The 2018 ESC/ESH Hypertension Guideline and the 2019 NICE Hypertension Guideline, How and Why They Differ

Bagua

Well-known member
Staff member
The 2018 ESC/ESH Hypertension Guideline and the 2019 NICE Hypertension Guideline, How and Why They Differ

Terry McCormack; Rebecca J. Boffa; Nicholas R. Jones; Serena Carville; Richard J. McManus




Eur Heart J. 2019;40(42):3456-3458.




Following the impressive results of the SPRINT study published in 2015,[1] international hypertension guideline committees have gradually updated their advice. In 2017 the American College of Cardiology and American Heart Association (ACC/AHA) were the first to do so,[2] followed by the European Society of Cardiology and European Society of Hypertension (ESC/ESH) in 2018,[3] and most recently the National Institute for Health and Care Excellence (NICE), who published their 'Hypertension in Adults' guideline in August 2019.[4] These three influential guidelines will inform global practice, yet, whilst agreeing on many points, there are also important differences in their recommendations. Here we focus on the European perspective, introducing the headline changes and then asking how and why the NICE guidelines differ from those of the ESC/ESH.


The ESC/ESH guidelines reiterate the importance of reducing blood pressure (BP) below 140/90 mmHg for all patients, but go further to suggest, where tolerated, that systolic blood pressure (SBP) for those aged under 65 should be reduced to between 120 and 129 mmHg (). The recommended treatment threshold was retained at an SBP of 140 mmHg, and recommended treatment for people with diabetes if BP is ≥140/90 mmHg but with a target of <130/80 mmHg. In terms of treatment, ESC/ESH recommend a three-step approach with single pill dual therapy if SBP is ≥150 mmHg and a single pill triple therapy if this is insufficient to obtain control. ESC/ESH also advocate low-dose spironolactone for resistant hypertension, where triple therapy is unsuccessful.

1575324365950.png
 
The updated NICE guideline continues to recommend treating to a threshold and target BP of 140/90 mmHg, as opposed to the lower treatment targets recommended by the ESC/ESH. Much of the guideline remains little changed from the 2011 guideline CG127,[5] with the major change being to reduce the risk threshold for treatment in uncomplicated stage 1 hypertension to 10% 10-year cardiovascular risk (previously 20%). The recommended treatment pathway remains similar to the previous guideline, with monotherapy at step 1 retained. Step 2 and 3 recommendations were amended so that medication choice focused on patient preferences. Similar to ESC/ESH, NICE recommends spironolactone, other diuretics, and alpha- or beta-blockers for resistant hypertension. Guidance for hypertension in those with diabetes was included in the NICE hypertension guideline for the first time, having previously fallen into the remit of the diabetes guideline. A patient decision aid accompanies the NICE treatment recommendations.



To understand how such differences can occur between the NICE and ESC/ESH guidelines, it is necessary to recognize that they use two different processes with different aims and methods.[6,7] NICE produces government-funded national guidelines intended for population treatment based on both clinical evidence and cost-effective analysis. NICE start with a series of questions, which can be quite specific, based on feedback from a broad range of stakeholders. ESC and ESH are medical societies who fund the clinical guideline development, with a broad scope, intended for treatment of individuals in many European countries with different socio-economic populations. The societies are largely made up of subject specialists whose needs drive the guidelines. The ESC/ESH guideline therefore encompasses nearly all aspects of BP control, including, for example, pregnancy and peri-operative management. NICE, on the other hand, produces a broad range of guidelines, and the scope of each is more focused in order to reduce overlap between guidelines. As a result, the management of hypertension in pregnancy and management of hypertension for secondary prevention of established cardiovascular disease, or in those with chronic kidney disease (CKD), were excluded from the scope of the hypertension guideline and covered in separate guidelines.



