Evaluating Long-Term Outcomes of Children Undergoing Surgical Treatment for Congenital Heart Disease for National Audit in England and Wales
There is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics. Informed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long-term outcome metrics suitable...
Saved in:
Published in | Journal of the American Heart Association Vol. 13; no. 21; p. e035166 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
29.10.2024
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | There is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics.
Informed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long-term outcome metrics suitable for routine monitoring. We then developed sentinel CHD phenotypes and algorithms for identifying treatment pathway procedures using clinical codes. Finally, we calculated the metrics within a retrospective national cohort analysis. The 9 selected sentinel CHDs had a higher-than-average prevalence, typically involved surgery in infancy, and were associated with an increased risk of late mortality. The selected metrics of survival and reinterventions at 1, 5, and 10 years were both important and feasible. The cohort included 29 319 (41.3% of all operated CHD births) English and Welsh children born with sentinel CHDs in 2000 to 2022. Example metrics at age 10 years included: survival-hypoplastic left heart syndrome: 57.6% (95% CI, 54.9%-60.4%), functionally univentricular heart: 86.7% (95% CI, 84.6%-88.9%), transposition of the great arteries: 93.1% (95% CI, 92.2%-93.9%), pulmonary atresia: 81.0% (95% CI, 79.1%-82.9%), atrioventricular septal defect: 88.5% (95% CI, 87.5%-89.5%), tetralogy of Fallot: 95.1% (95% CI, 94.4%-95.8%), aortic stenosis: 94.4% (95% CI, 93.3%-95.6%), coarctation: 96.7% (95% CI, 96.2%-97.3%), and ventricular septal defect: 96.9% 95% CI, (96.4%-97.3%); and (2) cumulative incidence of reintervention-hypoplastic left heart syndrome : 54.5% (95% CI, 51.5%-57.3%), functionally univentricular heart: 57.3% (95% CI, 53.9%-60.5%), transposition of the great arteries: 20.9% (95% CI, 19.5%-22.3%), pulmonary atresia: 66.8% (95% CI, 64.2%-69.1%), atrioventricular septal defect: 21.6% (20.3%-23.0%), tetralogy of Fallot: 26.6% (95% CI, 25.2%-28.0%), aortic stenosis: 31.2% (95% CI, 28.8%-33.6%), coarctation: 19.8% (95% CI, 18.6%-21.1%), and ventricular septal defect: 6.1% (95% CI, 5.5%-6.8%).
It is feasible to report important long-term outcomes of survival and reintervention for sentinel CHDs using routinely collected procedure records, adding value to national audit. |
---|---|
AbstractList | Background There is strong interest in the evaluation of longer‐term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics. Methods and Results Informed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long‐term outcome metrics suitable for routine monitoring. We then developed sentinel CHD phenotypes and algorithms for identifying treatment pathway procedures using clinical codes. Finally, we calculated the metrics within a retrospective