Bleeding Disorders

Professional Reference articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Blood Clotting Tests written for patients

Related synonyms: bleeding diathesis, clotting disorder, coagulation disorder, coagulopathy, haemostatic disorder

Bleeding disorders are usually taken to mean coagulopathies with reduced clotting of the blood but also encompass disorders characterised by abnormal platelet function or blood vessel walls that result in increased bleeding. Bleeding disorders may result from faults at many different levels in the coagulation cascade. They can range from severe and life-threatening conditions, such as haemophilia A, to much more mild variants. Some bleeding symptoms (eg, bruising without obvious cause, nosebleeds and heavy menstrual bleeding) are quite common in the general population and there is phenotypic variation even among individuals with defined bleeding problems. Investigation of mild bleeding problems often fails to provide a diagnosis.[1]

When a blood vessel is injured, a series of biochemical reactions is brought into play. This has been presented in the past as a coagulation 'cascade', describing a series of reactions necessary to achieve haemostasis by developing a clot, stopping its formation at the right time,and eventually facilitating clot dissolution when the vessel has healed. The scientific literature has moved towards the concept of a cell-based model which has more relevance to in vitro mechanisms (see below).[3]

Nevertheless, the coagulation cascade is still useful in describing the sequence of events that occur in vitro.

Most of the proteins required for the cascade are produced by the liver as inactive precursors (zymogens) which are then modified into clotting factors. There are two routes for activation of the coagulation system. The intrinsic pathway is activated by contact with collagen from damaged blood vessels (or indeed any negatively charged surface). The extrinsic pathway is activated by contact with tissue factor from the surface of extravascular cells.

Both routes end in a final common pathway - the proteolytic activation of thrombin and the cleaving of fibrinogen to form a fibrin clot. The intrinsic pathway is the main 'player' in this scenario, with the extrinsic pathway acting as an enhancer.


The cell-based model

The original cascade proposed by McFarlane in 1964 has been developed over the ensuing decades. A newer model describes the complex formed by tissue factor and factor VII. These participate in the activation of factor IX, indicating that the intrinsic and extrinsic coagulation pathways are linked almost from the outset.[4]The new cascade model identifies a role for endothelial cells and details the influence of host factors.[3]

Three stages are identified in the cell-based model in which it is envisaged that most of the processes involved occur at the cell surface level:[5]

  • Initiation - tissue factor-expressing cells and microparticles are exposed to plasma.
  • Amplification - small amounts of thrombin induce platelet activation and aggregation and promote activation of factors V, VIII and XI on platelet surfaces.
  • Propagation - this involves the formation of proteins (eg, tenase, prothrombinase) involved in the formation of the thrombin clot.

Platelets are identified as having three functions - control of thrombin generation, support of fibrin formation and regulation of fibrin clot retraction. Different populations of platelets with distinct surface properties are involved in these coagulant functions.[6]

Congenital bleeding disorders

  • Haemophilia A (factor VIII deficiency) and haemophilia B (factor IX deficiency or Christmas' disease) are the most well-known congenital bleeding disorders as well as celebrated examples of X-linked genetic disease.[7] Other inherited bleeding disorders affecting the coagulation pathway are much rarer and inherited in an autosomal recessive fashion; for example, prothrombin (factor II) deficiency is found in about 1 in 2 million individuals.
  • Von Willebrand's disease (vWD) is the most common inherited bleeding disorder. Usually the condition is mild without spontaneous bleeding. It occurs equally in men and women and is caused by reduced production or abnormality of Von Willebrand's factor (vWF) that both promotes normal platelet function and stabilises factor VIII.
  • Rare autosomal recessive disorders (Glanzmann's thrombasthenia and Bernard-Soulier syndrome) affecting platelet membrane glycoproteins and causing abnormal platelet binding and aggregation

Acquired disorders[8, 9]

