Long term respiratory morbidity in patients with vascular rings: a review

Abnormalities in position and/ or branching of the aortic arch can lead to a complete or incomplete vascular ring (VR) that encircles and compresses the trachea, the bronchi and/or the oesophagus. Vascular rings (VRs) account for < 1% of congenital cardiac defects [1, 2]. Their real incidence is difficult to establish as the clinical presentations are non-specific and range from early onset of symptoms to asymptomatic clinical setting into adulthood [3, 4]. Though most VRs are isolated, congenital heart defects and chromosomal abnormalities can be associated [5, 6]. Extrinsic airway compression (EAC) and malacia are common complications of vascular rings. Otherwise, tracheal stenosis due to complete cartilaginous rings is found in association with left pulmonary artery sling (LPA sling).

Apparent life-threatening events (ALTE), apnoea, respiratory distress during airway infection and need of intubation, recurrent respiratory infections, barky cough, stridor, wheezing, and dyspnoea on exertion are all symptoms affecting patients with airway compression, associated malacia and tracheal stenosis due to VR [7]. Additional symptoms such as failure to thrive and dysphagia are reported in patients with oesophagus compression [8]. When prenatal diagnosis is not available and reported symptoms are suspicious for EAC by VR, a complete diagnostic workup should be considered by clinicians [9].

Vascular rings

Due to the strong relationship of the thoracic vascular structures with the trachea and bronchi, any anatomic variation leading to complete or incomplete VR [Table 1] may produce several grade of EAC that appears typically pulsatile and located in characteristic positions [10].

Table 1 Type of vascular abnormalities of the aortic arch leading to airway compression

As reported by recent studies, right aortic arch (RAA) with aberrant left subclavian artery (ALSA) is the most common complete VR [7, 11,12,13], followed by double aortic arch (DAA) [7, 14]. Innominate artery (IA) compression accounts 3 to 20% of cases of incomplete vascular ring, followed by left pulmonary artery (LPA) sling [15]. Less common complete VR subtypes are: RAA with mirror-image branching (MB), and retro-oesophageal course of the left- sided arterial duct between the right-sided descending aorta and the left pulmonary artery; circumflex retro-oesophageal aortic arch, and left aortic arch (LAA) with aberrant right subclavian artery (rSa) when the arterial duct is right-sided (RLA) [16].

Among all patients with RAA, a total of 65% of them have a true vascular ring due to the presence of a retroesophageal left subclavian artery with a left ligamentum arteriosum (LLA) [Fig. 1] [17]. The aneurysmal dilatation at the base of the left subclavian artery is known as Kommerell diverticulum (KD), that can be an independent cause of airway compression when enlarged > 1.5 times the diameter of the subclavian artery [18, 19]. The division of the ligamentum arteriosum allows to free the trachea from the ring, giving relief of airway compression and promoting the normal development of tracheal cartilage. When dissection of KD is necessary, translocation of the aberrant left subclavian artery is also performed [19].

Fig. 1figure 1

3D volume rendering reconstruction of a cardiac CT in patient with Right Aortic Arch (RAA) and Aberrant Left Subclavian Artery (ALSA). The vascular structures together with the left duct ligament (not visible on CT) completely encircle the trachea (in blue) and the oesophagus (in violet). Panel A: front view. Panel B: back view. Panel C: trachea with the narrowing (red arrow) at the level of the ring

DAA [Fig. 2] with dominant right arch (80%), or dominant left arch (10%), or balanced arches (10%) [17] is a true vascular ring that accounts about 30 to 45% of all VRs [20]. The smaller of the two arches, or the atretic arch, should be divided [21].

