Hypertension after coarctation repair—a systematic review

Abstract

Background

Coarctation of the Aorta (CoA) leads to increased morbidity and mortality later in life despite early surgical or percutaneous treatment. Many long-term complications are related to hypertension (HT) which is a common finding late after coarctation repair.

Methods

A systematic Review was performed including articles published between February 2012 to December 2020. Systematic searches were conducted on PubMed and the Cochrane Controlled Trials Register to look for studies on HT after aortic CoA-repair. PRISMA guidelines were used.

Results

In this systematic review on HT after CoA Repair the mean prevalence of HT was 47.3% (20–70%). A progressive character was of the HT was found, furthermore if only studies are included with 24 h blood pressure (BP) recording in addition to standard BP measurements, the incidence of HT rose to 57.8%.

Discussion

Most clinical studies look at complications, mortality rate and residual pressure gradient rather than correlating hemodynamic indices with long-term outcome. Although HT is commonly based in measurement of peripheral BP, it has been shown that peripheral BP in CoA patients has a poor correlation with central aortic pressure. Central aortic hemodynamics are significantly altered in patients with repaired CoA, which can now adequately be investigated non-invasively. At the present time there are no studies linking long-term outcome with abnormal central hemodynamics.

Introduction

Coarctation of the Aorta (CoA) comprises approximately 5–8% of all structural congenital cardiac lesions. It occurs three times more commonly in males than females. CoA still leads to increased morbidity and mortality later in life despite early surgical or percutaneous treatment. Many long-term complications are related to hypertension (HT) which is a common finding late after coarctation repair.

Improved treatment and surveillance have shifted the emphasis from short-term to long-term outcome (1). Since the last systematic review on HT after CoA published in 2013 by Canniffe et al. (1), important new evidence has emerged on this topic. We therefore revisited a systematic review on HT after CoA Repair based on findings from 2012 to 2020, with additional focus on pathophysiology. The role of specific hemodynamic indicators of long-term outcome is currently not well understood. We touch on this subject with a brief discussion on ways of assessing central hemodynamics non-invasively. The objective of the systemic review was therefore to establish what has changed since the last systematic review on the topic and to assess whether novel ways of measuring central aortic hemodynamics have been incorporated into studies documenting HT after CoA repair.

The holy grail would be to identify preliminary signals of potentially harmful pathophysiologic changes, to find treatments that prevent the cascade ending towards established HT. In this way long-term complications related to HT in CoA patients might be anticipated.

We present the following article in accordance with the PRISMA reporting checklist (available at https://tp.amegroups.com/article/view/10.21037/tp-21-418/rc).

Methods

A systematic review on the subject of HT after CoA-repair was performed, with emphasis on articles published in the English language from February 2012 until December 2020. PRISMA guidelines (preferred reporting items for systematic reviews and meta-analysis) were used. Systematic searches were conducted on PubMed and the Cochrane Controlled Trials Register to look for studies on HT after aortic CoA-repair. No restrictions were applied to the status of publication other than the above-mentioned elements. Search Terms were HT, blood-pressure, coarctation repair, coarctation surgery, percutaneous treatment of coarctation, coarctation stenting, age-at-repair, and pathophysiology.

Inclusion and exclusion criteria

The novel data of this review was compared to these of the systematic review retrieved from 1987 to 2012 (1), based on the use of identical inclusion criteria. Studies were only included when blood pressure (BP) was an outcome measure after coarctation repair. CoA-repair could be either surgically or via catheter-based interventions. Studies also needed to be randomized controlled trials or case-controlled or cross-sectional studies yielding at least 35 patients. Observational studies were included if the study population comprised more than 120 study subjects, with more than 20 years follow-up. The paper of Meijs et al. (2) was excluded for comparison as this meta-analysis investigated the effect of stent therapy on BP changes in the short and medium term, rather than the incidence and prevalence of HT after treatment in the long term.

A PubMed search for articles on CoA initially led to 12,405 articles (Figure 1). Limiting the search to articles published since February 2012, retained 5,905 articles. By excluding duplicates, case reports and systematic reviews the total was brought to 1,913 articles. Of these, abstracts were read to eliminate inappropriate studies. This reduced the total to 358 articles requiring the reading of the full text to ascertain whether the inclusion criteria were fulfilled. Of the 358 articles, 352 were obtained via institutional online access. The remaining full texts were requested via our library, but only 4 published in English were used. After consulting the full content of these 356 articles, only 17 fulfilled the inclusion criteria as set out above (3-19) (Table 1).

