{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,11]],"date-time":"2026-08-11T20:30:28Z","timestamp":1786480228864,"version":"build-2736575974"},"reference-count":30,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"7","license":[{"start":{"date-parts":[[2025,3,4]],"date-time":"2025-03-04T00:00:00Z","timestamp":1741046400000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["Kidney360"],"published-print":{"date-parts":[[2025,7]]},"abstract":"<jats:sec>\n                    <jats:title>Key Points<\/jats:title>\n                    <jats:p>\n                      <jats:list list-type=\"bullet\">\n                        <jats:list-item>\n                          <jats:p>We created computable phenotypes to accurately identify cases of pediatric CKD by underlying diagnosis.<\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>Combined annual incidence of five leading causes of pediatric CKD was high, 47.07 (95% confidence interval, 45.96 to 48.20) per 100,000 children.<\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>Our computable phenotypes have the potential to be broadly implemented to advance epidemiologic research in pediatric CKD.<\/jats:p>\n                        <\/jats:list-item>\n                      <\/jats:list>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Incidence data on pediatric CKD are incomplete. We developed electronic health record\u2013based algorithms (e-phenotypes) to identify cases and provide incidence estimates of five leading causes of pediatric CKD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>E-phenotypes using common standardized clinical terminology were built and contained utilization, diagnostic, procedural, age, and time-period inclusion and exclusion criteria for autosomal dominant polycystic kidney disease (ADPKD), Alport syndrome (AS), congenital anomalies of the kidney and urinary tract (CAKUT), lupus nephritis (LN), and primary childhood nephrotic syndrome (NS). Cases diagnosed between 2014 and 2023 were identified from a pediatric health care system that is the sole pediatric nephrology provider serving the Atlanta Metropolitan Statistical Area. The performance of the e-phenotypes was tested using a cohort of 1000 pediatric patients. The cases identified were used to estimate incidences using population information from the Georgia Department of Health.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      The e-phenotypes demonstrated sensitivity ranging from 0.83 to 0.95, specificity 0.96 to 1.00, positive predictive value 0.81 to 1.00, and negative predictive value 0.98 to 1.00. The positive likelihood ratio was &gt;20, and the negative likelihood ratio was &lt;0.20. The 6814 combined cases of ADPKD (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =107), AS (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =31), CAKUT (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =6120), LN (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =161), and NS (\n                      <jats:italic toggle=\"yes\">n<\/jats:italic>\n                      =395) had an annual incidence of 47.07 (95% confidence interval, 45.96 to 48.20) per 100,000 children. Annual incidence per 100,000 children (95% confidence interval) for each condition was ADPKD 0.74 (0.61 to 0.89), AS 0.21 (0.15 to 0.30), CAKUT 42.28 (41.22 to 43.35), LN 1.11 (0.95 to 1.30), and NS 2.73 (2.47 to 3.01).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Our incidence estimates suggest that CKD conditions are common among children. The e-phenotypes require validation for use at other institutions but offer opportunities to examine determinants of CKD detection, management, and outcomes.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.34067\/kid.0000000753","type":"journal-article","created":{"date-parts":[[2025,3,4]],"date-time":"2025-03-04T12:09:39Z","timestamp":1741090179000},"page":"1096-1105","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":3,"title":["Incidence of Leading Causes of Pediatric CKD Using Electronic Health Record-Driven Computable Phenotype"],"prefix":"10.34067","volume":"6","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-0911-0823","authenticated-orcid":false,"given":"Jonathan M.","family":"Beus","sequence":"first","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katie","family":"Liu","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9309-6205","authenticated-orcid":false,"given":"Adrianna","family":"Westbrook","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6664-8630","authenticated-orcid":false,"given":"Jessica L.","family":"Harding","sequence":"additional","affiliation":[{"name":"Department of Surgery, Emory University School of Medicine, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3756-8575","authenticated-orcid":false,"given":"Evan W.","family":"Orenstein","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9894-0049","authenticated-orcid":false,"given":"H. Stella","family":"Shin","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2109-5769","authenticated-orcid":false,"given":"Swaminathan","family":"Kandaswamy","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-7749-6183","authenticated-orcid":false,"given":"Christel","family":"Wekon-Kemeni","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Meda E.","family":"Pavkov","sequence":"additional","affiliation":[{"name":"Division of Diabetes