Lalić-Ćosić, Sanja

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Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom

Lalić-Ćosić, Sanja

(Универзитет у Београду, Фармацеутски факултет, 2022)

TY  - THES
AU  - Lalić-Ćosić, Sanja
PY  - 2022
UR  - https://eteze.bg.ac.rs/application/showtheses?thesesId=9096
UR  - https://fedorabg.bg.ac.rs/fedora/get/o:29381/bdef:Content/download
UR  - https://plus.cobiss.net/cobiss/sr/sr/bib/76873993
UR  - https://nardus.mpn.gov.rs/handle/123456789/21434
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4850
AB  - Preeklampsija je multisistemski poremećaj koji se javlja kao komplikacija trudnoće ipredstavlja jedan od vodećih uzroka mortaliteta i morbiditeta majki, ali i njihovog potomstva.Smatra se da preeklampsija nastaje kao posledica poremećaja u ranom razvoju placente kojidovodi do aktivacije maternalnog vaskularnog endotela što rezultuje generalizovanomvazokonstrikcijom, značajnim metaboličkim promenama, disfunkcijom endotela, pojačaniminflamatornim odgovorom i aktivacijom koagulacije. TakoĎe, dokazano je da pojavapreeklampsije u trudnoći ukazuje na postojanje nepovoljnog kardio-metaboličkog profilaţene, te je u novijim vodičima preeklampsija uvrštena u dugoročne faktore rizika za razvojkardiovaskularnih bolesti (KVB). Pored toga, preeklampsija i KVB imaju zajedničke faktorerizika, a oba poremećaja su okarakterisana i zajedničkim patofiziološkim promenama.Klinički simptomi preeklampsije, hipertenzija i proteinurija, ispoljavaju se nakon 20. nedeljegestacije, mada dijagnoza preeklampsije moţe da se postavi i u odsustvu proteinurije ukolikoje novonastala hipertenzija udruţena sa pojavom trombocitopenije, poremećene funkcijejetre, novorazvijene bubreţne insuficijencije, plućnog edema ili novonastalih vizuelnihodnosno cerebralnih poremećaja, te uteroplacentalnog poremećaja koji rezultuje zastojem urastu ploda.S obzirom da je hiperkoagulabilno stanje u preeklampsiji dodatno pojačano u odnosuna normalnu trudnoću cilj ove studije je bio da se ispita korisnost globalnih testovahemostaze, endogenog trombinskog potencijala i ukupnog hemostatskog potencijala, uproceni poremećaja hemostaze u preeklampsiji, pre i nakon poroĎaja, kao i da se utvrdipovezanost ispitivanih parametara sa ishodima preeklamptične trudnoće. Analizirane sutakoĎe i karakteristike fibrinskih ugrušaka u normalnoj i preeklamptičnoj trudnoći. Poredtoga, odreĎivani su različiti fenotipovi ekstracelularnih vezikula i analizirana je njihovapovezanost sa ispitivanim hemostatskim parametrima.U studiju je uključeno 46 trudnica sa preeklampsijom i 80 zdravih trudnica...
AB  - Pre-eclampsia is a multisystem disorder that occurs as a complication of pregnancyand is one of the leading causes of maternal mortality and morbidity, as well as of theiroffspring. The major cause of pre-eclampsia is considered to be a defect in early placentaldevelopment leading to maternal vascular endothelial activation which results in generalizedvasoconstriction, significant metabolic changes, endothelial dysfunction, enhancedinflammatory response, and coagulation activation. Also, it has been proven that theoccurrence of pre-eclampsia in pregnancy indicates the existence of an unfavourable cardio-metabolic profile in women, and recent guidelines include pre-eclampsia as a long-term