1 Introduction

By definition ‘secondary’ hypertension (SH) comprises those forms of arterial hypertension (HT) that are due to an identified cause and, therefore, can be resolved by removing the underlying cause.

The European Societies of Cardiology and Hypertension (ESC/ESH) guidelines suggest that the screening for SH should be restricted to patients with certain features, such as younger age (i.e. < 40 years), acute worsening of HT in patients with previously documented chronically stable normotension, severe (grade 3) or drug-resistant HT, presence of extensive hypertension-mediated organ damage (HMOD) [1]. However, accumulating experiences in specialized tertiary referral centers have provided compelling evidence that if SH is systematically sought for, its prevalence is much higher [2], involving a proportion of the hypertensive patients that ranges from about 35% in general to higher rates in those with drug-resistant HT [3]. For example, amongst those with primary aldosteronism who were referred for adrenal vein sampling (AVS) in the Adrenal Vein sampling International Study (AVIS)-2, 20–50% had resistant hypertension depending on the criteria used to define this condition [4]. Even though specialized centers receive a selected cohort of patients, these figures indicate that the diagnosis of SH is probably missed in the majority of the patients. This is a disastrous situation, not only because it implies missing the opportunity of long-term cure and/or a better control of high blood pressure (BP), but also because identification of the cause and the underlying pathophysiological mechanisms allows a more targeted and effective pharmacological treatment, and, therefore, prevention of HMOD and cardiovascular (CV) events [5]. Given the unprecedented progress made in the last decades in the understanding, screening, work-up, and management of SH, the purpose of this mini-review is to furnish concise updated information on the diagnosis and treatment of the most common forms of SH, which are summarized in Table 1. For in depth information, the readers are referred to recent comprehensive reviews [6, 7].

Table 1 Causes of secondary hypertension
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2 Primary Aldosteronism

Keynote

PA is the most common curable form of HT. Its prior probability is higher in certain categories of patients, which makes its detection obligatory in such categories. However, several experts call for broader screening strategies with the aim to surgically cure or medically treat PA patients, thus avoiding or reverse HMOD and CV complications.

Primary aldosteronism (PA) is by far the most common curable form of HT and is associated with an excess rate of HMOD and CV complications as compared to primary essential HT with a similar degree of BP elevation [8, 9]. Its prevalence ranges from 6% in unselected hypertensive patients [10] to 11.2% in those referred to specialized centers [11], and to more 20% in the patients with drug-resistant HT [12, 13].

2.1 Screening and Diagnostic Tests

Table 2 reports the main clinical features of PA. When the PA patients were systematically subtyped by using adrenal vein sampling (AVS), about two-thirds of them were found to have a unilateral form of PA, mainly an aldosterone-producing adenoma (APA) or, much more rarely, unilateral adrenal hyperplasia, while a bilateral form (also known as idiopathic hyperaldosteronism) was diagnosed in the remaining third [11]. The main feature of patients with bilateral PA is multiple aldosterone-producing cell clusters (APCCs) or micro-aldosterone-producing adenomas, rather than bilateral adrenal hyperplasia (BAH) [14], which seems to be the more common form when AVS is not systematically exploited or it is interpreted with cutoffs for selectivity and lateralization that are too tight [15]. Much rarer are unilateral aldosterone-producing carcinomas [16], and the familial forms (FH) due to germline mutations, which cause BAH [17] and include several types (e.g. FH-I—also known as ‘glucocorticoid-remediable aldosteronism’, II, III, and IV).

Table 2 Clinical characteristics suggestive of primary aldosteronism
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Figure 1 shows a simplified algorithm for the initial work-up of PA [9], which performed extremely well at our center. Briefly, the diagnosis of PA entails demonstration of low or undetectable renin levels and inappropriately high secretion of aldosterone. Considering this, in 1982 Hiramatsu et al. proposed the aldosterone : renin ratio (ARR) [18], which can now be easily calculated using the freely downloadable ARR App (available for Android and iPhone) [19]. To effectively use the ARR one should, however, be aware that its values are influenced by many drugs and conditions (Table 3) [9, 20]. Thus, the usual recommendation is to switch antihypertensive therapy to doxazosin and/or a long-acting calcium-channel blocker, and also to keep the patients resting quietly (supine or sitting) for 60 min before collecting blood samples [9]. However, a major advancement in this field with profound implications for clinical practice has been the discovery that the mineralocorticoid receptor antagonists (MRAs), which for decades were forbidden during the screening, can be prescribed during the screening of PA [21], and also when PA patients undergo subtype differentiation because they did not cause false negative ARR values during the screening, neither they precluded the diagnosis of unilateral PA by AVS [22,23,24]. This novel evidence is of utmost practical importance particularly in the patients with severe hypokalemia and/or poor control of BP values, because the MRAs are the most effective agents to control BP and hypokalemia in PA patients.

