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Practical Guidelines: Lung Transplantation in Patients with Cystic Fibrosis

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-121569
  • There are no European recommendations on issues specifically related to lung transplantation (LTX) in cystic fibrosis (CF). The main goal of this paper is to provide CF care team members with clinically relevant CF-specific information on all aspects of LTX, highlighting areas of consensus and controversy throughout Europe. Bilateral lung transplantation has been shown to be an important therapeutic option for end-stage CF pulmonary disease. Transplant function and patient survival after transplantation are better than in most other indicationsThere are no European recommendations on issues specifically related to lung transplantation (LTX) in cystic fibrosis (CF). The main goal of this paper is to provide CF care team members with clinically relevant CF-specific information on all aspects of LTX, highlighting areas of consensus and controversy throughout Europe. Bilateral lung transplantation has been shown to be an important therapeutic option for end-stage CF pulmonary disease. Transplant function and patient survival after transplantation are better than in most other indications for this procedure. Attention though has to be paid to pretransplant morbidity, time for referral, evaluation, indication, and contraindication in children and in adults. This review makes extensive use of specific evidence in the field of lung transplantation in CF patients and addresses all issues of practical importance. The requirements of pre-, peri-, and postoperative management are discussed in detail including bridging to transplant and postoperative complications, immune suppression, chronic allograft dysfunction, infection, and malignancies being the most important. Among the contributors to this guiding information are 19 members of the ECORN-CF project and other experts. The document is endorsed by the European Cystic Fibrosis Society and sponsored by the Christiane Herzog Foundation.zeige mehrzeige weniger

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Metadaten
Autor(en): T. O. Hirche, C. Knoop, H. Hebestreit, D. Shimmin, A. Solé, J. S. Elborn, H. Ellemunter, P. Aurora, M. Hogardt, T. O. F. Wagner
URN:urn:nbn:de:bvb:20-opus-121569
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Kinderklinik und Poliklinik
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Pulmonary Medicine
ISSN:2090-1836
Erscheinungsjahr:2014
Band / Jahrgang:2014
Seitenangabe:621342
Originalveröffentlichung / Quelle:Pulmonary Medicine Volume 2014, Article ID 621342, 22 pages. http://dx.doi.org/10.1155/2014/621342
DOI:https://doi.org/10.1155/2014/621342
PubMed-ID:https://pubmed.ncbi.nlm.nih.gov/24800072
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):cystic fibrosis; lung transplantation
Datum der Freischaltung:19.02.2016
Urhebende Körperschaft:ECORN-CF Study Group
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung