International Incidence and Outcomes of Biliary Atresia
ABSTRACT Objectives: International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population‐based literature to assess international variation of BA incidence and outcomes, and to assess the evid...
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Published in | Journal of pediatric gastroenterology and nutrition Vol. 56; no. 4; pp. 344 - 354 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Hagerstown, MD
Copyright by ESPGHAN and NASPGHAN
01.04.2013
Lippincott Williams & Wilkins |
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Abstract | ABSTRACT
Objectives:
International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population‐based literature to assess international variation of BA incidence and outcomes, and to assess the evidence for seasonal variation in incidence, centralization of Kasai hepatoportoenterostomy, and newborn screening.
Methods:
We conducted a systematic review (registration number CRD42011001441) of observational or interventional research within MEDLINE, EMBASE, and the Cochrane Database, which reported incidence, prevalence, or outcomes of infants with BA. Population‐based studies, defined by inclusion of an entire population or representative sample, were included. Outcomes included overall survival, native liver survival (NLS), and time to Kasai hepatoportoenterostomy. Single‐ or multicenter studies were excluded unless those centers captured all potential patients within a jurisdiction. Two independent data extractors reviewed the s and articles.
Results:
A total of 40 studies were included following review of 3128 references. A wide range of incidence was reported internationally. Ten‐year overall survival ranged from 66.7% to 89%. NLS ranged from 20.3% to 75.8% at 1 to 3 years and 24% to 52.8% at 10 years. Earlier age at Kasai was a predictor of improved NLS. Seasonality was reported in 11 studies, and 3 reported an increased incidence during the months of August to March. The evidence for centralization of Kasai to high‐volume centers is promising but does not account for all case‐mix, provider, or health system factors involved in volume–outcome relations. Stool color card screening resulted in earlier Kasai and improved NLS in Taiwan.
Conclusions:
Large, international studies could help fill the gaps in knowledge identified by this review. |
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AbstractList | OBJECTIVES:International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population-based literature to assess international variation of BA incidence and outcomes, and to assess the evidence for seasonal variation in incidence, centralization of Kasai hepatoportoenterostomy, and newborn screening.
METHODS:We conducted a systematic review (registration number CRD42011001441) of observational or interventional research within MEDLINE, EMBASE, and the Cochrane Database, which reported incidence, prevalence, or outcomes of infants with BA. Population-based studies, defined by inclusion of an entire population or representative sample, were included. Outcomes included overall survival, native liver survival (NLS), and time to Kasai hepatoportoenterostomy. Single- or multicenter studies were excluded unless those centers captured all potential patients within a jurisdiction. Two independent data extractors reviewed the abstracts and articles.
RESULTS:A total of 40 studies were included following review of 3128 references. A wide range of incidence was reported internationally. Ten-year overall survival ranged from 66.7% to 89%. NLS ranged from 20.3% to 75.8% at 1 to 3 years and 24% to 52.8% at 10 years. Earlier age at Kasai was a predictor of improved NLS. Seasonality was reported in 11 studies, and 3 reported an increased incidence during the months of August to March. The evidence for centralization of Kasai to high-volume centers is promising but does not account for all case-mix, provider, or health system factors involved in volume–outcome relations. Stool color card screening resulted in earlier Kasai and improved NLS in Taiwan.
