Klinički značaj dijagnostičkog algoritma u detekciji blažih poremećaja hemostaze kod pacijentkinja sa menoragijom
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Djukić SM, Andjelković NV, Vukomanović VR, Simić Vukomanović IM, Djukić AL, Antović JP. Klinički značaj dijagnostičkog algoritma u detekciji blažih poremećaja hemostaze kod pacijentkinja sa menoragijom. Vojnosanit Pregl [Internet]. 12. April 2021. [citirano 20. Septembar 2026.];77(6). Dostupno na: https://test.aseestant.ceon.rs/index.php/vsp/article/view/17002

Sažetak

Uvod/Cilj. Poremećaji koagulacije mogu da budu uzrok menoragije kod žena u reproduktivnom periodu. Cilj istraživanja bio je utvrđivanje učestalosti poremećaja koagulacije kod žena sa menoragijom i kreiranje odgovarajućeg algoritma za detektovanje poremećaja koagulacije. Metode. Ispitivani su parametri koagulacije kod 115 žena (36,1 ± 9,6 godina) sa anamnestičkim podatkom o postojanju menoragije koja je verifikovana primenom semi-kvantitativne metode ˗ Pictorial Bleeding Assessment Chart (PBAC) sa skorom ≥ 100. Rezultati. Menoragija je bila objektivno verifikovana kod 55,7% ispitanica. Pacijentkinje sa menoragijom imale su viši PBAC skor [medijana (Md) = 150,0 vs. Md = 50,0; p < 0,001], ali ne i dužinu menstrualnog ciklusa (7,2 ± 2,1 dana vs. 7,3 ± 1,9 dana; p > 0,05). Poremećaji koagulacije bili su detektovani kod 12 (10,4%) ispitanica – snižene vrednosti faktora (F) IX: Ac kod 4 (3,5%), F VII: Ac kod 1 (0,9%), F X: Ac kod 1 (0,9%), F XI: Ac kod 1 (0,9%), a 5 (4,3%) pacijentkinja ispunjavalo je kriterijume blage forme von Willebrandove bolesti (VWB) tip 1. Ispitanice sa poremećajima koagulacije su imale produženo protrombinsko vreme (PT) [Md = 13,1 s (12,2–14,8 s) vs. Md = 12,5 s (10,6–18,3) s; p = 0,032]. Anemija je dijagnostikovana kod 61 (53,0%) pacijentkinje. Najjači prediktor poremećaja hemostaze bilo je postojanje objektivno verifikovane menoragije (količnik verovatnoće 0.018), a zatim prisustvo anemije (12.43), PT (2.35), dužina menstrualnog ciklusa (1.16) i vrednost PBAC skora (0.98). Zaključak. Rezultati istraživanja ukazuju na potrebu formiranja dijagnostičkog algoritma poremećaja hemostaze. Sofisticirane i skupe laboratorijske analize za dijagnozu poremećaja hemostaze bilo bi racionalno sprovesti kod pacijentkinja koje imaju menoraguju verifikovanu objektivnim metodama, PBAC skor > 100, produžen menstrualni ciklus, anemiju i produženo PT.

Ključne reči

von Willebrand-ova bolest
hemostaza, poremećaji
anemija
DOI: 10.2298/VSP180330123D

Reference

Shaw JA, Rivlin ME, Shaw HA. Menorrhagia. Medscape. Avail-able from: http://emedicine.medscape.com/article/255540-overview#showall [accessed 2012 November 27].

ACOG Committee on Practice Bulletins-Gynecology. American Col-lege of Obstetricians and Gynecologists. ACOG practice bulletin: management of anovulatory bleeding. Int J Gynaecol Obstet 2001; 72(3): 263–71.

Shapley M, Jordan K, Croft PR. An epidemiological survey of symptoms of menstrual loss in the community. Br J Gen Pract 2004; 54(502): 359–63.

Dilley A, Drews C, Lally C, Austin H, Barnhart E, Evatt B. A survey of gynecologists concerning menorrhagia: perceptions of bleeding disorders as a possible cause. J Womens Health Gend Based Med 2002; 11(1): 39–44.

Hallberg L, Nilsson L. Determination of menstrual blood loss. Scand J Clin Lab Invest 1964; 16(2): 244–48.

Higham JM, O'Brien PMS, Shaw RW. Assessment of menstrual blood loss using a pictorial chart. Br J Obstet Gynaecol 1990; 97(8): 734–9.

Vilos GA, Lefebvre G, Graves GR. SOGC clinical practice guidelines. Guidelines for the management of abnormal uter-ine bleeding. J Obstet Gynaecol Can 2001; 106: 1–6.

Albers JR, Hull SK, Wesley RM. Abnormal uterine bleeding. Am Fam Physician 2004; 69(8): 1915–26.

El-Hemaidi I, Gharaibeh A, Shehata H. Menorrhagia and bleed-ing disorders. Curr opin Obstet Gynecol 2007; 19(6): 513–20.

Kadir RA, Economides DL, Sabin CA, Owens D, Lee CA. Frequency of inherited bleeding disorders in women with menorrhagia. Lancet 1998; 351(9101): 485–89.

