Quality of life in adult patients with haemophilia--a single centre experience from Sweden.
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Quality of life in adult patients with haemophilia--a single centre experience from Sweden. / Lindvall, K; Mackensen von, Sylvia; Berntorp, E.
In: HAEMOPHILIA, Vol. 18, No. 4, 4, 2012, p. 527-531.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Quality of life in adult patients with haemophilia--a single centre experience from Sweden.
AU - Lindvall, K
AU - Mackensen von, Sylvia
AU - Berntorp, E
PY - 2012
Y1 - 2012
N2 - Increased or maintained health and quality of life (HRQoL) are essential goals in health care among patients with a chronic disease. To gain an understanding of HRQoL in patients with haemophilia at the Haemophilia Treatment Centre in Malmö, Sweden, patients seen from 2004-2008 were asked to complete the Short form Health Survey, SF-36, also answering to what extent haemophilia, physically and mentally, interferes with their daily life at their annual check-up. Data were extracted from the UMAS Haemophilia Database. Interference of haemophilia in daily life was estimated using a Visual Analogue Scale. A total of 105/144 haemophilia patients were included in the study (73%); 28 mildly, 21 moderately and 56 severely affected. The median age of patients at study entry was 44.0 years (range 18-84 years). The comparison of SF-36 data of Swedish haemophilia patients with the general Swedish male population yielded no significant differences in age groups 15-24, 25-34 and 65-74 years. Patients in age groups 35-44 years, 45-54 years and 55-64 years were significantly impaired in some of their HRQoL domains. For severely affected patients who filled in SF-36 over a period of 5 years no statistical differences in HRQoL were found. For patients undergoing orthopaedic surgery HRQoL increased in most SF-36 domains. Patients reported in general on the VAS that they feel 'somehow' interfered in their daily life due to haemophilia. The results indicate a need for continuous monitoring of HRQoL to identify an increased need of care in the ageing haemophilia population.
AB - Increased or maintained health and quality of life (HRQoL) are essential goals in health care among patients with a chronic disease. To gain an understanding of HRQoL in patients with haemophilia at the Haemophilia Treatment Centre in Malmö, Sweden, patients seen from 2004-2008 were asked to complete the Short form Health Survey, SF-36, also answering to what extent haemophilia, physically and mentally, interferes with their daily life at their annual check-up. Data were extracted from the UMAS Haemophilia Database. Interference of haemophilia in daily life was estimated using a Visual Analogue Scale. A total of 105/144 haemophilia patients were included in the study (73%); 28 mildly, 21 moderately and 56 severely affected. The median age of patients at study entry was 44.0 years (range 18-84 years). The comparison of SF-36 data of Swedish haemophilia patients with the general Swedish male population yielded no significant differences in age groups 15-24, 25-34 and 65-74 years. Patients in age groups 35-44 years, 45-54 years and 55-64 years were significantly impaired in some of their HRQoL domains. For severely affected patients who filled in SF-36 over a period of 5 years no statistical differences in HRQoL were found. For patients undergoing orthopaedic surgery HRQoL increased in most SF-36 domains. Patients reported in general on the VAS that they feel 'somehow' interfered in their daily life due to haemophilia. The results indicate a need for continuous monitoring of HRQoL to identify an increased need of care in the ageing haemophilia population.
KW - Adult
KW - Humans
KW - Male
KW - Aged
KW - Middle Aged
KW - Aged, 80 and over
KW - Adolescent
KW - Questionnaires
KW - Young Adult
KW - Health Status
KW - Longitudinal Studies
KW - Quality of Life
KW - Hemophilia A/psychology
KW - Sweden
KW - Adult
KW - Humans
KW - Male
KW - Aged
KW - Middle Aged
KW - Aged, 80 and over
KW - Adolescent
KW - Questionnaires
KW - Young Adult
KW - Health Status
KW - Longitudinal Studies
KW - Quality of Life
KW - Hemophilia A/psychology
KW - Sweden
M3 - SCORING: Journal article
VL - 18
SP - 527
EP - 531
JO - HAEMOPHILIA
JF - HAEMOPHILIA
SN - 1351-8216
IS - 4
M1 - 4
ER -