Translation, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3975-5131","authenticated-orcid":false,"given":"Fang","family":"Xu","sequence":"additional","affiliation":[{"name":"Division of Diabetes Translation, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6648-6301","authenticated-orcid":false,"given":"Edwin A.","family":"Smith","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7855-9168","authenticated-orcid":false,"given":"Kelly A.","family":"Rouster-Stevens","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3489-1756","authenticated-orcid":false,"given":"Sampath","family":"Prahalad","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2490-021X","authenticated-orcid":false,"given":"Larry A.","family":"Greenbaum","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6941-0057","authenticated-orcid":false,"given":"Chia-shi","family":"Wang","sequence":"additional","affiliation":[{"name":"Emory University and Children's Healthcare of Atlanta, Atlanta, Georgia"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,3,4]]},"reference":[{"issue":"4","key":"B1-20250801","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1007\/s004670050462","article-title":"Chronic renal insufficiency in children and adolescents: the 1996 annual report of NAPRTCS. North American Pediatric Renal Transplant Cooperative Study","volume":"12","author":"Fivush","year":"1998","journal-title":"Pediatr Nephrol."},{"issue":"11","key":"B8-20250801","doi-asserted-by":"crossref","first-page":"1728","DOI":"10.34067\/KID.0000852021","article-title":"A computable phenotype for autosomal dominant polycystic kidney disease","volume":"2","author":"Kalot","year":"2021","journal-title":"Kidney360."},{"issue":"1","key":"B9-20250801","doi-asserted-by":"crossref","first-page":"65","DOI":"10.2215\/CJN.07810621","article-title":"Using a multi-institutional pediatric learning health system to identify systemic lupus erythematosus and lupus nephritis: development and validation of computable phenotypes","volume":"17","author":"Wenderfer","year":"2022","journal-title":"Clin J Am Soc Nephrol."},{"issue":"12","key":"B10-20250801","doi-asserted-by":"crossref","first-page":"1979","DOI":"10.34067\/KID.0002892021","article-title":"Validating a computable phenotype for nephrotic syndrome in children and adults using PCORnet data","volume":"2","author":"Oliverio","year":"2021","journal-title":"Kidney360."},{"issue":"3","key":"B11-20250801","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1016\/j.ecl.2010.05.011","article-title":"Epidemiology of type 1 diabetes","volume":"39","author":"Maahs","year":"2010","journal-title":"Endocrinol Metab Clin North Am."},{"issue":"2","key":"B12-20250801","first-page":"83","article-title":"Childhood and adolescent cancer statistics, 2014","volume":"64","author":"Ward","year":"2014","journal-title":"CA Cancer J Clin."},{"issue":"37","key":"B13-20250801","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1146\/annurev-publhealth-032315-021353","article-title":"Using electronic health records for population health research: a review of methods and applications","volume":"37","author":"Casey","year":"2016","journal-title":"Annu Rev Public Health."},{"issue":"6","key":"B14-20250801","doi-asserted-by":"crossref","first-page":"1215","DOI":"10.1007\/s00467-021-05145-1","article-title":"Epidemiology of pediatric chronic kidney disease\/kidney failure: learning from registries and cohort studies","volume":"37","author":"Harada","year":"2022","journal-title":"Pediatr Nephrol."},{"issue":"3","key":"B15-20250801","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1007\/s00467-019-04458-6","article-title":"The CKiD study: overview and summary of findings related to kidney disease progression","volume":"36","author":"Atkinson","year":"2021","journal-title":"Pediatr Nephrol."},{"issue":"2","key":"B16-20250801","doi-asserted-by":"crossref","first-page":"173","DOI":"10.2215\/CJN.0000000000000051","article-title":"Evaluating kidney function decline in children with chronic kidney disease using a multi-institutional electronic health record database","volume":"18","author":"Gluck","year":"2023","journal-title":"Clin J Am Soc Nephrol."},{"issue":"6","key":"B17-20250801","doi-asserted-by":"crossref","first-page":"878","DOI":"10.1053\/j.ajkd.2015.01.008","article-title":"Predictors of rapid progression of glomerular and nonglomerular kidney disease in children and adolescents: the chronic kidney disease in children (CKiD) cohort","volume":"65","author":"Warady","year":"2015","journal-title":"Am J Kidney Dis."},{"issue":"3S2","key":"B18-20250801","first-page":"S50","article-title":"Chronic kidney disease emerging trends in children and what to do about it","volume":"114","author":"Beng-Ongey","year":"2022","journal-title":"J Natl Med Assoc."},{"issue":"4S","key":"B19-20250801","first-page":"S1","article-title":"KDIGO 2021 clinical practice guideline for the management of glomerular diseases","volume":"100","year":"2021","journal-title":"Kidney Int."},{"issue":"11","key":"B20-20250801","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1038\/s41581-019-0155-2","article-title":"International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people","volume":"15","author":"Gimpel","year":"2019","journal-title":"Nat Rev Nephrol."},{"issue":"1","key":"B21-20250801","doi-asserted-by":"crossref","first-page":"143","DOI":"10.2215\/CJN.04230321","article-title":"Guidelines for genetic testing and management of Alport syndrome","volume":"17","author":"Savige","year":"2022","journal-title":"Clin J Am Soc Nephrol."