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WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

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WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013
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Page 1: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

WOMEN WITH BLEEDING DISORDERS

Nairobi, Kenya

June 25, 2013

Page 2: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

OBJECTIVES

• Discuss the types of bleeding disorders affecting women

• Distinguish sex-linked inheritance from autosomal inheritance

• Explain carrier versus non-carrier states in women

• List common bleeding symptoms in women

• Identify approaches available to treat bleeding in women

• Examine ways to treat bleeding episodes specific to women

Page 3: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

TYPES OF BLEEDING DISORDERS IN WOMEN

- Hemophilia: very rare, more commonly symptomatic carrier

- Von Willebrand disease

- Other plasma protein (factor) deficiencies

- Platelet function defects

- Fibrinolysis inhibitor deficiencies

- Hereditary hemorrhagic telangiectasia (HHT)

- Ehlers-Danlos

ADDITIONAL TEXT EXAMPLE

Page 4: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

CARRIERS OF HEMOPHILIA

• For many years, people believed that only men could have symptoms of hemophilia

• We now know that women who carry the hemophilia gene can experience symptoms.

• A woman with < 40% factor levels is no different from a man with the same factor levels—she has hemophilia

• A woman with levels of 40-60% who experiences abnormal bleeding is called a symptomatic carrier

Page 5: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

CARRIER VERSUS NON-CARRIER

• Can occur on sex chromosomes and autosomes

• Trait generally not expressed in carriers

• Level of missing protein in carriers can be quite low; even in the mild range

• Some carriers may be symptomatic

• Remember: all daughters born to men with hemophilia are obligate carriers.

Page 6: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

PLASMA PROTEIN DEFICIENCIES

Sometimes called rare bleeding disorders (RBDs)1 or recessively-inherited coagulation defects (RICDs)2

Differ from hemophilia A & B1,2,3

• Genetics

• Epidemiology

• Clinical presentation

• Diagnostic evaluation

• Treatment

May lack specific protein concentrate for treatment

1Bolton-Maggs PHBet al. Haemophilia 2004; 10: 593-628.2Mannucci PM, Duga S, Peyvandi F. Blood 2004; 104: 1243-1252.3Munn, James E. Nursing Care of Children and Adolescents with Cancer and Blood Disorders, Fourth Edition, Glenview, IL; Association of Pediatric Hematology Oncology Nurses; 2011: 818-876.

Page 7: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

PLATELET DISORDERS

Giulio Bizzozero discovered function of platelets in 1882

Role of platelets in hemostasis:

• Primary hemostatic plug

• Secretion of substances to promote

• Platelet recruitment

• Vessel contraction

• Coagulation

• Provide optimal surface for coagulation to proceed

Giulio Bizzozero

Munn, James E. Nursing Care of Children and Adolescents with Cancer and Blood Disorders, Fourth Edition, Glenview, IL; Association of Pediatric Hematology Oncology Nurses; 2011: 818-876.

Page 8: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

PLATELETS

MegakaryocyteSpleen

1/3 pooled

2/3 in circulation

Normal: 150-450 X 103

Average life span: 7-10 days

Munn, James E. Rare Coagulopathies. In: National Hemophilia Foundation’s Nursing Working Group (ed): Nurses’ Guide to Bleeding Disorders, in print.

Page 9: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

PLATELET DISORDERS

Defects in any of the functions of platelets can result in bleeding

Clinical features: easy bruising, petechiae, mucocutaneous bleeding, menorrhagia, rarely intramuscular bleeding or hemarthrosis

Diagnosis: CBC with differential and platelet count, PFA testing, platelet aggregation and secretion studies, electron microscopy

Treatment

• Antifibrinolytics (IV, oral)

• Hormonal suppression (OCPs, IUD)

• Platelets

• Recombinant activated factor VII

Munn, James E. Rare Coagulopathies. In: National Hemophilia Foundation’s Nursing Working Group (ed): Nurses’ Guide to Bleeding Disorders, in print.

Page 10: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

FIBRINOLYSIS INHIBITOR PROTEIN DEFICIENCIES

Fibrinolysis is the body’s natural response to clot formation

Achieved principally through plasmin (enzyme that degrades clots)

Natural inhibitors help regulate this process

• α2-antiplasmin (α2-AP)

• Plasminogen activator inhibitor-1 (PAI-1)

Deficiencies in either can result in bleeding

Clinical bleeding is usually mucocutaneous

Treatment with antifibrinolytics (IV, oral)

Munn, James E. Rare Coagulopathies. In: National Hemophilia Foundation’s Nursing Working Group (ed): Nurses’ Guide to Bleeding Disorders, in print.

Page 11: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

OTHER BLEEDING DISORDERS

Hereditary hemorrhagic telangiectasia (HHT) (Osler-Weber-Rendu Syndrome)

• AVMs present in mucosal membranes and may involve other organs

• Bleeding can be mild or severe

• Treatment is symptomatic

1Dupuis-Girod S, Bailly S, Plauchu H. J Thromb

Haemost 2010; 8: 1447–1456.