Fig. 2figure 2

3D volume rendering reconstruction of a cardiac CT in patient with Double Aortic Arch, constituted by a dominant right aortic arch (RAA) and a diminutive Left Aortic Arch (LAA). The vascular structures together completely encircle the trachea (in blue) and the oesophagus (in orange). Pulmonary artery in violet. Panel A: front view. Panel B: back view

LPA sling is a rare vascular anomaly where the LPA does not arise from the pulmonary trunk but takes its origin distally from the posterior aspect of the right pulmonary artery [Fig. 3]. The LPA then makes a turn to the left, and courses toward the left lung passing between the lower trachea and oesophagus. Therefore, a vascular sling is formed around the right side of the trachea. The arterial duct, or its ligament, connects the pulmonary trunk to the descending aorta on the left side of the trachea, completing the vascular ring. The sling is almost always associated with an airway anomaly.

Fig. 3figure 3

3D volume rendering reconstruction of a cardiac CT in patient with Left Pulmonary arterial sling. The Left Pulmonary Artery (LPA) arises posteriorly and distally from the Right Pulmonary Artery (RPA), coursing posteriorly to the trachea (T). A tracheal bronchus (commonly associated to LPA sling) is also detected (red arrow)

LPA sling sometimes can lead to right lung hyperinflation [17]. Tracheal stenosis due to complete cartilaginous rings is detected in 75% of patients affected by LPA sling [3] and is often responsible of the poor prognosis of this vascular abnormality. Surgical repair with LPA reimplantation and slide tracheoplasty is required and the mortality and morbidity rate are directly related to the extent of the tracheal stenosis [3].

The innominate artery compression syndrome cannot be considered a true vascular ring because the trachea is crossed and compressed anteriorly (from the left to the right) by the IA rising abnormally from the aorta on the left side of midline and coursing rightward in front of the trachea [3]. The suspension of IA is indicated when there is the evidence of more than 80% compression of the tracheal lumen by bronchoscopy [3].

The mere presence of a vascular ring is not an indication in itself for surgical intervention. It is important to know that symptoms in small children may disappear as the child and chest cage grow. It is generally accepted, however, that surgical intervention should be undertaken if the patient is symptomatic, and or in presence of significant compromise to the airways. Unnecessary delay may cause further tracheobronchial damage, leading to chronic compromise of the airways, with poor outcome in term of symptoms relief even after the correction [3, 5, 16].

Some Authors advocate that the decision for surgery should be based on the severity of symptoms and not just the degree of airway compression [22]. Indeed, Myer and colleagues [23] included reflex apnoea, failure of medical management of severe respiratory distress after 48 h, and prolonged intubation among absolute criteria. At a later time, recurrent tracheobronchitis or bronchopneumonia, exercise intolerance, dysphagia, or failure to thrive with associated subglottic stenosis, asthma, cystic fibrosis, or prior tracheoesophageal fistula repair were considered relative criteria [10].

Very recently, Said and Biermann confirmed in two different papers the indication to treat surgically all complete VRs (DAA, RAA with LLA, LAA with RLA) and LPA sling, reserving surgery to symptomatic incomplete VRs or those without symptoms and associated cardiac defects [12, 19].

Respiratory symptoms

Most of the patients with complete VRs and LPA sling have respiratory symptoms that often occur early in life (1 – 6 months), becoming progressive with the growth of the intrathoracic structures. However, significant tracheal compression may be present in infants even without symptoms [3, 24].

Clinical manifestations vary with the severity of encroachment on the trachea, bronchus or oesophagus by the abnormal vascular structures. The severity of compression not only depends on the type of anomaly, but is also related to the size and shape of the thoracic cage enclosing the vascular structures and airway [16].

Symptoms vary from apnoea and cyanosis to stridor, barky cough, wheezing, shortness of breath and dysphagia especially for solid food [2, 3, 7, 10, 12, 25]. In addition, because the tracheal compression impairs the muco-ciliary clearance leading to the stagnation of secretions, patients and their parents report history of chronic cough poor response to medical treatment, recurrent bronchopneumonia, fatigue during physical exertion and need of invasive respiratory support during respiratory exacerbation in the most severe cases [26]. Reported symptoms usually become evident during expiration, when the intrathoracic pressure (Ppl) overcomes the intratracheal pressure (Ptr), leading to the worsening of airway narrowing [10]. Symptoms’ worsening is explained by Bernoulli’s principle, according to which the increase in the speed of a fluid occurs simultaneously with a decrease in pressure in the point where the channel narrows [Fig. 4].