Fig. 1
figure 1

Simplified algorithm for the work-up for primary aldosteronism. Please note the pivotal role of adrenal vein sampling (AVS) for patient’s assignment to surgery or medical treatment. In case of uncertain AVS results or unsuccessful AVS, the indication to unilateral adrenalectomy can be justified by in case of drug-resistant hypertension and/or unbearable side effects with the antihypertensive treatment. *Confirmatory tests are not explained in this simplified algorithm because their accuracy and diagnostic gain over a well-performed baseline ARR has not been proven in studies that fulfilled the Standards for Reporting of Diagnostic Accuracy (STARD) requirements [25]. Moreover, in the largest and only study that followed these requirements, the captopril test was not shown to provide any diagnostic gain over the baseline ARR [26]. PA primary aldosteronism, ARR aldosterone: renin ratio, PRA plasma renin activity, K+ potassium, Na+ sodium, CT computed tomography, MRI magnetic resonance imaging, AVS adrenal vein sampling, BP blood pressure

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Table 3 Drugs and conditions that affect aldosterone, renin, and aldosterone:renin ratio
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The use of confirmatory tests, such as the oral sodium loading test, the saline infusion test, the captopril challenge test, and the fludrocortisone plus salt loading test, remains controversial. They are based on the unproven premise that aldosterone secretion would be completely independent of renin and angiotensin II. Moreover, studies that supported their use did not comply with the Standards for Reporting of Diagnostic Accuracy (STARD) requirement for validation for diagnostic tests [25]. Furthermore, the largest study that examined the captopril test and fulfilled these requirements—the AQUARR Study—failed to show any diagnostic gain of this confirmatory test over a carefully done ARR [26]. Thus, if the screening is properly performed and shows an ARR consistently elevated, i.e. a florid PA phenotype (identified by a high aldosterone > 15 ng/dL, a DRC ≤ 2 mIU/L, with or without low potassium levels), they are useless, and patients can proceed to subtyping if they seek for surgery [27, 28].

2.2 Treatment

Unilateral laparoscopic adrenalectomy is the best treatment that can be offered to PA patients with proven unilateral disease. This means that patients should be referred for AVS to be performed by an expert team in a specialized tertiary center before considering surgery. MRAs, such as spironolactone, canrenone potassium, potassium canrenoate, eplerenone, alone or in combination with other antihypertensive drugs, are recommended for those patients with BAH or not suitable for surgery. MRAs are also indicated before adrenalectomy to control BP values and serum potassium levels [9, 27]. In both surgically and medically treated PA, follow-up is necessary to verify the ‘cure’ of PA and the effectiveness of treatment [29, 30].

A more in-depth discussion of the diagnostic work-up and treatment is available in the 2020 Italian Society of Arterial Hypertension (SIIA) practical guidelines [28].

3 Renovascular Hypertension (RVH)

Keynote

The main causes of renal artery stenosis in RVH patients are fibromuscular dysplasia (FMD) and atherosclerosis (ATS). FMD is most frequent in young-to-middle aged women, while ATS prevails in adult men with multiple risk factors.

Renovascular hypertension (RVH) defines a condition where renal artery occlusion or stenosis decreases renal perfusion pressure to levels that activates the renin–angiotensin–aldosterone system (RAAS), thereby raising BP. Its major causes are fibromuscular dysplasia (FMD) and atherosclerosis, which usually involve different cohorts of patients. FMD affects especially children and young-to-middle aged women [31], and is a systemic arterial disease. It causes RVH (FMD-RVH) when it involves the renal artery. Atherosclerotic renovascular hypertension (ATS-RVH) is the most common form in older adults, predominantly men, with multiple risk factors. Its prevalence in the general population of patients with HT ranges between 1 and 8%, depending on the selection of the population, but can be as high as 25–35% in patients with signs of multisite atherosclerosis [7].