riskfactor for the development of cardiovascular disease (CVD). Moreover, pre-eclampsia andCVD share common risk factors, and both disorders are characterized by commonpathophysiological changes. Clinical symptoms of preeclampsia, hypertension andproteinuria, can be seen after 20 weeks of gestation, although the diagnosis of pre-eclampsiacan be made in the absence of proteinuria if the new-onset hypertension is associated withthrombocytopenia, impaired liver function, new-onset renal failure, pulmonary oedema ornew-onset visual or cerebral disorders, and uteroplacental disorder that results in fetal growthretardation.Bearing in mind that the hypercoagulable state in pre-eclampsia is further enhancedcompared to normal pregnancy, the aim of this study was to evaluate the usefulness of globalhaemostatic assays, endogenous thrombin potential and overall haemostatic potential in theassessment of the haemostatic disorders in pre-eclampsia before and after delivery and toanalyse the results of these assays in relation to the outcomes of preeclamptic pregnancy. Thecharacteristics of fibrin clots in normal and preeclamptic pregnancies were also analyzed.Furthermore, different phenotypes of extracellular vesicles were determined and theirassociation with the investigated hemostatic parameters was analyzed.The study involved 46 pregnant women with pre-eclampsia and 80 healthy pregnantwomen...
PB  - Универзитет у Београду, Фармацеутски факултет
T2  - Универзитет у Београду
T1  - Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom
UR  - https://hdl.handle.net/21.15107/rcub_nardus_21434
ER  - 
@phdthesis{
author = "Lalić-Ćosić, Sanja",
year = "2022",
abstract = "Preeklampsija je multisistemski poremećaj koji se javlja kao komplikacija trudnoće ipredstavlja jedan od vodećih uzroka mortaliteta i morbiditeta majki, ali i njihovog potomstva.Smatra se da preeklampsija nastaje kao posledica poremećaja u ranom razvoju placente kojidovodi do aktivacije maternalnog vaskularnog endotela što rezultuje generalizovanomvazokonstrikcijom, značajnim metaboličkim promenama, disfunkcijom endotela, pojačaniminflamatornim odgovorom i aktivacijom koagulacije. TakoĎe, dokazano je da pojavapreeklampsije u trudnoći ukazuje na postojanje nepovoljnog kardio-metaboličkog profilaţene, te je u novijim vodičima preeklampsija uvrštena u dugoročne faktore rizika za razvojkardiovaskularnih bolesti (KVB). Pored toga, preeklampsija i KVB imaju zajedničke faktorerizika, a oba poremećaja su okarakterisana i zajedničkim patofiziološkim promenama.Klinički simptomi preeklampsije, hipertenzija i proteinurija, ispoljavaju se nakon 20. nedeljegestacije, mada dijagnoza preeklampsije moţe da se postavi i u odsustvu proteinurije ukolikoje novonastala hipertenzija udruţena sa pojavom trombocitopenije, poremećene funkcijejetre, novorazvijene bubreţne insuficijencije, plućnog edema ili novonastalih vizuelnihodnosno cerebralnih poremećaja, te uteroplacentalnog poremećaja koji rezultuje zastojem urastu ploda.S obzirom da je hiperkoagulabilno stanje u preeklampsiji dodatno pojačano u odnosuna normalnu trudnoću cilj ove studije je bio da se ispita korisnost globalnih testovahemostaze, endogenog trombinskog potencijala i ukupnog hemostatskog potencijala, uproceni poremećaja hemostaze u preeklampsiji, pre i nakon poroĎaja, kao i da