Bleeding diathesis

High tendency to bleed due to a blood clotting disorder

Medical condition

Bleeding diathesis

Other names| Haemorrhagic diathesis, Hemorrhagic diathesis
A bleeding wound in the finger
Specialty| Hematology

In medicine (hematology), bleeding diathesis is an unusual susceptibility to bleed (hemorrhage) mostly due to hypocoagulability (a condition of irregular and slow blood clotting), in turn caused by a coagulopathy (a defect in the system of coagulation). Therefore, this may result in the reduction of platelets being produced and leads to excessive bleeding.[1] Several types of coagulopathy are distinguished, ranging from mild to lethal. Coagulopathy can be caused by thinning of the skin (Cushing's syndrome), such that the skin is weakened and is bruised easily and frequently without any trauma or injury to the body.[2] Also, coagulopathy can be contributed by impaired wound healing or impaired clot formation.[3]

## Signs and symptoms

[edit]

Symptom | Disorders

|

Petechiae (red spots)  |

* Wiskott–Aldrich syndrome, where they may resemble a few bruises[4]
* Acute leukemia[5]
* Chronic leukemia[5]
* Vitamin K deficiency[6]

Purpura and ecchymoses |

* Acute leukemia[5]
* Chronic leukemia[5]
* Vitamin K deficiency[6]

Blood in stool |

* Wiskott–Aldrich syndrome, especially in infancy[4]
* Acute leukemia[5]

Bleeding gingiva (gums)  |

* Wiskott–Aldrich syndrome[4]
* Acute leukemia[5]
* Chronic leukemia[5]

Prolonged nose bleeds |

* Wiskott–Aldrich syndrome[4]

### Complications

[edit]

Following are some complications of coagulopathies, some of them caused by their treatments:

Complication | Disorders

|

Soft tissue bleeding, e.g. deep-muscle bleeding, leading to swelling, numbness or pain of a limb.  |

* Hemophilia[7]
* Von Willebrand disease[8]

Joint damage, potentially with severe pain and even destruction of the joint and development of arthritis |

* Hemophilia[7]
* Von Willebrand disease[8]

Retinal bleeding |

* Acute leukemia[5]

Transfusion transmitted infection, from blood transfusions that are given as treatment.  |

* Hemophilia[7]

Adverse reactions to clotting factor treatment.  |

* Hemophilia[7]

Anemia |

* Von Willebrand disease[8]

Exsanguination (bleeding to death)  |

* Von Willebrand disease[8]
* Acute leukemia[5]
* Vitamin K deficiency[6]

Cerebral hemorrhage |

* Wiskott–Aldrich syndrome[4]

## Causes

[edit]

While there are several possible causes, they generally result in excessive bleeding and a lack of clotting.[citation needed]

### Acquired

[edit]

Acquired causes of coagulopathy include anticoagulation with warfarin, liver failure, vitamin K deficiency and disseminated intravascular coagulation. Additionally, the hemotoxic venom from certain species of snakes can cause this condition, for example Bothrops, rattlesnakes and other species of viper. Viral hemorrhagic fevers include dengue hemorrhagic fever and dengue shock syndrome. Leukemia may also cause coagulopathy. Furthermore, cystic fibrosis has been known to cause bleeding diathesis, especially in undiagnosed infants, due to malabsorption of fat soluble vitamins like vitamin K.[citation needed]

### Autoimmune causes of acquired coagulation disorders

[edit]

There are autoimmune causes of coagulation disorders. They include acquired antibodies to coagulation factors, termed inhibitors of coagulation. The main inhibitor is directed against clotting factor VIII. Another example is antiphospholipid syndrome, an autoimmune, hypercoagulable state.[citation needed]

### Causes other than coagulation

[edit]

Bleeding diathesis may also be caused by impaired wound healing (as in scurvy), or by thinning of the skin, such as in Cushing's syndrome.[citation needed]

## Genetic

[edit]

