Thirty-year survival after cardiac surgery for patients with Turner syndrome
Open accessAbstract
Objective To evaluate long-term survival in patients with Turner syndrome after congenital heart surgery with a focus on left heart obstructive lesions (LHOLs).Study design We queried the Pediatric Cardiac Care Consortium, a US-based registry of congenital heart surgery, for patients with Turner syndrome undergoing congenital heart surgery at <21 years of age between 1982 and 2011. Outcomes were obtained from the Pediatric Cardiac Care Consortium and from national death and transplant registries through 2019. Survival of patients with Turner syndrome and nonsyndromic patients with similar LHOL was compared by Kaplan-Meier survival curves and Cox regression adjusted for age, congenital heart disease, and era.Results We identified 179 patients with Turner syndrome operated for LHOL: 161 with 2-ventricle lesions (coarctation n = 149, aortic stenosis n = 12) and 18 with hypoplastic left heart (HLH) variants. There were 157 with 2-ventricle LHOL and 6 with HLH survived to discharge. Among survivors to hospital discharge, the 30-year transplant-free survival was 90.4% for Turner syndrome with 2-ventricle lesions and 90.9% for nonsyndromic comparators (adjusted hazard ratio [aHR] 1.15, 95% CI 0.64-2.04). The postdischarge survival for HLH was 33% for Turner syndrome and 51% for nonsyndromic patients, with these numbers being too small for meaningful comparisons. There was a higher risk for cardiovascular disease events in patients with Turner syndrome vs male (aHR 3.72, 95% CI 1.64-8.39) and female comparators (aHR 4.55, 95% CI 1.87-11.06) excluding heart failure deaths.Conclusions The 30-year transplant-free survival is similar for patients with Turner syndrome and nonsyndromic comparators with operated 2-ventricle LHOL without excess congenital heart disease risk. However, patients with Turner Syndrome still face increased cardiovascular disease morbidity, stressing the importance of lifelong comorbidity surveillance in this population.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Several studies have reported 2-3-fold higher mortality in neonates with TS with hypoplastic left heart (HLH) compared to all cases of HLH, suggesting an independent risk of TS to mortality.
“Similarly, several studies have reported 2-3-fold higher mortality in neonates with TS with hypoplastic left heart (HLH) compared to all cases of HLH, suggesting an independent risk of TS to mortality.633-635”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [634]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Chromosomal microarray versus karyotyping for prenatal diagnosis
Wapner, R. J., Martin, C. L., Levy, B., Ballif, B. C., Eng, C. M., Zachary, J. M., Savage, M., Platt, L. D., Saltzman, D., Grobman, W. A., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1203382 · Cited by 1,412 · see citing works
Nielsen, J., & Wohlert, M. (1991) · Human Genetics · doi:10.1007/bf01213097 · Cited by 1,193 · see citing works
Gravholt, C. H., Andersen, N. H., Conway, G. S., Dekkers, O. M., Geffner, M. E., Klein, K. O., Lin, A. E., Mauras, N., Quigley, C. A., Rubin, K., et al. (2017) · European Journal of Endocrinology · doi:10.1530/eje-17-0430 · Cited by 1,101 · see citing works
Self-citationPierpont, M. E., Brueckner, M., Chung, W. K., Garg, V., Lacro, R. V., McGuire, A. L., Mital, S., Priest, J. R., Pu, W. T., Roberts, A., et al. (2018) · Circulation · doi:10.1161/cir.0000000000000606 · Cited by 654 · see citing works
Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome
Stochholm, K., Juul, S., Juel, K., Naeraa, R. W., & Højbjerg Gravholt, C. (2006) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2006-0558 · Cited by 652 · see citing works
