Prevalence and mortality among children with anorectal malformation: A multi-country analysis

被引:19
作者
Kancherla, Vijaya [2 ]
Sundar, Manasvi [2 ]
Tandaki, Lucita [1 ]
Lux, Anke [3 ]
Bakker, Marian K. [4 ]
Bergman, Jorieke Eh [4 ]
Bermejo-Sanchez, Eva [5 ]
Canfield, Mark A. [6 ]
Dastgiri, Saeed [7 ]
Feldkamp, Marcia L. [8 ]
Gatt, Miriam [9 ]
Groisman, Boris [10 ]
Hurtado-Villa, Paula [11 ]
Kallen, Karin [12 ]
Landau, Danielle [13 ]
Lelong, Nathalie [14 ]
Lopez-Camelo, Jorge [15 ]
Martinez, Laura Elia [16 ]
Mastroiacovo, Pierpaolo [17 ]
Morgan, Margery [18 ]
Mutchinick, Osvaldo M. [19 ]
Nance, Amy E. [20 ]
Nembhard, Wendy N. [21 ,22 ]
Pierini, Anna [23 ,24 ]
Sipek, Antonin [25 ]
Stallings, Erin B. [26 ]
Szabova, Elena [27 ]
Tagliabue, Giovanna [28 ]
Wertelecki, Wladimir [29 ]
Zarante, Ignacio [30 ,31 ]
Rissmann, Anke [1 ]
机构
[1] Otto von Guericke Univ, Med Fac, Malformat Monitoring Ctr Saxony Anhalt, Leipziger Str 44, D-39120 Magdeburg, Germany
[2] Emory Univ, Dept Epidemiol, Rollins Sch Publ Hlth, Atlanta, GA USA
[3] Otto von Guericke Univ, Med Fac, Inst Biometr & Med Informat, Magdeburg, Germany
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Eurocat Northern Netherlands, Groningen, Netherlands
[5] Inst Salud Carlos III, Inst Invest Enfermedades Raras IIER, ECEMC Spanish Collaborat Study Congenital Malform, UIAC Unidad Invest Anomalias Congenitas, Madrid, Spain
[6] Texas Dept State Hlth Serv, Birth Defects Epidemiol & Surveillance Branch, Austin, TX USA
[7] Tabriz Univ Med Sci, Tabriz Hlth Serv Management Res Ctr, Sch Med, Tabriz, Iran
[8] Univ Utah, Dept Pediat, Div Med Genet, Sch Med, Salt Lake City, UT USA
[9] Directorate Hlth Informat & Res, Malta Congenital Anomalies Registry, Guardamangia, Malta
[10] Natl Minist Hlth, Natl Adm Labs & Hlth Inst ANLIS, Natl Ctr Med Genet, Natl Network Congenital Anomalies Argentina RENAC, Buenos Aires, DF, Argentina
[11] Pontificia Univ Javeriana Cali, Sch Hlth, Dept Basic Sci Hlth, Cali, Colombia
[12] Natl Board Hlth & Welf, Stockholm, Sweden
[13] Soroka Med Ctr, Dept Neonatol, Beer Sheva, Israel
[14] Univ Paris, INSERM, U1153,Ctr Epidemiol & Stat Sorbonne Paris Cite CR, Obstet Perinatal & Pediat Epidemiol Res Team Epop, Paris, France
[15] Ctr Med Educ & Clin Res CEMIC CONICET, ECLAMC, Buenos Aires, DF, Argentina
[16] Univ Autonoma Nuevo Leon, Hosp Univ Dr Jose E Gonzalez, Dept Genet, Registro DAN Registro Defectos Nacimiento, Monterrey, Mexico
[17] Int Clearinghouse Birth Defects Surveillance & Re, Int Ctr Birth Defects, Rome, Italy
[18] Singleton Hosp, Publ Hlth Wales, Congenital Anomaly Register Wales, Swansea, W Glam, Wales
[19] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Genet, RYVEMCE, Mexico City, DF, Mexico
[20] Utah Dept Hlth, Utah Birth Defects Network, Bur Children Special Hlth Care Needs, Salt Lake City, UT USA
[21] Univ Arkansas Med Sci, Arkansas Ctr Birth Defects Res & Prevent, Little Rock, AR 72205 USA
[22] Univ Arkansas Med Sci, Arkansas Reprod Hlth Monitoring Syst, Fay Boozman Coll Publ Hlth, Dept Epidemiol, Little Rock, AR 72205 USA
[23] CNR, Inst Clin Physiol, Pisa, Italy
[24] Fdn Toscana Gabriele Monasterio, Tuscany Registry Congenital Defects, Pisa, Italy
[25] Thomayer Hosp, Dept Med Genet, Prague, Czech Republic
[26] US Ctr Dis Control, Div Birth Defects & Infant Disorders, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA USA
[27] Slovak Med Univ, Slovak Teratol Informat Ctr FPH, Bratislava, Slovakia
[28] Fdn IRCCS Ist Nazl Tumori, Canc Registry Unit, Lombardy, Italy
[29] OMNI Net Ukraine Programs, Rivne, Ukraine
[30] Pontificia Univ Javeriana, Human Genet Inst, Bogota, Colombia
[31] Hosp Univ San Ignacio, Bogota, Colombia
关键词
anorectal atresia; birth defect; epidemiology; mortality; prevalence; DESCRIPTIVE EPIDEMIOLOGY; CONGENITAL-ANOMALIES; RISK; DIAGNOSIS; BIRTH; CARE; ANUS;
D O I
10.1002/bdr2.2129
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: We examined the total prevalence, trends in prevalence, and age-specific mortality among individuals with anorectal malformation (ARM) Methods: We conducted a retrospective cohort study using data from 24 population- and hospital-based birth defects surveillance programs affiliated with the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR) from 18 countries and for births from 1974 to 2014. We estimated pooled and program-specific total prevalence per 10,000 total births. Poisson regression was used to assess time trends in prevalence from 2001 to 2012 when most programs contributed data. We calculated selected age-specific proportions of deaths, stratified by case status Results: The pooled total prevalence of ARM was 3.26 per 10,000 total births (95% Confidence Interval = 3.19, 3.32) for birth years 1974-2014. About 60% of cases were multiple or syndromic. Prevalence of multiple, syndromic, and stillborn cases decreased from 2001 to 2012. The first week mortality proportion was 12.5%, 3.2%, 28.3%, and 18.2% among all, isolated, multiple, and syndromic cases, respectively Conclusions: ARM is relatively rare, with multiple and syndromic cases showing decreasing prevalence during the study period. Mortality is a concern during the first week of life, and especially among multiple and syndromic cases. Our descriptive epidemiological findings increase our understanding of geographic variation in the prevalence of ARM and can be used to plan needed clinical services. Exploring factors influencing prevalence and mortality among individuals with ARM could inform future studies.
引用
收藏
页码:390 / 404
页数:15
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