Shankar M, Lee CA, Sabin CA, Economides DL, Kadir RA. Von Willebrand disease in women with menorrhagia: a sys-tematic review. BJOG 2004; 111(7): 734–40.

Plug I, Mauser-Bunchoten EP, Brocker-Vriends AH, van Am-stel HK, van der Bom JG, van Diemen-Homan JE, et al. Bleeding in carriers of hemophilia. Blood 2006; 108(1): 52–6.

Mannucci PM, Duga S, Peyvandi F. Recessively inherited coagu-lation disorders. Bood 2004; 104(5): 1243–52.

Philipp CS, Faiz A, Dowling N, Dilley A, Michaels LA, Ayers C, et al. Age and the prevalence of bleeding disorders in wom-en with menorrhagia. Obstet Gynecol 2005; 105(1): 61–6.

Dilley A, Drews C, Miller C, Lally C, Austin H, Ramaswamy D, et al. Von Willebrand disease and other inherited bleeding disorders in women with diagnosed menorrohagia. Obstet Gy-necol 2001; 97(4): 630–36.

Djukic SM, Lekovic D, Jovic N, Varjacic M. Unnecessary Hyster-ectomy due to Menorrhagia and Disorders of Hemostasis: An Example of Overuse and Excessive Demand for Medical Ser-vices. Front Pharmacol 2016; 7: 507.

Vercellini P, Vendola N, Ragni G, Trespidi L, Oldani S, Cro-signani PG. Abnormal Uterine Bleeding Associated with Iron-Deficiency Anemia. Etiology and role of hysteroscopy. J Re-prod Med 1993; 38 (7): 502–4.

Biron C, Bengler C, Gris JC, Schved JF. Acquired isolated factor VII deficiency during sepsis. Haemostasis 1997; 27(2): 51–6.

White B, Martin M, Kelleher S, Browne P, McCann SR, Smith OP. Successful use of recombinant FVIIa (Novoseven) in the management of pulmonary haemorrhage secondary to Asper-gillus infection in a patient with leukaemia and acquired FVII deficiency. Br J Haematol 1999; 106(1): 254–5.

Weisdorf D, Hasegawa D, Fair DS. Acquired factor VII defi-ciency associated with aplastic anaemia: correction with bone marrow transplantation. Br J Haematol 1989; 71(3): 409–13.

Toor AA, Slungaard A, Hedner U, Weisdorf DJ, Key NS. Ac-quired factor VII deficiency in hematopoietic stem cell trans-plant recipients. Bone Marrow Transplant 2002; 29(5): 403–8.

Raucourt E, Dumont MD, Tourani JM, Hubsch JP, Riquet M, Fischer AM. Acquired factor VII deficiency associated with pleural liposarcoma. Blood Coagul Fibrinolysis 1994; 5(5): 833–6.

Mehta J, Singhal S, Mehta BC. Factor VII inhibitor. J Assoc Physicians India 1992; 40(1): 44.

Brunod M, Chatot-Henry C, Mehdaoui H, Richer C, Fonteau C. Acquired anti-factor VII (proconvertin) inhibitor: hemorrhage and thrombosis. Thromb Haemost 1998; 79(5): 1065–6.

Okajima K, Ishii M. Life-threatening bleeding in a case of au-toantibody induced factor VII deficiency. Int J Hematol 1999; 69(2): 129–32.

Aguilar C, Lucia JF, Hernandez P. A case of an inhibitor auto-antibody to coagulation factor VII. Haemophilia 2003; 9(1): 119–20.

Pinotti M, Bertolucci C, Portaluppi F, Colognesi I, Frigato E, Foà A, et al. Daily and circadian rhythms of tissue factor pathway in-hibitor and factor VII activity. Arterioscler Thromb Vasc Biol 2005; 25(3): 646–9.

Colognesi I, Pasquali V, Foa`A, Renzi P, Bernardi F, Bertolucci C, et al. Temporal variations of coagulation factor VII activity in mice are influenced by lighting regime. Chronobiol Int 2007; 24(2): 305–13.

Siboni SM, Spreafico M, Calo L, Maino A, Santagostino E, Federici AB, et al. Gynaecological and obstetrical problems in women with different bleeding disorders. Haemophilia 2009; 15(6): 1291–9.

Hutspardol S, Sirachainan N, Soisamrong A, Atchararit N, O-Prasertsawat P, Chuansumrit A. Hemostatic defects in Thai ado-lescents with menorrhagia. J Med Assoc Thai 2010; 93(4): 436–42.

James A, Kouides P, Abdul-Kadir R, Edlund M, Federici AB, Halimeh S, et al. Von Willebrand disease and other bleeding disorders in women: consensus on diagnosis and management from an international expert panel. Am Obstet Gynecol 2009; 201(1): 12.e1–8.

Tosetto A, Castaman G, Rodeghiero F. Assessing bleeding in von Willebrand disease with bleeding score. Blood Rev 2007; 21(2): 89–97.

Rodeghiero F, Tosetto A, Abshire T, Arnold DM, Coller B, James P, et al. ISTH/SSC joint VWF and Perinatal/Pediatric Hemo-stasis Subcommittees Working Group. ISTH/SSC bleeding as-sessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders. J Thromb Haemost 2010; 8(9): 2063–5.