Turner's Syndrome in Adulthood
Elsheikh, M., Dunger, D. B., Conway, G. S., & Wass, J. A. H. (2002) · Endocrine Reviews · doi:10.1210/edrv.23.1.0457 · Cited by 397 · see citing works
Mortality in women with Turner syndrome in Great Britain: a national cohort study
Schoemaker, M. J., Swerdlow, A. J., Higgins, C. D., Wright, A. F., & Jacobs, P. A. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-1049 · Cited by 360 · see citing works
Cardiovascular Malformations and Complications in Turner Syndrome
Sybert, V. P. (1998) · PEDIATRICS · doi:10.1542/peds.101.1.e11 · Cited by 326 · see citing works
Left Ventricular Outflow Obstruction
Aboulhosn, J., & CHILD, J. S. (2006) · Circulation · doi:10.1161/circulationaha.105.592089 · Cited by 245 · see citing works
Cardiovascular Health in Turner Syndrome: A Scientific Statement From the American Heart Association
Silberbach, M., Roos‐Hesselink, J. W., Andersen, N. H., Braverman, A. C., Brown, N. M., Collins, R. T., Backer, J. F. A. D., Eagle, K. A., Hiratzka, L. F., Johnson, W. H., et al. (2018) · Circulation Genomic and Precision Medicine · doi:10.1161/hcg.0000000000000048 · Cited by 242 · see citing works
Self-citationSwerdlow, A. J., Hermon, C., Jacobs, P. A., Alberman, E. D., Beral, V., Daker, M. G., Fordyce, A., & Youings, S. A. (2001) · Annals of Human Genetics · doi:10.1046/j.1469-1809.2001.6520177.x · Cited by 238 · see citing works
Trends in long-term mortality after congenital heart surgery.
Spector, L. G., Menk, J. S., Knight, J. H., McCracken, C., Thomas, A. S., Vinocur, J. M., Oster, M. E., St Louis, J. D., Moller, J. H., & Kochilas, L. (2018) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2018.03.491 · Cited by 230 · see citing works
Self-citationMortality ratios, life expectancy, and causes of death in patients with Turner's syndrome.
Price, W. H., Clayton, J. F., Collyer, S., Mey, R. D., & Wilson, J. (1986) · Journal of Epidemiology & Community Health · doi:10.1136/jech.40.2.97 · Cited by 154 · see citing works
Congenital Cardiovascular Disease in Turner Syndrome
Bondy, C. A. (2008) · Congenital Heart Disease · doi:10.1111/j.1747-0803.2007.00163.x · Cited by 117 · see citing works
Long-term outcomes in patients with Turner syndrome: a 68-year follow-up
Fuchs, M. M., Attenhofer Jost, C., Babovic‐Vuksanovic, D., Connolly, H. M., & Egbe, A. (2019) · Journal of the American Heart Association · doi:10.1161/jaha.118.011501 · Cited by 88 · see citing works
Völkl, T. M. K., Degenhardt, K., Koch, A., Simm, D., Dörr, H. G., & Singer, H. (2005) · Clinical Cardiology · doi:10.1002/clc.4960280209 · Cited by 86 · see citing works
Cardiovascular abnormalities in Turner's syndrome: What prevention?
Dulac, Y., Pienkowski, C., Abadir, S., Tauber, M., & Acar, P. (2008) · Archives of cardiovascular diseases · doi:10.1016/j.acvd.2008.05.007 · Cited by 64 · see citing works
Cramer, J. W., Bartz, P. J., Simpson, P. M., & Zangwill, S. D. (2013) · Pediatric Cardiology · doi:10.1007/s00246-013-0766-5 · Cited by 62 · see citing works
Putting the Pediatric Cardiac Care Consortium in Context
Vinocur, J. M., Moller, J. H., & Kochilas, L. K. (2012) · Circulation Cardiovascular Quality and Outcomes · doi:10.1161/circoutcomes.111.964841 · Cited by 40 · see citing works
Self-citationMorales‐Demori, R. (2017) · Congenital Heart Disease · doi:10.1111/chd.12521 · Cited by 40 · see citing works
Spector, L. G., Menk, J. S., Vinocur, J. M., Oster, M. E., Harvey, B. A., St. Louis, J. D., Moller, J., & Kochilas, L. K. (2016) · Journal of the American Heart Association · doi:10.1161/jaha.116.003783 · Cited by 39 · see citing works
Self-citationFrequency and outcomes of cardiac operations and catheter interventions in Turner syndrome
