Complicanze ostetriche e trombofilia Valerio De Stefano Is# ... · PDF file• Abruptio...
Transcript of Complicanze ostetriche e trombofilia Valerio De Stefano Is# ... · PDF file• Abruptio...
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Complicanzeostetricheetrombofilia
ValerioDeStefano
Is#tutodiEmatologia,UniversitàCa7olica,
PoliclinicoA.Gemelli,Roma
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Complications of pregnancy and hemostasis
• Thrombophilic disorders • Hemorrhagic disorders • Confounding associated conditions
• Thrombosis • Early and late fetal loss and other
obstetric complications • Postpartum hemorrhage
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Outlines
• Inherited and acquired thrombophilia
• Thrombophilia and association with obstetric complications
• Heparin and prevention of obstetric complications
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Which test ?
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Inheritance: autosomal dominant, incomplete penetrance
Deficiency antithrombin protein C protein S Prevalence: 1:6001 -50002 1: 2003-6004 1: 800-40005
VTE
Prevalence: 1.9% 3.7% 2.3% (unselected pts.)
Prevalence: 4.3% 4.8% 4.3% (selected pts.)
1 AT activity 2 AT antigen 3 PC antigen 4 PC activity 5 free PS and total
PS
N Eng J Med 2001; 344: 1222 (modified)
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PREVALENCE OF FACTOR V LEIDEN De Stefano et al, Sem. Thromb. Hemostas. 24, 367,1998
Healthy individuals
European ancestry (n= 16.150) 4.8 % Middle East (n= 2.366) 5.4 % Africa (n= 717) 0 Asia (n= 2.274) 1.0 % (India and Nepal n= 220) 2.7 % Native Americans (n= 568) 0.3 % African Americans (n= 957) 1.2 %
Caucasian patients with venous thrombosis n= 2.456 18.4 % n= 1.142 (consecutive) 18.8 % n= 1.314 (selected) 18.1 %
Caucasian patients with arterial thromboembolic disease. n = 4.417 5.7 %
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Blood, 1996; 88: 3698
Pooled analysis of 14 case-control studies: 7.3% heterozygotes among 3.356 patients with venous thromboembolism 3% heterozygotes among 6.267 controls (pooled odds ratio 2.5) De Stefano et al, Haematologica 2003
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Odds ratio for VTE
Heterozygous FV Leiden 4.22
Heterozygous PT20210A 2.79
Double heterozygotes 3.42
Homozygous FV Leiden 11.45
Homozygous PT20210A 6.74
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Severe HyO (homocystinuria)
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Martinelli, De Stefano & Mannucci, Nature Rev Cardiology, 2014
Thrombophilic abnormality
Risk (Odds Ratio)
AT deficiency
10.2 - 18.3
PC deficiency
4.1 - 16.2
PS deficiency
7.6 - 16.2
FV Leiden
2.5 - 7.5
PT G20210A
1.7 - 5.2
Combined alterations
6.4 (FVL + PT)
Reviewed in Rossi et al, Thromb Haemost , 2011
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LABORATORY SCREENING Italian Cooperation on Inherited Thrombophilia
ICIT Working Group, October 2004
• AT heparin cofactor • PC (functional assay) • PS (immunologic assay) • APC-resistance (and/or FV Leiden) • PT 20210A • Fasting homocysteine • LAC and aPL
Routinary search for other polymorphisms in factor V, factor II, and MTHFR (as well as in other genes) is discouraged .