  • Liver disease and cirrhosis cause reduced synthesis of clotting proteins and thrombocytopenia.
  • Vitamin K deficiency due to dietary deficiency, gastrointestinal malabsorption or absence of gut bacteria in infancy (haemorrhagic disease of the newborn).[10]
  • Shock, sepsis or malignancy can all cause an increased bleeding tendency, often through the final common pathway of disseminated intravascular coagulopathy (DIC) where simultaneous microvascular thrombosis and generalised bleeding occur due to massive consumption of coagulation factors or damage to vessel walls (for example, in meningococcal septicaemia).
  • Renal disease causes platelet dysfunction and reduced aggregation.
  • Circulating autoantibodies to coagulation factors (eg, in lymphoma and systemic lupus erythematosus) or to platelets (as in immune thrombocytopenic purpura).
  • Amyloidosis where factor X deficiency occurs as well as local infiltration of blood vessels.
  • Vitamin C deficiency can cause diffuse haemorrhage in surgical patients.[11]
  • Advanced age can be associated with fragile veins.[12]
  • Prolonged steroid use is reputed to be associated with hypercoagulability and increased bleeding tendency. However, one study found that this effect was likely to be of limited clinical consequence.[13]

Remember that some diseases can be associated with both bleeding and thrombosis - eg, polycythaemia rubra vera and essential thrombocythaemia.[14]


  • Bruising may be spontaneous or recurrent:
    • Large bruises on sun-exposed areas of limbs in the elderly are usually due to cumulative ultraviolet vessel damage and are rarely significant.[18]
    • Large bruises on the trunk are more indicative of a bleeding disorder.
  • Prolonged bleeding:
    • After minor cuts or abrasions.
    • Nosebleeds lasting >10 minutes despite compression (especially in children).
    • Severe menorrhagia causing anaemia, with normal uterus.
    • Bleeding from gums without gingival disease and unrelated to brushing.
    • Following dental extraction.
    • Postpartum haemorrhage.
    • After injections or surgical procedures.

Also enquire regarding:

  • Current medication:
    • Including aspirin, non-steroidal anti-inflammatory drugs, warfarin and complementary/alternative preparations.
    • Remember drug interactions between warfarin and other medications that prolong the international normalised ratio (INR).
  • Family history of bleeding tendency.
  • Alcohol intake.
  • Other constitutional symptoms - eg, malaise, weight loss.
  • Past history or thrombosis (can be suggestive of thrombophilia).
  • Previous blood transfusions.
  • Renal or hepatic impairment.


Systemically look for:

  • Pallor.
  • Sepsis.
  • Haemodynamic status.
  • Lymphadenopathy or hepatosplenomegaly.