national cohort analysis. The 9 selected sentinel CHDs had a higher‐than‐average prevalence, typically involved surgery in infancy, and were associated with an increased risk of late mortality. The selected metrics of survival and reinterventions at 1, 5, and 10 years were both important and feasible. The cohort included 29 319 (41.3% of all operated CHD births) English and Welsh children born with sentinel CHDs in 2000 to 2022. Example metrics at age 10 years included: survival—hypoplastic left heart syndrome: 57.6% (95% CI, 54.9%–60.4%), functionally univentricular heart: 86.7% (95% CI, 84.6%–88.9%), transposition of the great arteries: 93.1% (95% CI, 92.2%–93.9%), pulmonary atresia: 81.0% (95% CI, 79.1%–82.9%), atrioventricular septal defect: 88.5% (95% CI, 87.5%–89.5%), tetralogy of Fallot: 95.1% (95% CI, 94.4%–95.8%), aortic stenosis: 94.4% (95% CI, 93.3%–95.6%), coarctation: 96.7% (95% CI, 96.2%–97.3%), and ventricular septal defect: 96.9% 95% CI, (96.4%–97.3%); and (2) cumulative incidence of reintervention—hypoplastic left heart syndrome : 54.5% (95% CI, 51.5%–57.3%), functionally univentricular heart: 57.3% (95% CI, 53.9%–60.5%), transposition of the great arteries: 20.9% (95% CI, 19.5%–22.3%), pulmonary atresia: 66.8% (95% CI, 64.2%–69.1%), atrioventricular septal defect: 21.6% (20.3%–23.0%), tetralogy of Fallot: 26.6% (95% CI, 25.2%–28.0%), aortic stenosis: 31.2% (95% CI, 28.8%–33.6%), coarctation: 19.8% (95% CI, 18.6%–21.1%), and ventricular septal defect: 6.1% (95% CI, 5.5%–6.8%). Conclusions It is feasible to report important long‐term outcomes of survival and reintervention for sentinel CHDs using routinely collected procedure records, adding value to national audit. There is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics. Informed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long-term outcome metrics suitable for routine monitoring. We then developed sentinel CHD phenotypes and algorithms for identifying treatment pathway procedures using clinical codes. Finally, we calculated the metrics within a retrospective national cohort analysis. The 9 selected sentinel CHDs had a higher-than-average prevalence, typically involved surgery in infancy, and were associated with an increased risk of late mortality. The selected metrics of survival and reinterventions at 1, 5, and 10 years were both important and feasible. The cohort included 29 319 (41.3% of all operated CHD births) English and Welsh children born with sentinel CHDs in 2000 to 2022. Example metrics at age 10 years included: survival-hypoplastic left heart syndrome: 57.6% (95% CI, 54.9%-60.4%), functionally univentricular heart: 86.7% (95% CI, 84.6%-88.9%), transposition of the great arteries: 93.1% (95% CI, 92.2%-93.9%), pulmonary atresia: 81.0% (95% CI, 79.1%-82.9%), atrioventricular septal defect: 88.5% (95% CI, 87.5%-89.5%), tetralogy of Fallot: 95.1% (95% CI, 94.4%-95.8%), aortic stenosis: 94.4% (95% CI, 93.3%-95.6%), coarctation: 96.7% (95% CI, 96.2%-97.3%), and ventricular septal defect: 96.9% 95% CI, (96.4%-97.3%); and (2) cumulative incidence of reintervention-hypoplastic left heart syndrome : 54.5% (95% CI, 51.5%-57.3%), functionally univentricular heart: 57.3% (95% CI, 53.9%-60.5%), transposition of the great arteries: 20.9% (95% CI, 19.5%-22.3%), pulmonary atresia: 66.8% (95% CI, 64.2%-69.1%), atrioventricular septal defect: 21.6% (20.3%-23.0%), tetralogy of Fallot: 26.6% (95% CI, 25.2%-28.0%), aortic stenosis: 31.2% (95% CI, 28.8%-33.6%), coarctation: 19.8% (95% CI, 18.6%-21.1%), and ventricular septal defect: 6.1% (95% CI, 5.5%-6.8%). It is feasible to report important long-term outcomes of survival and reintervention for sentinel CHDs using routinely collected procedure records, adding value to national audit. There is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics.BACKGROUNDThere is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative metrics.Informed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long-term outcome metrics suitable for routine monitoring. We then developed sentinel CHD phenotypes and algorithms for identifying treatment pathway procedures using clinical codes. Finally, we calculated the metrics within a retrospective national cohort analysis. The 9 selected sentinel CHDs had a higher-than-average prevalence, typically involved surgery in infancy, and were associated with an increased risk of late mortality. The selected metrics of survival and reinterventions at 1, 5, and 10 years were both important and feasible. The cohort included 29 319 (41.3% of all operated CHD births) English and Welsh children born with sentinel CHDs in 2000 to 2022. Example metrics at age 10 years included: survival-hypoplastic left heart syndrome: 57.6% (95% CI, 54.9%-60.4%), functionally univentricular heart: 86.7% (95% CI, 84.6%-88.9%), transposition of the great arteries: 93.1% (95% CI, 92.2%-93.9%), pulmonary atresia: 81.0% (95% CI, 79.1%-82.9%), atrioventricular septal defect: 88.5% (95% CI, 87.5%-89.5%), tetralogy of Fallot: 95.1% (95% CI, 94.4%-95.8%), aortic stenosis: 94.4% (95% CI, 93.3%-95.6%), coarctation: 96.7% (95% CI, 96.2%-97.3%), and ventricular septal defect: 96.9% 95% CI, (96.4%-97.3%); and (2) cumulative incidence of reintervention-hypoplastic left heart syndrome : 54.5% (95% CI, 51.5%-57.3%), functionally univentricular heart: 57.3% (95% CI, 53.9%-60.5%), transposition of the great arteries: 20.9% (95% CI, 19.5%-22.3%), pulmonary atresia: 66.8% (95% CI, 64.2%-69.1%), atrioventricular septal defect: 21.6% (20.3%-23.0%), tetralogy of Fallot: 26.6% (95% CI, 25.2%-28.0%), aortic stenosis: 31.2% (95% CI, 28.8%-33.6%), coarctation: 19.8% (95% CI, 18.6%-21.1%), and ventricular septal defect: 6.1% (95% CI, 5.5%-6.8%).METHODS AND RESULTSInformed by user online discussion forums and scoping of national data, we selected sentinel CHDs and long-term outcome metrics suitable for routine monitoring. We then developed sentinel CHD phenotypes and algorithms for identifying treatment pathway procedures using clinical codes. Finally, we calculated the metrics within a retrospective national cohort