Fig. 4figure 4

Effect of intrathoracic pressure (Ppl) variation on tracheal lumen during a) inspiration and b) expiration phases. Ppl overcomes intra-tracheal pressure (Ptr) during expiration, leading to the lumen collapse (black arrows)

Because the described clinical picture is often misinterpreted as laryngomalacia, bronchiolitis, asthma, and gastroesophageal reflux, clinician should keep in mind the possibility of a VR in children with recurrent respiratory symptoms with or without digestive symptoms and poor response to medical treatment [27,28,29,30].

Respiratory functional assessment

In addition to the clinical history, spirometry should be considered as non-invasive, fast, and available easily test in children aged over 6 years. It can help the physician to support the initial suspicion showing the abnormality of the flow-volume curve shape. Indeed, the diminished expiratory flow in the initial phase followed by an upward deflection and then the continuation of exhalation on the flow-volume curve is indicative of intra-thoracic obstruction [Fig. 5]. The notch, not variating after inhaler short bronchodilator administration, reflects the sudden diminution of flow at the beginning of expiration when the compressed airway collapses [31].

Fig. 5figure 5

Maximal expiratory flow-volume curve in a patient with complete vascular ring (RAA with mirror image branching and LLA). Note the flattening of the proximal portion of the expiratory flow-curve due to the external compression/tracheomalacia that affects to expiratory flow rates in the large airways but not in the peripheral ones. FEV1 2.12 L (85%), FVC 3.00 L (102%), FEV1/FVC 83%, FEF25-75% 1.82 L/s (65%)

Because spirometry provides a static measure of lung function, it doesn’t evaluate the respiratory abilities to perform exercise, which is considered very important in the psychological and physical development of children and adolescents. Therefore, the exercise challenge test is helpful to reproduce exercise induced symptoms reported by patient [32], giving a complete idea of the clinical situation. The test should be obviously suitable for the patient’s age (step test, six-minutes walking test, exercise test on treadmill or cycle ergometer). Because it can help to identify and quantify the limitations during exercise, the derived information can be helpful for the therapeutic choice which may include a conservative or not attitude [33]. Moreover, clinician may use both static and dynamic lung function tests during the post-operative period to monitor the obstructive pattern and detect the resolution of airflow limitation.

Diagnostic assessment of airway compression/collapse

VR can be accurately diagnosed by fetal ultrasound improving prognosis in these patients, as it enables proper timing of additional postnatal investigation and surgery [11]. Chest x-ray is not routinely recommended to diagnose VR, even though it can be useful to show the location of the aortic arch in relation to the trachea [34]. Both diagnostic tests are not able to study the impact of the vascular abnormality on airways, therefore additional investigations should be considered.

Computed tomography with angiography (CTA) is an important tool that has currently replaced barium contrast esophagogram as it allows a careful simultaneous assessment of vascular abnormalities and airway involvement [35]. In addition, dynamic image analysis during a complete respiratory cycle (inspiration and expiration) provides a fully evaluation of the airway collapse that shows a high correlation with the degree of respiratory impairment [36, 37]. Endoluminal volume rendering also allows virtual tracheobronchoscopic demonstration of the airway.

CTA is most widely used compared to magnetic resonance imaging (MRI) because of its fast scanning time, enabling to perform the investigation without sedation/anesthesia even in very small and uncooperative children, and the ability to thoroughly assess the airway [38]. Nevertheless indication to CTA investigation must be carefully assessed, valuing risk/benefit ratio, since radiation exposure remains a major concern [38]. Flexible laringotracheo-bronchoscopy performed under light sedation and spontaneous breathing allows the dynamic evaluation of the tracheobronchial tree, revealing the localization, extension and the estimation of the airway malacia severity [10]. This exam is often the first investigation performed in children effected by persistent stridor or recurrent respiratory symptoms despite medical treatment. The finding of a pulsatile narrowing raises the suspicion of vascular compression and requires further examinations defining the underlying vascular abnormality and the degree of airway compression. The spatial location of compression detected on flexible bronchoscopy can suggest the type of VR that in any case must be confirmed with imaging: right aortic arc (RAA) usually compresses the right posterior distal trachea; double aortic arch (DAA) usually compresses the right anterior and posterior distal trachea; LPA sling usually causes compression of the right anterior distal trachea and right mainstem bronchus as well as the posterior trachea; innominate artery compression usually presents as anterior mid-tracheal compression [10]. Differently, once the diagnosis has already been made, airway endoscopy represents a complementary exam to be performed during correction to verify the efficacy of surgical manoeuvre [39].