Figure 1.

Initial screening. *, PubMed, Cochrane Controlled Trials Register; **, records were excluded by a human not with any automation tools, except limiting by year of publication; no Controlled Trial had long-term BP data and/or included HT as an outcome measure; therefore all 117 trials were excluded; ***, 2 reports were not in English and were excluded. For more information, visit: http://www.prisma-statement.org/. BP, blood pressure; HT, hypertension.

Table 1. Articles meeting inclusion criteria.

Author	Group	Standarized def. HT	Follow-up (in years)	Age at surgery	24 h BP	Exercise test	Re-CoA or HAA data (%)	HT (%)	Surgery (%) vs. percutaneous	BAV (%)
Bambul Heck (4)	273	Yes	31.4 (14.1–39.9)	9.7 (0–56)	Yes	Yes	–	70	100	48
Brown (5)	819	Yes*	17.4±13.9	17.2±13.6	No	No	–	40 to >70**	100	–
Chen (6)	247	Yes	5.9	S: 6 (0–55), I: 25 (0.5–64)	No	No	31 re-CoA, 25.9 HAA	69.6	81	56
Choudhary (7)	151	Yes	26±13	5 (0–10)	No	No	31 re-CoA	44	Mixed	66
Dijkema (8)	206	Yes	12.5	0.1 (0–17)	No	No	21 HAA	20	86	39
Egbe (9)	546	Yes	Age 33±9	–	No	Yes	–	60	87	57
Giordano (10)	148	Yes	13.3±4.5	0.4 (0–11.8)	Yes	Yes	–	44	100	–
Lee (11)	834	Yes	27 [18–36]	3 (0.1–15)	No	No	59 re-CoA	57	83	58
Lillitos (12)	87	Yes	1.9 (0–9)	0–5.6**	No	No	15 re-CoA	7–40**	100	–
Luitingh (13)	41	Yes	13±3	0.03 (0.02–0.1)	Yes	Yes	32 HAA	39 (12 on exercise test)	100	61
Martins (14)	75	Yes	9–12**	S 6 [1–26], BD 5 [1–17], ST 15 [7–26]	Yes	Yes	–	30 S, 39 BD, 45 ST	Mixed	79 S, 45 B
Mery (15)	343	Yes	12 (0.5–19)	0.1 (0–0.75)	No	No	33 HAA	33	100	–
Rinnström (16)	653	Yes	27.4±12.8	9.5±11	No	No	49 re-CoA	52.7	94	–
Róg (3)	58	Yes	20.39±9.8	8.7±8.6	Yes	Yes	39 re-CoA, 46 HAA	48.3	86	62
Sendzikaite (17)	90	Yes	8.5 (6–11.8)	0.4 (0.05–2)	Yes	No	–	46.7	71	54
Smith-Parrish (18)	160	Yes	14 (4.6–36.7)	–	No	No	–	22–38**	86	–
Wu (19)	2,295	Not stated	Age 18–60	–	No	No	–	34.5	–	–

*, including self-reported HT; **, data divers in cohorts. HT, hypertension; BP, blood pressure; CoA, coarctation of the Aorta; HAA, hypoplastic aortic arch; BAV, bicuspid aortic valve; S, surgery; B, balloon dilatation; I, interventional treatment; BD, balloon dilatation; ST, stent.

The Cochrane Controlled Trials Register was searched for trials reporting on CoA, using BP as an outcome measure. One hundred seventeen trials were initially identified but only one article had data on long-term CoA outcome (20). The paper of Pádua et al. reported on the efficacy of surgery versus stenting as best treatment of CoA. As HT was not a specific outcome measure, this publication was not included (20).

Data extraction

One single reviewer extracted all data independently. The acquired information considered BP, HT, age-at-repair, type of repair, duration of follow-up, control group data, vascular measurements, aortic arch geometry, journal, year of publication and first author.

