info:eu-repo/semantics/article
Sternal torsion in pectus excavatum is related to cardiac compression and chest malformation indexes
Fecha
2020-04Registro en:
Capunay, Carlos; Martínez Ferro, Marcelo; Carrascosa, Patricia; Bellia Munzon, Gaston; Deviggiano, Alejandro; et al.; Sternal torsion in pectus excavatum is related to cardiac compression and chest malformation indexes; W B Saunders Co-Elsevier Inc; Journal Of Pediatric Surgery; 55; 4; 4-2020; 619-624
0022-3468
CONICET Digital
CONICET
Autor
Capunay, Carlos
Martínez Ferro, Marcelo
Carrascosa, Patricia
Bellia Munzon, Gaston
Deviggiano, Alejandro
Nazar, Maximiliano
Martinez, Jorge Luis
Rodriguez Granillo, Gaston Alfredo
Resumen
Background/purpose: The role of sternal torsion (ST) in patients with pectus excavatum (PEX) is unknown. We evaluated the relationship between ST and both chest malformation and cardiac compression (CC) indexes. Methods: We included consecutive patients with PEX who underwent chest computed tomography and cardiac magnetic resonance (CMR) to define surgical candidacy. Malformation indexes included the Haller index (HI), correction index (CI), and ST. CC and the tricuspid to mitral annulus width ratio were evaluated using CMR. Results: One-hundred and sixteen patients were included, with a mean HI of 5.8 ± 3.6 and a mean CI of 35.8 ± 18.0%. ST was significantly related to malformation indexes, being patients with absence of ST those showing the lowest HI (p = 0.048) and CI (p = 0.002). Right-sided ST was significantly related to the CC classification (p = 0.0001), and the tricuspid/mitral annulus width ratio was significantly lower among these patients (absence 0.98 ± 0.15, left-sided 0.91 ± 0.10, right-sided 0.80 ± 0.15, p < 0.0001). A significant inverse relationship between ST degrees and the tricuspid/mitral ratio was also identified (r = -0.47, p < 0.0001). Conclusions: We identified a significant relationship between ST and both chest malformation and CC indexes; the absence of ST being identified as a marker of an overall more benign phenotype.