12th Congress of the European Hematology ... - Haematologica
12th Congress of the European Hematology ... - Haematologica
12th Congress of the European Hematology ... - Haematologica
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
symptoms <strong>of</strong> DVT, 3 (7.89%) previous DVT, 6 (15.73%) surgery within<br />
4 weeks before, 7 (18.42%) active cancer, 1 (2.63%) refered OA intake.<br />
5 patients (13.15%) died. Group B characteristics: 29 patients (7 male/22<br />
female). Median age: 69 years (30-92). Median D-dimer at diagnosis<br />
2096 µg/L (237-7198). 14 patients (48.27%) showed signs or symptoms<br />
<strong>of</strong> DVT, 7 (24.13%) required immobilization in <strong>the</strong> previous 4 weeks, 2<br />
(6.89%) surgery within 4 weeks before, 5 (17.24%) active cancer, 1<br />
(3.44%) was pregnant. 2 patients (6.89%) died due to complications <strong>of</strong><br />
acute event. In group A we found a statistically significant between score<br />
<strong>of</strong> clinical assessment and OS. We found a positive correlation coefficient<br />
(r 0.508) statistically significant (p=0.005) between clinical score and troponin<br />
levels in group B. There were no differences between <strong>the</strong> two Ddimer<br />
assays with regard <strong>of</strong> severity <strong>of</strong> PE, PaO2, troponin, pulmonary<br />
hypertension and o<strong>the</strong>r features. Conclusions. a) The score <strong>of</strong> clinical<br />
assessment employed in our series may be useful as a right ventricular<br />
dysfunction marker; neverthless <strong>the</strong> prognostic value <strong>of</strong> this score need<br />
to be evaluated in properly designed pospective studies. b) Results <strong>of</strong> <strong>the</strong><br />
two D-dimer assays are not related to <strong>the</strong> severity <strong>of</strong> PE assessed by<br />
various markers in our serie.<br />
0828<br />
ORAL ANTICOAGULATION REVERSAL: FRESH FROZEN PLASMA OR PROTHROMBIN<br />
COMPLEX CONCENTRATE?<br />
B. Soria Santabarbara, N. Fernandez-Mosteirin, F. Sevil, C. Salvador-<br />
Osuna, A. Godoy, N. Padron, M. Torres, J.F. Lucia, M. Giralt<br />
Hospital Universitario Miguel Servet, ZARAGOZA, Spain<br />
Background. Oral anticoagulation (OA) reversal may be required due to<br />
bleeding, asymptomatic over anticoagulation or surgical procedures. The<br />
anticoagulant effect may be reversed by a variety <strong>of</strong> Methods. vitamin K,<br />
fresh frozen plasma (FFP) and prothrombin complex concentrates (PCCs).<br />
Aims. To analize <strong>the</strong> characteristics <strong>of</strong> patients that have required rapid<br />
OA reversal and to evaluate <strong>the</strong> results <strong>of</strong> <strong>the</strong> aplication <strong>of</strong> an OA reversal<br />
guidelines. Patients and Methods. We reviewed <strong>the</strong> clinical files, demographic<br />
and clinical parameters, and complications <strong>of</strong> patientes who<br />
requiered OA reversal during a period <strong>of</strong> twelve months in our center.<br />
According to our guidelines all patients received vitamin K and FFP (rapid<br />
but no immediate reversal required) or PCC (immediate reversal).<br />
Results. 73277 samples from 6464 anticoagulated patients were processed.<br />
75 pacientes (1.16%) (33 male / 42 female), median age 76 years (range<br />
38-86) received PCC; 40 patients (0.63%) (14 male / 26 female), median<br />
age 79 years (range 49-92) received FFP. All patients were under<br />
acenocumarol treatment but 3 (2 in PCC group and 1 in FFP taking warfarin).<br />
OA indications in PCC patients: atrial fibrillation (FA) 45 (60%),<br />
pros<strong>the</strong>tic heart valve (PV) 19 (25.3%), deep venous thrombosis<br />
(DVT)/pulmonary embolism (PE) 8 (10.6%), myocardiopathy 3 (4%),<br />
stroke 1 (1.3%), acute arterial ischemia (AAI) 1 (1.3%). OA indications in<br />
FFP patients: FA 22 (55%), PV 9 (22.5%), DVT/PE 5 (12.5%), stroke 2<br />
(5%) and mitral stenosis (MS) 2 (5%). In PCC group 8 (10.6%) patients<br />
pressented a time from starting OA to PCC administration less than 4<br />
weeks, in <strong>the</strong> remaining 67 patients median <strong>of</strong> OA treatment was 37.5<br />
months (range 2-168). In FFP median time <strong>of</strong> OA was 47 months (0-168).<br />
Median INR at <strong>the</strong> moment <strong>of</strong> PCC administration 3.18 (range 1.44-9.8)<br />
and 3.93 (range 1.55-12) in FFP group. 22 patients in FFP group and 29 in<br />
PCC group were over <strong>the</strong>rapeutic anticoagulation levels.<br />
Table 1.<br />
FFP PCC<br />
Indication/Number OA Indication/Number OA<br />
Gastrointestinal Bleeding/16 10 AF, 4 PV, Intracraneal Bleeding/19 11 FA, 7 PV<br />
1 DVT, 1 MS 1 DVT<br />
Urgent surgery/11 4 FA, 3 DVT, Gastrointestinal 10 FA, 5 PV,<br />