Results

Standardized definitions

All studies used as definition for HT a value of ≥140/90 mmHg or >the 95^th percentile in children. In the previous review by Canniffe (1), the definition of HT was not standardized across articles yet.

24 h BP was measured in some studies but there was no standardization of the type of BP devices. Significant differences have been shown when using two different 24 h BP devices (21).

Medication for HT confounded the results. Some patients were identified as having HT if they were taking medication for HT, even with normal BP measurements, for example by Bambul Heck et al. (4). Furthermore, it is possible that some antihypertensive medications were started for an indication other than HT, with insufficient data in the studies to test this hypothesis. Mery et al. (15) noted that the usage of cardiac medications for other cardiac conditions might have influenced BP.

BP phenotypes, as outlined in the 2016 European Society of Hypertension guidelines (22), were not routinely categorized. Sendzikaite et al. (17) did find that isolated systolic HT was the dominant phenotype in CoA patients.

The definition of re-CoA used was an invasive gradient of 20 mmHg, however this gradient was estimated in various ways. In some studies, re-CoA was diagnosed by echocardiography (15), in others via magnetic resonance imaging (MRI) (6,9,11) or clinically measuring a non-invasive BP gradient (16).

The definition of exercise induced HT was systolic blood pressure (SBP) >200 mmHg, however Luitingh et al. identified a cut-off of 190 mmHg as a more suitable value to identify those with HT in children (13).

Prevalence of HT in CoA

The mean prevalence of HT in this systematic review was 47.3% (range, 20–70%). However, the prevalence was as low as 7% in a specific cohort (12). In a previous review Canniffe et al. found a prevalence of 32,5% (range, 25–68%) (1).

There is a progressive character to HT after CoA repair. In a study by Bambul Heck et al. (4), a group of 273 patients were studied previously (COALA study) and re-assessed 14 years later. All patients had ambulatory 24 h BP measurements. In this study, 23% of patients were found to have HT with 25% taking anti-hypertensive drugs initially. 14 years later 53% of the same patient group were found to have HT with nearly half receiving antihypertensive medication. Furthermore, the studies with the longest follow-up found the highest incidence of HT (5,7,9,16,17).

Influence of re-CoA

HT developing in CoA patients without documented residual narrowing was not viewed separately from those with residual obstruction. A limitation in extracting BP data from these studies is that in most cases the BP data does not differentiate between those with re-CoA and those without. Some studies report on the incidence of re-CoA or hypoplastic arches, but failed to separate the BP data. However, Choudhary et al. (7) and Chen et al. (6) found no clear correlation in the prevalence of HT in those with and without re-stenosis.

24. h BP

24 h BP was performed in 6 studies (3,4,10,13,14,17). It is interesting to note that Luitingh et al. compared the incidence of HT in patients at rest, after 24 h BP recording and during exercise (13). They found that of the 41 patients, 5% showed resting HT while 39% had HT on 24 h BP measurements. As expected, a higher prevalence of HT was found if 24 h BP registration was performed but no additional cases were identified by exercise testing. If only studies are included recording 24 h BP recording in addition to standard BP measurements, the incidence of HT rises to 57.8%, which is 10% higher compared to only standard BP measurement.

Exercise testing

Exercise Tests were performed in 6 studies (3,4,9,10,13,14). Luitingh et al. found an overall reduced exercise endurance in CoA patients compared to the control group (13). The mean SBP at peak exercise was higher in the coarctation population (164±26 vs. 148±19 mmHg, P=0.003). Five of the 41 (12%) coarctation patients had a peak exercise SBP >200 mmHg and were therefore considered to have exercise-induced HT, although they went on to propose a cut-off value of >190 mmHg in children. Róg et al. found lower values of peak VO₂/kg, heart rate peak and % max heart rate (HR) in CoA patients during exercise testing compared to controls (3). They postulated that most of the findings were due to chronotropic incompetence.

Other factors influencing HT

Age at repair was the main determinant of HT in various studies, with older age at repair being associated with an increased incidence of HT (5,7,12,17), but not in the studies of Bambul Heck et al. (4) and Rinnström et al. (16).

