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[Home infusion therapy for Pompe disease: Recommendations for German-speaking countries]. / Heiminfusionstherapie bei Morbus Pompe: Konsensusempfehlungen für den deutschsprachigen Raum.
Hahn, Andreas; Lampe, Christina; Boentert, Matthias; Hundsberger, Thomas; Löscher, Wolfgang; Wenninger, Stephan; Ziegler, Andreas; Lagler, Florian; Ballhausen, Diana; Schlegel, Thomas; Schoser, Benedikt.
Affiliation
  • Hahn A; Abteilung Kinderneurologie, Sozialpädiatrie und Epileptologie, Universitätsklinikum Gießen und Marburg GmbH Standort Gießen, Deutschland.
  • Lampe C; Abteilung Kinderneurologie, Sozialpädiatrie und Epileptologie, Universitätsklinikum Gießen und Marburg GmbH Standort Gießen, Deutschland.
  • Boentert M; Klinik für Neurologie mit Institut für Translationale Neurologie, Universitätsklinikum Münster; Klinik für Innere Medizin, Bereich Neurologie, UKM-Marienhospital Steinfurt, Deutschland.
  • Hundsberger T; Klinik für Neurologie, Kantonsspital St. Gallen, Schweiz.
  • Löscher W; Department Neurologie, Medizinische Universität Innsbruck, Österreich.
  • Wenninger S; Friedrich-Baur- Institut der Neurologischen Klinik , Klinikum der Universität München, Deutschland.
  • Ziegler A; Sektion für Neuropädiatrie und Stoffwechselmedizin, Zentrum für Kinder- und Jugendmedizin, Universitätsklinikum Heidelberg, Deutschland.
  • Lagler F; Universitätsklinik für Kinder- und Jugendheilkunde Paracelsus Medizinische Privatuniversität Salzburg, Österreich.
  • Ballhausen D; Unité pédiatrique des maladies métaboliques, Département Femme-Mère-Enfant, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Schweiz.
  • Schlegel T; Kanzlei für Medizinrecht (Prof. Schlegel, Hohmann & Partner), Frankfurt am Main, Deutschland.
  • Schoser B; Friedrich-Baur- Institut der Neurologischen Klinik , Klinikum der Universität München, Deutschland.
Fortschr Neurol Psychiatr ; 89(12): 630-636, 2021 Dec.
Article in De | MEDLINE | ID: mdl-33561874
ABSTRACT

BACKGROUND:

Pompe disease is a lysosomal multisystem disorder with predominant proximal myopathy. Treatment with enzyme replacement therapy (ERT) is available requiring life-long biweekly infusions of recombinant α-glucosidase. To minimize the burden of ERT patients ask for home infusion therapy. AIMS AND

METHODS:

Pompe disease experts from Germany, Austria, and Switzerland discussed in two consensus meetings in 2019 and 2020 requirements for home infusion therapy, adequate execution of treatment, and the legal situation for delegating physicians. RESULTS AND

DISCUSSION:

Home infusion therapy is principally feasible for patients with Pompe disease if certain preconditions are fulfilled, but the decision to implement has to be made on an individual basis. The treating physician delegates the execution of ERT ad personam to nursing staff but retains full legal responsibility. Home infusion therapy has to be carried out by specially trained and qualified staff. Infusion-related risks comprise mainly allergic reactions, and adequate medical treatment must be warranted. In German-speaking countries, clear rules for conducting home infusion therapy are needed to reduce psychosocial stress for patients with Pompe disease, and providing legal certainty for delegating physicians.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Home Infusion Therapy Type of study: Guideline Limits: Humans Country/Region as subject: Europa Language: De Journal: Fortschr Neurol Psychiatr Year: 2021 Type: Article

Full text: 1 Database: MEDLINE Main subject: Glycogen Storage Disease Type II / Home Infusion Therapy Type of study: Guideline Limits: Humans Country/Region as subject: Europa Language: De Journal: Fortschr Neurol Psychiatr Year: 2021 Type: Article