Article

Stable Angina Medical Therapy Management Guidelines: A Critical Review of Guidelines from the European Society of Cardiology and National Institute for Health and Care Excellence

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Abstract

Most patients with stable angina can be managed with lifestyle changes, especially smoking cessation and regular exercise, along with taking antianginal drugs. Randomised controlled trials show that antianginal drugs are equally effective and none of them reduced mortality or the risk of MI, yet guidelines prefer the use of beta-blockers and calcium channel blockers as a first-line treatment. The European Society of Cardiology guidelines for the management of stable coronary artery disease provide classes of recommendation with levels of evidence that are well defined. The National Institute for Health and Care Excellence (NICE) guidelines for the management of stable angina provide guidelines based on cost and effectiveness using the terms first-line and second-line therapy. Both guidelines recommend using low-dose aspirin and statins as disease-modifying agents. The aim of this article is to critically appraise the guidelines’ pharmacological recommendations for managing patients with stable angina.

Keywords

Antianginals, ESC, guidelines, NICE, pharmacotherapy, stable angina,

Disclosure:UT received honoraria for consulting from Clovis pharmaceuticals and Gilead sciences; from the speakers’ bureau of Gilead sciences and Amgen, and received research grants and is the local principal investigator for NIH and VA Coop studies and for multicenter trials with AstraZeneca and Novartis. TR has no conflicts of interest to declare.

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DOI:https://doi.org/10.15420/ecr.2018.26.1

Correspondence Details:Udho Thadani, University of Oklahoma Health Sciences Center and VA Medical Center, 800 Stanton L Young Blvd, COM 5400, Oklahoma City, OK 73104, US. E: udho-thadani@ouhsc.edu

Open Access:

This work is open access under the CC-BY-NC 4.0 License which allows users to copy, redistribute and make derivative works for non-commercial purposes, provided the original work is cited correctly.

Background

Definition of Stable Angina

Angina pectoris was first defined by William Heberden in 1768. He described it as a smothering sensation or tightness across the front of the chest which may radiate to the left arm or to both arms as well as the jaw or back. It is usually triggered by exercise or emotional stress and it may be aggravated by the ingestion of a heavy meal.1 The pain usually resolves by stopping exercise or with sublingual nitroglycerin. Angina is arbitrarily defined as stable when the angina episodes are stable over a period of 3–6 months.2,3 Atypical features, such as shortness of breath during exercise in the absence of pulmonary disease or extreme fatigue during exertion, have been considered as angina equivalents.4 These atypical presentations in the absence of chest pain are often found in women, older people and people with diabetes.

Causes of Stable Angina

The exact aetiology of stable angina is not well defined; however, it is thought to be secondary to a mismatch between myocardial supply and demand.5 The majority of patients with angina have significant narrowing of one or more epicardial coronary arteries. It is also recognised that many patients with stable angina have non-obstructive or even normal coronary arteries.

Prognosis for Patients with Stable Angina

The prognosis for patients with stable angina varies, but there is an annual mortality rate of up to 3.2%. Long-term prognosis is influenced by left ventricular systolic function, extent of coronary artery disease (CAD), exercise duration or effort tolerance, and comorbid conditions.3 The published data does not account for medical interventions, such as statins and aspirin, which reduce mortality and morbidity in coronary artery disease, and it is likely that the prognosis of stable angina without medical therapy may be very different.4

Pharmaceutical Therapy

Nitrates, Beta-blockers and Calcium Channel Blockers

Nitrates are available in different formulations and both short- and long-acting organic nitrates have been shown to be effective in treating angina when used appropriately to avoid nitrate tolerance.3,6,7 Nitrates are as effective as beta-blockers (BB) and calcium channel blockers (CCB).8 Sublingual nitroglycerin tablets and oral nitroglycerin spray are rapidly absorbed and when taken prophylactically can improve exercise tolerance and reduce the incidence of MI.9,10 One of the major side-effects of nitrate use is headaches that may be severe enough to necessitate discontinuation of the therapy.11 Tachyphylaxis, or tolerance to continuous use of nitrates is another limiting factor, but can be avoided by allowing prolonged nitrate-free intervals for nitrate levels to decline before the next dose.6,7,9,12 Long-acting nitrates have been downgraded to second-line therapy in guidelines because of their side-effects and the incidence of tachyphylaxis.

The first reported use of BBs to treat hypertension and angina was in the 1970s in the UK.13,14 BBs are an effective therapy in the management of stable angina.14–17 Many BB are available for clinical use. They have the common property of blocking beta-adrenergic receptors and selective and non-selective BB can be chosen for their different properties. Although BB can reduce mortality and morbidity in patients with heart failure with reduced ejection fraction and in patients with recent MI, these agents have a limited effect on mortality and the incidence of MI when used in patients with stable angina.18–26

CCBs, both dihydropyridine (DHP) agents and non-DHP agents, have been used for more than five decades, and are very effective for the treatment of stable angina. They significantly reduce the episodes of angina, increase exercise duration and decrease the frequency of nitroglycerin use.27–30 When combined with BB, they have been shown to significantly delay the onset of ST-segment depression using an exercise treadmill test.31 Patients with asthma or chronic obstructive pulmonary disease (COPD) are good candidates for treatment with CCB, given the risk of bronchospasm in these patients when taking BB.32 A combination of BB and non-DHP CCB should be avoided due to the risk of symptomatic bradycardia and atrioventricular block.33

Nicorandil, Ranolazine, Trimetazidine, Ivabradine and Allopurinol

Nicorandil, which is a nitrate-moiety nicotinamide ester and adenosine-sensitive potassium channel opener, increases coronary blood flow and prevents coronary artery spasm.34 It has been approved for clinical use in Japan and many European countries on the basis of small trials in patients with stable angina.35,36 This medication is not used in the US because placebo-controlled studies from Australia and the US failed to confirm antianginal efficacy of nicorandil compared with placebo.37 In Europe, it has been used instead of nitrates or in combination with other antianginals.37 Side-effects of gastrointestinal ulcerations and headache limit the long-term use of nicorandil in patients with stable angina.38,39

Ranolazine is an orally active piperazine derivative.40 The exact mechanism its antianginal action is unknown, but animal studies have shown that it inhibits late sodium inward current during periods of ischaemia, reducing intracellular calcium overload.41,42 Ranolazine is an effective antianginal and anti-ischaemic agent compared with placebo and is as equally effective as atenolol.43,44 Extended-release ranolazine compared with placebo, as monotherapy or in combination with other antianginals, has been shown to significantly increased total exercise time by 116 seconds and 23.7 seconds, respectively.43,44 It also increased treadmill walking time for people with angina and delayed the onset of exercise-induced MI.43,45,46 Ranolazine has been shown to be ineffective in the treatment of women with microvascular angina compared with placebo.47

Trimetazidine is available in Europe and several countries in Asia as an adjunct therapy for angina, but it is not used in the US.4,35,48 In patients who remain symptomatic despite treatment with first-line therapy drugs, trimetazidine decreases angina frequency without exerting any effects on heart rate or blood pressure, as shown in the TRIMetazidine in POLand (TRIMPOL) trials I and II.49,50

Chronic Stable Angina Pharmacotherapy Comparison Of Guideline Recommendations

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Allopurinol is a pyrazolopyrimidine and an analogue of hypoxanthine.51,52 It has been demonstrated that high-dose allopurinol is associated with a significant improvement in endothelium-dependent vasodilation and exercise tolerance. The effects of high-dose allopurinol (600 mg daily) have been shown to be similar to conventional antianginal medications.53 While recommended in the European Society of Cardiology (ESC) guidelines as a second- or third-line agent for symptom control, allopurinol is not endorsed in the National Institute for Health and Care Excellence (NICE) guidelines.35,54,55 Allopurinol is not approved by the Food and Drug Administration to treat angina in the US.

Ivabradine lowers heart rate and inhibits the primary sinoatrial node current.56 It is use-dependent, meaning that its effect is the highest in high heart rate and vice versa; bradycardia is less commonly encountered in patients on ivabradine because its effect is ameliorated at lower heart rates.57 Studies have shown that ivabradine as an add-on therapy to atenolol significantly increased exercise time and reduces the number of angina attacks compared with atenolol alone or other BB and it did not cause significant bradycardia.58–61 However, symptomatic bradycardia remains a concern when using combination therapy, and it may adversely affect outcome in severely symptomatic patients.33 In patients with stable angina without heart failure, ivabradine added to background therapy was shown not to decrease the incidence of death from cardiovascular causes or non-fatal MI, but in a subgroup of patients with severe angina, ivabradine performed worse than placebo with regards to hard endpoints.62

Combination Antianginal Therapy

Monotherapy in optimal doses,is often as effective as combination therapy using two or more agents.3,4,35,63,64 There is a lack of well-designed studies showing that treatment with more than one class of drug is superior to combination treatment with a different class of antianginal drugs.65,66 Adding either a long-acting nitrate or a CCB to BB therapy is often useful and reduces angina frequency, improves exercise tolerance and reduces MI.63,65 A combination of BB and ivabradine has been shown to be effective in patients with a heart rate greater than 60 BPM, but safety concerns have been raised.62,67 As discussed earlier, extended release ranolazine monotherapy, or in combination with BB or CCB, is effective.43,45,46 Trimetazidine as an add-on to older antianginal drugs has also been shown to be effective.44,45

None of the trials involving a combination of antianginal drugs have been adequately blinded to make firm conclusions regarding the superiority of a combination of two antianginal drugs to doses of monotherapy. Data on the efficacy of triple therapy with three different classes of antianginal drugs are not available.