RAAS activation occurs when the narrowing of the renal artery lumen in one or both renal arteries attains a certain threshold, usually estimated > 75%, or can be presumed even at a lower degree of stenosis if there is post-stenotic dilatation. The increased renin synthesis aims at maintaining glomerular filtration rate (GFR) through a prominent constriction of the post-glomerular arterioles and via the elevation of systemic BP. In the majority of the patients, however, at the time of diagnosis, the activation of the RAAS is no longer detectable for multiple reasons, as discussed elsewhere [32].

In fact, it has to be reckoned that stenosis of the renal arteries may be hemodynamically insignificant and can result from accelerated atherosclerosis in patients with primary HT. Hence, confirming the diagnosis of RVH is a challenging undertaking, as this can only be made retrospectively if revascularization results in the cure or improvement of HT [5].

3.1 Screening and Diagnostic Tests

For the reason just mentioned, the work-up of RVH, which has to be undertaken in a clinically selected high-risk population (Table 4 and Fig. 2), cannot rely solely on the biochemical assessment, i.e. measurement of serum potassium levels, 24-h urinary sodium and potassium excretion, and active renin concentration or plasma renin activity, but should also entail instrumental tests. The latter comprise: (1) Duplex sonography with bilateral assessment of the most relevant indexes, (e.g. renal arterial resistive, pulsatility indexes, acceleration time, peak systolic velocity, renal-aortic ratio) and evaluation of their homogeneity throughout the different thirds of each kidney; (2) computed tomography (CT) or magnetic resonance angiography, and (3) renal catheter-based contrast angiography. The latter can be implemented with a simultaneous, unstimulated trans-lesional pressure gradient (between the distal renal artery and the aorta) measurement that has been suggested for determining the severity and hemodynamic significance of renal artery stenosis. A pressure gradient threshold of 10% of the mean (aortic) pressure (or a trans-lesional gradient of at least 20 mmHg) has been proposed to decide whether or not to perform balloon angioplasty (see “Treatment” section below) [33]. While there are no randomized clinical trials supporting the superiority of this approach in terms of outcome, its pitfalls are both theoretical and practical: positioning a catheter through a tight stenosis by itself creates a gradient, which can lead to an overestimation of the stenosis severity. Moreover, in the presence of multiple lesions, as typically in FMD, estimation of pressure gradient can be challenging. Finally, the measurement of the trans-lesional pressure gradient is not widely available, even in centers that perform a substantial number of percutaneous procedures for RVH.

Table 4 Clinical findings suggestive of renovascular hypertension (RVH) according to the etiology
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Fig. 2
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Diagnostic algorithm for identification and treat renovascular hypertension (RVH). As no single test is sensitive and specific enough to detect and ruled out RVH, a comprehensive assessment based on biochemical (↓ K+, ↑ renin, ↑ plasma aldosterone concentration) and instrumental tests (Duplex sonography and renal post-captopril scintigraphy) is necessary. Imaging by angio-CT or angio-MR plays a key role to assess the localization of stenosis and multivessel involvement, and to plan revascularization, by angioplasty in FMD-RVH and angioplasty + stenting in case of ATS-RVH. RVH renovascular hypertension, FMD fibromuscular dysplasia, CT computed tomography, MR magnetic resonance, PTRA percutaneous transluminal renal angioplasty, BP blood pressure

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3.2 Treatment

The first-choice treatment for FMD-RVH is renal artery angioplasty without stenting. Its effect on BP reduction is greater in younger patients, with ‘short history’ of HT, and without comorbidities (such as diabetes mellitus or obesity). In patients with ATS-RVH angioplasty should be performed with stenting, and there are compelling indications to undertake such treatment (Table 5). However, it remains controversial if percutaneous transluminal renal angioplasty (PTRA) plus stenting is superior to an aggressive medical treatment in the patients without such compelling indications (Class of Recommendation IIb, Level of Evidence C) (Fig. 2) [33,34,35]. According to a guideline, renal artery angioplasty would be ‘rarely appropriate’ in: (1) asymptomatic unilateral hemodynamically significant RAS in a viable kidney; (2) patients with small (< 7 cm pole to pole) nonviable kidneys; (3) patients with moderate RAS (50–69% diameter stenosis) with translesional gradients that fail to achieve the threshold [35].

