SciELO - Scientific Electronic Library Online

 
vol.88 número5Células madre: buscando marcadores de superficie celular que predispongan compromiso de diferenciación cardiacaHipertensión arterial pulmonar asociada al virus de inmunodeficiencia humana. A 3 décadas de su descripción índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay artículos similaresSimilares en SciELO

Compartir


Archivos de cardiología de México

versión On-line ISSN 1665-1731versión impresa ISSN 1405-9940

Resumen

BURBOA-NORIEGA, Luis; BURBOA-NORIEGA, Jesús; CRISTANCHO-ROJAS, César  y  CRIALES-VERA, Sergio. Evaluation of the characteristics of aortic dissection by computed angio-tomography in the Mexican population. Arch. Cardiol. Méx. [online]. 2018, vol.88, n.5, pp.496-502.  Epub 04-Dic-2020. ISSN 1665-1731.  https://doi.org/10.1016/j.acmx.2018.05.009.

Objective:

To review aortic dissection (AD) in the Mexican population.

Method:

A retrospective study was conducted using 434 medical records of patients with aortic angio-tomography between November 2014 and October 2015. A sample was obtained of 32 patients with a first time diagnosis of AD. An analysis was performed of the dissections according to gender, age group, Stanford/De Bakey classification, and mortality rate 6 months after diagnosis. Statistical analysis was performed by obtaining the Chi squared index for the independent variables of gender, Marfan syndrome, systemic arterial hypertension, as well as calcified atheromatous disease in association with dissection subtypes, re-entry sites, and hypo-perfusion signs.

Results:

The patients included 65.6% males with a mean age of 54.5 years, and 34.4% females with mean age of 42.5 years. The most common dissection subtype was B/3. Mortality rate at 6 months was 18.7%. There was a significant association, with a marginal P in patients with Marfan syndrome and Stanford subtypes of AD (P = .0506). There was a significant association in patients with abdominal aortic aneurysm, when compared with Stanford subtypes of AD (P = .047104).

Conclusions:

AD is an emergency in which diagnosis and timely management are essential to improve prognosis. In the sample presented here, a significant association was found in patients with a history of Marfan syndrome and abdominal aneurysms with dissections according to the Stanford classification. The rest of the independent variables did not show any significant association, probably related to the size of the sample.

Palabras llave : Aortic dissection; Aorticangio-computed tomography; Marfan syndrome; Aortic aneurysm; Mexico.

        · resumen en Español     · texto en Español     · Español ( pdf )