Guidelines for Stable Angina

There are published guidelines for the management of patients with stable ischaemic heart disease and stable angina. The ESC and NICE guidelines have been updated regularly to provide a clear set of guidelines for management for healthcare professionals in the UK and Europe.35,54,55 ESC guidelines (Table 1) provide recommendations divided into classes:

  • Class I where the evidence and/or general agreement that a given treatment or procedure is beneficial, useful and effective.
  • Class IIa where the weight of evidence or opinion is in favour of usefulness/efficacy.
  • Class IIb where usefulness/efficacy is less well established by evidence or opinion.
  • Class III where there is evidence or general agreement that the given treatment or procedure is not useful/effective and in some cases may be harmful.35

In addition, for each class of recommendation, a level of evidence is included:

  • Level of evidence A denotes that data were derived from multiple randomised clinical trials or meta-analyses.
  • Level of evidence B indicates that data were derived from a single randomised clinical trial or large non-randomised studies.
  • Level of evidence C is where a consensus of opinion of the experts and/or small studies, retrospective studies or registries were available.35

NICE guidelines (Table 1) are based on extensive reviews of published data and take into consideration cost-effectiveness and the adverse effects of medications. The terms first-line treatment and second-line treatment are used and guidance is given on the most appropriate use of antianginal therapy, taking co-morbidities into consideration when selecting therapy.54,55

Guidelines for Antianginal Therapy

A previously published article compared the American and Canadian guidelines.65 This article compares the recommendations for antianginal therapy in ESC and NICE guidelines (Table 1). Both sets of guidelines agree that optimal medical therapy includes antianginal therapy and medications to prevent MI and stroke, including aspirin and statins. They both favour the use of sublingual short-acting nitrates for the relief of an established attack of angina or for prophylaxis. Both guidelines recommend the use of BB or CCB as first-line therapy with the notion that non-DHP CCB should not be combined with ivabradine or BB.

NICE guidelines recommend a trial of a maximally tolerated dose of either a BB or a CCB as initial therapy. If there are contraindications to one class of drugs or no response, switching to a CCB from a BB and vice versa should be considered. If the response to one class of these antianginal drugs is sub-optimal, NICE recommends a combination of a BB with a DHP-CCB as preferred combination therapy. Use of second-line drugs (long-acting nitrates, nicorandil, ranolazine or ivabradine) as monotherapy or in combination therapy is only recommended when there are contraindications to first-line drugs. Triple therapy is only recommended when patients are being considered for possible revascularisation and remain symptomatic despite treatment with first-line agents. ESC guidelines are more liberal on the use of combination therapy with two or more agents.

ESC guidelines specify certain subsets of patients who would benefit from BB (patients with previous MI and patients with reduced left ventricular ejection fraction), while NICE guidelines do not have any specific patient subgroups. Ranolazine, ivabradine, and nicorandil are considered to be second-line treatments based on both guideline documents. While trimetazidine and allopurinol are recommended as second- or third- line therapy in the ESC guidelines, NICE guidelines do not endorse the use of those medications for patients with stable angina.

Co-morbidities and Stable Angina

Both guidelines recommend use of specific antianginal medications, taking into consideration the presence or absence of comorbidities such as COPD, hypertension, peripheral vascular disease and diabetes, despite the lack of randomised controlled trials to support this.64,65,68

Guidelines to Reduce MI and Sudden Cardiac Death

Lifestyle Changes

Smoking cessation or abstinence reduces the risk of CAD mortality by 50% in 1 year and after 5–15 years the coronary mortality risk reaches that of non-smokers.69 In addition to decreasing cardiovascular mortality and morbidity, stopping smoking in patients with angina also increases exercise performance.64 Although based on small observational studies, exercise training was shown to have favourable outcomes in patients with stable angina.70 Both guidelines emphasise the importance of smoking cessation and regular exercise. NICE guidelines do not specify any special diets, while ESC guidelines recommend a Mediterranean diet. Cardiac rehabilitation is recommended in ESC guidelines, but not in NICE guidelines.