Table 5 ACC/AHA recommendations to perform angioplasty and stent in ATS-RVH
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4 Pheochromocytoma/Paraganglioma

Keynote

More than 80% of PPGLs patients have paroxysmal or sustained high BP. Screening test includes measurement of urinary metanephrines. When the tumor is detected by imaging, antihypertensive treatment is based on α1-adrenergic receptor blockade followed by association with β-blockers.

About 80–85% of chromaffin-cell tumors are pheochromocytomas (PHEO), and 15–20% are paragangliomas (PGL). Owing to their common embryologic origin and clinical similarities, they are usually jointly defined as pheochromocytomas and paragangliomas, in short PPGLs. On the whole, PPGLs are rare, as they comprise less than 0.2–0.6% of the patients with HT. Due to the huge variation of clinical presentation, PPGLs have been defined as ‘the great simulators’ as symptoms can range from none to many. Symptoms are usually due to a mass effect and/or derive from catecholamines excess. Paroxysmal or sustained high BP is the most common sign of PPGLs and involves up to 80% of patients (Table 6). In syndromic cases, the concurrence of physical signs (see later) should suggest the diagnosis (Table 6) [36,37,38]. However, PPGLs occurring in the head and neck district are usually parasympathetic, and therefore do not secrete catecholamines. Hence, these patients usually present to the otolaryngologist and/or to the vascular surgeon for the detection of cervical masses or nodules [37].

Table 6 Most frequent clinical manifestations of PPGLs and their distribution
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4.1 Screening and Diagnostic Tests

Syndromic PPGLs, including neurofibromatosis type 1, multiple endocrine neoplasia type 2, von Hippel-Lindau syndrome, renal cell carcinoma with SDHB mutation, Carney triad, and Carney-Stratakis syndrome, are rare and characterized by typical clinical phenotypes and associated comorbidities, which render the clinical suspicion quite obvious. The work-up for HT patients with non-syndromic and syndromic PPGLs is shown in Fig. 3. Biochemical tests for suspected cases include measurements of urinary and/or plasma free normetanephrines and metanephrines that are the most accurate tests to detect or exclude PPGLs. Detection of plasma metanephrines must be performed under standardized conditions such as stress-free conditions (e.g. after rest in the supine position), and with positioning an indwell cannula to avoid the pain of venipuncture, to limit false-positive results. The measurement of conjugated metanephrines in 24-h urine has been demonstrated to cause false positive test results, and thus free metanephrines should be preferred [38]. Imaging is recommended when the screening is positive (e.g. magnetic resonance imaging-MRI or CT); due to their high vascularization PPGLs usually show up as hyperintense lesions on T2-weighed MRI.

Fig. 3.
figure 3

A schematic algorithm suggested for diagnosis and treatment of hypertensive patients with suspected of pheochromocytoma and paraganglioma. CT has been suggested as the first-choice imaging modality because of its excellent spatial resolution for thorax, abdomen, and pelvis. MRI is recommended in patients with metastatic PPGLs, for detection of skull base and neck paragangliomas. *Biochemical screening should be performed after withdrawing of interfering drugs and substances, including acetaminophen, labetalol, sotalol, α-methyldopa, tricyclic antidepressants, MAO-inhibitors, sympathomimetics, cocaine. **A quarter of patients with PPGLs show borderline biochemical results, likely due to inappropriate sampling. If results remain elevated after repeating the measurement, the clonidine suppression test with detecting of plasma normetanephrine can be used. This test has been claimed to have a 100% diagnostic specificity with a 97% sensitivity; however, it has not been validated in prospective studies. HT hypertension, CT computed tomography, MRI magnetic resonance imaging, MIBG metaiodobenzylguanidine, 18F-FDG [18F]-fluoro-fluorodeoxyglucose, 18F-FDOPA 6-[18F]-l-fluoro-l-3,4-dihydroxyphenylalanine, PET positron-emission tomography

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In all patients with sporadic (non-familial) PPGLs genetic testing is recommended for the following reasons: (1) about one-third of these patients have germline mutations; (2) some of the mutations, for example, those of succinate dehydrogenase subunit B (SDHB), are associated to a higher risk of malignant/metastatic disease; (3) a germline mutation in the proband, unless occurring de novo, indicates a familial form, which can allow earlier diagnosis and treatment of PPGLs in the relatives [36].

