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Published on: July 18, 2014
The heart after surviving twin-to-twin transfusion syndrome
Ximena Torres1, Mar Bennasar1, Carles Bautista-Rodríguez2
1Fetal Medicine Research Center, BCNatal - Barcelona Center for Maternal-Fetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Deu), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, and Centre for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain.
Insights
Twin-to-twin transfusion syndrome causes cardiac remodeling in both fetuses. While fetal therapy improves function, persistent cardiac changes are seen postnatally in survivors of this complex pregnancy condition.
Area of Science:
- Cardiology
- Fetal Medicine
- Neonatology
Background:
- Twin-to-twin transfusion syndrome (TTTS) causes significant cardiac structural and functional changes in affected fetuses.
- Understanding the long-term cardiac impact on survivors is crucial for clinical management.
Purpose of the Study:
- To detail echocardiographic alterations in monochorionic fetuses with TTTS (recipient and donor).
- To track these changes before and after laser photocoagulation, through the third trimester, and into the first year of life.
Main Methods:
- Observational study of 55 uncomplicated and 78 TTTS-affected monochorionic diamniotic twins.
- Comprehensive fetal echocardiography at four time points: pre-surgery, 24-72 hours post-surgery, 28-30 weeks gestation, and 6-12 months post-birth.
- Echocardiographic parameters were normalized using z-scores or indexed to heart area, estimated fetal weight, or body surface area.
Main Results:
- At diagnosis, recipients showed enlarged hearts, ventricular hypertrophy, and impaired systolic/diastolic function; donors had smaller ventricular dimensions and reduced longitudinal motion.
- Post-laser therapy, functional parameters improved in both.
- Prenatally, morphometric changes persisted, particularly in donors. Postnatally, recipients exhibited persistent cardiac remodeling, while donors showed decreased longitudinal motion.
Conclusions:
- Cardiac remodeling is evident in both TTTS fetuses at diagnosis, with significant diastolic dysfunction in recipients.
- Fetal therapy ameliorates most echocardiographic parameters, but residual cardiac changes persist postnatally in both fetuses.
Background:
The persistent changes in cardiac structure and function in children who survived twin-to-twin transfusion syndrome remain a matter of concern and controversy. Current fetal echocardiographic parameters and their postnatal evolution can help improve our understanding of the subject.
Objective:
To describe the echocardiographic changes of monochorionic fetuses affected by twin-to-twin transfusion syndrome, the recipient and the donor, before and after laser photocoagulation and to determine their evolution in the third trimester and during their first year of life.
Study Design:
An observational study was conducted including 55 uncomplicated monochorionic diamniotic twins and 78 pairs with twin-to-twin transfusion syndrome, 44 stage I-II and 34 stage III-IV, prospectively enrolled from 2015 until 2018. Comprehensive echocardiography was performed at 4 time periods: before laser photocoagulation, at 24 to 72 hours after surgery, at 28 to 30 weeks of gestation, and at 6 to 12 months after birth. Echocardiographic parameters were transformed to z-scores or indexed for heart area, estimated fetal weight, or body mass surface.
Results:
At diagnosis, recipients in all stages presented larger hearts (cardiothoracic ratio z-score: 2.77 [0.8] vs controls: -0.03 [0.5]; P<.001) and signs of ventricular hypertrophy (left end-diastolic ventricle wall thickness: 2.68 [0.7] vs controls -0.03 [0.7]; P<.001), along with systolic (cardiac index recipients: 317 [114] mL/min/kg vs controls: 400 [120] mL/min/kg, P<.001) and diastolic impairment (isovolumetric relaxation time z-score: 2.76 [0.6] vs controls: 0.05 [0.6]; P<.001). Donors presented smaller ventricular areas and diameters when compared with controls (left end-diastolic ventricle area z-score: -1.48 [1] vs 0.03 [0.9]; P<.001), along with decreased longitudinal motion (tricuspid annular plane systolic excursion z-score: -0.9 [1] vs controls -0.04 [1]; P<.001) and shorter ejection time z-score (-1.5 [0.7] vs controls: 0.0 [0.7]; P<.001). After surgery, an improvement in functional parameters was observed in both fetuses, whereas most morphometric changes prevailed in donors and recipients in the prenatal period. Postnatally, cardiac remodeling persisted in recipients (left relative wall thickness: 0.34 [0.02] vs controls: 0.30 [0.02]; P<.001), whereas donors mainly presented a decreased longitudinal motion in infancy (tricuspid annular plane systolic excursion z-score: -0.72 [0.7] vs controls: 0.23 [0.9]; P<.05).
Conclusion:
Cardiac remodeling is present in both fetuses at the twin-to-twin transfusion syndrome diagnosis, whereas diastolic dysfunction is only significant in the recipient. Fetal therapy improves most echocardiographic parameters, although postnatally, the echocardiographic changes persist in both fetuses.
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