Antiplatelet Therapy

Both guidelines recommend daily use of low-dose aspirin because it has been shown to reduce the incidence of acute MI and sudden death in patients with known CAD.71 This has only been shown to be effective for patients with stable angina in a small study.72 The use of aspirin in patients with stable angina in the absence of CAD is uncertain.65 In patients who are allergic to aspirin, clopidogrel may be used instead according to ESC guidelines, but is not evidence-based; although routine combination of aspirin and a P2Y12 inhibitor is not recommended due to an excessive risk of bleeding.73

Treatment of Dyslipidaemia

There are no specific trials of statins in patients with stable angina, however this class of drugs reduce all-cause mortality, acute coronary events, and the need for revascularisation in patients with CAD and in those at high risk of CAD.74,75 ESC guidelines recommend the use of statins to achieve the ideal low-density lipoprotein goal (<1.8 mmol/l), while NICE guidelines recommend the use of high-dose statins, such as 80 mg atorvastatin (Table 1).

Control of Hypertension

There are no specific trials of antihypertensive medications in patients with stable angina who also have hypertension. But given the documented beneficial effects of controlling blood pressure on hard outcomes, especially stroke and heart failure, both guidelines recommend optimal control of blood pressure in patients with stable angina to reduce the incidence of stroke and MI. The blood pressure goal is <140 mmHg for systolic, however recent data suggest that lowering systolic blood pressure to 120 mmHg may be a desirable option if tolerated by the patient.76,77

Management of Diabetes

Diabetes is commonly found in patients with stable angina. Control of diabetes reduces micro- as well as macrovascular complications. Based on the Action to Control Cardiovascular Risk in Type 2 Diabetes (ACCORD) trial, an HbA1C level <7% is desirable.78 Both guidelines recommend routine use of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (ARB) for patients with stable angina who have diabetes.

Concomitant Management of Patients with Angina and Heart Failure With Reduced Ejection Fraction

There are no randomised controlled trials that have studied patients with stable angina and heart failure with reduced ejection fraction. Based on the available outcome trials showing survival benefit, the use of BB and angiotensin-converting enzyme inhibitors or ARB is recommended in patients with reduced left ventricular ejection fraction <40% and concomitant angina.4,19,79–82

Treatment of Patients with Stable Angina and Normal Coronary Arteries or Microvascular Angina

NICE does not make any specific pharmacotherapy recommendations for patients with stable angina and normal coronary arteries or microvascular angina, while ESC guidelines recommend a trial of antianginal drugs. There are no efficacy trials regarding hard outcomes in patients with stable angina who have normal coronary arteries.65 Current evidence does not support the routine use of aspirin or statins in patients with microvascular angina who have normal coronary arteries.

Identification of High-Risk Patients with Left main or Severe Triple Vessel Coronary Artery Disease

Updated NICE guidelines recommend use of coronary CT angiography for an initial investigation for all patients with typical and atypical angina to define coronary anatomy non-invasively, even if the patients are adequately treated with pharmacotherapy.83 This is based on available data showing that coronary artery bypass surgery is superior to medical treatment in this group of patients. ESC guidelines, on the other hand, use non-invasive stress testing to define a high-risk group.83

Conclusion

The current guidelines are largely based on expert opinion and consensus rather than high-quality randomised controlled trials. The two documents discussed in this article make different recommendations for first-line treatment, as well as add-on treatment with two or three antianginal drugs, without objective data.

Secondary prevention strategies vary; however, the use of low-dose aspirin and statin therapy seem to be justified based on the available data. The management of patients with microvascular disease or normal coronary arteries and angina remains uncertain especially in the absence of randomised controlled trials. The guideline recommendations rely mostly on assumptions and extrapolations and expert opinion based on the available data regarding patients with obstructive CAD.