analysis. The 9 selected sentinel CHDs had a higher-than-average prevalence, typically involved surgery in infancy, and were associated with an increased risk of late mortality. The selected metrics of survival and reinterventions at 1, 5, and 10 years were both important and feasible. The cohort included 29 319 (41.3% of all operated CHD births) English and Welsh children born with sentinel CHDs in 2000 to 2022. Example metrics at age 10 years included: survival-hypoplastic left heart syndrome: 57.6% (95% CI, 54.9%-60.4%), functionally univentricular heart: 86.7% (95% CI, 84.6%-88.9%), transposition of the great arteries: 93.1% (95% CI, 92.2%-93.9%), pulmonary atresia: 81.0% (95% CI, 79.1%-82.9%), atrioventricular septal defect: 88.5% (95% CI, 87.5%-89.5%), tetralogy of Fallot: 95.1% (95% CI, 94.4%-95.8%), aortic stenosis: 94.4% (95% CI, 93.3%-95.6%), coarctation: 96.7% (95% CI, 96.2%-97.3%), and ventricular septal defect: 96.9% 95% CI, (96.4%-97.3%); and (2) cumulative incidence of reintervention-hypoplastic left heart syndrome : 54.5% (95% CI, 51.5%-57.3%), functionally univentricular heart: 57.3% (95% CI, 53.9%-60.5%), transposition of the great arteries: 20.9% (95% CI, 19.5%-22.3%), pulmonary atresia: 66.8% (95% CI, 64.2%-69.1%), atrioventricular septal defect: 21.6% (20.3%-23.0%), tetralogy of Fallot: 26.6% (95% CI, 25.2%-28.0%), aortic stenosis: 31.2% (95% CI, 28.8%-33.6%), coarctation: 19.8% (95% CI, 18.6%-21.1%), and ventricular septal defect: 6.1% (95% CI, 5.5%-6.8%).It is feasible to report important long-term outcomes of survival and reintervention for sentinel CHDs using routinely collected procedure records, adding value to national audit.CONCLUSIONSIt is feasible to report important long-term outcomes of survival and reintervention for sentinel CHDs using routinely collected procedure records, adding value to national audit. |
Author | Taylor, Julie A Huang, Qi Brown, Kate L van Doorn, Carin Espuny-Pujol, Ferran Pagel, Christina Wray, Jo Stoica, Serban Franklin, Rodney C G Crowe, Sonya |
Author_xml | – sequence: 1 givenname: Kate L orcidid: 0000-0002-0729-4959 surname: Brown fullname: Brown, Kate L organization: Great Ormond Street Hospital Biomedical Research Centre London UK – sequence: 2 givenname: Qi orcidid: 0000-0003-4456-2999 surname: Huang fullname: Huang, Qi organization: Clinical Operational Research Unit University College London UK – sequence: 3 givenname: Ferran orcidid: 0000-0001-9085-7400 surname: Espuny-Pujol fullname: Espuny-Pujol, Ferran organization: Clinical Operational Research Unit University College London UK – sequence: 4 givenname: Julie A orcidid: 0000-0002-7698-6991 surname: Taylor fullname: Taylor, Julie A organization: Clinical Operational Research Unit University College London UK – sequence: 5 givenname: Jo orcidid: 0000-0002-4769-1211 surname: Wray fullname: Wray, Jo organization: Great Ormond Street Hospital Biomedical Research Centre London UK – sequence: 6 givenname: Carin orcidid: 0000-0003-2721-3279 surname: van Doorn fullname: van Doorn, Carin organization: Paediatric