  • Skin, palate and gums for:
    • Bruising
    • Petechia (non-blanching haemorrhagic spot <2 mm diameter)
    • Purpura (2-10 mm diameter)
    • Ecchymosis (>10 mm diameter)
  • Fundi for retinal haemorrhages.
  • Joints for haemarthrosis.
  • Rectal or vaginal examinations where appropriate.
Comparing coagulation factor and platelet defects[19, 20]
 Coagulation factor defectsPlatelet disorders and von Willebrand's disease
Bruising on trunk and limbsLarge bruisesSmall bruises
Bleeding from cutsRelatively slightProfuse
NosebleedsUncommonCommon, frequently profuse and of long duration
Gastrointestinal bleedingUncommonCommon
HaemarthrosisIn severe haemophiliaVery rare
Bleeding after surgery or dental extractionUp to a day's delay before bleeding occursImmediate bleeding
  • FBC, blood film and platelet count - may detect leukaemia, lymphoma or thrombocytopenia or abnormal platelets.
  • Consider checking U&Es to exclude uraemia causing a platelet disorder.
  • Consider LFTs to detect hepatic cause of acquired coagulation factor deficiency and alcohol-related damage.
  • Bone marrow biopsy.
  • A coagulation screen usually involves taking blood in a mixture of citrate, EDTA and clotted sample bottles. It includes:
    • Activated partial thromboplastin time (APTT):
      • This measures the intrinsic pathway (which includes factors I, II, V, VIII, IX, X, XI and XII) and the common pathway.
      • A plasma sample is used and the intrinsic pathway is activated by adding phospholipid, an activator such as kaolin (which acts as a negatively charged surface) and calcium ions. The formation of prothrombinase complexes on the surface of the phospholipid enables the formation of thrombin and a subsequent clot. The result is reported as the time in seconds for this reaction.
      • The test is used to assess the overall competence of the coagulation system, as a routine test to monitor heparin therapy and as a pre-operative screen for bleeding tendencies. It will also reveal possible coagulation factor deficiencies, as in haemophilia A and B.
    • Prothrombin time (PT):
      • This assesses the extrinsic and final common pathway of the coagulation cascade, thus can detect factor I, II, V, VII or X deficiency or the effects of warfarin.
      • It is performed by adding thromboplastin and calcium ions to a plasma sample. The time for clot formation is measured.
      • Prolonged time suggests the presence of an inhibitor to, or a deficiency of, one or more coagulation factors, the presence of warfarin, the existence of vitamin K deficiency or liver dysfunction.
      • The INR, used to monitor warfarin, is derived by comparing the patient's clotting time to that of a standardised sample.
    • Thrombin clotting time test:
      • This measures the rate of a patient's clot formation compared with a normal plasma control. The plasma is first depleted of platelets and a standard amount of thrombin added.
      • The test is used in the diagnosis of DIC and other conditions that can affect fibrinogen level, such as liver disease.
    If the above tests are all normal, the vast majority of common haemostatic disorders will have been excluded. However, if symptoms persist and/or there is a suggestion of family history, patients should be referred to a haematologist for further tests which may include:
    • Bleeding time - this tests the interaction between the platelets and the vessel walls. A standardised spring-loaded lancet is used to make a small cut in the patient's forearm and the time for the bleeding to stop is then measured. The test is not useful as a screening test, as it has a high false positive result. It is sometimes used in the investigation of vWD although even here it has poor specificity.
    • The platelet function analyser is a relatively new technique. It has largely replaced the in vivo bleeding time test although it is not specific for, nor predictive of, any particular disorder and its limitations need to be taken into account.[21, 22]
    • Fibrinogen - the level can be determined by immunological or functional assay. It is usually performed when APTT or PT screening tests are prolonged. The main disorders detected are afibrinogenaemia or hypofibrinogenaemia (due to absence or a low level of fibrinogen production) and dysfibrinogenaemia (due to a molecular alteration of fibrinogen, causing poor function). Differences in the level of fibrinogen measured by the two methods are suggestive of dysfibrinogenaemia.[1]
    • Specific factor assays - factors VIII or IX to determine severity of haemophilia; factor VIII and vWF in vWD.
    • Gene analysis looking for specific gene defects.
Haemostasis tests in bleeding disorders[1, 23]
 Platelet countProthrombin timeActivated partial thromboplastin timeBleeding timeThrombin timeAdditional tests
Haemophilia ANormalNormalProlongedNormal Factor VIII low
Haemophilia BNormalNormalProlongedNormal Factor IX low
Von Willebrand's diseaseNormalNormalProlonged or normalProlonged VWF and factor VIII activity low and
impaired ristocetin-induced platelet aggregation
Liver diseaseLowProlongedProlonged Normal (rarely prolonged) 
Disseminated intravascular coagulopathyLowProlongedProlonged Grossly prolonged 
Massive transfusionLowProlongedProlonged Normal 
Oral anticoagulantsNormalGrossly prolongedProlonged Normal 
HeparinNormal (rarely low)Mildly prolongedProlonged Prolonged 

Management is dependent on the underlying condition - see separate articles on Haemophilia A (Factor VIII Deficiency) and Haemophilia B (Factor IX Deficiency) and the separate article Von Willebrand's Disease.

Whilst the sex-linked nature of haemophilia results in mostly male sufferers, women are much more likely to present with mild bleeding disorders due to the demands of menstruation and childbirth. Menorrhagia can be tackled by standard means. For further details see the separate article on Menorrhagia.

Those with serious inherited bleeding disorders may wish for genetic counselling and prenatal diagnosis.[24]

Did you find this information useful?

