How I treat age-related morbidities in elderly persons with hemophilia

被引:142
作者
Mannucci, Pier M. [1 ]
Schutgens, Roger E. G. [2 ]
Santagostino, Elena [1 ]
Mauser-Bunschoten, Evelien P. [2 ]
机构
[1] Maggiore Hosp, A Bianchi Bonomi Hemophilia & Thrombosis Ctr, Ist Ricovero & Cura Carattere Sci, Mangiagalli & Regina Elena Fdn,Dept Med & Med Spe, I-20122 Milan, Italy
[2] Univ Med Ctr Utrecht, Dept Hematol, Van Creveldkliniek, Utrecht, Netherlands
关键词
SEROTONIN REUPTAKE INHIBITORS; INHERITED BLEEDING DISORDERS; FACTOR-VIII INHIBITORS; ACTIVATED FACTOR-VII; ATRIAL-FIBRILLATION; LIFE EXPECTANCY; RISK-FACTORS; ANTITHROMBOTIC THERAPY; THROMBOLYTIC THERAPY; MULTICENTER COHORT;
D O I
10.1182/blood-2009-07-215665
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In persons with hemophilia, life expectancy is now approaching that of the general male population, at least in countries that can afford regular replacement therapy with coagulation factor concentrates. The new challenges for comprehensive treatment centers are thus to provide optimal health care for this aging population of patients, who often present not only with the comorbidities typically associated with hemophilia (arthropathy, chronic pain, blood-borne infections), but also with common age-related illnesses such as cardiovascular disease and cancer. There are no evidence-based guidelines for the management of these conditions, which often require drugs that interfere with hemostasis, enhance the bleeding tendency, and warrant more intensive replacement therapy. At the moment, elderly patients with hemophilia affected by other diseases should be managed like their age-group peers without hemophilia, provided replacement therapy is tailored to the heightened risk of bleeding associated with the need for invasive procedures and drugs that further compromise the deranged hemostasis. More detailed advice is provided on the schedules of replacement therapy needed to tackle cardiovascular diseases, such as acute coronary syndromes and nonvalvular atrial fibrillation, because these conditions will become more and more frequent challenges for the comprehensive treatment centers. (Blood. 2009; 114: 5256-5263)
引用
收藏
页码:5256 / 5263
页数:8
相关论文
共 71 条
  • [1] Ahlberg A., 1965, Acta Orthop Scand Suppl, P3, DOI DOI 10.3109/ORT.1965.36.SUPPL-77.01
  • [2] Antithrombotic and thrombolytic therapy for ischemic stroke
    Albers, Gregory W.
    Amarenco, Pierre
    Easton, J. Donald
    Sacco, Ralph L.
    Teal, Philip
    [J]. CHEST, 2008, 133 (06) : 630S - 669S
  • [3] Mortality rates and causes of death among all HIV-positive individuals with hemophilia in Canada over 21 years of follow-up
    Arnold, Donald M.
    Julian, Jim A.
    Walker, Irwin R.
    [J]. BLOOD, 2006, 108 (02) : 460 - 464
  • [4] Treatment of atrial fibrillation
    Bajpai, Abhay
    Savelieva, Irina
    Camm, A. John
    [J]. BRITISH MEDICAL BULLETIN, 2008, 88 (01) : 75 - 94
  • [5] Economic evaluation of major knee surgery with recombinant activated factor VII in hemophilia patients with high titer inhibitors and advanced knee arthropathy: exploratory results via literature-based modeling
    Ballal, Rahul D.
    Botteman, Marc F.
    Foley, Isaac
    Stephens, Jennifer M.
    Wilke, Caitlyn T.
    Joshi, Ashish V.
    [J]. CURRENT MEDICAL RESEARCH AND OPINION, 2008, 24 (03) : 753 - 768
  • [6] Modulation of human platelet aggregation by the phosphodiesterase type 5 inhibitor sildenafil
    Berkels, R
    Klotz, T
    Sticht, G
    Englemann, U
    Klaus, W
    [J]. JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2001, 37 (04) : 413 - 421
  • [7] Potency, selectivity, and consequences of nonselectivity of PDE inhibition
    Bischoff, E
    [J]. INTERNATIONAL JOURNAL OF IMPOTENCE RESEARCH, 2004, 16 (Suppl 1) : S11 - S14
  • [8] Experimental melanoma metastasis in lungs of mice with congenital coagulation disorders
    Bruggemann, Lois W.
    Versteeg, Henri H.
    Niers, Tatjana M.
    Reitsma, Pieter H.
    Spek, C. Arnold
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (6B) : 2622 - 2627
  • [9] Prophylaxis in people with haemophilia
    Coppola, Antonio
    Franchini, Massimo
    Tagliaferri, Annarita
    [J]. THROMBOSIS AND HAEMOSTASIS, 2009, 101 (04) : 674 - 681
  • [10] Currier Judith S, 2008, Circulation, V118, pe29, DOI 10.1161/CIRCULATIONAHA.107.189624