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Diagnostic panel for thrombophilia of a Public Hospital in Rome (2017)
• Factor V Leiden • Factor V H1299R • Factor II G20210A • Factor XIII V34L • Beta Fbg -455GA • Plt Ag HPA1 a/b • MTHFR C677T • MTHFR A1298C
• ApoLp B-100 R3500Q • Beta-thromboglobulin • PAI 4G/5G • Homocysteine • AT, PC, PS • APC-resistance • LAC / ACA
Unappropriate tests are written in red
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677 TT MTHFR POLYMORPHISM AND RISK FOR DVT
• Controls: 390 / 2.856 (13.6%)
• Patients with DVT and inherited thrombophilia: 74 / 527 (14.0%)
• Patients with DVT and no inherited thrombophilia:
224 / 1.564 (14.3%) De Stefano et al, Sem Thromb Haemost 26,305,2000 (pooled analysis of 8 published series)
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C677T polymorphism is associated with
Increased risk for • Basal cell carcinoma • Cerebral hemorrhage • Chronic allograft nephropathy • Essential hypertension • Ischemic stroke • Lung cancer • Male infertility • Migraine • Pancreatic cancer • Primary open-angle glaucoma • Sqamous cell carcinoma of the
head and neck • Sudden hearing loss • Schizophrenia • Steatosis and fibrosis in chronic
hepatitiS C • Type 2 diabetes • Venous thromboembolism
Decreased risk • Acute lymphoblastic leukemia • Colorectal cancer • Multiple myeloma
Simone et al, Eur J Epidemiol, 2013
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Copyright ©2005 American Heart Association
Smith, G. D. et al. Arterioscler Thromb Vasc Biol 2005;25:2228-2233
Differences in mean plasma fibrinogen between those in control groups with different genotypes
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Copyright ©2005 American Heart Association
Smith, G. D. et al. Arterioscler Thromb Vasc Biol 2005;25:2228-2233
Studies reporting association between {beta}-fibrinogen genotype and CHD
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Lancet, 22 May 2004
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CARRIER CASES
CARRIER CONTROLS
ODDS RATIO (95%CI)
P
100 / 152 (65.7%)
90 / 152 (59.2%)
1.32 (0.83-2.11)
0.28
105 / 152 (69.0%)
90 / 152 (59.2%)
1.53 (0.95-2.46)
0.09
110 / 152 (72.3%)
90 / 152 (59.2%)
1.80 (1.11-2.91)
0.02
+ 22% cases in respect to the baseline prevalence
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CARRIER CASES
CARRIER CONTROLS
ODDS RATIO (95%CI)
P
30 / 829 (3.6%)
25 / 829 (3.0%)
1.41 (0.84-2.39)
0.23
40 / 829 (4.8%)
25 / 829 (3.0%)
1.63 (0.97-2.71)
0.07
50 / 829 (6.0%)
25 / 829 (3.0%)
2.06 (1.26-3.37)
0.004
+ 100% cases in respect to the baseline prevalence
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Martinelli, De Stefano & Mannucci, Nature Rev Cardiology, 2014
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Who ?
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REASONS FOR TESTING FOR INHERITED THROMBOPHILIA
Venous thromboembolism 44% Premature arterial thrombosis 23% Obstetric complications 17% Asymptomatic individuals 16%
Coppens et al. Blood 2007 Gartner et al. Contraception 2008 Laberge et al. Genet Med 2009 Suthers et al. Royal Coll Path Australasia 2009
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Obstetric complications
• Recurrent miscarriage: Ø three (two) or more Ø (consecutive) miscarriages Ø before 20 (24) weeks of gestation
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Obstetric complications
• Recurrent miscarriage: Ø anatomic factors (uterine septum,
cervical incompetence) 10-15% Ø thrombophilia 3-15% Ø chromosomal abnormalities 2-4% Ø hormonal abnormalities (hypotiroidism,
hyperprolactinemia, luteal phase defect) 25-40%
Ø unexplained 50%
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Obstetric complications
• Abruptio placentae: separation of the normally located
placenta after the 20th week of pregnancy of gestation and prior to birth.
Ø Class 1 (48%) mild, no coagulopathy, no fetal distress Ø Class 2 (27%) fetal distress, hyofibrinogenemia Ø Class 3 (24%) severe, maternal shock, coagulopathy, fetal death
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Obstetric complications
• Intrauterine growth retardation (IUGR): IUGR occurs when the unborn baby is at or below the 10th weight percentile for his or her age in weeks bruptio placentae
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Obstetric complications • Preeclampsia: new onset hypertension (>140 mm
Hg systolic or > 90 mm Hg diastolic) and proteinuria (> 300 mg in a 24 hour collection).
eclampsia, HELLP syndrome • Heritable patterns • Heterogeneity of the pathogenetic mechanisms (hemodynamic
factors, oxidative stress, thrombophilia, genetic factors, angiogenic factors),
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Inherited thrombophilia and obstetric complications • In Western countries up to 18% of pregnancies
ends in fetal loss (0.8% as stillbirth) • 5% of women experienced 2 or more fetal losses
(1% > 2 fetal losses) • Abruptio placentae complicates 1% of births • Preeclampsia complicates 5-7% of births and in
5-10% of cases HELLP can arise (0.5 per cent deliveries)
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Inherited thrombophilia and obstetric complications
• Women with AT, PC or PS deficiency were first recognized at higher risk of fetal loss in 1996
(Preston et al, Lancet 1996, Sanson et al, Thromb Haemost 1996)
• Overall, inherited thrombophilia was diagnosed in 38% of 110 women with obstetrical complications
(Kupferminc et al, New Engl J Med 1999)
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Copyright restrictions may apply.
Kovalevsky, G. et al. Arch Intern Med 2004;164:558-563.
Association of factor V Leiden mutation and recurrent pregnancy loss
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Copyright restrictions may apply.
Kovalevsky, G. et al. Arch Intern Med 2004;164:558-563.