Differences in recommendations within the treatment pathway were in part due to differences in the guideline scopes. The ESC/ESH recommendations for initial single pill combinations were justified by evidence of improved adherence.[8,9] Gupta et al., using urine analysis to indicate the absence of prescribed drugs, demonstrated a linear relationship between the number of pills a patient was expected to take and their lack of adherence.[9] This evidence was not included in the NICE guideline due to adherence not being within the scope, and instead there is a cross-reference to the NICE Medicines Adherence Guideline.[10] Recommendations for resistant hypertension were similar between the guidelines although based on different rationales. The ESC/ESH based recommendations on the PATHWAY-2 study, which found a short-term benefit of spironolactone for BP outcomes.[11] NICE instead based recommendations for resistant hypertension on consensus in the absence of evidence. These recommendations were also consistent with the findings of PATHWAY-2, although this trial was excluded from the review due to only having short-term, surrogate outcomes.

The guideline development process also differed between guidelines. The ESC/ESH guideline is based on a 'Task Force' of 21, mostly specialist, physicians who review five classes of graded evidence. The Committee for Practice Guidelines oversees this process. ESC/ESH is very inclusive of all available evidence, including health economics papers, but has no in-house health economics capability. After publication, it is the individual 'National Societies' who are responsible for endorsement, translations, and implementation.

On the other hand, NICE guidelines involve a slightly smaller committee, representing a diverse composition of knowledge and experience, tailored to each guideline topic. A chair is appointed before scoping who should not have direct reputational or financial conflicts of interest, and is thus usually a non-specialist. The committee includes a mix of people from primary and secondary care, as well as patients. A technical team including systematic reviewers and health economists assists the committee and undertakes the systematic reviews rating evidence according to the GRADE process. NICE emphasize the importance of pre-specifying the areas covered within the guideline in order to reduce bias. As a result, the protocols for each systematic review are pre-defined early in the development process, and the committee determine the evidence level that would be required to inform recommendations. The committee also select the areas of the scope that require original health economics analyses, based on where recommendations may have the highest resource impact. NICE guidelines undergo internal quality assurance and a public consultation phase before the final document is published, whereas ESC/ESH utilize internal peer review.



The evidence base and its interpretation also differed within each guideline, which had implications for recommendations. This fundamental difference in interpretation is exemplified by the SPRINT trial. NICE considered that the methodology of measuring BP could not be translated into UK clinical practice and so did not lower the recommended treatment target. The use of automated devices set on a time delay, with an unaccompanied rest period, is not common practice in the UK and was considered likely to result in significantly lower BP readings than those taken in routine clinical practice. Other concerns related to the heterogeneity of study populations (inclusion of patients with established cardiovascular or renal disease), and limited long-term safety data at lower achieved BPs. The NICE committee therefore could not confidently recommend a lower BP target for the UK population. However, the NICE guideline acknowledges the possible benefits of lower BP targets, and recommendations now emphasize the importance of maintaining BP below 140/90 mmHg. ESC/ESH considered the limitations of the BP measurement and made the interpretation that the lower and higher targets in SPRINT would correspond to 130–140 mmHg vs. 140–150 mmHg, respectively. Both guideline committees considered the risk of harms of treatment vs. the benefits. In both guidelines, recommendations related to targets in the type 2 diabetes population were based on the results of the ACCORD study, which was similar to SPRINT in design but did not show similar benefits of lower targets.[12]



Both guidelines made similar recommendations on when to initiate treatment, including all adults with stage 2 or 3 hypertension, as well as people with persistent stage 1 hypertension who have at least moderate 10-year cardiovascular risk. In support of this recommendation, the ESC/ESH guideline cited the results of the HOPE-3 primary prevention study, which showed that treatment for people with stage 1 hypertension and intermediate cardiovascular risk resulted in a significant reduction in major cardiovascular outcomes.[13] The NICE guideline was more prescriptive with the specific risk threshold at which to initiate treatment, suggesting that this should be based on 10-year cardiovascular risk assessment using a tool such as QRISK2. NICE based this advice on the results of an original health economics model produced for the guideline, incorporating the treatment effects from the meta-analysis of Brunstrom et al.[14] This found that treatment initiation at a 10% QRISK2 threshold gave an incremental cost-effectiveness ratio (ICER) of £10 000 for males at age 60 and was therefore deemed cost-effective. Treatment initiation was not strongly recommended below this threshold because the benefit of treatment was less certain, with evidence from observational research that treating low-risk stage hypertension (<10% 10-year cardiovascular disease risk), a group not included in previous randomized controlled trials, could result in harm from treatment side effects.[15]



