TY - JOUR
T1 - Acromegaly management in the Nordic countries: A Delphi consensus survey
AU - Arlien-Søborg, Mai C.
AU - Dal, Jakob
AU - Heck, Ansgar
AU - Stochholm, Kirstine
AU - Husted, Eigil
AU - Feltoft, Claus Larsen
AU - Rasmussen, Åse Krogh
AU - Feldt-Rasmussen, Ulla
AU - Andreassen, Mikkel
AU - Klose, Marianne Christina
AU - Nielsen, Torben Leo
AU - Andersen, Marianne Skovsager
AU - Christensen, Louise Lehmann
AU - Krogh, Jesper
AU - Jarlov, Anne
AU - Bollerslev, Jens
AU - Nermoen, Ingrid
AU - Oksnes, Marianne
AU - Dahlqvist, Per
AU - Olsson, Tommy
AU - Berinder, Katarina
AU - Hoybye, Charlotte
AU - Petersson, Maria
AU - Akerman, Anna karin
AU - Wahlberg, Jeanette
AU - Ekman, Bertil
AU - Engstrom, Britt Eden
AU - Johannsson, Gudmundur
AU - Ragnarsson, Oskar
AU - Olsson, Daniel
AU - Sigurjónsdóttir, Helga Ágústa
AU - Fougner, Stine Lyngvi
AU - Matikainen, Niina
AU - Vehkavaara, Satu
AU - Metso, Saara
AU - Jaatinen, Pia
AU - Hämäläinen, Päivi
AU - Rintamäki, Reeta
AU - Yliaska, Iina
AU - Immonen, Heidi
AU - Mäkimattila, Sari
AU - Cederberg-Tamminen, Henna
AU - Viukari, Marianna
AU - Nevalainen, Pasi
AU - Nuutila, Pirjo
AU - Schalin-Jäntti, Camilla
AU - Burman, Pia
AU - Jørgensen, Jens Otto Lunde
PY - 2024/9
Y1 - 2024/9
N2 - Objective: Acromegaly is associated with increased morbidity and mortality if left untreated. The therapeutic options include surgery, medical treatment, and radiotherapy. Several guidelines and recommendations on treatment algorithms and follow-up exist. However, not all recommendations are strictly evidence-based. To evaluate consensus on the treatment and follow-up of patients with acromegaly in the Nordic countries. Methods: A Delphi process was used to map the landscape of acromegaly management in Denmark, Sweden, Norway, Finland, and Iceland. An expert panel developed 37 statements on the treatment and follow-up of patients with acromegaly. Dedicated endocrinologists (n = 47) from the Nordic countries were invited to rate their extent of agreement with the statements, using a Likert-type scale (1−7). Consensus was defined as ≥80% of panelists rating their agreement as ≥5 or ≤3 on the Likert-type scale. Results: Consensus was reached in 41% (15/37) of the statements. Panelists agreed that pituitary surgery remains first line treatment. There was general agreement to recommend first-generation somatostatin analog (SSA) treatment after failed surgery and to consider repeat surgery. In addition, there was agreement to recommend combination therapy with first-generation SSA and pegvisomant as second- or third-line treatment. In more than 50% of the statements, consensus was not achieved. Considerable disagreement existed regarding pegvisomant monotherapy, and treatment with pasireotide and dopamine agonists. Conclusion: This consensus exploration study on the management of patients with acromegaly in the Nordic countries revealed a relatively large degree of disagreement among experts, which mirrors the complexity of the disease and the shortage of evidence-based data.
AB - Objective: Acromegaly is associated with increased morbidity and mortality if left untreated. The therapeutic options include surgery, medical treatment, and radiotherapy. Several guidelines and recommendations on treatment algorithms and follow-up exist. However, not all recommendations are strictly evidence-based. To evaluate consensus on the treatment and follow-up of patients with acromegaly in the Nordic countries. Methods: A Delphi process was used to map the landscape of acromegaly management in Denmark, Sweden, Norway, Finland, and Iceland. An expert panel developed 37 statements on the treatment and follow-up of patients with acromegaly. Dedicated endocrinologists (n = 47) from the Nordic countries were invited to rate their extent of agreement with the statements, using a Likert-type scale (1−7). Consensus was defined as ≥80% of panelists rating their agreement as ≥5 or ≤3 on the Likert-type scale. Results: Consensus was reached in 41% (15/37) of the statements. Panelists agreed that pituitary surgery remains first line treatment. There was general agreement to recommend first-generation somatostatin analog (SSA) treatment after failed surgery and to consider repeat surgery. In addition, there was agreement to recommend combination therapy with first-generation SSA and pegvisomant as second- or third-line treatment. In more than 50% of the statements, consensus was not achieved. Considerable disagreement existed regarding pegvisomant monotherapy, and treatment with pasireotide and dopamine agonists. Conclusion: This consensus exploration study on the management of patients with acromegaly in the Nordic countries revealed a relatively large degree of disagreement among experts, which mirrors the complexity of the disease and the shortage of evidence-based data.
KW - acromegaly
KW - Delphi
KW - dopamine agonist
KW - growth hormone
KW - growth hormone receptor antagonist
KW - insulin-like growth factor i
KW - somatostatin
KW - Humans
KW - Consensus
KW - Scandinavian and Nordic Countries/epidemiology
KW - Delphi Technique
KW - Acromegaly/therapy
KW - Human Growth Hormone/therapeutic use
KW - Surveys and Questionnaires
KW - Somatostatin/analogs & derivatives
U2 - 10.1111/cen.15095
DO - 10.1111/cen.15095
M3 - Journal article
C2 - 38865284
AN - SCOPUS:85195918201
SN - 0300-0664
VL - 101
SP - 263
EP - 273
JO - Clinical Endocrinology
JF - Clinical Endocrinology
IS - 3
ER -