The type of repair was also found to be important. Giordano et al. (10), compared a group of patients with isolated CoA (148 patients) with patients having CoA as part of a complex congenital heart disease (CHD) (87 patients). Although patients with isolated CoA were significantly younger, they had a markedly higher incidence of HT (44% vs. 24%). They postulated that in the complex CHD group, the incidence of HT was lower because the aortic repair was more effective than in those with isolated CoA, possibly due to less residual aortic arch hypoplasia through aortic arch enlargement with a pulmonary homograft patch. Martins et al. failed to demonstrate that the type of repair was predictive for vascular function differences and HT when comparing surgery vs. balloon dilatation (BD) vs. stents (14).

Patients treated in different eras were compared by Dijkema et al. (8). They now favor enlarging the transverse arch, as it has been shown that catch-up growth of arch hypoplasia after end-to-end anastomosis does not always occur (23).

Obesity was studied as a separate outcome measurement by Smith-Parrish et al. in a cross-sectional study involving coarctation patients (18). They found an alarming and increasing prevalence of obesity of 26% at the age of 10 years, and 63% at the age of 20 years. There was good correlation between obesity and HT in their study. Rinnström et al. (16) also revealed an association between HT and obesity.

The increased risk of a cerebro-vascular accident (CVA) after coarctation repair was found to be three-fold, with HT the single best predictor of CVA [Wu et al. (19)].

Arterial hemodynamic factors

Pulse wave velocity (PWV) is commonly used to assess vascular hemodynamics in the clinical setting. It mainly assesses aortic stiffness. Luitingh et al. found a significantly higher PWV in CoA patients compared to controls (13). However, carotid artery distensibility and arterial stiffness index were similar in both groups. Carotid intima media thickness (IMT) was also measured and found to be significantly raised in CoA patients even without HT (3). In a multicenter, cross-sectional, observational comparison of vascular function in CoA patients, Martins et al. (14) found that major vascular outcomes (prevalence of HT, global aortic stiffness, central BP and endothelial function) were similar in CoA patients treated with BD, stenting or surgery. Through segmental assessment of PWV and distensibility measures by cardiac magnetic resonance (CMR) they revealed that proximal aortic stiffness was lowest in the BD patients and highest in the stenting group.

Cardiac hemodynamic factors

Selected studies measured left ventricle (LV) hemodynamic factors, usually systolic and sometimes diastolic LV function with echocardiography (4,9,13,17). Martins et al. looked at LV mass, usually derived from echo-measurements (14). There was an important prevalence of left ventricular hypertrophy (LVH) in the absence of HT. Sendzikaite et al. found a similar proportion of LVH in normotensive (31%) and hypertensive patients (33%) with repaired CoA (17). Chen et al. measured LV function and mass with CMR (6). They found a strong relation between an increased LV mass and the risk of hospitalization. Egbe et al. looked at LV diastolic dysfunction and found that the aortic isthmus ratio (ratio of the aortic isthmus diameter to the descending aorta diameter at the level of the diaphragm ≤0.5) had a strong correlation with diastolic dysfunction and exertional symptoms (9).

Discussion

Despite successful treatment of aortic CoA, long-term morbidity and mortality remains higher in this patient population compared to controls. Frequent problems found in the long-term follow-up of these patients are early onset of cardiovascular diseases like myocardial infarction, cardiac failure, stroke, and even sudden death, often in the setting of arterial HT. The incidence of HT found in this systematic review, is high at 47.3%.

Various factors influence the development of HT. Cohen and colleagues already reported in 1989 that the most important determinant of long-term survival and HT in CoA patients was the age of patients at the time of the initial repair (24). This finding was confirmed in many studies (5,7,12,17), except for a few recent studies (4,16). Rinnström et al. followed up patients during 3 decades after CoA repair and found that the age at intervention was less important than the age at follow-up, postulating that the beneficial effect of early repair might eventually wear off as patients age (16).

In general, HT is based on measurement of the peripheral BP, being the simplest measure of afterload. However, peripheral BP can deviate from central aortic pressure in patients with repaired CoA, limiting thereby its value in assessing properly the vascular and cardiac hemodynamics after CoA repair (25).