Regarding the elderly and very elderly, both guidelines acknowledge the distinction between frailty and simply advancing age, and take into account the uncertainty around the evidence for treatment effects. However, ESC/ESH conclude that less intensive treatment in the elderly could be too conservative for those who are active and independent rather than frail. NICE decided to retain recommendations for a less intensive initiation threshold and treatment target of 150/90 mmHg based on HYVET,[16] due to the lack of direct comparative evidence for the influence of frailty in this population. Both NICE and ESC/ESH recommend the use of standing BP measurements for people with diabetes, symptoms of postural hypotension, or age above 80.



There are therefore both similarities and differences between the two guidelines. Both guidelines seek to direct health professionals to the most clinically effective treatments, but some discrepancies exist due to differences in the aims, context, and methodologies of each guideline.
 
References

  1. Sprint Research Group, Wright JT Jr, Williamson JD, Whelton PK, Snyder JK, Sink KM, Rocco MV, Reboussin DM, Rahman M, Oparil S, Lewis CE, Kimmel PL, Johnson KC, Goff DC Jr, Fine LJ, Cutler JA, Cushman WC, Cheung AK, Ambrosius WT. A randomized trial of intensive versus standard blood-pressure control. N Engl J Med 2015;373:2103–2116.
  2. Whelton PK, Carey RM, Aronow WS, DE Casey Jr, Collins KJ, Dennison Himmelfarb C, DePalma SM, Gidding S, Jamerson KA, Jones DW, MacLaughlin EJ, Muntner P, Ovbiagele B, Smith SC Jr, Spencer CC, Stafford RS, Taler SJ, Thomas RJ, Williams KA Sr, Williamson JD, Wright JT Jr. 2017 ACC/AHA/AAPA/ABC/ACPM/AGS/APhA/ASH/ASPC/NMA/PCNA Guideline for the prevention, detection, evaluation, and management of high blood pressure in adults: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. J Am Coll Cardiol 2018;71:e127–e248.
  3. Williams B, Mancia G, Spiering W, Agabiti Rosei E, Azizi M, Burnier M, Clement DL, Coca A, de Simone G, Dominiczak A, Kahan T, Mahfoud F, Redon J, Ruilope L, Zanchetti A, Kerins M, Kjeldsen SE, Kreutz R, Laurent S, Lip GYH, McManus R, Narkiewicz K, Ruschitzka F, Schmieder RE, Shlyakhto E, Tsioufis C, Aboyans V, Desormais I; ESC Scientific Document Group. 2018 ESC/ESH Guidelines for the management of arterial hypertension. Eur Heart J 2018;39:3021–3104.
  4. National Institute for Health and Care Excellence. Hypertension in adults: diagnosis and management. NICE Guideline 136. August, 2019. https://www.nice.org.uk/guidance/ng136.
  5. Krause T, Lovibond K, Caulfield M, McCormack T, Williams B, Guideline Development Group. Management of hypertension: summary of NICE guidance. BMJ 2011;343:d4891.
  6. National Institute for Health and Care Excellence. Developing NICE guidelines: the manual. Process and Methods [PMG20]. https://www.nice.org.uk/process/pmg20/chapter/introduction-and-overview2018.
  7. European Society of Cardiology. Writing ESC Guidelines: ESC issued recommendations for formulating Guidelines. http://www.escardio.org/Guidelines-...s/Guidelinesdevelopment/Writing-ESCGuidelines.
  8. Corrao G, Parodi A, Nicotra F, Zambon A, Merlino L, Cesana G, Mancia G. Better compliance to antihypertensive medications reduces cardiovascular risk. J Hypertens 2011;29:610–618.
