| Literature DB >> 29040454 |
Thomas Syburra1, Ed Nicol2, Stuart Mitchell3, Denis Bron4, Ulrich Rosendahl5, John Pepper5.
Abstract
Aircrew are responsible for safe and reliable aircraft operations. Cardiovascular disease accounts for 50% of all pilot licences declined or withdrawn for medical reasons in Western Europe and is the most common cases of sudden incapacitation in flight. Aircrew retirement age is increasing (up to age 65) in a growing number of airlines and the burden of subclinical, but potentially significant, coronary atherosclerosis is unknown in qualified pilots above age 40. Safety considerations are paramount in aviation medicine, and the most dreaded cardiovascular complications are thromboembolic events and rhythm disturbances due to their potential for sudden incapacitation. In aviation, the current consensus risk threshold for an acceptable level of controlled risk of acute incapacitation is 1% (for dual pilot commercial operations), a percentage calculated using engineering principles to ensure the incidence of a fatal air accident is no greater than 1 per 107 h of flying. This is known as the '1% safety rule'. To fly as a pilot after cardiac surgery is possible; however, special attention to perioperative planning is mandatory. Choice of procedure is crucial for license renewal. Licensing restrictions are likely to apply and the postoperative follow-up requires a tight scheduling. The cardiac surgeon should always liaise and communicate with the pilot's aviation medicine examiner prior to and following cardiac surgery.Entities:
Mesh:
Year: 2018 PMID: 29040454 PMCID: PMC6019020 DOI: 10.1093/ejcts/ezx346
Source DB: PubMed Journal: Eur J Cardiothorac Surg ISSN: 1010-7940 Impact factor: 4.191
Figure 1:Calculation of the 1% safety rule, from [1, 3].
Figure 2:Monkey in centrifuge: chest X-rays of a chimpanzee undergoing centrifuge testing at + 1Gz, +2Gz, +4Gz and +6Gz. Mediastinal elongation with topographic changes [30].
Follow-up investigations after aortic valve surgery
| Items | Value |
|---|---|
| Prosthetic valve function | Δ |
| Transvalvular flow pattern and in LVOT | Laminar |
| Dimensions of sinus portion and aorta | <4 cm and <4.5 cm, respectively |
| Other heart valves | No pathologies |
| Dimensions of the heart chambers | LVEDD <5.6 cm |
| LV muscle mass, free wall and septum | <1.1 cm |
| LV biplane ejection fraction | ≥50% |
| No rhythm disturbances | 48 h Holter recording |
LV: left ventricular; LVOT: left ventricular outflow tract; LVEDD: left ventricular end-diastolic diameter.
Follow-up investigations after coronary revascularization
| Items | Value |
|---|---|
| Exercise ECG | No myocardial ischaemia |
| No conduction disturbances | |
| Echocardiogram | No dyskinesia, no akinesia |
| LV biplane ejection fraction ≥50% | |
| Holter ECG 24 h | No significant rhythm disturbances |
| After PCI | Myocardial perfusion scan |
| Alternatively: stress echocardiogram | |
| After CABG | Within 5 years of surgery: perfusion scan |
| or equivalent | |
| If any doubt about perfusion | Myocardial perfusion scan |
| Symptoms or signs of ischaemia | In all cases, coronary angiography at any time |
CABG: coronary artery bypass grafting; ECG: electrocardiogram; LV: left ventricular; PCI: percutaneous coronary intervention.
Management of the aortic dilation in relationship to diameter, comorbidities and concomitant surgical procedures
| Diameter (cm) of ascending aorta | Condition | Action |
|---|---|---|
| Any | At the time of diagnosis of Marfan syndrome | TTE then repeat TTE 6 months after to determine the rate of enlargement of the aorta |
| >4.0 | All, asymptomatic | Search for connective tissue disorder |
| Initiate ß-blocker therapy | ||
| Strict blood pressure control <120/80 mmHg | ||
| Moderately restrict physical activity | ||
| Provide pregnancy counselling | ||
| Yearly imaging with TTE and/or CT/MRI | ||
| >4.0 | Bicuspid aortic valve | Yearly imaging with TTE and/or CT/MRI |
| Initiate ß-blocker therapy | ||
| >4.0 | Women with Marfan | Operative treatment: repair aortic root and replace ascending aorta |
| >4.2 by TOE (internal diameter) | Connective tissue disorder | Operative treatment |
| Loeys–Dietz syndrome | ||
| >4.4 by CT/MRI (external diameter) | ||
| TGFBR1/TGFBR2 mutation | ||
| Desired pregnancy | ||
| Family history of aortic dissection | ||
| Growth >0.5 cm/year | ||
| >4.5 | Concomitant aortic valve surgery | Operative treatment |
| <5.0 | In Marfan patients: if maximal cross-sectional area (cm2) of root or ascending aorta divided by patient’s height (m) exceeds a ratio of 10 | Operative treatment |
| >5.0 | Any connective tissue disorder | Operative treatment: repair aortic root and replace ascending aorta |
| Bicuspid aortic valve | ||
| >5.5 | All, asymptomatic | Operative treatment |
CT: computed tomography; MRI: magnetic resonance imaging; TOE: transoesophageal echocardiography; TTE: transthoracic echocardiography.
Management of the aortic arch dilation in relationship to diameter
| Diameter (cm) of aortic arch | Condition | Action |
|---|---|---|
| <4.0 | All | CT or MRI every 12 months |
| >4.0 | All | CT or MRI every 6 months |
| >5.5 | Patients with low operative risk with isolated degenerative or atherosclerotic aneurysm | Operative treatment |
CT: computed tomography; MRI: magnetic resonance imaging.