},{"issue":"9","key":"B22-20250801","doi-asserted-by":"crossref","first-page":"1654","DOI":"10.1681\/ASN.V491654","article-title":"The spectrum of autosomal dominant polycystic kidney disease in children","volume":"4","author":"Fick","year":"1994","journal-title":"J Am Soc Nephrol."},{"issue":"5","key":"B23-20250801","doi-asserted-by":"crossref","first-page":"2218","DOI":"10.1111\/j.1523-1755.2005.00678.x","article-title":"Autosomal-dominant polycystic kidney disease in infancy and childhood: progression and outcome","volume":"68","author":"Shamshirsaz","year":"2005","journal-title":"Kidney Int."},{"issue":"10","key":"B24-20250801","doi-asserted-by":"crossref","first-page":"e038005","DOI":"10.1136\/bmjopen-2020-038005","article-title":"'A sword of Damocles': patient and caregiver beliefs, attitudes and perspectives on presymptomatic testing for autosomal dominant polycystic kidney disease: a focus group study","volume":"10","author":"Logeman","year":"2020","journal-title":"BMJ Open."},{"issue":"9","key":"B25-20250801","doi-asserted-by":"crossref","first-page":"2273","DOI":"10.1681\/ASN.2020071065","article-title":"Prevalence estimates of predicted pathogenic COL4A3-COL4A5 variants in a population sequencing database and their implications for Alport syndrome","volume":"32","author":"Gibson","year":"2021","journal-title":"J Am Soc Nephrol."},{"issue":"1","key":"B26-20250801","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1681\/ASN.2017050483","article-title":"Genetic complexity of autosomal dominant polycystic kidney and liver diseases","volume":"29","author":"Cornec-Le Gall","year":"2018","journal-title":"J Am Soc Nephrol."},{"issue":"5","key":"B27-20250801","doi-asserted-by":"crossref","first-page":"723","DOI":"10.2215\/CJN.12581019","article-title":"A primer on congenital anomalies of the kidneys and urinary tracts (CAKUT)","volume":"15","author":"Murugapoopathy","year":"2020","journal-title":"Clin J Am Soc Nephrol."},{"issue":"1","key":"B28-20250801","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1053\/j.ackd.2014.07.002","article-title":"Socioeconomic disparities in chronic kidney disease","volume":"22","author":"Nicholas","year":"2015","journal-title":"Adv Chronic Kidney Dis."},{"issue":"6","key":"B29-20250801","doi-asserted-by":"crossref","first-page":"1085","DOI":"10.1007\/s00467-020-04470-1","article-title":"Racial and health insurance disparities in pediatric acute kidney injury in the USA","volume":"35","author":"Bjornstad","year":"2020","journal-title":"Pediatr Nephrol."},{"issue":"10","key":"B30-20250801","doi-asserted-by":"crossref","first-page":"1841","DOI":"10.3390\/medicina59101841","article-title":"Lupus nephritis in children: novel perspectives","volume":"59","author":"Pennesi","year":"2023","journal-title":"Medicina (Kaunas)."},{"issue":"2","key":"B31-20250801","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1007\/s40620-021-01108-9","article-title":"Estimation of childhood nephrotic syndrome incidence: data from the atlanta metropolitan statistical area and meta-analysis of worldwide cases","volume":"35","author":"Londeree","year":"2022","journal-title":"J Nephrol."},{"issue":"1","key":"B32-20250801","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1038\/s41572-018-0047-y","article-title":"Polycystic kidney disease","volume":"4","author":"Bergmann","year":"2018","journal-title":"Nat Rev Dis Primers."},{"issue":"2","key":"B33-20250801","doi-asserted-by":"crossref","first-page":"272","DOI":"10.1053\/j.ajkd.2020.03.026","article-title":"Alport syndrome: achieving early aiagnosis and treatment","volume":"77","author":"Kashtan","year":"2021","journal-title":"Am J Kidney Dis."},{"issue":"6","key":"B34-20250801","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1002\/acr.21664","article-title":"American College of Rheumatology guidelines for screening, treatment, and management of lupus nephritis","volume":"64","author":"Hahn","year":"2012","journal-title":"Arthritis Care Res (Hoboken)."},{"issue":"3","key":"B35-20250801","doi-asserted-by":"crossref","first-page":"877","DOI":"10.1007\/s00467-022-05739-3","article-title":"IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome","volume":"38","author":"Trautmann","year":"2023","journal-title":"Pediatr Nephrol."},{"issue":"8","key":"B36-20250801","doi-asserted-by":"crossref","first-page":"1529","DOI":"10.1007\/s00467-020-04519-1","article-title":"IPNA clinical practice recommendations for the diagnosis and management of children with steroid-resistant nephrotic syndrome","volume":"35","author":"Trautmann","year":"2020","journal-title":"Pediatr Nephrol."}],"container-title":["Kidney360"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.34067\/KID.0000000753","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,11]],"date-time":"2026-08-11T19:58:59Z","timestamp":1786478339000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.34067\/KID.0000000753"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,3,4]]},"references-count":30,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2025]]}},"URL":"https:\/\/doi.org\/10.34067\/kid.0000000753","relation":{},"ISSN":["2641-7650"],"issn-type":[{"value":"2641-7650","type":"electronic"}],"subject":[],"published":{"date-parts":[[2025,3,4]]},"assertion":[{"value":"2024-11-01","name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2025-02-26","name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}}]}}