Some people lack genes that typically produce the protein coagulation factors that allow normal clotting. Various types of hemophilia and von Willebrand disease are the major genetic disorders associated with coagulopathy. Rare examples are Bernard–Soulier syndrome, Wiskott–Aldrich syndrome and Glanzmann's thrombasthenia. Gene therapy treatments may be a solution as they involve in the insertion of normal genes to replace defective genes causing for the genetic disorder. Gene therapy is a source of active research that hold promise for the future.[9]

## Diagnosis

[edit]

### Comparing coagulation tests

[edit]

Laboratory findings in various platelet and coagulation disorders  Condition  | Prothrombin time | Partial thromboplastin time | Bleeding time | Platelet count

|
|
|
|

Vitamin K deficiency or warfarin | Prolonged | Normal or mildly prolonged | Unaffected  | Unaffected
Disseminated intravascular coagulation | Prolonged | Prolonged | Prolonged | Decreased
Von Willebrand disease | Unaffected  | Prolonged or unaffected | Prolonged | Unaffected
Hemophilia | Unaffected  | Prolonged | Unaffected  | Unaffected
Aspirin | Unaffected  | Unaffected  | Prolonged | Unaffected
Thrombocytopenia | Unaffected  | Unaffected  | Prolonged | Decreased
Liver failure, early  | Prolonged | Unaffected  | Unaffected  | Unaffected
Liver failure, end-stage  | Prolonged | Prolonged | Prolonged | Decreased
Uremia | Unaffected  | Unaffected  | Prolonged | Unaffected
Congenital afibrinogenemia | Prolonged | Prolonged | Prolonged | Unaffected
Factor V deficiency  | Prolonged | Prolonged | Unaffected  | Unaffected
Factor X deficiency as seen in amyloid purpura | Prolonged | Prolonged | Unaffected  | Unaffected
Glanzmann's thrombasthenia | Unaffected  | Unaffected  | Prolonged | Unaffected
Bernard–Soulier syndrome | Unaffected  | Unaffected  | Prolonged | Decreased or unaffected
Factor XII deficiency | Unaffected  | Prolonged | Unaffected  | Unaffected
C1INH deficiency | Unaffected  | Shortened | Unaffected  | Unaffected

## Treatments

[edit]

Consult a hematologist and have regular blood check ups. Have an early diagnostic test for any blood disorders or blood diseases including hemophilia, hemorrhage, and sickle-cell anemia. Prothrombin time and partial thromboplastin time blood tests are useful to investigate the reason behind the excessive bleeding. The PT evaluates coagulation factors I, II, V, VII and X, while the PTT evaluates coagulation factors I, II, V, VIII, IX, X, XI and XII. The analysis of both tests thus helps to diagnose certain disorders.[10]

Blood transfusion involves the transfer of plasma containing all the necessary coagulating factors (fibrinogen, prothrombin, thromboplastin) to help restore them and to improve the immune defense of the patient after excessive blood loss. Blood transfusion also caused the transfer of platelets that can work along with coagulating factors for blood clotting to commence.[11]

Different drugs can be prescribed depending on the type of disease. Vitamins (K, P and C) are essential in case of obstruction to walls of blood vessels. Also, vitamin K is required for the production of blood clotting factors, hence the injection of vitamin K (phytomenadione) is recommended to boost blood clotting.[12]

## References

[edit]

