-
Something wrong with this record ?
Survival and Freedom From Reinterventions in Patients With Repaired Tetralogy of Fallot: Up to 42-Year Follow-Up of 917 Patients
R. Gebauer, V. Chaloupecký, B. Hučín, T. Tláskal, A. Komárek, J. Janoušek
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 2012
Free Medical Journals
from 2012
PubMed Central
from 2012
Europe PubMed Central
from 2012
Open Access Digital Library
from 2012-01-01
Open Access Digital Library
from 2012-01-01
Open Access Digital Library
from 2015-01-01
Wiley-Blackwell Open Access Titles
from 2012
ROAD: Directory of Open Access Scholarly Resources
from 2012
- MeSH
- Child MeSH
- Tetralogy of Fallot * surgery MeSH
- Infant MeSH
- Humans MeSH
- Follow-Up Studies MeSH
- Pulmonary Valve * surgery MeSH
- Reoperation MeSH
- Retrospective Studies MeSH
- Risk Factors MeSH
- Freedom MeSH
- Treatment Outcome MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Background To evaluate long-term outcome of tetralogy of Fallot repair analyzing an unbiased country-wide surgically treated population with tetralogy of Fallot. Methods and Results Retrospective analysis of consecutive patients aged <18 years who underwent tetralogy of Fallot repair at a single nationwide pediatric cardiac center. Death from any cause and need for surgical or catheter reintervention were the study end points. Cox regression analysis was used to identify related risk factors. A total of 917 patients (male, 56.3%) were analyzed. Staged repair was performed in 16.9%. Early mortality (24/917, 2.62% patients) was confined to the early surgical eras. Late mortality was 4.5% (40/893 patients). Survival probability was 95.1%, 93.8% and 91.9% at 10, 20 and 30 years after repair, respectively. Early surgical era (P=0.013) and surgical/catheter reinterventions (P<0.001) were multivariable predictors of late death. A total of 487 reinterventions were performed after initial repair in 253/917 patients (27.6%), with pulmonary artery revalvulation (196/917 patients, 21.4%) being most frequent. Probability of freedom from first reintervention was 89.0%, 73.3%, and 55.1% at 10, 20, and 30 years after primary repair, respectively. Transannular repair was associated with the need for pulmonary artery revalvulation (P<0.001). Patients who underwent staged repair were more likely to need reinterventions on pulmonary arteries (P<0.001). Conclusions In an unbiased nationwide cohort, tetralogy of Fallot repair carried a favorable survival of >90% at 30 years. Each reintervention significantly incrementally increased the risk of mortality. Type of initial repair predicted the need for specific surgical or catheter reinterventions.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24001038
- 003
- CZ-PrNML
- 005
- 20240213093555.0
- 007
- ta
- 008
- 240109s2023 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1161/JAHA.121.024771 $2 doi
- 035 __
- $a (PubMed)37823375
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Gebauer, Roman $u Children's Heart Center, 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic $1 https://orcid.org/000900010758338X
- 245 10
- $a Survival and Freedom From Reinterventions in Patients With Repaired Tetralogy of Fallot: Up to 42-Year Follow-Up of 917 Patients / $c R. Gebauer, V. Chaloupecký, B. Hučín, T. Tláskal, A. Komárek, J. Janoušek
- 520 9_
- $a Background To evaluate long-term outcome of tetralogy of Fallot repair analyzing an unbiased country-wide surgically treated population with tetralogy of Fallot. Methods and Results Retrospective analysis of consecutive patients aged <18 years who underwent tetralogy of Fallot repair at a single nationwide pediatric cardiac center. Death from any cause and need for surgical or catheter reintervention were the study end points. Cox regression analysis was used to identify related risk factors. A total of 917 patients (male, 56.3%) were analyzed. Staged repair was performed in 16.9%. Early mortality (24/917, 2.62% patients) was confined to the early surgical eras. Late mortality was 4.5% (40/893 patients). Survival probability was 95.1%, 93.8% and 91.9% at 10, 20 and 30 years after repair, respectively. Early surgical era (P=0.013) and surgical/catheter reinterventions (P<0.001) were multivariable predictors of late death. A total of 487 reinterventions were performed after initial repair in 253/917 patients (27.6%), with pulmonary artery revalvulation (196/917 patients, 21.4%) being most frequent. Probability of freedom from first reintervention was 89.0%, 73.3%, and 55.1% at 10, 20, and 30 years after primary repair, respectively. Transannular repair was associated with the need for pulmonary artery revalvulation (P<0.001). Patients who underwent staged repair were more likely to need reinterventions on pulmonary arteries (P<0.001). Conclusions In an unbiased nationwide cohort, tetralogy of Fallot repair carried a favorable survival of >90% at 30 years. Each reintervention significantly incrementally increased the risk of mortality. Type of initial repair predicted the need for specific surgical or catheter reinterventions.
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a kojenec $7 D007223
- 650 12
- $a Fallotova tetralogie $x chirurgie $7 D013771
- 650 _2
- $a retrospektivní studie $7 D012189
- 650 _2
- $a následné studie $7 D005500
- 650 _2
- $a reoperace $7 D012086
- 650 _2
- $a rizikové faktory $7 D012307
- 650 _2
- $a svoboda $7 D005610
- 650 _2
- $a výsledek terapie $7 D016896
- 650 12
- $a plicní chlopeň $x chirurgie $7 D011664
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Chaloupecký, Václav $u Children's Heart Center, 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic $1 https://orcid.org/0000000329429575
- 700 1_
- $a Hučín, Bohumil $u Children's Heart Center, 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic
- 700 1_
- $a Tláskal, Tomáš $u Children's Heart Center, 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic $1 https://orcid.org/0000000203882390
- 700 1_
- $a Komárek, Arnošt $u Department of Probability and Mathematical Statistics, Faculty of Mathematics and Physics Charles University Prague Czech Republic $1 https://orcid.org/0000000187783762 $7 mzk2008434100
- 700 1_
- $a Janoušek, Jan $u Children's Heart Center, 2nd Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic $1 https://orcid.org/0000000249321150 $7 jo2003180379
- 773 0_
- $w MED00188127 $t Journal of the American Heart Association $x 2047-9980 $g Roč. 12, č. 20 (2023), s. e024771
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/37823375 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20240109 $b ABA008
- 991 __
- $a 20240213093552 $b ABA008
- 999 __
- $a ok $b bmc $g 2049573 $s 1210732
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 12 $c 20 $d e024771 $e 20231012 $i 2047-9980 $m Journal of the American Heart Association $n J Am Heart Assoc $x MED00188127
- LZP __
- $a Pubmed-20240109