References

  1. Heberden W. Some account of a disorder of the breast. Medical Transactions 1772;2:59–67.
  2. Abrams J, Thadani U. Therapy of stable angina pectoris: the uncomplicated patient. Circulation 2005;112: e255–9.
    Crossref | PubMed
  3. Thadani U. Current medical management of chronic stable angina. J Cardiovasc Pharmacol Ther 2004;9(Suppl 1):S11–29.
    PubMed
  4. Fihn SD, Gardin JM, Abrams J, et al. 2012 ACCF/AHA/ACP/AATS/PCNA/SCAI/STS guideline for the diagnosis and management of patients with stable ischemic heart diseases. J Am Coll Cardiol 2012; 60:e44–e164.
    Crossref | PubMed
  5. Opie LH. Angina pectoris: the evolution of concepts. J Cardiovasc Pharmacol Ther 2004;9:S3–9.
    Crossref | PubMed
  6. Thadani U, Lipicky RJ. Short and long-acting oral nitrates for stable angina pectoris. Cardiovasc Drugs Ther 1994;8:611–23.
    Crossref | PubMed
  7. Thadani U, Lipicky RJ. Ointments and transdermal nitroglycerin patches for stable angina pectoris. Cardiovasc Drugs Ther 1994;8:625–33.
    Crossref | PubMed
  8. Heidenreich PA, McDonald KM, Hastie T, et al. Meta-analysis of trials comparing beta-blockers, calcium antagonists, and nitrates for stable angina. JAMA 1999;281:1927–36.
    Crossref | PubMed
  9. Thadani U. Challenges with nitrate therapy and nitrate tolerance: prevalence, prevention, and clinical relevance. Am J Cardiovasc Drugs 2014;14:287–301.
    Crossref | PubMed
  10. Thadani U, Wittig T. A randomized, double-blind, placebo-controlled, crossover, dose-ranging multicenter study to determine the effect of sublingual nitroglycerin spray on exercise capacity in patients with chronic stable angina. Clin Med Insights Cardiol 2012;6:87–95.
    Crossref | PubMed
  11. Thadani U, Rodgers T. Side effects of using nitrates to treat angina. Expert Opin Drug Saf 2006;5:667–74.
    Crossref | PubMed
  12. Steering Committee, Transdermal Nitroglycerin Cooperative Study. Acute and chronic antianginal efficacy of continuous twenty-four-hour application of transdermal nitroglycerin. Am J Cardiol 1991;68:1263–73.
    Crossref | PubMed
  13. Prichard BN, Owens CW. Mode of action of beta-adrenergic blocking drugs in hypertension. Clin Physiol Biochem 1990;8:1–10.
    PubMed
  14. Prichard BN. Beta-adrenergic receptor blocking drugs in angina pectoris. Drugs 1974;7:55–84.
    Crossref | PubMed
  15. Thadani U, Davidson C, Singleton W, Taylor SH. Comparison of the immediate effects of five beta-adrenoreceptor-blocking drugs with different ancillary properties in angina pectoris. N Engl J Med 1979;300:750–5.
    Crossref | PubMed
  16. Thadani U, Davidson C, Singleton W, Taylor SH. Comparison of five beta-adrenoreceptor antagonists with different ancillary properties during sustained twice daily therapy in angina pectoris. Am J Med 1980;68:243–50.
    Crossref | PubMed
  17. Thadani U, Sharma B, Meeran MK, et al. Comparison of adrenergic beta-receptor antagonists in angina pectoris. Br Med J 1973;1:138–42.
    Crossref | PubMed
  18. CIBIS-II Investigators and Committees. The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial. Lancet 1999;353:9–13.
    Crossref | PubMed
  19. MERIT-HF Study Group. Effect of metoprolol CR/XL in chronic heart failure: Metoprolol CR/XL Randomised Intervention Trial in Congestive Heart Failure (MERIT-HF). Lancet 1999;353:2001–7.
    Crossref | PubMed
  20. Packer M, Bristow MR, Cohn JN, et al. The effect of carvedilol on morbidity and mortality in patients with chronic heart failure. N Engl J Med 1996;334:1349–55.
    Crossref | PubMed
  21. Beta-Blocker Heart Attack Study Group. The beta-blocker heart attack trial. JAMA 1981;246:2073–4.
    Crossref | PubMed
  22. Hjalmarson A, Herlitz J, Holmberg S, et al. The Göteborg metoprolol trial. Effects on mortality and morbidity in acute myocardial infarction. Circulation 1983;67(6 Pt 2):I26–32.
    PubMed
  23. Huang HL, Fox KA. The impact of beta-blockers on mortality in stable angina: a meta-analysis. Scott Med J 2012;57:69–75.
    Crossref | PubMed