1. ^ "Bleeding Diathesis: Causes, Symptoms, and Treatments". Doctors Health Press - Daily Free Health Articles and Natural Health Advice. 2017-06-23. Retrieved 2018-09-17.
2. ^ Douglas H (April 1949). "Cushing' Syndrome and Thymic Carcinoma". QJM: An International Journal of Medicine. 18 (2): 133–147\. doi:10.1093/oxfordjournals.qjmed.a066529.
3. ^ Amin C, Sharathkumar A, Griest A (2014-01-01). "Bleeding diathesis and hemophilias". Neurologic Aspects of Systemic Disease Part II. Handbook of Clinical Neurology. Vol. 120\. pp. 1045–59\. doi:10.1016/B978-0-7020-4087-0.00070-X. ISBN 9780702040870. PMID 24365370.
4. ^ a b c d e Wiskott–Aldrich Syndrome Archived 2010-12-21 at the Wayback Machine The International Patient Organisation for Primary Immunodeficiencies (IPOPI).
5. ^ a b c d e f g h i Disorders of thrombosis and hemostasis: clinical and laboratory practice. Page  Rodger L. Bick. Edition 3, illustrated. ISBN 0-397-51690-8, ISBN 978-0-397-51690-2. 446 pages
6. ^ a b c Vitamin K Deficiency eMedicine. Author: Pankaj Patel, MD. Coauthor(s): Mageda Mikhail, MD, Assistant Professor. Updated: Dec 18, 2008
7. ^ a b c d Hemophilia Complications By Mayo Clinic staff. May 16, 2009
8. ^ a b c d Von Willebrand disease --> Complications By Mayo Clinic staff. Feb. 7, 2009
9. ^ McCain J (June 2005). "The future of gene therapy". Biotechnology Healthcare. 2 (3): 52–60\. PMC 3564347. PMID 23393464.
10. ^ "Prothrombin Time (PT) w/INR and Partial Thromboplastin Time (PTT) Blood Test". Walk-In Lab. Retrieved 2018-09-17.
11. ^ "Hemorrhagic diathesis: causes, symptoms, diagnosis, treatment | Competently about health on iLive". iliveok.com. Retrieved 2018-09-17.
12. ^ "Treatments for bleeding disorders". Netdoctor. 2015-11-03. Retrieved 2018-09-17.

## External links

[edit]

Classification|

* ICD-10: D69.9
* ICD-9-CM: 287.9
* MeSH: D006474
* DiseasesDB: 1442

|

* v
* t
* e

Disorders of bleeding and clotting

* Coagulation
* coagulopathy
* Bleeding diathesis

Clotting|

| By cause|

* Clotting factors
* Antithrombin III deficiency
* Protein C deficiency
* Activated protein C resistance
* Protein S deficiency
* Factor V Leiden
* Prothrombin G20210A
* Platelets
* Sticky platelet syndrome
* Thrombocytosis
* Essential thrombocythemia
* DIC
* Purpura fulminans
* Antiphospholipid syndrome

|

Clots|

* Thrombophilia
* Thrombus
* Thrombosis
* Virchow's triad
* Trousseau sign of malignancy

By site|

* Deep vein thrombosis
* Bancroft's sign
* Homans sign
* Lisker's sign
* Louvel's sign
* Lowenberg's sign
* Peabody's sign
* Pratt's sign
* Rose's sign
* Pulmonary embolism
* Renal vein thrombosis

Bleeding|

| By cause|

| Thrombocytopenia|

* Thrombocytopenic purpura: ITP
* Evans syndrome
* TM
* TTP
* Upshaw–Schulman syndrome

* Heparin-induced thrombocytopenia (HIT)
* May–Hegglin anomaly
* Monoclonal gammopathy of thrombotic significance (MGTS)

|

Platelet function|

* adhesion
* Bernard–Soulier syndrome
* aggregation
* Glanzmann's thrombasthenia
* platelet storage pool deficiency
* Hermansky–Pudlak syndrome
* Gray platelet syndrome

Clotting factor|

* Hemophilia
* A/VIII
* B/IX
* C/XI
* von Willebrand disease
* Hypoprothrombinemia/II
* Factor VII deficiency
* Factor X deficiency
* Factor XII deficiency
* Factor XIII deficiency
* Dysfibrinogenemia
* Congenital afibrinogenemia

Signs and symptoms|

* Bleeding
* Bruise
* Hematoma
* Petechia
* Purpura
* Nonthrombocytopenic purpura

By site|

* head
* Epistaxis
* Hemoptysis
* Intracranial hemorrhage
* Hyphema
* Subconjunctival bleeding
* torso
* Hemothorax
* Hemopericardium
* Pulmonary hematoma
* abdomen
* Gastrointestinal bleeding
* Hemobilia
* Hemoperitoneum
* Hematocele
* Hematosalpinx
* joint
* Hemarthrosis

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