Further reading & references

  1. Hayward CP; Diagnosis and management of mild bleeding disorders. Hematology Am Soc Hematol Educ Program. 2005:423-8.
  2. Adams RL, Bird RJ; Review article: Coagulation cascade and therapeutics update: relevance to nephrology. Part 1: Overview of coagulation, thrombophilias and history of anticoagulants. Nephrology (Carlton). 2009 Aug 14(5):462-70. doi: 10.1111/j.1440-1797.2009.01128.x.
  3. McMichael M; New models of hemostasis. Top Companion Anim Med. 2012 May 27(2):40-5. doi: 10.1053/j.tcam.2012.07.005. Epub 2012 Aug 29.
  4. De Caterina R, Husted S, Wallentin L, et al; Anticoagulants in heart disease: current status and perspectives. Eur Heart J. 2007 Apr 28(7):880-913. Epub 2007 Apr 10.
  5. De Caterina R, Husted S, Wallentin L, et al; General mechanisms of coagulation and targets of anticoagulants (Section I). Position Paper of the ESC Working Group on Thrombosis--Task Force on Anticoagulants in Heart Disease. Thromb Haemost. 2013 Apr 109(4):569-79. doi: 10.1160/TH12-10-0772. Epub 2013 Feb 28.
  6. Heemskerk JW, Mattheij NJ, Cosemans JM; Platelet-based coagulation: different populations, different functions. J Thromb Haemost. 2013 Jan 11(1):2-16. doi: 10.1111/jth.12045.
  7. Bolton-Maggs PH, Pasi KJ; Haemophilias A and B. Lancet. 2003 May 24 361(9371):1801-9.
  8. van Herrewegen F, Meijers JC, Peters M, et al; Clinical practice: the bleeding child. Part II: disorders of secondary hemostasis and fibrinolysis. Eur J Pediatr. 2012 Feb 171(2):207-14. doi: 10.1007/s00431-011-1571-x. Epub 2011 Sep 17.
  9. Bleeding Disorders
  10. Chalmers EA; Neonatal coagulation problems. Arch Dis Child Fetal Neonatal Ed. 2004 Nov 89(6):F475-8.
  11. Blee TH, Cogbill TH, Lambert PJ; Hemorrhage associated with vitamin C deficiency in surgical patients. Surgery. 2002 Apr 131(4):408-12.
  12. Leibovitch I, Modjtahedi S, Duckwiler GR, et al; Lessons learned from difficult or unsuccessful cannulations of the superior ophthalmic vein in the treatment of cavernous sinus dural fistulas. Ophthalmology. 2006 Jul 113(7):1220-6.
  13. Turan A, Dalton JE, Turner PL, et al; Preoperative prolonged steroid use is not associated with intraoperative blood transfusion in noncardiac surgical patients. Anesthesiology. 2010 Aug 113(2):285-91. doi: 10.1097/ALN.0b013e3181e6a195.
  14. Schafer AI; Molecular basis of the diagnosis and treatment of polycythemia vera and essential thrombocythemia. Blood. 2006 Jun 1 107(11):4214-22. Epub 2006 Feb 16.
  15. Bolton-Maggs PH, Chalmers EA, Collins PW, et al; A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol. 2006 Dec 135(5):603-33.
  16. Tosetto A; The Role of Bleeding History and Clinical Markers for the Correct Diagnosis of VWD. Mediterr J Hematol Infect Dis. 2013 Jul 12 5(1):e2013051. doi: 10.4084/MJHID.2013.051. Print 2013.
  17. Textbook of Haemophilia
  18. Webster GF; Common skin disorders in the elderly. Clin Cornerstone. 2001 4(1):39-44.
  19. Karnath B; Easy Bruising and Bleeding in the Adult Patient, 2005
  20. Federici AB; Clinical diagnosis of von Willebrand disease. Haemophilia. 2004 Oct 10 Suppl 4:169-76.
  21. Franchini M; The platelet function analyzer (PFA-100): an update on its clinical use. Clin Lab. 2005 51(7-8):367-72.
  22. Naik S, Teruya J, Dietrich JE, et al; Utility of platelet function analyzer as a screening tool for the diagnosis of von Willebrand disease in adolescents with menorrhagia. Pediatr Blood Cancer. 2013 Jul 60(7):1184-7. doi: 10.1002/pbc.24456. Epub 2013 Jan 17.
  23. Handbook of Diagnostic Hemostasis and Thrombosis Tests; University of Washington Department of Laboratory Medicine Reference Laboratory Services, 2005
  24. Street AM, Ljung R, Lavery SA; Management of carriers and babies with haemophilia. Haemophilia. 2008 Jul 14 Suppl 3:181-7.
Original Author:
Dr Chloe Borton
Current Version:
Dr Laurence Knott
Peer Reviewer:
Dr John Cox
Document ID:
1872 (v22)
Last Checked:
13 January 2014
Next Review:
12 January 2019

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.