  24. Bangalore S, Steg G, Deedwania P, et al. Beta-blocker use and clinical outcomes in stable outpatients with and without coronary artery disease. JAMA 2012;308:1340–9.
    Crossref | PubMed
  25. Bangalore S, Bhatt DL, Steg PG, et al. Beta blockers and cardiovascular events in patients with and without myocardial infarction: post hoc analysis from the CHARISMA trial. Circ Cardiovasc Qual Outcomes 2014;7:872–81.
    Crossref | PubMed
  26. Bangalore S, Makani H, Radford M, et al. Clinical outcomes with beta-blockers for myocardial infarction: a meta-analysis of randomized trials. Am J Med 2014;127:939–53.
    Crossref | PubMed
  27. Singh BN, Ellrodt G, Peter CT. Verapamil: a review of its pharmacological properties and therapeutic use. Drugs 1978;15:169–97.
    Crossref | PubMed
  28. Chaffman M, Brogden RN. Diltiazem: a review of its pharmacological properties and therapeutic efficacy. Drugs 1985;29:387–454.
    Crossref | PubMed
  29. Ezekowitz MD, Hossack K, Mehta JL, et al. Amlodipine in chronic stable angina: results of a multicenter double-blind crossover trial. Am Heart J 1995;129:527–35.
    Crossref | PubMed
  30. Glasser SP, West TW. Clinical safety and efficacy of once-a-day amlodipine for chronic stable angina pectoris. Am J Cardiol 1988;62:518–22.
    Crossref | PubMed
  31. Van Der Vring JA, Daniëls MC, Holwerda NJ, et al. Combination of calcium channel blockers and beta-adrenoceptor blockers for patients with exercise-induced angina pectoris: a double-blind parallel-group comparison of different classes of calcium channel blockers. Br J Clin Pharmacol 1999;47:493–8.
    Crossref | PubMed
  32. Husted SE, Ohman EM. Pharmacological and emerging therapies in the treatment of chronic angina. Lancet 386(9994):691–701.
    Crossref | PubMed
  33. Rousan TA, Mathew ST, Thadani U. The risk of cardiovascular side effects with anti-anginal drugs. Expert Opin Drug Saf 2016;15:1609–23.
    Crossref | PubMed
  34. Drug and Therapeutics Bulletin. Nicorandil for angina. Drug Ther Bull 1995;33:89–92.
    Crossref | PubMed
  35. Montalescot G, Sechtem U, Achenbach S, et al. 2013 ESC guidelines on the management of stable coronary artery diseas. Eur Heart J 2013;34:2949–3003.
    Crossref | PubMed
  36. Camm AJ, Maltz MB. A controlled single-dose study of the efficacy, dose response and duration of action of nicorandil in angina pectoris. Am J Cardiol 1989;63:J61–5.
    Crossref | PubMed
  37. Thadani U. Can nicorandil treat angina pectoris effectively? Nat Clin Pract Cardiovasc Med 2005;2:186–7.
    Crossref | PubMed
  38. IONA Study Group. Effect of nicorandil on coronary events in patients with stable angina: the Impact Of Nicorandil in Angina (IONA) randomised trial. Lancet 2002;359:1269–75.
    Crossref | PubMed
  39. Pisano U, Deosaran J, Leslie SJ et al. Nicorandil, gastrointestinal adverse drug reactions and ulcerations: a systematic review. Adv Ther 2016;33:320–44.
    Crossref | PubMed
  40. Cocco G, Rousseau MF, Bouvy T, et al. Effects of a new metabolic modulator, ranolazine, on exercise tolerance in angina pectoris patients treated with beta-blocker or diltiazem. J Cardiovasc Pharmacol 1992;20:131–8.
    PubMed
  41. Thadani U. Should ranolazine be used for all patients with ischemic heart disease or only for symptomatic patients with stable angina or for those with refractory angina pectoris? A critical appraisal. Expert Opin Pharmacother 2012;13:2555–63.
    Crossref | PubMed
  42. Codolosa JN, Acharjee S, Figueredo VM. Update on ranolazine in the management of angina. Vasc Health Risk Manag 2014;10:353–62.
    Crossref | PubMed
  43. Chaitman BR, Skettino SL, Parker JO, et al. Anti-ischemic effects and long-term survival during ranolazine monotherapy in patients with chronic severe angina.J Am Coll Cardiol 2004;43:1375–82.
    Crossref | PubMed
  44. Chaitman BR, Pepine CJ, Parker JO, et al. Effects of ranolazine with atenolol, amlodipine, or diltiazem on exercise tolerance and angina frequency in patients with severe chronic angina: a randomized controlled trial. JAMA 2004;291:309–16.
    Crossref | PubMed