1 PE, 1 MS Bleeding/17 1 DVT,<br />
1 AAI<br />
Mucous Bleeding/6 3 AF, 2 Stroke, Urgent 16 FA, 7 PV,<br />
1 PV surgery/28 2 DVT, 1 PE<br />
2 DM<br />
Hemoptysis/2 1 AF, 1 PV Hemoptysis/2 2 FA<br />
Intestinal obstruction 1 PV Hematuria/2 1 FA, 1 PV<br />
Intracraneal Bleeding/1 1 FA Invasive procedure 7 4 FA, 2 PV,<br />
1 DVT<br />
Retroperitoneal Bleeding/1 1 FA<br />
DIC/1 1 PV<br />
Thigh hematoma/1 1 FA<br />
12 th <strong>Congress</strong> <strong>of</strong> <strong>the</strong> <strong>European</strong> <strong>Hematology</strong> Association<br />
38 (50.6%) patients received PCC and 18 (45%) received FFP due to<br />
major bleeding. Incidence <strong>of</strong> major bleeding in our serie 0.86%. After<br />
PCC all patients normalized INR whereas 7 (17%) patients treated<br />
with FFP pressented INR over 1.5 after administration. Thrombotic<br />
complications after PCC administration were not observed. 3 (7.5%)<br />
patiens treated with FFP presented complications due to volume overload<br />
(cardiogenic shock, congestive heart failure and pulmonary edema).<br />
In <strong>the</strong> group <strong>of</strong> PCC 6 (8%) patients died due to complications <strong>of</strong><br />
<strong>the</strong> acute event and 4 (10%) in <strong>the</strong> group <strong>of</strong> FFP. Conclusions. a) Anual<br />
incidence <strong>of</strong> major bleeding in OA patients in our serie is slightly less<br />
than described in literature. b) Administration <strong>of</strong> PCC is a safety and<br />
effective treatment, able to achieve immediate reversal <strong>of</strong> OA. c)<br />
According our results FFP takes more time to correct anticoagulation;<br />
at <strong>the</strong> same time we must consider volume overload complications<br />
due FFP administration.<br />
0829<br />
ELUSIVE ASSOCIATION BETWEEN THE ANTICARDIOLIPIN ANTIBODIES AND THE VENOUS<br />
THROMBOEMBOLISM<br />
J. Gonzalez-Ordonez, 1 C. Fernández-Canal, 2 M.E. Gonzalez, 2<br />
M. Moran-Alcala, 1 D. Macias, 1 M.A. Arias1 1 Hospital San Agustin, AVILES; 2 Hospital de Cabueñes, GIJON, Spain<br />
Background. The association <strong>of</strong> some antiphospholipid antibodies and<br />
<strong>the</strong> venous thromboembolism (VTE) seems categorically established for<br />
<strong>the</strong> lupus anticoagulant but is less conclusive for <strong>the</strong> o<strong>the</strong>r related autoantibodies.<br />
Among <strong>the</strong>m, <strong>the</strong> possible thrombogenic role attributed to<br />
<strong>the</strong> anticardiolipin antibodies (ACA) is one <strong>of</strong> <strong>the</strong> most controversial<br />
mainly due to methodological issues. In fact, <strong>the</strong> available clinical data<br />
are influenced by <strong>the</strong> absence <strong>of</strong> reference material for calibration and<br />
by discrepancies about <strong>the</strong> cut-<strong>of</strong>f values used for <strong>the</strong> interpretation <strong>of</strong><br />
Results. We aim to know any possible association between anticardiolipin<br />
antibodies (using methods for IgG and IgM isotypes) and <strong>the</strong> VTE<br />
with regards to <strong>the</strong> influence <strong>of</strong> different cut-<strong>of</strong>f levels. Population and<br />
methods. We studied 574 subjects, 297 consecutive patients suffering an<br />
episode <strong>of</strong> VTE objectively diagnosed (105 with pulmonary embolism<br />
and 192 with deep venous thrombosis) and 277 healthy controls <strong>of</strong> similar<br />
gender and age [in overall 61.9(13.9) y, 50.8% males]. The 21.5% <strong>of</strong><br />
<strong>the</strong> thrombotic episodes were recurrences. The blood sample <strong>of</strong> patients<br />
was obtained several weeks after <strong>the</strong> oral anticoagulation withdraw<br />
(around seven months after <strong>the</strong> acute thrombotic episode). We performed<br />
a commercial enzyme-linked immunoabsorbant assay (ELISA)<br />
for both isotypes (IgG and IgM) <strong>of</strong> <strong>the</strong> anticardiolipin antibodies (ACA)<br />
in serum and a molecular identification <strong>of</strong> <strong>the</strong> main thrombophilic mutations<br />
(FV Leiden or prothrombin 20210A). Results. ACA <strong>of</strong> IgG isotype.<br />
Using <strong>the</strong> manufacturer criteria <strong>the</strong> 5% <strong>of</strong> samples (19 patients and 10<br />
controls) were considered as positives (>15 U/mL) (non-significant difference).<br />
We tested several arbitraries and statistical cut-<strong>of</strong>f values (90th,<br />
95th, 97.5th, 99th percentiles) obtaining a non-significant association<br />
with <strong>the</strong> exception <strong>of</strong> a very weak one using <strong>the</strong> value <strong>of</strong> 20 U/mL [OR=<br />
3.1 (1.1-9.2) (p