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Haemophilia A
Classification and external resources

Deficiency in coagulation factor VIII is the cause of haemophilia A.]
ICD-10 D66.
ICD-9 286.0
OMIM 306700
DiseasesDB 5555
eMedicine emerg/239
MeSH D006467

Haemophilia A (also spelled hemophilia A) is the most common form of haemophilia which is the most common genetic disorder associated with serious bleeding. It is caused by a reduction in the amount or activity of factor VIII. This protein serves as a cofactor for factor IX in the activation of factor X in the coagulation cascade. The lack of this section of the coagulation cascade results in the formation of fibrin deficient clots which makes coagulation much more prolonged, and the clot more unstable.

Haemophilia A is inherited as an X-linked recessive trait, and thus occurs in males and in homozygous females. However, mild haemophilia A has been described in heterozygous females, presumably due to extremely unfavourable lyonization (inactivation of the normal X chromosome in most of the cells). Approximately 30% of patients have no family history; their disease is presumably caused by new mutations [1]. Approximately, 1 in 5,000 males are affected.

Contents

Severity

There are numerous different mutations which cause haemophilia A. Due to differences in changes to the gene involved (and the subsequent resulting protein), patients with haemophilia often have some level of active clotting factor. Individuals with less than 1% active factor are classified as having severe haemophilia, those with 1-5% active factor have moderate haemophilia, and those with mild haemophilia have between 5-40% of normal levels of active clotting factor.[2]

Signs and symptoms

Characteristic symptoms vary with severity. In general symptoms are internal or external bleeding episodes, which are called "bleeds".[3][4] Patients with more severe hemophilia suffer more severe and more frequent bleeds. While patients with mild haemophilia typically suffer more minor symptoms except after surgery or serious trauma. Moderate haemophiliacs have variable symptoms which manifest along a spectrum between severe and mild forms.

If forceps or vacuum extraction are used in vaginal births, the first signs of haemophilia may be severe head bruising or haematomas or even intercranial haemorrhage.[5] Prolonged bleeding from a circumcision wound or a venipuncture or heelprick is another common early sign of haemophilia. These signs may lead to blood tests which indicates haemophilia. In other patients, especially those with moderate or mild haemophilia a later trauma will lead to the first serious bleed.

Haemophilia leads to a severely increased risk of prolonged bleeding from common injuries, or in severe cases bleeds may be spontaneous and without obvious cause. Bleeding may occur anywhere in the body. Superficial bleeding such as those cause by abrasions, or shallow lacerations may be prolonged and the scab may easily be broken up due to the lack of fibrin, which may cause re-bleeding. While superficial bleeding may be troublesome, by far the most serious sites of bleeding are:

The muscle and joint haemorrhages are indicative of haemophilia, while digestive tract and cerebral haemorrhages are also germane to other coagulation disorders.

Though typically not life threatening, joint bleeds are one of the most serious symptoms of haemophilia. Repeated bleeds into the a joint capsule can cause permanent joint damage and disfigurement resulting in chronic arthritis and disability. Joint damage is not a result of blood in the capsule but rather the healing process. When blood in the joint is broken down by enzymes in the body, the bone in that area is also degraded. Therefore this exerts mass amounts of pain the person afflicted with the disease.

Diagnosis

The diagnosis may be suspected as coagulation testing reveals an increased PTT in the context of a normal PT and bleeding time. PTT test are the first blood test done when haemophilia is indicated. However, the diagnosis is made in the presence of very low (<10 IU) levels of Factor VIII.

A family history is frequently present, although not essential. Recently, genetic testing has been made available to determine an individual's risk of attaining or passing on haemophilia.

Diagnosis of haemophilia A also includes a severity level which can range from mild to severe based on the amount of active and functioning factor VIII detected in the blood. Factor VIII levels do not typically change throughout an individual's life. Severe haemophilia a is the most common form occurring in 60% of patients. Severe haemophilia A is indicated by active Factor VIII levels less than 1 or 2%. Severe haemophiliacs have frequent serious bleeds (20+ times per year), these bleeds often occur spontaneously without trauma or injury. Moderate haemophilia is indicated by active Factor VIII levels between 1-5% and a lower, but variable frequency of bleeding episodes, particularly of spontaneous bleeds. Mild haemophilia is indicated by active Factor VIII levels between 5-25%. Patients with mild haemophilia often experience few or no bleeding episodes except in the case of serious trauma (i.e. compound fracture of a bone), tooth extraction, or surgery.

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Differential diagnosis

The two most common differential diagnoses are haemophilia B (also known as Christmas disease) which is a deficiency in Factor IX, are von Willebrand Disease which is a deficiency in von Willebrand factor, which is needed for the proper functioning of Factor VIII. Haemophilia C is also a possible, but rare, differential diagnosis.

Therapy

Most severe haemophilia patients require regular supplementation with intravenous recombinant or plasma concentrate Factor VIII. The prophylactic treatment regime is highly variable and individually determined. Apart from "routine" supplementation, extra factor concentrate is given around surgical procedures and after trauma. In children, an easily accessible intravenous port (e.g. Port-a-Cath) may have to be inserted to minimise frequent traumatic intravenous cannulation. These devices have made prophylaxis in haemophilia much easier for families because the problems of "finding a vein" for infusion two to three times a week are eliminated. However, there are risks involved with their use, the most worrisome being that of infection. Studies differ but some show an infection rate as high as 50 per cent. These infections can usually be treated with intravenous antibiotics but sometimes the device must be removed. Also, there are other studies that show a risk of clots forming at the tip of the catheter. Still, many families choose to use the device because of the benefits.

Some patients with severe haemophilia and most with moderate and mild haemophilia treat only as needed without a regular prophylactic schedule. Due to risk of permanent disability, prophylactic treatment is always indicated if a "target joint" (a joint which has repeated bleeding episodes) is identified.

Mild haemophiliacs often manage their condition with desmopressin, which releases stored factor VIII from blood vessel walls.

Complications

A particular therapeutic conundrum is the development of "inhibitor" antibodies against factor VIII due to frequent infusions. These develop as the body recognises the "normal form" factor VIII as foreign, as the body does not have its own "copy". The problem is that in these patients, factor VIII infusions are ineffective. Recently activated factor VII (NovoSeven) has become available as a treatment for haemorrhage in patients with haemophilia and factor inhibitors.

Prior to the use of modern blood screening methods and the advent of recombinant Factor VIII, blood born diseases such as hepatitis and HIV were very common in patients with haemophilia as a result of treatment.

See also

External links

References

  1. ^ Bowen DJ: Haemophilia A and haemophilia B: molecular insights. Mol Pathol 2002; 55:1
  2. ^ Hemophilia overview Emedicine.medscape.com, Dimitrios P Agaliotis, Robert A Zaiden, and Saduman Ozturk. Jan. 2, 2008.
  3. ^ Types of Bleeds National Hemophilia Federation.
  4. ^ Key facts: what is haemophilia? The Haemophilia Society.
  5. ^ Kelley, L.A. 2007 "Raising a child with hemophilia: a practical guide for parents, 4th edition." LA Kelley Communications, Inc. USA. Sponsored by CSL Behring.

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