se utvrdipovezanost ispitivanih parametara sa ishodima preeklamptične trudnoće. Analizirane sutakoĎe i karakteristike fibrinskih ugrušaka u normalnoj i preeklamptičnoj trudnoći. Poredtoga, odreĎivani su različiti fenotipovi ekstracelularnih vezikula i analizirana je njihovapovezanost sa ispitivanim hemostatskim parametrima.U studiju je uključeno 46 trudnica sa preeklampsijom i 80 zdravih trudnica..., Pre-eclampsia is a multisystem disorder that occurs as a complication of pregnancyand is one of the leading causes of maternal mortality and morbidity, as well as of theiroffspring. The major cause of pre-eclampsia is considered to be a defect in early placentaldevelopment leading to maternal vascular endothelial activation which results in generalizedvasoconstriction, significant metabolic changes, endothelial dysfunction, enhancedinflammatory response, and coagulation activation. Also, it has been proven that theoccurrence of pre-eclampsia in pregnancy indicates the existence of an unfavourable cardio-metabolic profile in women, and recent guidelines include pre-eclampsia as a long-term riskfactor for the development of cardiovascular disease (CVD). Moreover, pre-eclampsia andCVD share common risk factors, and both disorders are characterized by commonpathophysiological changes. Clinical symptoms of preeclampsia, hypertension andproteinuria, can be seen after 20 weeks of gestation, although the diagnosis of pre-eclampsiacan be made in the absence of proteinuria if the new-onset hypertension is associated withthrombocytopenia, impaired liver function, new-onset renal failure, pulmonary oedema ornew-onset visual or cerebral disorders, and uteroplacental disorder that results in fetal growthretardation.Bearing in mind that the hypercoagulable state in pre-eclampsia is further enhancedcompared to normal pregnancy, the aim of this study was to evaluate the usefulness of globalhaemostatic assays, endogenous thrombin potential and overall haemostatic potential in theassessment of the haemostatic disorders in pre-eclampsia before and after delivery and toanalyse the results of these assays in relation to the outcomes of preeclamptic pregnancy. Thecharacteristics of fibrin clots in normal and preeclamptic pregnancies were also analyzed.Furthermore, different phenotypes of extracellular vesicles were determined and theirassociation with the investigated hemostatic parameters was analyzed.The study involved 46 pregnant women with pre-eclampsia and 80 healthy pregnantwomen...",
publisher = "Универзитет у Београду, Фармацеутски факултет",
journal = "Универзитет у Београду",
title = "Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom",
url = "https://hdl.handle.net/21.15107/rcub_nardus_21434"
}
Lalić-Ćosić, S.. (2022). Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom. in Универзитет у Београду
Универзитет у Београду, Фармацеутски факултет..
https://hdl.handle.net/21.15107/rcub_nardus_21434
Lalić-Ćosić S. Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom. in Универзитет у Београду. 2022;.
https://hdl.handle.net/21.15107/rcub_nardus_21434 .
Lalić-Ćosić, Sanja, "Ispitivanje značaja markera hiperkoagulabilnosti i globalnih hemostatskih testova u trudnoći komplikovanoj preeklampsijom" in Универзитет у Београду (2022),
https://hdl.handle.net/21.15107/rcub_nardus_21434 .

Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients

Kovač, Mirjana; Basarić, Dušica; Tomić, Branko; Gvozdenov, Maja; Backović, Dragana; Lalić-Ćosić, Sanja

(Inst. Sci. inf., Univ. Defence in Belgrade, 2022)

TY  - JOUR
AU  - Kovač, Mirjana
AU  - Basarić, Dušica
AU  - Tomić, Branko
AU  - Gvozdenov, Maja
AU  - Backović, Dragana
AU  - Lalić-Ćosić, Sanja
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4437
AB  - Background/Aim. Direct oral anticoagulants (DOACs) administration significantly interferes with coagulation as-says. The aim of the study was to evaluate the effect of DOACs and DOAC-Remove® on coagulation assays dur-ing thrombophilia testing. Methods. The study was car-ried out from January 2019 to the end of June 2020. It in-cluded 30 DOAC-treated patients, 14 females and 16 males aged 23 to 63 (median age 47.6 years), tested for thrombophilia due to venous thromboembolism (VTE). Thrombophilia testing was performed using DOAC-Remove® tablets (activated charcoal). The results before and after DOAC-Remove® were compared. Results. Posi-tive lupus anticoagulant (LA) results were observed in 20% apixaban, 100% dabigatran, and 70% rivaroxaban-treated patients, while in samples after DOAC-Remove®, the LA positivity was observed only in one from the apix-aban group. Before DOAC-Remove®, the activated pro-tein C (APC) resistance (APC-R) was measurable in 40% dabigatran and 80% rivaroxaban-treated patients, while, after using DOAC-Remove®, the APC-R was measurable in all cases. Comparing the results obtained from the sam-ples before and after DOAC-Remove®, a difference was noted in relation to all dilute Russell's viper venom time (dRVVT) coagulation tests, except for the dRVVT ratio in the apixaban group. Clot-based methods for detecting the APC resistance were significantly affected by dabigatran and less by rivaroxaban. Conclusion. DOACs were prac-tically inactivated after the addition of the DOAC-Remove®, which made it possible to perform analyses for the LA and APC-R testing freely and obtain relevant re-sults.
AB  - Uvod/Cilj. Primena direktnih oralnih antikoagulansa (DOAK)
značajno utiče na testove koagulacije. Cilj rada bio je da se pro-
ceni uticaj DOAK i DOAC-Remove® tableta (aktivni ugalj) na
testove koagulacije tokom ispitivanja trombofilije. Metode.
Istraživanjem, sprovedenim od januara 2019. do juna 2020.
godine, obuhvaćeno je 30 bolesnika lečenih DOAK-om i
testiranih na trombofiliju zbog venskog tromboembolzma
(VTE). Bilo je 14 žena i 16 muškaraca, starosti od 23 do 63
godine (medijana 47,6 godina). Ispitivanje trombofilije izvršeno
je upotrebom DOAC-Remove® tableta (aktivni ugalj).
Upoređivani su rezultati pre i posle primene DOAC-Remove®.
Rezultati. Pozitivni rezultati za lupus antikoagulantni (LA) test
dobijeni su kod 20% bolesnika lečenih apiksabanom, kod
100% bolesnika lečenih dabigatranom i kod 70% lečenih riva-
roksabanom, a u uzorcima posle DOAC-Remove® pozitivnost
na LA dobijena je samo kod jednog bolesnika iz grupe lečnih
apiksabanom. Pre primene DOAC-Remove®, rezistencija na
aktivisani protein C (activated protein C resistance – APC-R) bila je
merljiva kod 40% i 80% bolesnika lečenih dabigatranom, od-
nosno rivaroksabanom, dok je posle primene DOAC-
Remove®, APC-R bila merljiva u svim slučajevima.
Upoređivanjem rezultata dobijenih iz uzoraka pre i posle
primene DOAC-Remove®, primećena je razlika u odnosu na
sve testove vremena koagulacije izvršene razblaženim Russell-
ovim zmijskim otrovom (dilute Russell’s viper venom time –
dRVVT), osim dRVVT u grupi bolesnika lečenih apiksabanom.
Na koagulacionu metodu za otkrivanje APC-R značajno je uti-
cao dabigatran, a manje rivaroksaban. Zaključak. Nakon
primene DOAC-Remove® tableta, DOAK su praktično
inaktivisani što je omogućilo izvođenje analiza za LA i APC-R i
dobijanje relevantnih rezultata testova.
PB  - Inst. Sci. inf., Univ. Defence in Belgrade
T2  - Vojnosanitetski Pregled
T1  - Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients
T1  - Uticaj DOAK i DOAC-REMOVE® na testove koagulacije u toku testiranja
trombofilije kod bolesnika lečenih primenom DOAK
VL  - 79
IS  - 12
SP  - 1248
EP  - 1254
DO  - 10.2298/VSP210217101K
ER  - 
@article{
author = "Kovač, Mirjana and Basarić, Dušica and Tomić, Branko and Gvozdenov, Maja and Backović, Dragana and Lalić-Ćosić, Sanja",
year = "2022",
