Therapeutic problems in elderly patients with hemophilia

被引:11
作者
Zawilska, Krystyna [1 ]
Podolak-Dawidziak, Maria [2 ]
机构
[1] Strus Hosp, Dept Hematol & Internal Dis, Poznan, Poland
[2] Wroclaw Med Univ, Dept Hematol Blood Neoplasms & Bone Marrow Transp, Wroclaw, Poland
来源
POLSKIE ARCHIWUM MEDYCYNY WEWNETRZNEJ-POLISH ARCHIVES OF INTERNAL MEDICINE | 2012年 / 122卷 / 11期
关键词
cardiovascular diseases; hemophilia; neoplasms; quality of life; renal failure; INHERITED BLEEDING DISORDERS; CHRONIC HEPATITIS-C; QUALITY-OF-LIFE; LIVER-TRANSPLANTATION; HEPATOCELLULAR-CARCINOMA; ATRIAL-FIBRILLATION; MORTALITY; DISEASE; MULTICENTER; MANAGEMENT;
D O I
10.20452/pamw.1466
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since the introduction of clotting factor concentrates, the life expectancy of patients with hemophilia has increased from 40 years in the 1960s to 60 or even 70 years today. In Poland, almost all elderly patients with hemophilia have arthropathy, the majority are infected with hepatitis C virus (HCV), and some even with hepatitis B or human immunodeficiency virus. Liver cirrhosis associated with HCV infection develops within 15 to 20 years in 20% to 30% of these patients. Coexistent diseases related to aging and affecting the heart, kidneys, and other organs constitute another challenge. To prevent ischemic heart disease, cardiovascular risk factors should be carefully monitored. The present paper describes the current recommendations for the use of antithrombotic therapy for acute coronary syndromes and atrial fibrillation in patients with hemophilia. Changes in the urinary system in hemophiliacs develop with age, often leading to dialysis. There is an urgent need for intensive physiotherapy and improved access to orthopedic treatment for patients with arthropathy. High-risk surgical procedures in these patients should be performed in specialized centers with an experienced team and a coagulation laboratory. Older patients with mild hemophilia are at an increased risk for inhibitor development following intensive factor replacement therapy for surgical or invasive procedures. Pain control is a particular challenge due to contraindications to the use of many effective analgesics; another concern is the quality of life of these patients. An increasing number of older patients with hemophilia requires a comprehensive diagnostic and therapeutic approach, preferably at hematological centers.
引用
收藏
页码:567 / 575
页数:9
相关论文
共 63 条
[1]   The growing burden of chronic disease in America [J].
Anderson, G ;
Horvath, J .
PUBLIC HEALTH REPORTS, 2004, 119 (03) :263-270
[2]   Living donor liver transplantation for hepatitis C related hepatocellular carcinoma in a haemophilia A patient [J].
Au, WY ;
Liu, CL ;
Lo, CM ;
Fan, ST ;
Lam, CK .
HAEMOPHILIA, 2005, 11 (04) :405-407
[3]  
Bajo M A, 2000, Adv Perit Dial, V16, P170
[4]   Sexual evaluation and treatment of ageing males with haemophilia [J].
Bar-Chama, N. ;
Snyder, S. ;
Aledort, L. .
HAEMOPHILIA, 2011, 17 (06) :875-883
[5]   Cardiovascular risk assessment in haemophilia patients [J].
Biere-Rafi, Sara ;
Baarslag, Manuel A. ;
Peters, Marjolein ;
Kruip, Marieke J. H. A. ;
Kraaijenhagen, Roderik A. ;
Den Heijer, Martin ;
Buller, Harry R. ;
Kamphuisen, Pieter W. .
THROMBOSIS AND HAEMOSTASIS, 2011, 105 (02) :274-278
[6]  
BONTEMPO FA, 1987, BLOOD, V69, P1721
[7]  
Central Statistical Office, 2009, CONC STAT YB POL
[8]   Mortality rates, life expectancy, and causes of death in people with hemophilia A or B in the United Kingdom who were not infected with HIV [J].
Darby, Sarah C. ;
Kan, Sau Wan ;
Spooner, Rosemary J. ;
Giangrande, Paul L. F. ;
Hill, Frank G. H. ;
Hay, Charles R. M. ;
Lee, Christine A. ;
Ludlam, Christopher A. ;
Williams, Michael .
BLOOD, 2007, 110 (03) :815-825
[9]   The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99 [J].
Darby, SC ;
Keeling, DM ;
Spooner, RJD ;
Kan, SW ;
Giangrande, PLF ;
Collins, PW ;
Hill, FGH ;
Hay, CRM .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (07) :1047-1054
[10]   The challenge of an ageing haemophilic population [J].
Dolan, G. .
HAEMOPHILIA, 2010, 16 :11-16