Unfortunately, there are no guidelines on the better diagnostic work up for children suspected of VR. However, it’s reasonable that children with history of recurrent respiratory symptoms poor response to medical treatment, symptoms and physical examination of airway obstruction, dysphagia, and failure to thrive should undergo to flexible laryngo-tracheo-bronchoscopy to assess for laryngomalacia, vocal fold mobility, tracheal stenosis or malacia [40]. The compression or collapse of 33% or less of the tracheal length is considered suggestive of extrinsic compression, while intrinsic tracheomalacia is considered when more of the trachea (> 33%) is involved [10]. In addition, the detection of compression of the right anterior and posterior tracheal walls or mainstem bronchus is considered indicative of complete VRs or pulmonary artery sling for which other imaging investigations are required. The grade of tracheal lumen reduction on flexible bronchoscopy (FBs) is another factor to consider when choosing whether to perform additional investigations. Indeed, the patient should undergo a chest angio-CT or MRI when anterior or posterior tracheal compression greater than 50% is found. When less than 50% of tracheal collapse id observed, the decision to make CTA or MRI to avoid misdiagnosis should be based on reported symptoms [10].

Long term respiratory outcomes

Morbidity and mortality in patients after surgical correction have been reported to a greater extent, in those with respiratory distress at presentation, underlying genetic condition, associated congenital tracheal stenosis or severe bronchomalacia, tetralogy of Fallot with absent pulmonary valve syndrome, underlying complex cyanotic heart disease and need of early respiratory support [7].

Since obstructive respiratory symptoms may persist for weeks or months after surgical intervention, a careful respiratory evaluation is required both in the short and long-term period. Anyway, it should be considered that symptoms’ persistence depends on timing and technique of surgical correction as well as the presence of residual malacia.

Studies describing respiratory symptoms trend after surgery correction are quite scarce, and reported follow up period ranges between six months and eleven years [2, 12, 14, 25, 26, 41,42,43,44,45,46,47,48,49]. A review of scientific literature was carried out using PubMed. The search was limited to the paediatric age. The search terms “respiratory outcomes” and “vascular rings” were used, and only English language articles were selected. The search resulted in 43 articles from 1992 to present; all titles and abstracts were reviewed. Only fourteen met our goal of assessing the course of symptoms after treatment [Table 2].

Table 2 Papers reporting long term respiratory outcomes in symptomatic children affected by VRs

Chun and colleagues evaluated the outcomes of 37 survivors affected by VRs. None of these patients required prolonged ventilatory support or tracheostomy in the short term. Respiratory arrest, pneumonia and pneumothorax were recorded among respiratory complications immediately after surgery. Median length of follow-up of survivors was 12.5 months. Five patients were lost in the follow up; 12/32 were asymptomatic and 15/32 had mild respiratory symptoms at 6 months to 1 year after repair [41].

Bonnard et al. described their experience on 62 children affected by VRs. Authors reported a complete improvement in 68%, a partial improvement in 17%, and no improvement in 15% of cases after intervention, followed up for a mean period of 37.4 months (range 12 to 159 months) [2].

Respiratory sequelae were also retrospectively examined by two different groups of researchers belonging to the same institution. Despite a small difference in the sample size, Authors reported a good trend of respiratory symptoms during a period of nearly 2 years with symptoms resolution in more than 70% of patients [42,

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