Cardiac Surgery, Leeds General Infirmary Leeds UK – sequence: 7 givenname: Serban orcidid: 0000-0002-0456-1249 surname: Stoica fullname: Stoica, Serban organization: Paediatric Cardiac Surgery Bristol Children's Hospital Bristol UK – sequence: 8 givenname: Christina orcidid: 0000-0002-2857-1628 surname: Pagel fullname: Pagel, Christina organization: Clinical Operational Research Unit University College London UK – sequence: 9 givenname: Rodney C G orcidid: 0000-0002-1096-6242 surname: Franklin fullname: Franklin, Rodney C G organization: Paediatric Cardiology Royal Brompton and Harefield NHS Foundation Trust London UK – sequence: 10 givenname: Sonya orcidid: 0000-0003-1882-5476 surname: Crowe fullname: Crowe, Sonya organization: Clinical Operational Research Unit University College London UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39470033$$D View this record in MEDLINE/PubMed |
BookMark | eNpNUU1v2zAMFYYMa5v1vFuhYy9O9OHI0TFIs2ZFsByWYkdDkShXhS2lkl1g_2E_evLSFRNAkcB7fCT4rtDEBw8IfaFkRqmg84fVdjWjrJwRvqBCfECXjJRVIeWSTP6rL9B1Ss8kP8EqvpCf0AWXZUUI55fo9-ZVtYPqnW_wLvimOEDs8H7odegg4WDx-sm1JoLHj95AbMLI_DHExmnV4kME1Xfge2xDxOssAN71GdiCij2-cwlUgr_g9zwk-AytBuN67Dze-KZV3uAxfqoW0mf00ao2wfVbnqLHr5vDelvs9vff1qtdoSmvRGE4t6ri0rCSgVwsS7rMPxHALRHSCCuMZBWjmoFlaimOVldH0JpKq8Awyqfo9qx7iuFlgNTXnUsa2rwNhCHVnDK6kLQqy0ydn6k6hpQi2PoUXafir5qSenShHl2oswv12YXccfMmPhw7MO_8fzfnfwDbz4UT |
Cites_doi | 10.1016/j.jtcvs.2022.11.018 10.1017/S104795112100281X 10.4103/apc.APC_32_19 10.1016/j.jtcvs.2016.05.019 10.1017/S1047951117002244 10.1017/S1047951114001450 10.1161/CIRCULATIONAHA.123.065647 10.1016/j.athoracsur.2015.12.039 10.1161/CIRCULATIONAHA.117.028784 10.1053/j.semtcvs.2018.02.004 10.1136/openhrt-2022-002147 10.1161/JAHA.115.002846 10.1016/j.jtcvs.2022.07.025 10.1055/s-0042-1757175 10.1016/S0140-6736(01)05404-6 10.1016/j.athoracsur.2016.12.013 10.1002/bdr2.1400 10.1017/S1047951112001369 10.1136/heartjnl-2018-312958 10.1136/heartjnl-2021-319677 10.1007/s00246-022-02954-5 10.1136/bmjopen-2018-028533 10.1136/openhrt-2014-000157 10.1016/j.athoracsur.2019.05.081 10.1093/ejcts/ezaa184 10.1016/j.jacc.2011.09.022 10.1016/j.athoracsur.2020.01.002 10.1016/j.cjca.2022.04.021 10.1161/CIRCULATIONAHA.120.046962 10.1177/2150135121991528 10.1093/ejcts/ezad284 10.1161/CIRCULATIONAHA.123.064400 10.1016/j.jtcvs.2009.03.071 |
ContentType | Journal Article |
DBID | NPM AAYXX CITATION 7X8 |
DOI | 10.1161/JAHA.124.035166 |
DatabaseName | PubMed CrossRef MEDLINE - Academic |
DatabaseTitle | PubMed CrossRef MEDLINE - Academic |
DatabaseTitleList | CrossRef PubMed MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 2047-9980 |
ExternalDocumentID | 10_1161_JAHA_124_035166 39470033 |
Genre | Journal Article |
GroupedDBID | 0R~ 1OC 24P 53G 5VS 8-1 AAZKR ACGFO ACXQS ADBBV ADKYN ADZMN AEGXH AENEX AIAGR ALAGY ALMA_UNASSIGNED_HOLDINGS AOIJS AVUZU BAWUL BCNDV DIK EBS EMOBN GODZA GROUPED_DOAJ GX1 HYE KQ8 M~E NPM OK1 RAH RHF RNS RPM WIN AAYXX CITATION 7X8 |
ID | FETCH-LOGICAL-c1376-d33fa739d242e95841895806e3f069d6f6d92721c2ef2a86bfc7becc19faed213 |
ISSN | 2047-9980 |