Already in 1971, O’Rourke and Cartmill suggested that morbidity in CoA patients was related to abnormal hemodynamics and vascular biomechanics (26). Recent developments in experimental and computational methods seem to support this theory (27). Factors contributing to an increased LV afterload are (I) a residual narrowing leading to additional resistance and (II) a less distensible aorta interfering with the buffer function of the aorta. The proximal aortic wall in patients with repaired CoA has been shown to have different histology, containing more collagen, less elastin fibers, and less smooth muscle cells. Compliance and distensibility of the aorta are therefore impaired in comparison with healthy individuals. Schäfer et al. found increased stiffness of the ascending aorta on MRI after CoA Repair with higher central aortic BP (28).

Central aortic pressure can be predicted by using the descending aortic distension waveform as a substitute for the pressure waveform and by scaling it to the measured brachial pressure in a fluid-structure interaction (FSI) (29). Quail et al. demonstrated the ability to assess central aortic SBP (c-SBP) non-invasively using a combination of phase-contrast magnetic resonance and oscillometric brachial artery BP (30). They also showed that it was possible to use the same high temporal-resolution phase-contrast magnetic resonance data to perform non-invasive wave intensity analysis (WIA) in patients with repaired CoA. Using this technique, the central aortic pressure was significantly higher in patients with repaired CoA compared to controls (30). Patients with repaired CoA had reduced total arterial compliance, increased pulse wave velocity, and larger backward compression waves, resulting in a higher left ventricular mass (LVM) index. The magnitude of the backward compression waves was independently associated with variation in LVM (31). Egbe et al. also showed that SBP may underestimate LV afterload after CoA repair since CoA patients have a higher arterial afterload compared with controls, even with similar SBP (25,32).

Recently abnormal diastolic LV function on echocardiography was shown to be related to proximal aortic elasticity (33,34). The authors postulated that in children who had a successful CoA repair very early in life, persistently elevated aortic stiffness may lead to diastolic impairment. We also found decreased diastolic LV function in children with repaired CoA, despite early repair and absence of residual stenosis (35). It has long been proposed that (early) arterial reflection waves generated by scar tissue at the repair site or by a stent leads to a new pressure wave reflection, generating LVH, considered as an adaptive response to maintain wall stress. Histologically cardiomyocyte size and density increase and fibrosis ensues. This leads to changes in the viscoelastic properties and results in increased LV filling pressures. This is clinically translated in the development of LVH, regardless of HT in CoA patients (17).

We showed in an experimental animal study that despite adequate relief of aortic coarctation, the Ventricular-Arterial (VA) hemodynamic relationship is compromised, depending on the sequelae of aortic treatment varying from a short residual stenosis to long non-stenotic aortic stiffening as by aortic stenting. Moreover, the impaired VA coupling is enhanced after inotropic stimulation, suggesting that the ventricular adaptation to the altered vascular dynamics may be underestimated, becoming unmasked during exercise. Although the therapeutic approach aims for complete elimination of the transaortic pressure gradient, the impact on other components of aortic hemodynamics or LV function often remains unsolved (36).

The role of specific hemodynamic indicators of long-term outcome is currently not well understood and unfortunately, none of the included studies assessed aortic and ventricular hemodynamics comprehensively by using currently available techniques, like the MRI-based assessment demonstrated by Quail et al. outlined previously (30). It would have been interesting to correlate these comprehensive parameters of central aortic hemodynamics with long-term outcome, but so far, such studies are lacking.

Most of the clinical studies on CoA look at complications, mortality rate and residual pressure gradient rather than correlating hemodynamic indices with long-term outcome (2,5,20,24,37,38). In this systematic review, many of the included studies only briefly touch on the underlying vascular mechanisms involved in the pathophysiology of HT (as can be seen in Table 2), with one exception where detailed vascular function was compared in three groups of CoA-repair (14). The relevance of the hemodynamic factors can be divided into arterial- and cardiac components. Various studies tried to assess arterial hemodynamic factors with PWV, carotid IMT, endothelial function, aortic distensibility and, in one study, with central BP (14). Ventricular function was assessed with echocardiographic and occasionally CMR measurements of systolic and diastolic function, degree of LVH and exercise testing with metabolic measurements.

Table 2. Data acquisition from the included articles to investigate the etiology of HT after CoA-repair.

