Skip to main content
Log in

Medikamentöse antihypertensive Therapie

Wo stehen wir?

Antihypertensive drug therapy

Where do we stand?

  • Schwerpunkt
  • Published:
Der Internist Aims and scope Submit manuscript

Zusammenfassung

Die medikamentöse antihypertensive Therapie ist auf allen Ebenen der Prävention eine der erfolgreichsten medizinischen Maßnahmen überhaupt. In Deutschland hat sich die Behandlungssituation in den letzten Jahren deutlich verbessert. Heute steht uns eine breite Palette gut wirksamer und gut verträglicher antihypertensiver Substanzen zur Verfügung. Die Kombinationstherapie hat in der Hypertoniebehandlung eine lange und erfolgreiche Tradition, insbesondere mit sinnvollen fixen Kombinationen. Die Verwendung von fixen Kombinationen ist darüber hinaus der Therapieadhärenz sehr förderlich, denn diese hängt ganz wesentlich von der Anzahl der einzunehmenden Medikamente ab. Zur Diskussion stehen der Stellenwert der β-Blocker und die doppelte Blockade des Renin-Angiotensin-Aldosteron-Systems. Hier muss die Interpretation der entsprechenden Studien sehr sorgfältig betrieben werden. Die blutdrucksenkende Wirkung einer Substanz kann ohne Berücksichtigung der Tageszeit, des Messzeitpunkts und des Zeitpunkts der Einnahme nicht umfassend beurteilt werden. Dies ist besonders wichtig mit Blick auf die 24-h-Wirkung. Ebenso muss eine optimale antihypertensive Therapie hinsichtlich der Dosis und Dosierungsintervalle den individuellen Blutdruckrhythmus über die Zeit berücksichtigen. Die Bedeutung des zentralen (aortalen) Blutdrucks als Zielblutdruck wird zunehmen.

Abstract

Antihypertensive drug therapy is one of the most successful medical measures ever, at all levels. The treatment situation in Germany has clearly improved in recent years. Nowadays, a wide range of very effective and well-tolerated hypertensive substances is available. Combination therapy has a long and successful tradition in hypertensive treatment, especially with suitable fixed combinations. Furthermore, the administration of fixed combinations is very beneficial to therapy adherence because it is essentially dependent on the number of drugs to be taken. The value of beta blockers and the double blockade of the renin-angiotensin-aldosterone system are under discussion and the interpretation of corresponding studies must be conducted very carefully. The hypertensive effect of a substance cannot be comprehensively assessed without taking the time of day, the time point of measurement and the time point of intake into consideration. This is particularly important with respect to the effect over 24 h. Optimal antihypertensive therapy must also take into consideration the individual blood pressure rhythm with respect to the dose and dosing intervals. The importance of the central (aortic) blood pressure as target blood pressure will increase.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Abb. 1
Abb. 2
Abb. 3
Abb. 4
Abb. 5
Abb. 6

Literatur

  1. Brixius K, Middeke M, Lichtenthal A et al (2007) Nitric oxide, erectile dysfunction and beta-blocker treatment (MR NOED study): benefit of nebivolol versus metoprolol in hypertensive men. Clin Exp Pharmacol Physiol 34(4):327–331

    Article  CAS  PubMed  Google Scholar 

  2. Chapman N, Chang CL, Dahlof B et al (2008) Effect of doxazosin gastrointestinal therapeutic system as third-line antihypertensive therapy on blood pressure and lipids in the Anglo-Scandinavian Cardiac Outcomes Trial. Circulation 118:42–48

    Article  CAS  PubMed  Google Scholar 

  3. Diederichs C, Neuhauser H (2014) Regional variations in hypertension prevalence and management in Germany: results from the German Health Interview and Examination Survey (DEGS 1). J Hypertens 32(7):1405–1414

  4. Gesundheitsberichterstattung des Bundes. http://www.gbe-bund.de

  5. Haller H, Ito S, Izzo JL Jr et al (2011) Olmesartan for the delay or prevention of microalbuminuria in type 2 diabetes. N Engl J Med 364(10):907–917

  6. Holzgreve H (2003) Combination versus monotherapy as initial treatment in hypertension. Herz 28:725–732

    Article  PubMed  Google Scholar 

  7. Law MR, Wald NJ, Morris JK et al (2003) Value of low dose combination treatment with blood pressure lowering drugs: analysis of 354 randomised trials. BMJ 326:1427–1431

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  8. Lane DA, Shah S, Beevers DG (2007) Low-dose spironolactone in the management of resistant hypertension: a surveillance study. J Hypertens 25:891–894

  9. Li NC, Lee A, Whitmer RA et al (2010) Use of angiotensin receptor blockers and risk of dementia in a predominantly male population: prospective cohort analysis. BMJ 340:b5465

    Article  PubMed Central  PubMed  Google Scholar 

  10. Lindholm LH et al (2005) Should betablockers remain first choice in the treatment of primary hypertension? A meta-analysis. Lancet 366:1545

    Article  CAS  PubMed  Google Scholar 

  11. Mann JF, Schmieder RE, McQueen M et al (2008) Renal outcomes with telmisartan, ramipril, or both, in people at high vascular risk (the ONTARGET study): a multicentre, randomised, double-blind, controlled trial. Lancet 372(9638):547–553

    Article  CAS  PubMed  Google Scholar 

  12. McMurray JJV, Packer M, Desai AS et al (2014) Angiotensin-neprilysin inhibition versus enalapril in heart failure. N Engl J Med 371:993–1004