Page 12: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

OTHER BLEEDING DISORDERS

Ehlers-Danlos Syndrome (EDS)

• Connective tissue (collagen) defect

• Clinical features– Joint hypermobility– Skin hyperelasticity– Hypertrophic scarring

• Bruising, spontaneous joint subluxations, poor wound healing

• Treatment is geared toward prevention or is symptomatic2

2Faber P, Craig WL, Duncan JL, Holliday K. Acta Anaesthesiol Scand 2007; 9: 1277-1279.3Munn, James E. Rare Coagulopathies. In: National Hemophilia Foundation’s Nursing Working Group (ed): Nurses’ Guide to Bleeding Disorders, in print.

Page 13: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

INHERITANCE OF BLEEDING DISORDERS

• Sex-linked: hemophilia, Wiskott-Aldrich Syndrome (platelet disorder)

• Autosomal: VWD, other factor deficiencies, most platelet disorders, fibrinolysis inhibitor deficiencies, HHT, Ehlers-Danlos

- Dominant

- Recessive

- Heterozygous

- Homozygous

Page 14: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

COMMON BLEEDING SYMPTOMS IN WOMEN WITH BLEEDING DISORDERS

• Mucocutaneous bleeding

• Petechiae

• Easy bruising

• Bleeding after trauma or surgery (including dental procedures)

• Menorrhagia

• Post-partum hemorrhage

• Rarely, intramuscular bleeding or hemarthrosis

Page 15: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

TREATMENT FOR BLEEDING

• Avoid IM injections if possible

• Avoid ASA and ASA-containing products

• Prepare for surgeries/deliveries in advance

• No invasive procedures without consultation of HTC team

Minor bleeding Major bleedingR.I.C.E Factor concentrates

Direct pressure Platelets

Topical hemostatic agents Cryoprecipitate

DDAVP FFP

Antifibrinolytics

Page 16: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

MENORRHAGIA

• Excessive uterine bleeding occurring at the expected intervals of the menstrual periods.

• The bleeding from the uterus starts on schedule but is heavier than usual and may last longer than usual.

• Menorrhagia may be a sign of an underlying disorder, such as hormone imbalance, endometriosis, uterine fibroids or, rarely, cancer of the uterus.

“MedicineNet.com” – We bring doctors’ knowledge to you.http://www.medterms.com/script/main/art.asp?articlekey=4353

Page 17: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

MENORRHAGIA

• Common symptom of women with bleeding disorders1

• Obstetricians/gynecologists may not associate menorrhagia with an inherited bleeding disorder2

• May result in unnecessary surgery if not treated appropriately

• Remember: the index patient identified by Erik von Willebrand in his discovery of a new bleeding disorder was a young girl who eventually died of hemorrhage in her 4th menstrual cycle3

1NHF “For You and Your Doctor” pamphlet (2001).2Dilley, A., et al (2001) “Obst. And Gyn: 97 (4), 630-636. April.3von Willebrand, E. (1926)

Page 18: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

TREATMENT OF MENORRHAGIA

• DDAVP

• Antifibrinolytics

• Oral contraceptive pills

• Factor replacement/Blood products

• IUDs

• Surgical interventions

Page 19: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

TREATMENT OF EXCESSIVE MENORRHAGIA

• OCP “Formula” to stop recalcitrant menorrhagia

Lo-ovral:

– 1 pill QID x 2 days

– 1 pill TID x 3 days

– 1 pill BID x 4 days

• Resume suppression therapy, usually 1-2 pills per day

• Use of anti-emetics, analgesics a must

Page 20: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

OBSTETRICAL/POST-PARTUM BLEEDING TREATMENT

For the mother:

• Previous bleeding history and response to therapy usually best indicator of OB/post-partum bleeding/treatment

• Consider treatment at delivery and again at days 5-7

• Factor concentrates to raise factor levels to >30%

• DDAVP – give immediately after delivery or at delivery of baby’s head

• NSVD is fine; consider cesarean for known carriers

Page 21: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

OBSTETRICAL/POST-PARTUM BLEEDING

For the baby:

- Avoid suction or forceps delivery and fetal scalp monitoring

- Take cord blood samples to avoid venipuncture bleeding

- Consider cranial ultrasound in boys suspected to have hemophilia prior to discharge from hospital

- Pediatrician should be available

Page 22: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

SUMMARY

• Women may have a variety of bleeding disorders that require specialized care

• Inheritance patterns are different for different bleeding disorders

• Carriers may be symptomatic and require treatment for bleeding

• Menorrhagia is one of the most common bleeding manifestations in women

• Treatments are available

• Special care must be taken with pregnancy and delivery

Page 23: WOMEN WITH BLEEDING DISORDERS Nairobi, Kenya June 25, 2013.

WFH RESOURCES

• Carriers and Women with Hemophilia

• Reproductive Health in Women with Bleeding Disorders

• Symptomatic Carriers of Hemophilia

Visit the Publications Library at www.wfh.org/publications for free copies


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