Author	Group	Patho-physiology of HT investigated?	Assessment central hemodynamics?	Assessment of arterial factors?	Assessment of cardiac factors?	Assessment of 3D aortic arch?	Retrospective data such as age at Rx and type of Rx
Bambul Heck (4)	273	No	No	No	No	No	Yes
Brown (5)	819	No	No	No	No	No	Yes
Chen (6)	247	Yes	No	Only anatomical data MRI	LV syst fx (MRI)	No	Yes
Choudhary (7)	151	No	No	No	No	No	Yes
Dijkema (8)	206	No	No	No	No	No	Yes
Egbe (9)	546	Yes	No	Only anatomical data, CT/MRI	LV diast fx, LV mass (echo)	No	Limited data
Giordano (10)	148	Yes	No	No	LV mass, LV syst and diast fx (echo)	No	Yes
Lee (11)	834	No	No	No	No	No	Yes
Lillitos (12)	87	No	No	No	No	No	Yes
Luitingh (13)	41	Yes	Partially via carotid echo	Yes, carotid IMT, stiffness and distensibility, PWV	LV syst fx, LV mass (echo)	No	Yes
Martins (14)	75	Yes	Yes, but not comprehensively	Aortic stiffness (applanation tonometry, MRI, PWV), endothelial fx (endo-PAT), biomarkers enothelial fx	LV mass, LV syst fx (MRI)	Yes	Limited
Mery (15)	343	No	No	No	No	No	Yes
Rinnström (16)	653	Yes with BMI	No	No	No	No	Yes
Róg (3)	58	Yes	Partially via carotid echo	Anatomical data (echo), carotid IMT	LV mass, LV syst fx, LV diast fx (echo)	No	Yes
Sendzikaite (17)	90	Yes also BMI	No	No	LV mass (echo)	No	Yes
Smith-Parrish (18)	160	Yes with BMI	No	No	No	No	Yes
Wu (19)	2295	No	No	No	No	No	Yes

HT, hypertension; CoA, coarctation of the Aorta; MRI, magnetic resonance imaging; LV, left ventricle; CT, computed tomography; diast, diastolic; echo, transthoracic or transoesophageal; syst, systolic function; IMT, intima media thickness; PWV, pulse wave velocity; PAT, peripheral arterial tone; BMI, brain natriuretic peptide.

Aortic arch morphology has been found to contribute to abnormal vascular remodelling various studies, with a gothic arch having the greatest effect, Quail et al. showed recently in an MRI based study that while there are many variations in 3D aortic shape after coarctation repair, there was only a modest association between variation in aortic radius and pathological wave reflections, but not with 3D curvature. This suggests that 3D shape is not the major determinant of vascular load following coarctation repair, calibre being more important than curvature (31). It is known that Aortic size mismatch between the ascending and descending aorta (DAAo/DDAo) can be predictive for exercise intolerance in repaired coarctation (39).

Finally, we must not forget that factors leading to HT unrelated to the heart or the aorta itself have also been identified. As an interesting example, Rodrigues et al. showed that vertebral artery hypoplasia (VAH) with an incomplete posterior circle of Willis (ipCoW) led to an increase in cerebrovascular resistance before the onset of increased sympathetic nerve activity in borderline hypertensive humans (40). To increase cerebral blood flow, BP had to rise, leading to the description “the selfish brain”. They found that CoA patients were 5.8 times more likely to have VAH + ipCoW than controls, as identified by MRI.

Conclusions

1. The prevalence of HT after CoA-repair is substantial and progressive, and higher than previously reported by Canniffe et al. (1).

2. Routine 24 h BP measurement is recommended in the follow-up of patients after CoA repair to identify HT.

3. LV diastolic dysfunction and LVH are common in patients with repaired CoA, even in the absence of HT, and correlates with worse long-term outcome.

4. There is poor correlation between peripheral BP and central aortic BP in CoA patients. Central aortic hemodynamics are significantly altered in patients with repaired CoA, and can now be investigated comprehensively and non-invasively through MRI-based analysis. At the present time there are no studies linking long-term outcome with abnormal central hemodynamics. However, it is expected that abnormal central aortic hemodynamics and pressure should have an even more deleterious effect on the heart and brain than peripherally raised BP. Further studies are needed to elucidate whether it might be beneficial to treat patients with abnormal central aortic hemodynamics with anti-hypertensive medication.

Supplementary

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