CONCLUSIONS:Large, international studies could help fill the gaps in knowledge identified by this review. ABSTRACT Objectives: International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population‐based literature to assess international variation of BA incidence and outcomes, and to assess the evidence for seasonal variation in incidence, centralization of Kasai hepatoportoenterostomy, and newborn screening. Methods: We conducted a systematic review (registration number CRD42011001441) of observational or interventional research within MEDLINE, EMBASE, and the Cochrane Database, which reported incidence, prevalence, or outcomes of infants with BA. Population‐based studies, defined by inclusion of an entire population or representative sample, were included. Outcomes included overall survival, native liver survival (NLS), and time to Kasai hepatoportoenterostomy. Single‐ or multicenter studies were excluded unless those centers captured all potential patients within a jurisdiction. Two independent data extractors reviewed the s and articles. Results: A total of 40 studies were included following review of 3128 references. A wide range of incidence was reported internationally. Ten‐year overall survival ranged from 66.7% to 89%. NLS ranged from 20.3% to 75.8% at 1 to 3 years and 24% to 52.8% at 10 years. Earlier age at Kasai was a predictor of improved NLS. Seasonality was reported in 11 studies, and 3 reported an increased incidence during the months of August to March. The evidence for centralization of Kasai to high‐volume centers is promising but does not account for all case‐mix, provider, or health system factors involved in volume–outcome relations. Stool color card screening resulted in earlier Kasai and improved NLS in Taiwan. Conclusions: Large, international studies could help fill the gaps in knowledge identified by this review. OBJECTIVESInternational trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population-based literature to assess international variation of BA incidence and outcomes, and to assess the evidence for seasonal variation in incidence, centralization of Kasai hepatoportoenterostomy, and newborn screening.METHODSWe conducted a systematic review (registration number CRD42011001441) of observational or interventional research within MEDLINE, EMBASE, and the Cochrane Database, which reported incidence, prevalence, or outcomes of infants with BA. Population-based studies, defined by inclusion of an entire population or representative sample, were included. Outcomes included overall survival, native liver survival (NLS), and time to Kasai hepatoportoenterostomy. Single- or multicenter studies were excluded unless those centers captured all potential patients within a jurisdiction. Two independent data extractors reviewed the abstracts and articles.RESULTSA total of 40 studies were included following review of 3128 references. A wide range of incidence was reported internationally. Ten-year overall survival ranged from 66.7% to 89%. NLS ranged from 20.3% to 75.8% at 1 to 3 years and 24% to 52.8% at 10 years. Earlier age at Kasai was a predictor of improved NLS. Seasonality was reported in 11 studies, and 3 reported an increased incidence during the months of August to March. The evidence for centralization of Kasai to high-volume centers is promising but does not account for all case-mix, provider, or health system factors involved in volume-outcome relations. Stool color card screening resulted in earlier Kasai and improved NLS in Taiwan.CONCLUSIONSLarge, international studies could help fill the gaps in knowledge identified by this review. International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We reviewed the population-based literature to assess international variation of BA incidence and outcomes, and to assess the evidence for seasonal variation in incidence, centralization of Kasai hepatoportoenterostomy, and newborn screening. We conducted a systematic review (registration number CRD42011001441) of observational or interventional research within MEDLINE, EMBASE, and the Cochrane Database, which reported incidence, prevalence, or outcomes of infants with BA. Population-based studies, defined by inclusion of an entire population or representative sample, were included. Outcomes included overall survival, native liver survival (NLS), and time to Kasai hepatoportoenterostomy. Single- or multicenter studies were excluded unless those centers captured all potential patients within a jurisdiction. Two independent data extractors reviewed the abstracts and articles. A total of 40 studies were included following review of 3128 references. A wide range of incidence was reported internationally. Ten-year overall survival ranged from 66.7% to 89%. NLS ranged from 20.3% to 75.8% at 1 to 3 years and 24% to 52.8% at 10 years. Earlier age at Kasai was a predictor of improved NLS. Seasonality was reported in 11 studies, and 3 reported an increased incidence during the months of August to March. The evidence for centralization of Kasai to high-volume centers is promising but does not account for all case-mix, provider, or health system factors involved in volume-outcome relations. Stool color card screening resulted in earlier Kasai and improved NLS in Taiwan. Large, international studies could help fill the gaps in knowledge identified by this review. |