abstract = "Background/Aim. Direct oral anticoagulants (DOACs) administration significantly interferes with coagulation as-says. The aim of the study was to evaluate the effect of DOACs and DOAC-Remove® on coagulation assays dur-ing thrombophilia testing. Methods. The study was car-ried out from January 2019 to the end of June 2020. It in-cluded 30 DOAC-treated patients, 14 females and 16 males aged 23 to 63 (median age 47.6 years), tested for thrombophilia due to venous thromboembolism (VTE). Thrombophilia testing was performed using DOAC-Remove® tablets (activated charcoal). The results before and after DOAC-Remove® were compared. Results. Posi-tive lupus anticoagulant (LA) results were observed in 20% apixaban, 100% dabigatran, and 70% rivaroxaban-treated patients, while in samples after DOAC-Remove®, the LA positivity was observed only in one from the apix-aban group. Before DOAC-Remove®, the activated pro-tein C (APC) resistance (APC-R) was measurable in 40% dabigatran and 80% rivaroxaban-treated patients, while, after using DOAC-Remove®, the APC-R was measurable in all cases. Comparing the results obtained from the sam-ples before and after DOAC-Remove®, a difference was noted in relation to all dilute Russell's viper venom time (dRVVT) coagulation tests, except for the dRVVT ratio in the apixaban group. Clot-based methods for detecting the APC resistance were significantly affected by dabigatran and less by rivaroxaban. Conclusion. DOACs were prac-tically inactivated after the addition of the DOAC-Remove®, which made it possible to perform analyses for the LA and APC-R testing freely and obtain relevant re-sults., Uvod/Cilj. Primena direktnih oralnih antikoagulansa (DOAK)
značajno utiče na testove koagulacije. Cilj rada bio je da se pro-
ceni uticaj DOAK i DOAC-Remove® tableta (aktivni ugalj) na
testove koagulacije tokom ispitivanja trombofilije. Metode.
Istraživanjem, sprovedenim od januara 2019. do juna 2020.
godine, obuhvaćeno je 30 bolesnika lečenih DOAK-om i
testiranih na trombofiliju zbog venskog tromboembolzma
(VTE). Bilo je 14 žena i 16 muškaraca, starosti od 23 do 63
godine (medijana 47,6 godina). Ispitivanje trombofilije izvršeno
je upotrebom DOAC-Remove® tableta (aktivni ugalj).
Upoređivani su rezultati pre i posle primene DOAC-Remove®.
Rezultati. Pozitivni rezultati za lupus antikoagulantni (LA) test
dobijeni su kod 20% bolesnika lečenih apiksabanom, kod
100% bolesnika lečenih dabigatranom i kod 70% lečenih riva-
roksabanom, a u uzorcima posle DOAC-Remove® pozitivnost
na LA dobijena je samo kod jednog bolesnika iz grupe lečnih
apiksabanom. Pre primene DOAC-Remove®, rezistencija na
aktivisani protein C (activated protein C resistance – APC-R) bila je
merljiva kod 40% i 80% bolesnika lečenih dabigatranom, od-
nosno rivaroksabanom, dok je posle primene DOAC-
Remove®, APC-R bila merljiva u svim slučajevima.
Upoređivanjem rezultata dobijenih iz uzoraka pre i posle
primene DOAC-Remove®, primećena je razlika u odnosu na
sve testove vremena koagulacije izvršene razblaženim Russell-
ovim zmijskim otrovom (dilute Russell’s viper venom time –
dRVVT), osim dRVVT u grupi bolesnika lečenih apiksabanom.
Na koagulacionu metodu za otkrivanje APC-R značajno je uti-
cao dabigatran, a manje rivaroksaban. Zaključak. Nakon
primene DOAC-Remove® tableta, DOAK su praktično
inaktivisani što je omogućilo izvođenje analiza za LA i APC-R i
dobijanje relevantnih rezultata testova.",
publisher = "Inst. Sci. inf., Univ. Defence in Belgrade",
journal = "Vojnosanitetski Pregled",
title = "Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients, Uticaj DOAK i DOAC-REMOVE® na testove koagulacije u toku testiranja
trombofilije kod bolesnika lečenih primenom DOAK",
volume = "79",
number = "12",
pages = "1248-1254",
doi = "10.2298/VSP210217101K"
}
Kovač, M., Basarić, D., Tomić, B., Gvozdenov, M., Backović, D.,& Lalić-Ćosić, S.. (2022). Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients. in Vojnosanitetski Pregled
Inst. Sci. inf., Univ. Defence in Belgrade., 79(12), 1248-1254.
https://doi.org/10.2298/VSP210217101K
Kovač M, Basarić D, Tomić B, Gvozdenov M, Backović D, Lalić-Ćosić S. Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients. in Vojnosanitetski Pregled. 2022;79(12):1248-1254.
doi:10.2298/VSP210217101K .
Kovač, Mirjana, Basarić, Dušica, Tomić, Branko, Gvozdenov, Maja, Backović, Dragana, Lalić-Ćosić, Sanja, "Influence of DOACS and DOAC-REMOVE® on coagulation assays during thrombophilia testing in DOAC-treated patients" in Vojnosanitetski Pregled, 79, no. 12 (2022):1248-1254,
https://doi.org/10.2298/VSP210217101K . .