4.2 Treatment

The gold-standard therapy for PPGLs is surgery for solitary or multiple tumors clustered in one area (Fig. 3) [36, 38]. Patients with hormonally functional PPGLs should undergo preoperative α1-blockade, followed by β-blockade and volume expansion to prevent perioperative CV complications. Antihypertensive treatment must include β1-blockers, as doxazosin or terazosin. Β-blockers can be used to controlled tachycardia and BP values, but only after α1-blockade. Likely because of α1-mediated vasoconstriction [5] PPGLs patients have a relative hypovolemia, i.e. a redistribution of blood volume from the periphery to the cardiopulmonary district. Hence, once the diagnosis has been made, before surgery and anesthesia, it is fundamental to correct this hypovolemia to avoid prominent hemodynamic instability.

Malignant forms are generally treated by meta-I-benzyl guanidine (MIBG) (for patients with metastatic disease who are MIBG positive) and/or chemo- or radiotherapy.

5 Cushing’s Syndrome

Keynote

ACTH-dependent or -independent hypercortisolism is a rare cause of SH but, in these patients, the BP control is often difficult to achieve when the surgical removal of cortisol-producing tumors is not performed.

Excessive autonomous production of cortisol is the hallmark of Cushing’s syndrome (CS) but accounts for less than 1% of endocrine causes of HT. However, high BP is reported in more than 80% of adults affected by CS [7].

5.1 Screening and Diagnostic Tests

On history, excessive use of exogenous glucocorticoid leading to iatrogenic CS must be ruled out before considering screening tests, which are indicated in the following categories of hypertensives: (1) patients with unusual features, for example, osteoporosis at a young age; (2) patients with suggestive signs and symptoms (Table 7); (3) adrenal incidentaloma compatible with adenoma [39]. The initial testing includes repeated (at least twice) measurements of 24-h urine free cortisol, late-night salivary cortisol, and 1-mg overnight dexamethasone suppression test. For the 1-mg overnight dexamethasone suppression test, a normal response is a serum cortisol less than 1.8 μg/dL; when values are between 1.8 and 5 μg/dL subclinical CS should be considered. The absence of cortisol suppression after dexamethasone (serum cortisol higher than 5 μg/dL or  >140 nmol/L) indicates a CS diagnosis. Once a diagnosis of CS has been made the next step is to distinguish between ACTH-dependent CS (that accounts for 80–85% of cases), which show normal or increased plasma ACTH values and are due to pituitary or ectopic ACTH-secreting tumors, and the less common ACTH-independent CS [40], in which ACTH is low. Uncertainties can be resolved by the CRH stimulation test as ACTH-independent cases show persistently suppressed ACTH values. Patients with ACTH-dependent CS should be evaluated in specialized tertiary referred centers by gadolinium-enhanced pituitary MRI, followed, when clinical, biochemical or radiological studies are discordant, by bilateral inferior petrosal sinus sampling. If ACTH is suppressed, abdominal CT scan or MRI should be done to identify the adrenal mass (90% are unilateral adrenal tumors) or hyperplasia (unilateral or bilateral) [41].

Table 7 Signs and symptoms associated with Cushing’s syndrome and their prevalence
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5.2 Treatment

Controlling cortisol hypersecretion by surgery or by cortisol lowering drugs or glucocorticoid receptor antagonists, can effectively lower BP in most hypertensive CS patients and normalize it in ~ 50% of cases [42]. Definitive therapy for CS is surgical excision of ACTH- or cortisol-producing tumor with a post-operative cure rate of 65–90%. In patients with contraindications to surgery, or with ectopic disease and persistent hypercortisolism, BP values are often difficult to control, and the most frequent causes of death are the CV complications. In these patients and in those with persistent high BP after surgery, an association of multiple antihypertensive drugs, including renin–angiotensin–aldosterone system (RAAS) modulators (i.e. ACE-inhibitors, angiotensin II receptor blockers—ARBs, and MRAs), is usually necessary [41].

6 Obstructive Sleep Apnea

Keynote

OSA is a frequent cause of SH and ‘difficult-to-treat’ HT. Patients with obesity, snoring, upper airway abnormalities, excessive daytime sleepiness, reduced sleep-related quality of life should be screened for OSA. The effect of PAP on BP is still controversial but, if associated with sleep hygiene and specific antihypertensive drugs, it can ameliorate BP control with the largest effect on nocturnal BP.

