Text-34890-2-10-20220126.pdf] Text
5320-Article Text-34890-2-10-20220126.pdf - Published Version

Download (289kB)

Abstract

Objectives: Ileosigmoid knotting (ISK) is a rare intestinal obstruction form worldwide. The aim of this study was to investigate changing trends in ISK.

Methods: The Web of Science and PubMed databases were electronically searched to find all publications to evaluate all epidemiological, etiological, clinical, laboratory, radiological, therapeutic, and prognostic factors in ISK.

Results: Most of the cases were reported from Asian and African countries. Mean age was 43.9 years with a 79.9%/20.1% of male/female ratio. Main symptom period was 48.1 hours, while the most common clinical features were abdominal pain/tenderness (99.1%), distention (88.3%), and obstipation/constipation (58.8%). Abdominal X-ray radiography, computerized tomography (CT), and magnetic resonance imaging (MRI) were diagnostic in 8.2%, 96.2%, and 100.0%, respectively, while the total diagnostic accuracy rate was 20.8%. Bowels were gangrenous in 85.6% of the patients. Ileum resection was applied in 14.0% of the cases, while sigmoid colon resection in 7.6%, and both segment resection in 67.1%. The mortality rate was 22.7%, while the morbidity rate was also 22.7%.

Conclusion: ISK is a rare disease, but it is still catastrophic despite its two-century recognised past. As an exception, diagnostic convenience arising from CT or MRI looks like the most important change over the last half-century.

Item Type: Article
Subjects: Oalibrary Press > Medical Science
Depositing User: Managing Editor
Date Deposited: 10 Apr 2023 04:58
Last Modified: 24 Jan 2024 04:10
URI: http://asian.go4publish.com/id/eprint/1825

Actions (login required)

View Item
View Item