TY - JOUR
T1 - Deep vein thrombosis after monoclonal gammopathy of undetermined significance and multiple myeloma
AU - Kristinsson, Sigurdur Y.
AU - Fears, Thomas R.
AU - Gridley, Gloria
AU - Turesson, Ingemar
AU - Mellqvist, Ulf Henrik
AU - Björkholm, Magnus
AU - Landgren, Ola
PY - 2008/11/1
Y1 - 2008/11/1
N2 - Patients with multiple myeloma (MM) have an increased risk of deep venous thrombosis (DVT), particularly when treated with immunomodulatory drugs. Recently, 2 small hospital-based studies observed persons with the MM precursor condition, monoclonal gammopathy of undetermined significance (MGUS), to be at increased risk of developing DVT. Among 4 196 197 veterans hospitalized at least once at US Veterans Affairs hospitals, we identified a total of 2374 cases of MGUS, and 39 272 persons were diagnosed with DVT (crude incidence 0.9 per 1000 person-years). A total of 31 and 151 DVTs occurred among MQUS and MM patients, respectively (crude incidence 3.1 and 8.7 per 1000 person-years, respectively; P < .01). Compared with the entire study population, the relative risk (RR) of DVT after a diagnosis of MGUS and MM was 3.3 (95% confidence interval [Cl], 2.3-4.7) and 9.2 (95% Cl, 7.9-10.8), respectively. The most prominent excess risk of DVT was found during the first year after diagnosis of MGUS (RR = 8.4; 95% Cl, 5.7-12.2) and MM (RR = 11.6; 95% Cl, 9.2-14.5). Among 229 MGUS cases (9.5%) that progressed to MM, only one person had a DVT diagnosis before transformation. Our findings suggest the operation of shared underlying mechanisms causing coagulation abnormalities among patients with MGUS and MM.
AB - Patients with multiple myeloma (MM) have an increased risk of deep venous thrombosis (DVT), particularly when treated with immunomodulatory drugs. Recently, 2 small hospital-based studies observed persons with the MM precursor condition, monoclonal gammopathy of undetermined significance (MGUS), to be at increased risk of developing DVT. Among 4 196 197 veterans hospitalized at least once at US Veterans Affairs hospitals, we identified a total of 2374 cases of MGUS, and 39 272 persons were diagnosed with DVT (crude incidence 0.9 per 1000 person-years). A total of 31 and 151 DVTs occurred among MQUS and MM patients, respectively (crude incidence 3.1 and 8.7 per 1000 person-years, respectively; P < .01). Compared with the entire study population, the relative risk (RR) of DVT after a diagnosis of MGUS and MM was 3.3 (95% confidence interval [Cl], 2.3-4.7) and 9.2 (95% Cl, 7.9-10.8), respectively. The most prominent excess risk of DVT was found during the first year after diagnosis of MGUS (RR = 8.4; 95% Cl, 5.7-12.2) and MM (RR = 11.6; 95% Cl, 9.2-14.5). Among 229 MGUS cases (9.5%) that progressed to MM, only one person had a DVT diagnosis before transformation. Our findings suggest the operation of shared underlying mechanisms causing coagulation abnormalities among patients with MGUS and MM.
UR - http://www.scopus.com/inward/record.url?scp=55749097953&partnerID=8YFLogxK
U2 - 10.1182/blood-2008-04-151076
DO - 10.1182/blood-2008-04-151076
M3 - Article
C2 - 18559977
AN - SCOPUS:55749097953
SN - 0006-4971
VL - 112
SP - 3582
EP - 3586
JO - Blood
JF - Blood
IS - 9
ER -