Obstructive sleep apnea (OSA) is an independent risk factor for HT and cardiovascular diseases [43] and is common in adults, particularly in patients with difficult-to-treat HT [44]. Its identification as the underlying cause of HT, followed by specific treatment, can render high BP responsive to treatment [44]. Fragmented, albeit rather consistent, evidence suggested that OSA can coexist with PA and that target treatment of the latter can ameliorate OSA [45]. However, results of a recent multicenter study seem to have challenged this view [46]; therefore, whether OSA is a presenting sign of PA or vice versa, remains somewhat controversial. Nonetheless, there are no doubts that patients with difficult-to-treat HT should be screened for either condition because identification of one or both can allow to better control their high BP and improve their quality of life.

6.1 Screening and Diagnostic Tests

Well recognized signs and symptoms (Table 8) should lead to screen hypertensive patients for OSA [47,48,49]. In-laboratory full-night polysomnography is the diagnostic gold standard for OSA patients [48, 49]. It allows to identify the severity of disease (i.e. through apnea/hypopnea index—AHI—measurement), the associated sleep disorders, and the response to treatment. When unfeasible, the home sleep apnea testing can be used, particularly for uncomplicated adults with suspect of OSA (Fig. 4).

Table 8 Clinical presentation of OSA
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Fig. 4
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Schematic algorithm summarizing the steps for recognition of obstructive sleep apnea and its diagnostic and therapeutic work-up. *Upper airway surgery and oral appliances are indicated only for specific cases with objective upper airways abnormalities. OSA obstructive sleep apnea, PSG polysomnography, AHI apnea/hypopnea index, PAP positive airway pressure, MRAs mineralocorticoid receptor antagonists

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6.2 Treatment

The proper work-up of OSA patients varies according to individual features. The first steps are the lifestyle changes and sleep hygiene (Fig. 4) (i.e. avoiding alcohol, caffeine or stimulants of wakefulness before sleep; increased physical activity during the day and obesity control; avoiding naps at unusual hours; discontinuation of hypnotic drugs). An ear–nose–throat (ENT) evaluation is recommended for OSA subjects with suspected upper airway abnormalities. The ENT specialist could also perform drug-induced sleep endoscopy examination that allows an accurate identification and correction of the obstruction [50]. In moderate-to-severe OSA (i.e. AHI ≥ 15 events per hour), especially in patients with symptoms of excessive daytime sleepiness, reduced sleep-related quality of life, and/or hypertension positive airway pressure (PAP) therapy, including continuous, self-titrated systems, and bilevel (as a second-level option), is the recommended treatment [51], which allows to maintain the upper airway patency and lower sympathetic [52] and RAAS activation [53, 54], by improving oxyhemoglobin saturation. PAP treatment improves signs and symptoms of OSA, and lowers BP values, more strongly in OSA patients with resistant hypertension [51, 55,56,57,58]. However, its effectiveness on BP and cardiovascular profile depends on patients’ adherence to treatment, which is often poor. Interestingly, recent data demonstrated a clinically significant improvement in PAP adherence and thereby improve symptom control in the treatment of OSA in adults with the use of telemonitoring intervention [51].

Only a few studies have evaluated the effects of antihypertensive agents on OSA. Their results were variable and statistical power was usually poor [47]. Growing evidence supports the role of high levels of plasma aldosterone in OSA that appear to contribute to poor control of BP values in these patients through peri-pharyngeal fluid retention [59]. By reducing parapharyngeal edema and upper airway obstruction, diuretics (i.e. MRAs) improve OSA severity and BP control [45, 60, 61]. Further studies are necessary to confirm this suggestion. A promising therapeutic strategy is the electrical stimulation of upper airway via hypoglossal nerve [62, 63], but data on its effect on BP are still preliminary.

7 Conclusions

The detection of SH can be simplified and made cost-effective by estimating the patient’s prior (pre-test) probability of the disease, which can be established by knowing the prevalence of the most common forms and by following few rules, as herein presented. Once a form of SH has been detected, knowledge of the underlying pathophysiology warrants a more rational and more effective treatment, which can allow to achieve long-term cure of arterial hypertension or a better control of the high BP values when cure is not accomplished. These outcomes are rewarding for the doctor, but even more so for the patient, who will avoid the complications of life-long exposure to high BP values, will enjoy a better quality of life, as convincingly documented in PA and OSA, and ultimately will no longer be life-long labelled as ‘patient’.