IngestDate | Wed Nov 06 16:47:55 EST 2024 Wed Oct 30 12:31:06 EDT 2024 Sat Nov 02 12:09:23 EDT 2024 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 21 |
Keywords | congenital heart disease pediatric cardiac surgery outcomes transparency |
Language | English |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c1376-d33fa739d242e95841895806e3f069d6f6d92721c2ef2a86bfc7becc19faed213 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ORCID | 0000-0002-0729-4959 0000-0003-4456-2999 0000-0002-0456-1249 0000-0003-1882-5476 0000-0001-9085-7400 0000-0002-4769-1211 0000-0003-2721-3279 0000-0002-1096-6242 0000-0002-2857-1628 0000-0002-7698-6991 |
OpenAccessLink | https://doi.org/10.1161/jaha.124.035166 |
PMID | 39470033 |
PQID | 3121591744 |
PQPubID | 23479 |
ParticipantIDs | proquest_miscellaneous_3121591744 crossref_primary_10_1161_JAHA_124_035166 pubmed_primary_39470033 |
PublicationCentury | 2000 |
PublicationDate | 2024-Oct-29 |
PublicationDateYYYYMMDD | 2024-10-29 |
PublicationDate_xml | – month: 10 year: 2024 text: 2024-Oct-29 day: 29 |
PublicationDecade | 2020 |
PublicationPlace | England |
PublicationPlace_xml | – name: England |
PublicationTitle | Journal of the American Heart Association |
PublicationTitleAlternate | J Am Heart Assoc |
PublicationYear | 2024 |
References | e_1_3_2_26_2 e_1_3_2_27_2 e_1_3_2_28_2 e_1_3_2_29_2 e_1_3_2_20_2 e_1_3_2_21_2 e_1_3_2_22_2 e_1_3_2_23_2 e_1_3_2_24_2 e_1_3_2_25_2 e_1_3_2_9_2 e_1_3_2_15_2 e_1_3_2_38_2 e_1_3_2_8_2 e_1_3_2_16_2 e_1_3_2_37_2 e_1_3_2_7_2 e_1_3_2_17_2 e_1_3_2_6_2 e_1_3_2_18_2 e_1_3_2_39_2 e_1_3_2_19_2 e_1_3_2_30_2 e_1_3_2_32_2 e_1_3_2_10_2 e_1_3_2_31_2 e_1_3_2_5_2 e_1_3_2_11_2 e_1_3_2_34_2 e_1_3_2_4_2 e_1_3_2_12_2 e_1_3_2_33_2 e_1_3_2_3_2 e_1_3_2_13_2 e_1_3_2_36_2 e_1_3_2_2_2 e_1_3_2_14_2 e_1_3_2_35_2 |
References_xml | – ident: e_1_3_2_13_2 doi: 10.1016/j.jtcvs.2022.11.018 – ident: e_1_3_2_14_2 doi: 10.1017/S104795112100281X – ident: e_1_3_2_22_2 doi: 10.4103/apc.APC_32_19 – ident: e_1_3_2_27_2 doi: 10.1016/j.jtcvs.2016.05.019 – ident: e_1_3_2_15_2 doi: 10.1017/S1047951117002244 – ident: e_1_3_2_36_2 doi: 10.1017/S1047951114001450 – ident: e_1_3_2_30_2 doi: 10.1161/CIRCULATIONAHA.123.065647 – ident: e_1_3_2_9_2 doi: 10.1016/j.athoracsur.2015.12.039 – ident: e_1_3_2_12_2 – ident: e_1_3_2_29_2 doi: 10.1161/CIRCULATIONAHA.117.028784 – ident: e_1_3_2_31_2 doi: 10.1053/j.semtcvs.2018.02.004 – ident: e_1_3_2_37_2 doi: 10.1136/openhrt-2022-002147 – ident: e_1_3_2_34_2 doi: 10.1161/JAHA.115.002846 – ident: e_1_3_2_18_2 doi: 10.1016/j.jtcvs.2022.07.025 – ident: e_1_3_2_3_2 – ident: e_1_3_2_25_2 doi: 10.1055/s-0042-1757175 – ident: e_1_3_2_4_2 doi: 10.1016/S0140-6736(01)05404-6 – ident: e_1_3_2_7_2 – ident: e_1_3_2_16_2 doi: 10.1016/j.athoracsur.2016.12.013 – ident: e_1_3_2_38_2 doi: 10.1002/bdr2.1400 – ident: e_1_3_2_8_2 doi: 10.1017/S1047951112001369 – ident: e_1_3_2_10_2 doi: 10.1136/heartjnl-2018-312958 – ident: e_1_3_2_11_2 doi: 10.1136/heartjnl-2021-319677 – ident: e_1_3_2_24_2 doi: 10.1007/s00246-022-02954-5 – ident: e_1_3_2_6_2 doi: 10.1136/bmjopen-2018-028533 – ident: e_1_3_2_2_2 doi: 10.1136/openhrt-2014-000157 – ident: e_1_3_2_26_2 doi: 10.1016/j.athoracsur.2019.05.081 – ident: e_1_3_2_17_2 doi: 10.1093/ejcts/ezaa184 – ident: e_1_3_2_28_2 doi: 10.1016/j.jacc.2011.09.022 – ident: e_1_3_2_33_2 – ident: e_1_3_2_5_2 doi: 10.1016/j.athoracsur.2020.01.002 – ident: e_1_3_2_19_2 doi: 10.1016/j.cjca.2022.04.021 – ident: e_1_3_2_35_2 doi: 10.1161/CIRCULATIONAHA.120.046962 – ident: e_1_3_2_20_2 doi: 10.1177/2150135121991528 – ident: e_1_3_2_23_2 doi: 10.1093/ejcts/ezad284 – ident: e_1_3_2_39_2 doi: 10.1161/CIRCULATIONAHA.123.064400 – ident: e_1_3_2_32_2 – ident: e_1_3_2_21_2 doi: 10.1016/j.jtcvs.2009.03.071 |
SSID | ssj0000627359 |
Score | 2.4014251 |
Snippet | There is strong interest in the evaluation of longer-term outcome metrics for congenital heart diseases (CHDs); however, registries focus on postoperative... Background There is strong interest in the evaluation of longer‐term outcome metrics for congenital heart diseases (CHDs); however, registries focus on... |
SourceID | proquest crossref pubmed |
SourceType | Aggregation Database Index Database |
StartPage | e035166 |
Title | Evaluating Long-Term Outcomes of Children Undergoing Surgical Treatment for Congenital Heart Disease for National Audit in England and Wales |
URI | https://www.ncbi.nlm.nih.gov/pubmed/39470033 https://www.proquest.com/docview/3121591744 |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Li9swEBbpFkovpe-mL1ToobB4G1uyvDqGkBC222wLDs3N-CEt6cFeHPvQ_ob-if7Tzkiynd3uwraHmCAnkvF8zHwz0swQ8j7UeZhOcu6FWiqPC-Z7ksnMS3UBVI5hOWhzQHYllmt-sgk3o9HvvVNLbZMd5T-vzSv5H6nCGMgVs2T_QbL9pDAA30G-cAUJw_VWMp67Ut2YqFSV514MavbwrG1gLVtLdtalapv2RueVKb_d1lbbxf0ZczxqOKswy2rb2GLDdYN1OXHrxtxcdSHDKSZxYIzENf8wew_fwMjsbmC5e5krpZv4KiL2gwGfgPoeDvHw1kWzv2575r-7aMsf3pf2u20NtlB1PQB8iD9g3rdygVoX1Ag4WgMX-TC6L8ACEuAJ2i0bdc1Yp7zZHkhtrrVTxQr3SG1Hl7_NhEAzcTJdYiyYHw2_vFyQe3WWLNanp0k838R3yN0AdJnY89qtsQf-Z1ry9Y_nCkjBGh-vrHCZ-9zg0BhiEz8kD5ys6NTC6xEZqfIxuffZnbl4Qn4NKKM9ymiHMlpp2qGMDiijHcpojzIKQKIDyqgBA3UoMzc7lFGDMrotqUMZxY9B2VOyXszj2dJzPTy83Afb5RWM6TRisgAqqCSwXf8YrhOhmJ4IWQgtChlEgZ8HSgfpsch0HqFa8aVOVRH47Bk5KKtSvSB0EqVCZcCXdZBxzorUjyJwP_w84nkYFNGYfOjebnJhS7UkxsUVfoKCSEAQiRXEmLzr3n4C6hT3yNJSVe0uYVhtRYKbzsfkuRVLPxmTPMLehy9v8e9X5P6A69fkoKlb9Qboa5O9NQD6AxmYnGc |
link.rule.ids | 315,783,787,867,27936,27937 |
linkProvider | Directory of Open Access Journals |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Evaluating+Long-Term+Outcomes+of+Children+Undergoing+Surgical+Treatment+for+Congenital+Heart+Disease+for+National+Audit+in+England+and+Wales&rft.jtitle=Journal+of+the+American+Heart+Association&rft.au=Brown%2C+Kate+L&rft.au=Huang%2C+Qi&rft.au=Espuny-Pujol%2C+Ferran&rft.au=Taylor%2C+Julie+A&rft.date=2024-10-29&rft.issn=2047-9980&rft.eissn=2047-9980&rft.volume=13&rft.issue=21&rft.spage=e035166&rft_id=info:doi/10.1161%2FJAHA.124.035166&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2047-9980&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2047-9980&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2047-9980&client=summon |