Aktuelle Kardiologie 2016; 5(01): 27-31
DOI: 10.1055/s-0041-109629
Übersichtsarbeit
Georg Thieme Verlag KG Stuttgart · New York

Pulmonalklappe

Pulmonary Valve
E. S. Kehmeier
1   Klinik für Kardiologie, Pneumologie und Angiologie, Herzzentrum der Heinrich-Heine-Universität Düsseldorf
,
F. de Haan
2   Kardiologische Gemeinschaftspraxis Solingen
,
O. Kretschmar
3   Pädiatrische Kardiologie, Kinder-Herzzentrum, Kinderspital Zürich, Schweiz
› Author Affiliations
Further Information

Publication History

Publication Date:
23 February 2016 (online)

Zusammenfassung

Pulmonalklappenerkrankungen (PK-Erkrankungen) treten nach wie vor meist im Rahmen komplexer angeborener Herzfehler oder nach deren Korrektur auf, mit einer relevanten Zahl erworbener PK-Erkrankungen ist auch zukünftig nicht zu rechnen. Das Auftreten einer klinischen Beschwerdesymptomatik zeigt i. d. R. den medizinischen Handlungsbedarf an. Symptomatische PK-Fehler und hochgradige Vitien müssen meist zeitnah behandelt werden, zwecks Erhalt der myokardialen Funktion und der Lebensqualität/körperlichen Belastbarkeit des Patienten. Hier kommt der interventionellen Therapie eine führende Rolle zu, die Weiterentwicklung von Transkatheter-Herzklappen erlaubt die Versorgung auch komplexer anatomischer Veränderungen im rechtsventrikulären Ausflusstrakt (RVOT). Operative Verfahren hingegen behalten ihren Stellenwert in der Therapie kombinierter Vitien. Zukunftsperspektiven bietet das „tissue engineering“ durch mitwachsende Herzklappen.

Abstract

Pulmonary valve disease is a common finding in complex congenital heart disease, either native or after corrective surgery in childhood. In contrast, acquired pulmonic valve disease is rare and numbers will not increase in future. Symptom onset mostly indicates the need for therapy. Generally, symptomatic pulmonic valve disease and/or severe malformations require therapy, in order to preserve myocardial function and quality of life/exercise capacity of the patient. Meanwhile, interventional procedures gain profound impact, as further development of transcatheter heart valves offers a broad application even in complex anatomic RVOT morphologies. However, operative procedures maintain their role in the treatment of combined cardiac lesions. Future perspectives are offered by tissue engineering with self-growing human heart valves.

 
  • Literatur

  • 1 Baumgartner H, Bonhoeffer P, De Groot NM et al. ESC Guidelines for the management of grown-up congenital heart disease (new version 2010). Eur Heart J 2010; 31: 2915-2957
  • 2 Nelson JS, Pasquali SK, Pratt CN et al. Long-term survival and reintervention after the Ross procedure across the pediatric age spectrum. Ann Thorac Surg 2015; 99: 2086-2095
  • 3 Bansal N, Kumar SR, Baker CJ et al. Age-related outcomes of the Ross procedure over 20 years. Ann Thorac Surg 2015; 99: 2077-2085
  • 4 Warnes CA, Williams RG, Bashore TM et al. ACC/AHA 2008 Guidelines for the Management of Adults with Congenital Heart Disease: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (writing committee to develop guidelines on the management of adults with congenital heart disease). Circulation 2008; 118: e714-833
  • 5 Loogen F, Seipel L, Gleichmann U et al. IV. Erworbene Herzklappenfehler. In: Diethelm L, Olsson O, Strnad F, Vieten H, Zuppinger A, Hrsg. Handbuch der medizinischen Radiologie. Heidelberg: Springer; 1977: 207-210
  • 6 Ananthakrishna A, Balasubramonium VR, Thazhath HK et al. Balloon pulmonary valvuloplasty in adults: immediate and long-term outcomes. J Heart Valve Dis 2014; 23: 511-515
  • 7 Bonhoeffer P, Boudjemline Y, Saliba Z et al. Percutaneous replacement of pulmonary valve in a right-ventricle to pulmonary-artery prosthetic conduit with valve dysfunction. Lancet 2000; 356: 1403-1405
  • 8 Cheatham JP, Hellenbrand WE, Zahn EM et al. Clinical and Hemodynamic Outcomes up to 7 Years After Transcatheter Pulmonary Valve Replacement in the US Melody Valve Investigational Device Exemption Trial. Circulation 2015; 131: 1960-1970
  • 9 Malekzadeh-Milani S, Ladouceur M, Patel M et al. Incidence and predictors of Melody® valve endocarditis: a prospective study. Arch Cardiovasc Dis 2015; 108: 97-106
  • 10 Meadows JJ, Moore PM, Berman DP et al. Use and performance of the Melody Transcatheter Pulmonary Valve in native and postsurgical, nonconduit right ventricular outflow tracts. Circ Cardiovasc Interv 2014; 7: 374-380
  • 11 Ewert P, Horlick E, Berger F. First implantation of the CE-marked transcatheter Sapien pulmonic valve in Europe. Clin Res Cardiol 2011; 100: 85-87
  • 12 Cao QL, Kenny D, Zhou D et al. Early clinical experience with a novel self-expanding percutaneous stent-valve in the native right ventricular outflow tract. Catheter Cardiovasc Interv 2014; 84: 1131-1137
  • 13 Sierra J, Christenson JT, Lahlaidi NH et al. Right ventricular outflow tract reconstruction: what conduit to use? Homograft or Contegra?. Ann Thorac Surg 2007; 84: 606-610
  • 14 Shin HJ, Kim YH, Ko JK et al. Outcomes of mechanical valves in the pulmonic position in patients with congenital heart disease over a 20-year period. Ann Thorac Surg 2013; 95: 1367-1371
  • 15 Cebotari S, Lichtenberg A, Tudorache I et al. Clinical application of tissue engineered human heart valves using autologous progenitor cells. Circulation 2006; 114 (1 Suppl.) I132-137