Association of prothrombin mutation and recurrent pregnancy loss
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Kovalevsky, G. et al. Arch Intern Med 2004;164:558-563
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Kovalevsky, G. et al. Arch Intern Med 2004;164:558-563
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VENOUS THROMBOEMBOLIC DISEASE (VTE) AND OBSTETRIC COMPLICATIONS (OC)
MULTICAUSAL MODEL
Gene defect(s) Gene defect(s) Age Dietary habit Triggering event Acquired factors
VTE
OC
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Clinical phenotype of the proband
Kindreds Relatives Carriers
Venous thromboembolism
344 1,088 625
Premature arterial thrombosis
30 113 51
Obstetric complication
86 257 146
Asymptomatic 106 262 145
Total 566 1,720 967
PARTICIPANTS TO THE STUDY
Rossi et al, Thromb Haemost 2011
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Clinical phenoype of the proband
Hazard ratio for DVT
in carriers vs. non-carriers
Log-rank test
Venous thromboembolism 3.11 (95% CI 1.40-4.67)
0.002
Premature arterial thrombosis
0.55 (95% CI 0.05-5.46)
0.62
Obstetric complication not applicable 0.07
Asymptomatic not applicable 0.17
Analysis according to Cox proportional hazards model
Rossi et al, Thromb Haemost 2011
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Inherited thrombophilia and obstetric complications
• The relative risk for recurrent fetal losses (> 2) is double among the carriers of AT, PC, and PS or factor V Leiden .
• The risk for stillbirth was 2 to 7 fold increased among carriers of factor V Leiden
• The risk associated with PT 20210A is more uncertain
Rey et al, Lancet 2003 Kovalevsky et al, Arch Intern Med 2004
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IUGR Howley et al, AJOG 2005
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IUGR Howley et al, AJOG 2005
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Inherited thrombophilia and obstetric complications – uncertain associations
• Severe preeclampsia Morrison et al, Thromb Haemost 2002 kosmas et al, J Hypetens 2003 Lin et al, Obstetr Gynecol 2005
• Intrauterine growth restriction Howley et al, AJOG 2005
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Inherited thrombophilia and obstetric complications – uncertain associations
• Abruptio placentae Only 3 studies available (on 20, 27, and 50
cases) reporting inherited thrombophilia present in 30 to 50% of cases)
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CANDIDATES FOR SCREENING
• A l l w o m e n w i t h r e c u r r e n t unexplained fetal losses and non recurrent late unexplained fetal loss are candidates for screening.
• The population study “NOHA first” found a 2 to 3-fold increase in risk for miscarriage after 10 weeks of gestation among carriers of factor V Leiden or PT 20210A (JTH 2005)
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IS LMWH TREATMENT JUSTIFIED FOR PREGNANT WOMEN WITH PREVIOUS (RECURRENT) FETAL LOSS ?
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Ø It has been estimated that after one miscarriage the risk of another is 20%;
Ø after two miscarriages it is 25%,
Ø and after three miscarriages 30%.
i.e.: the probability of deliver a viable newborn after three miscarriages is 70% without any pharmacological intervention
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2003
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2004
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2007
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2008
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• Heparin and aspirin may be effective in preventing miscarriages in women with antiphopsholipid antibodies, but not in those without, as shown in two recent randomized controlled trials in women with at least two consecutive unexplained miscarriages (Clark et al, Blood 2010; Kaandorp et al, NEJM 2010)
• Efficacy of heparin has been demonstrated in two randomized pilot studies on women with a history of previous obstetric complications (Rey et al, J Thromb Haemost 2009; Gris et al, Thromb and Haemost 2010)
• Large studies on women with inheri ted thrombophilia and previous obstetric complications are urgently needed
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Low-molecular-weight heparin and recurrent placenta-mediated pregnancy complications: a meta-analysis of individual patient data from randomised controlled trials (Rodger et al, Lancet 2016)
• Data from 963 eligible women in eight trials: 480 randomly assigned to LMWH and 483 randomly assigned to no LMWH; 403/963 (42%) had thrombophilia.
• In the primary analysis, LMWH did not significantly reduce the risk of recurrent placenta-mediated pregnancy complications (LMWH 62/444 [14%] versus no LMWH 95/443 (22%), p=0·09; relative risk 0·64, 95% CI 0·36–1·11, p=0·11).
• In subgroup analyses, lLMWH in multicentre trials reduced the primary outcome in women with previous abruption (p=0·006) but not in any of the other subgroups of previous complications.
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9 th ACCP Conference, Chest 2012
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Thrombosis and Haemostasis, 2012; 107: 477
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CONCLUSIONS
• The pregnancy-related thrombotic risk of
thrombophilic women is dependent on history but also on type of thrombophilia.
• Extreme caution should be adopted for women with rare thrombophilic abnormalities, in whom reports offer controversial data.
• LMWH is not justified for prevention of recurrent fetal loss in women without thrombophilia. But results of RCT cannot applied to thrombophilic women, in whom there is evidence of benefit.