Madriago, E., Nguyen, T., McFerson, M., Larson, E. V., Airhart, N., Moller, J. H., & Silberbach, M. (2012) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2012.04.036 · Cited by 34 · see citing works
Self-citationThe Pediatric Cardiac Care Consortium–Revisited
Moller, J. H., Powell, C. B., Joransen, J. A., & Borbas, C. (1994) · The Joint Commission Journal on Quality Improvement · doi:10.1016/s1070-3241(16)30115-8 · Cited by 31 · see citing works
Namachivayam, S. P., d’Udekem, Y., Millar, J., Cheung, M. M. H., & Butt, W. W. (2016) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2016.05.006 · Cited by 24 · see citing works
Chew, J. D., Hill, K. D., Jacobs, M. L., Jacobs, J. P., Killen, S. A. S., Godown, J., Wallace, A. S., Thibault, D., Chiswell, K., Bichell, D. P., et al. (2019) · The Annals of Thoracic Surgery · doi:10.1016/j.athoracsur.2019.05.047 · Cited by 19 · see citing works
Chou, Y., Wang, C., Lin, C.-H., Chung, H., & Lo, F. (2019) · Pediatrics & Neonatology · doi:10.1016/j.pedneo.2019.10.001 · Cited by 17 · see citing works
Outcomes in hospitalisations of women with Turner syndrome compared to women without Turner syndrome
Singh, I., Duca, L. M., Kao, D. P., Chatfield, K. C., & Khanna, A. D. (2021) · Cardiology in the Young · doi:10.1017/s1047951121000858 · Cited by 5 · see citing works
Electrophysiological effects and clinical utility of propafenone in children
Singh, M., McKenzie, K., Hudak, M. L., et al. (2021) · Cardiology in the Young · doi:10.1017/s1047951121002857 · Cited by 2 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Clinical practice guidelines for the care of girls and women with Turner syndrome.
Gravholt, C. H., Andersen, N. H., Christin-Maitre, S., Davis, S. M., Duijnhouwer, A., Gawlik, A., Maciel-Guerra, A. T., Gutmark-Little, I., Fleischer, K., Hong, D., et al. (2024) · European Journal of Endocrinology · doi:10.1093/ejendo/lvae050 · Cited by 224 · see citing works
Andersen, A. R., Urhoj, S. K., Tan, J., Cavero‐Carbonell, C., Gatt, M., Gissler, M., Klungsoyr, K., Khoshnood, B., Morris, J., Neville, A. J., et al. (2023) · Birth Defects Research · doi:10.1002/bdr2.2222 · Cited by 4 · see citing works
- Authors
- Alam, S., Claxton, J. S., Mortillo, M., Sassis, L., Kefala-Karli, P., Silberbach, M., Kochilas, L., & Wechsler, S. B.
- Affiliations
- Emory University (US)
- University of Nicosia (CY)
- Oregon Health & Science University (US)
- Corresponding author
- Alam, Sabikha
- ORCID
- Venue
- The Journal of Pediatrics
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 239
- Pages
- 187-192.e1
- ISSN
- 0022-3476 (ISSN-L)
- PMC
- PMC8626205
- OpenAlex
- W3195693214
- Cited by
- 8
- References
- 28
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 1
- FWCI
- 0.90
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (am, 349 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- The Journal of Pediatrics (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- U.S. Department of Defense (PR180683)
- National Heart, Lung, and Blood Institute (R01 HL122392)
- Topics
- Health Sciences › Medicine › Epidemiology › Congenital Heart Disease Studies
- Health Sciences › Medicine › Surgery › Cardiac and Coronary Surgery Techniques
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Valve Diseases and Treatments
- Keywords
- Turner syndrome, congenital heart surgery, coarctation of the aorta, aortic stenosis, hypoplastic left heart syndrome, long-term survival, transplant-free survival, cardiovascular morbidity, lifelong surveillance
- MeSH terms
- Adolescent, Child, Child, Preschool, Female, Follow-Up Studies, Cardiac Surgical Procedures, Humans, Infant, Infant, Newborn, Male, Registries, Retrospective Studies, Turner Syndrome, Survival Analysis, Treatment Outcome, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review