Literature DB >> 7373460

Incidence of cholelithiasis in sickle cell anemia using the ultrasonic gray-scale technique.

S Sarnaik, T L Slovis, D P Corbett, A Emami, C F Whitten.   

Abstract

Gray-scale ultrasound examination of the gallbladder was successfully performed in 226 patients with sickle cell hemoglobinopathy from 2 to 18 years of age. Sixty-three (27%) demonstrated the presence of gallstones; 14 additional patients had "sludge." The incidence of gallstones increased significantly with age, from 12% in the 2- to 4-year age group to 42% in the 15- to 18-year-old group. The proportion of females with gallstones increased significantly in adolescence. Patients with gallstones had higher mean bilirubin levels, but their mean hemoglobin values and reticulocyte counts were not significantly different from those in patients without gallstones. Ultrasound examination of the gallbladder is a simple, noninvasive technique for evaluating the biliary system. The incidence of gallstones in patients below the age of 10 is higher than expected and raises management questions that must be resolved.

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Year:  1980        PMID: 7373460     DOI: 10.1016/s0022-3476(80)80626-3

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  33 in total

1.  Hepatobiliary Complications of Sickle Cell Disease among Children Admitted to Al Wahda Teaching Hospital, Aden, Yemen.

Authors:  Hana A Qhalib; Gamal H Zain
Journal:  Sultan Qaboos Univ Med J       Date:  2014-10-14

2.  Laparoscopic cholecystectomy in adults with sickle cell disease.

Authors:  G Bonatsos; K Birbas; K Toutouzas; N Durakis
Journal:  Surg Endosc       Date:  2001-05-14       Impact factor: 4.584

3.  The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.

Authors:  Suad AlFadhli; Hassan Al-Jafer; Mays Hadi; Mashael Al-Mutairi; Rasheeba Nizam
Journal:  PLoS One       Date:  2013-10-30       Impact factor: 3.240

4.  Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up.

Authors:  B A I Attalla; Z A Karrar; G Ibnouf; A O Mohamed; O Abdelwahab; E M Nasir; M A El Seed
Journal:  Afr Health Sci       Date:  2013-03       Impact factor: 0.927

5.  Gall stones in sickle cell disease in the United Kingdom.

Authors:  L R Bond; S R Hatty; M E Horn; M Dick; H B Meire; A J Bellingham
Journal:  Br Med J (Clin Res Ed)       Date:  1987-07-25

Review 6.  Sickle cell states and the anaesthetist.

Authors:  D W Esseltine; M R Baxter; J C Bevan
Journal:  Can J Anaesth       Date:  1988-07       Impact factor: 5.063

7.  Biliary scintigraphy in children with sickle cell anemia and acute abdominal pain.

Authors:  W A D'Alonzo; S Heyman
Journal:  Pediatr Radiol       Date:  1985

8.  Sickle cell cholangiopathy: an endoscopic retrograde cholangiopancreatography evaluation.

Authors:  Hussain Issa; Ali Al-Haddad; Ahmed Al-Salem
Journal:  World J Gastroenterol       Date:  2009-11-14       Impact factor: 5.742

9.  Cholecystitis and cholelithiasis in children and adolescents.

Authors:  E R Cheng; M I Okoye
Journal:  J Natl Med Assoc       Date:  1986-11       Impact factor: 1.798

10.  Sonographic pattern of gallbladder disease in children with sickle cell anaemia.

Authors:  D A Nzeh; M A Adedoyin
Journal:  Pediatr Radiol       Date:  1989
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