  45. Stone PH, Gratsiansky NA, Blokhin A, et al. Antianginal efficacy of ranolazine when added to treatment with amlodipine: the ERICA (Efficacy of Ranolazine in Chronic Angina) trial. J Am Coll Cardiol 2006;48:566–75.
    Crossref | PubMed
  46. Kosiborod M, Arnold SV, Spertus JA, et al. Evaluation of ranolazine in patients with type 2 diabetes mellitus and chronic stable angina: results from the TERISA randomized clinical trial (Type 2 Diabetes Evaluation of Ranolazine in Subjects With Chronic Stable Angina). J Am Coll Cardiol 2013;61:2038–45.
    Crossref | PubMed
  47. Bairey Merz CN, Handberg EM, Shufelt CL, et al. A randomized, placebo-controlled trial of late Na current inhibition (ranolazine) in coronary microvascular dysfunction (CMD): impact on angina and myocardial perfusion reserve. Eur Heart J 2016;37:1504–13.
    Crossref | PubMed
  48. Gupta AK, Winchester D, Pepine CJ. Antagonist molecules in the treatment of angina. Expert Opin Pharmacother 2013;14:2323–42.
    Crossref | PubMed
  49. Thadani U. Modified-release formulation of trimetazidine for exceptional control of angina pectoris: fact or fiction. Am J Cardiovasc Drugs 2005;5:331–4.
    Crossref | PubMed
  50. Szwed H, Sadowski Z, Elikowski W, et al. Combination treatment in stable effort angina using trimetazidine and metoprolol: results of a randomized, double-blind, multicentre study (TRIMPOL II). TRIMetazidine in POLand. Eur Heart J 2001;22:2267–74.
    Crossref | PubMed
  51. Kelkar A, Kuo A, Frishman WH. Allopurinol as a cardiovascular drug. Cardiol Rev 2011; 19:265–71.
    Crossref | PubMed
  52. Day RO, Graham GG, Hicks M, et al. Clinical pharmacokinetics and pharmacodynamics of allopurinol and oxypurinol. Clin Pharmacokinet 2007;46:623–44.
    Crossref | PubMed
  53. Noman A, Ang DS, Ogston S, et al. Effect of high-dose allopurinol on exercise in patients with chronic stable angina: a randomised, placebo controlled crossover trial. Lancet 2010;375:2161–7.
    Crossref | PubMed
  54. O’Flynn N, Timmis A, Henderson R, et al. Management of stable angina: summary of NICE guidance. BMJ 2011;343:d4147.
    Crossref | PubMed
  55. National Institute for Health and Care Excellence. Stable Angina: Management. London: NICE, 2011. Available at: https://www.nice.org.uk/guidance/cg126 (accessed 23 February 2019).
  56. Borer JS, Fox K, Jaillon P, et al. Antianginal and antiischemic effects of ivabradine, an I(f) inhibitor, in stable angina: a randomized, double-blind, multicentered, placebo-controlled trial. Circulation 2003;107:817–23.
    Crossref | PubMed
  57. Ferrari R, Ceconi C, Selective and specific I(f) inhibition with ivabradine: new perspectives for the treatment of cardiovascular disease. Expert Rev Cardiovasc Ther 2011;9:959–73.
    Crossref | PubMed
  58. Tardif JC, Ponikowski P, Kahan T, ASSOCIATE Study Investigators. Efficacy of the I(f) current inhibitor ivabradine in patients with chronic stable angina receiving beta-blocker therapy: a 4-month, randomized, placebo-controlled trial. Eur Heart J 2009;30:540–8.
    Crossref | PubMed
  59. Werdan K, Ebelt H, Nuding S, et al. Ivabradine in combination with beta-blocker improves symptoms and quality of life in patients with stable angina pectoris: results from the ADDITIONS study. Clin Res Cardiol 2012;101:365–73.
    Crossref | PubMed
  60. Köster R, Kaehler J, Meinertz T. Treatment of stable angina pectoris by ivabradine in every day practice: the REDUCTION study. Am Heart J 2009;158:e51–7.
    Crossref | PubMed
  61. Müller-Werdan U, Stöckl G, Ebelt H, et al. Ivabradine in combination with beta-blocker reduces symptoms and improves quality of life in elderly patients with stable angina pectoris: age-related results from the ADDITIONS study. Exp Gerontol 2014;59:34–41.
    Crossref | PubMed
  62. Fox K, Ford I, Steg PG, et al. Ivabradine in stable coronary artery disease without clinical heart failure. N Engl J Med 2014;371:1091–9.
    Crossref | PubMed
  63. Thadani U. Chronic stable angina pectoris. In: Crawford MH, DiMarco JP, Paulus WJ (eds). Cardiology. 3rd ed. Philadelphia: Saunders. 2010 283–99.
  64. Rousan TA, Mathew ST, Thadani U. Drug therapy for stable angina pectoris. Drugs 2017;77:265–84.