  9. Gupta P, Patel P, Strauch B, Lai FY, Akbarov A, Gulsin GS, Beech A, Maresova V, Topham PS, Stanley A, Thurston H, Smith PR, Horne R, Widimsky J, Keavney B, Heagerty A, Samani NJ, Williams B, Tomaszewski M. Biochemical screening for nonadherence is associated with blood pressure reduction and improvement in adherence. Hypertension 2017;70:1042–1048.
  10. National Institute for Health and Care Excellence. Medicines adherence: involving patients in decisions about prescribed medicines and supporting adherence [CG76]. https://www.nice.org.uk/guidance/cg76/chapter/1-Guidance#supportingadherence2009.
  11. Williams B, MacDonald TM, Morant S, Webb DJ, Sever P, McInnes G, Ford I, Cruickshank JK, Caulfield MJ, Salsbury J, Mackenzie I, Padmanabhan S, Brown MJ; British Hypertension Society's PATHWAY Studies Group. Spironolactone versus placebo, bisoprolol, and doxazosin to determine the optimal treatment for drug-resistant hypertension (PATHWAY-2): a randomised, double-blind, crossover trial. Lancet 2015;386:2059–2068.
  12. Accord Study Group, Cushman WC, Evans GW, Byington RP, Goff DC, Jr., Grimm RH, Jr., Cutler JA, Simons-Morton DG, Basile JN, Corson MA, Probstfield JL, Katz L, Peterson KA, Friedewald WT, Buse JB, Bigger JT, Gerstein HC, Ismail-Beigi F. Effects of intensive blood-pressure control in type 2 diabetes mellitus. N Engl J Med 2010;362:1575–1585.
  13. Lonn EM, Bosch J, Lopez-Jaramillo P, Zhu J, Liu L, Pais P, Diaz R, Xavier D, Sliwa K, Dans A, Avezum A, Piegas LS, Keltai K, Keltai M, Chazova I, Peters RJ, Held C, Yusoff K, Lewis BS, Jansky P, Parkhomenko A, Khunti K, Toff WD, Reid CM, Varigos J, Leiter LA, Molina DI, McKelvie R, Pogue J, Wilkinson J, Jung H, Dagenais G, Yusuf S; HOPE-3 Investigators. Blood-pressure lowering in intermediate-risk persons without cardiovascular disease. N Engl J Med 2016;374:2009–2020.
  14. Brunstrom M, Carlberg B. Association of blood pressure lowering with mortality and cardiovascular disease across blood pressure levels: a systematic review and meta-analysis. JAMA Intern Med 2018;178:28–36.
  15. Sheppard JP, Stevens S, Stevens R, Martin U, Mant J, Hobbs FDR, McManus RJ. Benefits and harms of antihypertensive treatment in low-risk patients with mild hypertension. JAMA Intern Med 2018;178:1626–1634.
  16. Beckett N, Peters R, Tuomilehto J, Swift C, Sever P, Potter J, McCormack T, Forette F, Gil-Extremera B, Dumitrascu D, Staessen JA, Thijs L, Fletcher A, Bulpitt C, HYVET Study Group. Immediate and late benefits of treating very elderly people with hypertension: results from active treatment extension to Hypertension in the Very Elderly randomised controlled trial. BMJ 2011;344:d7541.



Disclaimer
The NICE guideline referred to in this article was produced by the National Guideline Centre for the National Institute for Health and Care Excellence (NICE). The views expressed in this article are those of the authors and not necessarily those of NICE.
National Institute for Health and Care Excellence (2019) Hypertension in adults. Available from https://www.nice.org.uk/guidance/ng136.

Eur Heart J. 2019;40(42):3456-3458. © 2019 Oxford University Press
Copyright 2007 European Society of Cardiology. Published by Oxford University Press. All rights reserved.
 
Top