  13. Middeke M (2013) Chronopathologie der Hypertonie und antihypertensive Chronotherapie. Akt Kardiol 2:183–188

    Article  Google Scholar 

  14. Middeke M (2013) Augmentation des aortalen Blutdruckes – Ursachen, kardiale Folgen und Konsequenzen für die antihypertensive Therapie. Akt Kardiol 2:151–156

    Article  Google Scholar 

  15. Middeke M et al (2013) Blood pressure and heart rate in hypertensives under nebivolol and metoprolol – a double blind cross over study. ESH, Mailand

  16. Middeke M (2014) Resistente Hypertonie: was tun? Nieren- und Hochdruckkrankheiten 43(4):177–186

  17. National Institute for Health and Clinical Excellence (o J) Hypertension: clinical management of primary hypertension in adults. Clinical guidelines: methods, evidence and recommendations. http://www.nice.org.uk/guidance/CG127

  18. Parving HH, Brenner BM, McMurray JJ et al (2012) Cardiorenal end points in a trial of aliskiren for type 2 diabetes. N Engl J Med 367:2204–2213

  19. Pischon T, Sharma AM, Mansmann U, Agrawal R (2003) Effect of forced titration of nebivolol on response rate in obese hypertensive patients. Am J Hypertens 16:98–100

    Article  PubMed  Google Scholar 

  20. Poirier L, Cléroux J, Nadeau A, Lacourcière Y (2001) Effects of nebivolol and atenolol on insulin sensitivity and haemodynamics in hypertensive patients. J Hypertens 19:1429–1435

  21. Predel HG et al (2001) Integrated effects of the vasodilating betablocker nebivolol on exercise performance, energy metabolism, cardiovascular and neurohormonal parameters in physically active patients. J Hum Hyp 15:715–721

  22. Ruilope LM, Dukat A, Böhm M et al (2010) Blood-pressure reduction with LCZ696, a novel dual-acting inhibitor of the angiotensin II receptor and neprilysin: a randomised, double-blind, placebo-controlled, active comparator study. Lancet 375:1255–1266

    Article  CAS  PubMed  Google Scholar 

  23. Van Bortel LM, Baak MA van (1992) Exercise tolerance with nebivolol and atenolol. Cardiovasc Drugs 6:239–247

    Article  Google Scholar 

  24. Van Nueten L, Schelling A, Vertommen C et al (1997) Nebivolol vs enalapril in the treatment of essential hypertension: a double-blind randomised trial. J Hum Hypertens 11:813–819

  25. Van Nueten L, Lacourcière Y, Vyssoulis G et al (1998) Nebivolol versus nifedipine in the treatment of essential hypertension: a double-blind, randomized, comparative trial. Am J Ther 5:237–243

    Article  Google Scholar 

  26. Rapsomaniki E, Timmis A, George J et al (2014) Blood pressure and incidence of twelve cardiovascular diseases: lifetime risks, healthy life-years lost, and age-specific associations in 1.25 million people. Lancet 383:1899–1911

    Article  PubMed Central  PubMed  Google Scholar 

  27. The Blood Pressure Lowering Treatment Trialist’s Collaboration (2014) Blood pressure-lowering treatment based on cardiovascular risk: a meta-analysis of individual patient data. Lancet 384:591–598

    Article  Google Scholar 

  28. Thomopoulos C, Parati G, Zanchetti A (2014) Effects of blood pressure lowering on outcome incidence in hypertension. 1. Overview, meta-analyses, and meta-regression analyses of randomized trials. J Hypertens 32:2285–2295

  29. Weber MA, Schiffrin EL, White WB et al (2014) Clinical practice guidelines for the management of hypertension in the community. A statement by the American Society of Hypertension and the International Society of Hypertension. J Hypertens 32:3–15

  30. Williams B, Lacy PS, Thom SM et al (2006) Differential impact of blood pressure-lowering drugs on central aortic pressure and clinical outcomes: principal results of the Conduit Artery Function Evaluation (CAFE) study. Circulation 113:1213–1225

    Article  CAS  PubMed  Google Scholar 

  31. Yusuf S, Teo KK, Pogue J et al (2008) Telmisartan, ramipril, or both in patients at high risk for vascular events. N Engl J Med 358:1547–1559

  32. Mancia G, Fagard R, Narkiewicz K et al (2013) 2013 ESH/ESC guidelines for the management of arterial hypertension. J Hypertens 31:1281–1357

  33. James PA, Oparil S, Carter BL et al (2014) 2014 Evidence-based guideline for the management of high blood pressure in adults: report from the Panel members appointed to the Eighth Joint National Committee (JNC 8). JAMA 311:507–520

    Article  CAS  PubMed  Google Scholar 

  34. Middeke M (2010) Hypertensiologie. Dtsch Med Wochenschr 135:1772–1774

    Google Scholar 

Download references

Einhaltung ethischer Richtlinien

Interessenkonflikt. M. Middeke: in den letzten 5 Jahren Vortragshonorare von Berlin-Chemie, Daichii, Novartis, Bayer, Takeda, Glaxo, Servier und Pfizer sowie Honorare für wissenschaftliche Beratung von Novartis.

Dieser Beitrag beinhaltet keine Studien an Menschen oder Tieren.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. Middeke.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Middeke, M. Medikamentöse antihypertensive Therapie. Internist 56, 230–239 (2015). https://doi.org/10.1007/s00108-014-3570-2

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00108-014-3570-2

Schlüsselwörter

Keywords

Navigation