| Literature DB >> 28716062 |
Kálmán Benke1,2, Bence Ágg3,4,5, Miklós Pólos3, Alex Ali Sayour3, Tamás Radovits3, Elektra Bartha3,4, Péter Nagy6, Balázs Rákóczi7, Ákos Koller8, Viola Szokolai6, Julianna Hedberg4, Béla Merkely3, Zsolt B Nagy6, Zoltán Szabolcs3,4.
Abstract
BACKGROUND: Marfan syndrome is a genetic disease, presenting with dysfunction of connective tissues leading to lesions in the cardiovascular and skeletal muscle system. Within these symptoms, the most typical is weakness of the connective tissue in the aorta, manifesting as aortic dilatation (aneurysm). This could, in turn, become annuloaortic ectasia, or life-threatening dissection. As a result, life-saving and preventative cardiac surgical interventions are frequent among Marfan syndrome patients. Aortic aneurysm could turn into annuloaortic ectasia or life-threatening dissection, thus life-saving and preventive cardiac surgical interventions are frequent among patients with Marfan syndrome. We hypothesized that patients with Marfan syndrome have different level of anxiety, depression and satisfaction with life compared to that of the non-clinical patient population.Entities:
Keywords: Anxiety; Cardiac surgery; Depression; Marfan syndrome; Questionnaire
Mesh:
Year: 2017 PMID: 28716062 PMCID: PMC5512884 DOI: 10.1186/s12888-017-1417-9
Source DB: PubMed Journal: BMC Psychiatry ISSN: 1471-244X Impact factor: 3.630
Clinical data
| 1. Aortic dissection | 2. Annuloaortic ectasia | 3. Prophylactic | 4. Non-operated | |
|---|---|---|---|---|
| Patients | 10 | 9 | 9 | 17 |
| Male | 4 | 6 | 6 | 3 |
| Anthropometric (measured) | ||||
| Height | 180.1 ± 10.1 | 183.9 ± 13.2 | 186.4 ± 13.7 | 180.2 ± 9.2 |
| Lower segment (cm) | 95.8 ± 8.6 | 100 ± 11.8 | 99.1 ± 6.8 | 94.3 ± 5.9 |
| Arm span (cm) | 190.3 ± 11.6 | 186 ± 17 | 192.6 ± 11.4 | 184.8 ± 7.5 |
| Footsize | 42.9 ± 2.2 | 43 ± 3.3 | 44.2 ± 4.1 | 42.2 ± 2.5 |
| Weight (kg) | 78.3 ± 13.4 | 71.9 ± 18.6 | 75.1 ± 19.3 | 69.6 ± 13.4 |
| Anthropometric (calculated) | ||||
| Upper segment (cm) | 84.3 ± 8.3 | 83.9 ± 9.2 | 87.3 ± 9.2 | 85.6 ± 6.8 |
| Body Mass Index (BMI; kg/m2) | 24.2 ± 3.7 | 21 ± 4.2 | 21.5 ± 4.5 | 21.3 ± 3 |
| Body surface area (m2) | 1.97 ± 0.2 | 1.91 ± 0.3 | 1.96 ± 0.3 | 1.86 ± 0.2 |
| Upper segment - Lower segment ratio (USLS) | 0.89 ± 0.12 | 0.85 ± 0.14 | 0.88 ± 0.09 | 0.91 ± 0.09 |
| Arm span - Height ratio (ASHR) | 1.06 ± 0.04 | 1.01 ± 0.04 | 1.04 ± 0.04 | 1.03 ± 0.03 |
| Ghent nosology (%) | ||||
| Mitral valve prolapse | 60 | 78 | 80 | 75 |
| Pectus carinatum | 40 | 44 | 80 | 63 |
| Pectus excavatum requiring surgery | 10 | 11 | 0 | 0 |
| Reduced upper to lower segment ratio | 40 | 44 | 20 | 19 |
| Increased arm span to height ratio | 70 | 11 | 10 | 19 |
| Wrist sign | 90 | 67 | 80 | 81 |
| Thumb sign | 80 | 67 | 100 | 94 |
| Scoliosis of >20° or spondylolisthesis | 80 | 56 | 90 | 94 |
| Severe scoliosis | 60 | 44 | 50 | 44 |
| Reduced extension at the elbows | 20 | 0 | 0 | 13 |
| Medial displacement of the medial malleolus causing pes planus | 30 | 22 | 70 | 69 |
| Heel deformity | 0 | 11 | 10 | 13 |
| Pectus excavatum of moderate severity | 20 | 22 | 40 | 31 |
| Asymetric chest | 40 | 22 | 70 | 44 |
| Joint hypermobility | 70 | 33 | 60 | 63 |
| Highly arched palate with crowding of teeth | 60 | 33 | 70 | 56 |
| Facial appearance | 50 | 22 | 60 | 38 |
| Ectopia lentis | 30 | 11 | 30 | 31 |
| Myopia over 3 diopters | 10 | 11 | 50 | 44 |
| Spontaneous pneumothorax | 0 | 11 | 0 | 13 |
| Striae atrophicae (stretch marks) | 100 | 44 | 70 | 56 |
Types of intervention in Marfan patients
| Name of the sample group | Cardiovascular diagnosis | Number of the patients (female/male) | Percentage of the patients |
|---|---|---|---|
| Acute aortic surgery | Aortic dissection | 10 (6/4) | 22% (10/45) |
| Annuloaortic ectasia | 9 (3/6) | 20% (9/45) | |
| Preventive prophylactic surgery | Prophylactic aortic-root reconstruction | 9 (3/6) | 20% (9/45) |
| No surgery | --------- | 17 (14/3) | 38% (17/45) |
Fig. 1The average STAI (Spielberger’s anxiety) scores of normal patient population and Marfan syndrome patients with acute aortic surgery. The scores of trait anxiety - which determines the predisposition for anxiety - of this group of Marfan syndrome (n = 10) patients, are significantly (p < .01) higher, than the scores of the normal patient population (n = 376. Source: [10])
Fig. 2Complex program of cardiac and psychological examination, consultation and treatment of Marfan syndrome patients. After an aortic-root reconstruction surgery, psychological consultation is recommended alongside cardiac surgical control, and if necessary, psychological treatment. The psychological consultation and control is justified by the high anxiety level experienced in Marfan syndrome patients after life-saving aortic surgery as showed in this study