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dc.contributor.authorJiraporn Khoranaen_US
dc.contributor.authorJayanton Patumanonden_US
dc.contributor.authorNuthapong Ukarapolen_US
dc.contributor.authorMongkol Laohapensangen_US
dc.contributor.authorPannee Visrutaratnaen_US
dc.contributor.authorJesda Singhavejsakulen_US
dc.date.accessioned2018-09-05T02:54:55Z-
dc.date.available2018-09-05T02:54:55Z-
dc.date.issued2016-09-13en_US
dc.identifier.issn1178203Xen_US
dc.identifier.issn11766336en_US
dc.identifier.other2-s2.0-84988985676en_US
dc.identifier.other10.2147/TCRM.S115253en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84988985676&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55372-
dc.description.abstract© 2016 Khorana et al. Purpose: The nonoperative reduction of intussusception in children can be performed safely if there are no contraindications. Many risk factors associated with failed reduction were defined. The aim of this study was to develop a scoring system for predicting the failure of nonoperative reduction using various determinants. Patients and methods: The data were collected from Chiang Mai University Hospital and Siriraj Hospital from January 2006 to December 2012. Inclusion criteria consisted of patients with intussusception aged 0–15 years with no contraindications for nonoperative reduction. The clinical prediction rules were developed using significant risk factors from the multivariable analysis. Results: A total of 170 patients with intussusception were included in the study. In the final analysis model, 154 patients were used for identifying the significant risk factors of failure of reduction. Ten factors clustering by the age of 3 years were identified and used for developing the clinical prediction rules, and the factors were as follows: body weight,12 kg (relative risk [RR] =1.48, P=0.004), duration of symptoms .48 hours (RR =1.26, P,0.001), vomiting (RR =1.63, P<0.001), rectal bleeding (RR =1.50, P<0.001), abdominal distension (RR =1.60, P=0.003), temperature .37.8°C (RR =1.51, P<0.001), palpable mass (RR =1.26, P<0.001), location of mass (left over right side RR =1.48, P<0.001), ultrasound showed poor prognostic signs (RR =1.35, P<0.001), and the method of reduction (hydrostatic over pneumatic, RR =1.34, P=0.023). Prediction scores ranged from 0 to 16. A high-risk group (scores 12–16) predicted a greater chance of reduction failure (likelihood ratio of positive [LR+] =18.22, P<0.001). A low-r sk group (score 0–11) predicted a lower chance of reduction failure (LR+ =0.79, P<0.001). The performance of the scoring model was 80.68% (area under the receiver operating characteristic curve). Conclusion: This scoring guideline was used to predict the results of nonoperative reduction and forecast the prognosis of the failed reduction. The usefulness of these prediction scores is for informing the parents before the reduction. This scoring system can be used as a guide to promote the possible referral of the cases to tertiary centers with facilities for nonoperative reduction if possible.en_US
dc.subjectChemical Engineeringen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.subjectSocial Sciencesen_US
dc.titleClinical prediction rules for failed nonoperative reduction of intussusceptionen_US
dc.typeJournalen_US
article.title.sourcetitleTherapeutics and Clinical Risk Managementen_US
article.volume12en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsThammasat University Hospitalen_US
article.stream.affiliationsMahidol Universityen_US
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