Evaluation of global haemostatic assays and fibrin structure in patients with pre-eclampsia

Lalić-Ćosić, Sanja; Dopsaj, Violeta; Kovač, Mirjana; Pruner, Iva; Littmann, Karin; Mandić-Marković, Vesna; Miković, Željko; Antović, Aleksandra

(Wiley-Blackwell, 2020)

TY  - JOUR
AU  - Lalić-Ćosić, Sanja
AU  - Dopsaj, Violeta
AU  - Kovač, Mirjana
AU  - Pruner, Iva
AU  - Littmann, Karin
AU  - Mandić-Marković, Vesna
AU  - Miković, Željko
AU  - Antović, Aleksandra
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3609
AB  - Introduction: Haemostatic balance shifted towards hypercoagulability in normal pregnancy is even more pronounced in pre-eclampsia (P-EC). The aim of this study was to analyse haemostatic disturbances and fibrin clot properties in women with pre-eclampsia and to investigate their association with maternal and foetal outcomes. Methods: Forty-six pregnant women diagnosed with pre-eclampsia were included in the study, with blood sampling done on the morning following admission to hospital, as well as after delivery (mean duration 4.8 days). Two global haemostatic assays—endogenous thrombin potential (ETP) and assay of overall haemostatic potential (OHP)—were employed, including fibrin clot turbidity measurements and scanning electron microscopy (SEM) of representative samples. Results: Three thrombin generation parameters (ETP, t_lag and peak height) and OHP were significantly increased in pre-eclampsia compared with controls, whereas overall fibrinolytic potential (OFP—determined as a parameter of the OHP assay) had significantly lower values. Clot lysis time was significantly prolonged in patients with pre-eclampsia. In the pre-eclamptic group after delivery, we observed a significant elevation in the peak height and a reduction in the time to peak and OFP compared with values before delivery. Pre-eclamptic patients with renal complications had significantly higher values for ETP, peak height and D-dimer. Turbidity measurements and SEM revealed dense fibrin structure in patients with pre-eclampsia. Conclusion: Patients with pre-eclampsia have enhanced coagulation and impaired fibrinolysis before, and even after, delivery. In particular, the presence of multi-organ dysfunction, such as renal dysfunction, may be associated with increased thrombin generation in pre-eclampsia.
PB  - Wiley-Blackwell
T2  - International Journal of Laboratory Hematology
T1  - Evaluation of global haemostatic assays and fibrin structure in patients with pre-eclampsia
VL  - 42
IS  - 3
SP  - 322
EP  - 330
DO  - 10.1111/ijlh.13183
ER  - 
@article{
author = "Lalić-Ćosić, Sanja and Dopsaj, Violeta and Kovač, Mirjana and Pruner, Iva and Littmann, Karin and Mandić-Marković, Vesna and Miković, Željko and Antović, Aleksandra",
year = "2020",
abstract = "Introduction: Haemostatic balance shifted towards hypercoagulability in normal pregnancy is even more pronounced in pre-eclampsia (P-EC). The aim of this study was to analyse haemostatic disturbances and fibrin clot properties in women with pre-eclampsia and to investigate their association with maternal and foetal outcomes. Methods: Forty-six pregnant women diagnosed with pre-eclampsia were included in the study, with blood sampling done on the morning following admission to hospital, as well as after delivery (mean duration 4.8 days). Two global haemostatic assays—endogenous thrombin potential (ETP) and assay of overall haemostatic potential (OHP)—were employed, including fibrin clot turbidity measurements and scanning electron microscopy (SEM) of representative samples. Results: Three thrombin generation parameters (ETP, t_lag and peak height) and OHP were significantly increased in pre-eclampsia compared with controls, whereas overall fibrinolytic potential (OFP—determined as a parameter of the OHP assay) had significantly lower values. Clot lysis time was significantly prolonged in patients with pre-eclampsia. In the pre-eclamptic group after delivery, we observed a significant elevation in the peak height and a reduction in the time to peak and OFP compared with values before delivery. Pre-eclamptic patients with renal complications had significantly higher values for ETP, peak height and D-dimer. Turbidity measurements and SEM revealed dense fibrin structure in patients with pre-eclampsia. Conclusion: Patients with pre-eclampsia have enhanced coagulation and impaired fibrinolysis before, and even after, delivery. In particular, the presence of multi-organ dysfunction, such as renal dysfunction, may be associated with increased thrombin generation in pre-eclampsia.",
publisher = "Wiley-Blackwell",
journal = "International Journal of Laboratory Hematology",
title = "Evaluation of global haemostatic assays and fibrin structure in patients with pre-eclampsia",
volume = "42",
number = "3",
pages = "322-330",
doi = "10.1111/ijlh.13183"
}
Lalić-Ćosić, S., Dopsaj, V., Kovač, M., Pruner, I., Littmann, K., Mandić-Marković, V., Miković, Ž.,& Antović, A.. (2020). Evaluation of global haemostatic assays and fibrin structure in patients with pre-eclampsia. in International Journal of Laboratory Hematology
Wiley-Blackwell., 42(3), 322-330.
https://doi.org/10.1111/ijlh.13183
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