Author | Jolin‐Dahel, Kheira S. Fortinsky, Kyle J. Jimenez‐Rivera, Carolina Gozdyra, Peter Benchimol, Eric I. |
AuthorAffiliation | Division of Gastroenterology, Hepatology and Nutrition, Childrenʼs Hospital of Eastern Ontario, Ottawa, ON, Canada †Institute for Clinical Evaluative Sciences, Toronto, ON, Canada |
AuthorAffiliation_xml | – name: Division of Gastroenterology, Hepatology and Nutrition, Childrenʼs Hospital of Eastern Ontario, Ottawa, ON, Canada †Institute for Clinical Evaluative Sciences, Toronto, ON, Canada |
Author_xml | – sequence: 1 givenname: Carolina surname: Jimenez‐Rivera fullname: Jimenez‐Rivera, Carolina email: cajimenez@cheo.on.ca organization: Children's Hospital of Eastern Ontario – sequence: 2 givenname: Kheira S. surname: Jolin‐Dahel fullname: Jolin‐Dahel, Kheira S. organization: Children's Hospital of Eastern Ontario – sequence: 3 givenname: Kyle J. surname: Fortinsky fullname: Fortinsky, Kyle J. organization: Children's Hospital of Eastern Ontario – sequence: 4 givenname: Peter surname: Gozdyra fullname: Gozdyra, Peter organization: Institute for Clinical Evaluative Sciences – sequence: 5 givenname: Eric I. surname: Benchimol fullname: Benchimol, Eric I. organization: Children's Hospital of Eastern Ontario |
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Keywords | Human Pediatrics Biliary atresia screening Prognosis Metabolic diseases Medical screening Epidemiology Incidence outcomes Gastroenterology Digestive diseases Child Liver transplantation |
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Notes | This article has been developed as a Journal CME Activity by NASPGHAN. Visit to view instructions, documentation, and the complete necessary steps to receive CME credit for reading this article. E.I.B. was supported by a Career Development Award from the Canadian Child Health Clinician Scientist Program. http://www.naspghan.org/wmspage.cfm?parm1=361 www.jpgn.org Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Website . The authors report no conflicts of interest. SourceType-Scholarly Journals-1 ObjectType-Feature-4 ObjectType-Undefined-1 content type line 23 ObjectType-Review-2 ObjectType-Article-3 |
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References | 1995; 30 2004; 363 2011; 158 1985; 290 1982; 307 2011; 53 1982; 100 1994; 29 2009; 48 2011; 128 1997; 99 2009; 94 2002; 141 1988; 43 2008; 23 2009; 123 2011; 21 1999; 53 2001; 138 1996; 22 2009; 62 2000; 355 2010; 169 2002; 35 1968; 102 1984; 105 2011; 31 2005; 41 1988; 12 2003; 38 1997; 181 1998; 20 2006; 117 1996; 129 2011; 9 2010; 86 1990; 25 2004; 18 2007; 151 2006; 44 2008; 47 2008; 46 1994; 13 1999; 31 2011; 46 1999; 30 2007; 42 1994; 1 2012; 47 2006; 149 2006; 148 1999; 319 2010; 51 1981; 56 23799456 - J Pediatr Gastroenterol Nutr. 2013 Sep;57(3):e20 23799455 - J Pediatr Gastroenterol Nutr. 2013 Sep;57(3):e19-20 e_1_2_8_24_1 e_1_2_8_47_1 e_1_2_8_26_1 e_1_2_8_49_1 e_1_2_8_3_1 e_1_2_8_5_1 e_1_2_8_7_1 e_1_2_8_9_1 e_1_2_8_20_1 e_1_2_8_43_1 e_1_2_8_22_1 e_1_2_8_45_1 e_1_2_8_41_1 e_1_2_8_17_1 e_1_2_8_19_1 e_1_2_8_13_1 e_1_2_8_36_1 e_1_2_8_15_1 Perisic VN (e_1_2_8_30_1) 1994; 13 e_1_2_8_38_1 e_1_2_8_57_1 Houwen RH (e_1_2_8_28_1) 1988; 43 Carvalho E (e_1_2_8_6_1) 2010; 86 e_1_2_8_32_1 e_1_2_8_55_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_53_1 e_1_2_8_51_1 e_1_2_8_29_1 e_1_2_8_25_1 e_1_2_8_46_1 e_1_2_8_48_1 e_1_2_8_2_1 e_1_2_8_4_1 e_1_2_8_8_1 e_1_2_8_21_1 e_1_2_8_42_1 e_1_2_8_23_1 e_1_2_8_44_1 e_1_2_8_40_1 e_1_2_8_18_1 e_1_2_8_39_1 e_1_2_8_14_1 e_1_2_8_35_1 e_1_2_8_16_1 e_1_2_8_37_1 e_1_2_8_58_1 Vic P (e_1_2_8_27_1) 1994; 1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_56_1 e_1_2_8_12_1 e_1_2_8_33_1 e_1_2_8_54_1 e_1_2_8_52_1 e_1_2_8_50_1 |
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International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported... OBJECTIVES:International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide.... International trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide. We... OBJECTIVESInternational trends in incidence and outcomes of biliary atresia (BA) are controversial and a wide range of estimates have been reported worldwide.... |
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SubjectTerms | biliary atresia Biliary Atresia - diagnosis Biliary Atresia - epidemiology Biliary Atresia - physiopathology Biliary Atresia - therapy Biological and medical sciences Child epidemiology Feeding. Feeding behavior Fundamental and applied biological sciences. Psychology Global Health Humans Incidence liver transplantation Liver, biliary tract, pancreas, portal circulation, spleen Medical sciences outcomes pediatrics Prognosis Referral and Consultation screening Seasons Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Survival Analysis Vertebrates: anatomy and physiology, studies on body, several organs or systems |
Title | International Incidence and Outcomes of Biliary Atresia |
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