    Crossref | PubMed
  65. Thadani U. Management of stable angina – current guidelines: a critical appraisal. Cardiovasc Drugs Ther 2016;30:419–26.
    Crossref | PubMed
  66. Ferrari R, Pavasini R, Camici PG, et al. Anti-anginal drugs-beliefs and evidence: systematic review covering 50 years of medical treatment. Eur Heart J 2019;40:190–4.
    Crossref | PubMed
  67. Fox K, Ford I, Steg PG, et al. Ivabradine for patients with stable coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): a randomised, double-blind, placebo-controlled trial. Lancet 2008;372:807–16.
    Crossref | PubMed
  68. Ferrari R, Camici PG, Crea F, et al. Expert consensus document: A ‘diamond’ approach to personalized treatment of angina. Nat Rev Cardiol 2018;15: 120–32.
    Crossref | PubMed
  69. Critchley JA, Unal B. Is smokeless tobacco a risk factor for coronary heart disease? A systematic review of epidemiological studies. Eur J Cardiovasc Prev Rehabil 2004;11:101–12.
    Crossref | PubMed
  70. Hambrecht R, Walther C, Möbius-Winkler S, et al. Percutaneous coronary angioplasty compared with exercise training in patients with stable coronary artery disease: a randomized trial. Circulation 2004;109:1371–8.
    Crossref | PubMed
  71. Second International Study of Infarct Survival Collaborative Group. Randomised trial of intravenous streptokinase, oral aspirin, both, or neither among 17,187 cases of suspected acute myocardial infarction: ISIS-2. Lancet 1988;2;349–60.
    PubMed
  72. Juul-Moller S, Edvardsson N, Jahnmatz B, et al. Double-blind trial of aspirin in primary prevention of myocardial infarction in patients with stable chronic angina pectoris. The Swedish Angina Pectoris Aspirin Trial (SAPAT) Group. Lancet 1992;340:1421– 5.
    Crossref | PubMed
  73. Bhatt DL, Fox KA, Hacke W, et al. Clopidogrel and aspirin versus aspirin alone for the prevention of atherothrombotic events. N Engl J Med 2006;354:1706–17.
    Crossref | PubMed
  74. Heart Protection Study Collaborative. MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20,536 high-risk individuals: a randomised placebo-controlled trial. Lancet 2002;360:7–22.
    Crossref | PubMed
  75. LaRosa JC, Grundy SM, Waters DD, et al. Intensive lipid lowering with atorvastatin in patients with stable coronary disease. N Engl J Med 2005;352:1425–35.
    Crossref | PubMed
  76. ACCORD Study Group, Cushman WC, Evans GW, et al. Effects of intensive blood-pressure control in type 2 diabetes mellitus. N Engl J Med 2010;362;1575–85.
    Crossref | PubMed
  77. SPRINT Research Group, Wright JT Jr, Williamson JD, et al. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med 2015;373:2103–16.
    Crossref | PubMed
  78. Action to Control Cardiovascular Risk in Diabetes Study Group, Gerstein HC, Miller ME, et al. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med 2008;358:2545–59.
    Crossref | PubMed
  79. CIBS II Stud Group. The Cardiac Insufficiency Bisoprolol Study II. Lancet 1999;353:1361.
    Crossref | PubMed
  80. The CONSENSUS Trial Study Group. Effects of enalapril on mortality in severe congestive heart failure. Results of the Cooperative North Scandinavian Enalapril Survival Study (CONSENSUS). The CONSENSUS Trial Study Group. N Engl J Med 1987;316:1429–35. PMID: 2883575" target="_blank">PubMed
  81. McMurray JJ, Ostergren J, Swedberg K, et al. Effects of candesartan in patients with chronic heart failure and reduced left-ventricular systolic function taking angiotensin-converting-enzyme inhibitors: the CHARM-Added trial. Lancet 2003;362:767–71.
    Crossref | PubMed
  82. Pfeffer MA, Braunwald E, Moyé LA, et al. Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction. Results of the survival and ventricular enlargement trial. The SAVE Investigators. N Engl J Med 1992:327;669–77.
    Crossref | PubMed
  83. Moss AJ, Williams MC, Newby DE, Nicol ED. The updated NICE guidelines: cardiac CT as the first-line test for coronary artery disease. Curr Cardiovasc Imaging Rep 2017;10:15.
    Crossref | PubMed
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