World Haemophilia Day: Odisha Needs More Centres For Diagnosing Bleeding Disorders

Whenever there is an injury or cut, it bleeds. However, the bleeding stops after some time. That’s normal. But when bleeding continues for a prolonged time, it may be abnormal. One needs to pay attention to it. One may be suffering from some inherited bleeding disorder and have to pay with one’s life due to excessive blood loss or haemorrhage following an accident, surgery or childbirth.

According to a report published, severe trauma results in 5 million deaths annually. At least 20% of severely injured patients are already coagulopathic upon arrival in the emergency room, which means they are suffering from some form of a bleeding disorder, either acquired or inherited. But awareness of this problem is low, leading to late recognition and delayed treatment of coagulopathy.

Inherited bleeding disorders are rare in the general population, but the total number of cases diagnosed is actually less than the actual number of cases prevalent in the population. Many times, it becomes apparent post-operatively. Despite the worldwide prevalence of rare bleeding disorders, knowledge of these conditions and their management is suboptimal.

Health care professionals often have little diagnostic and therapeutic experience with variable access to diagnostic modalities required for accurate identification. Therefore, patients often experience morbidity and mortality due to delayed diagnosis. You can assess the gravity of the problem by looking into the actual numbers of available facilities for diagnosing these disorders in our state Odisha.

Facilities in Odisha

We have less than 10 centres that are performing special coagulation testing like ‘Factor VIII’ or IX assay. We have less than five centres that are performing the von Willebrand factor assay. We have two odd centres doing inhibitor assay for haemophilia patients and have only one centre that is performing platelet function test.

There is a lack of awareness among the general population about different bleeding disorders and when to seek medical advice. Secondly, the lack of diagnostic facility for bleeding disorders makes the situation worse. Many patients have to travel outside the state to different central institutions for diagnosis and treatment. The cost of travel, stay and regular treatment at a far off place is prohibitive for many patients suffering from bleeding. Let’s understand it more.

The normal process to keep the blood in a fluid state and form a clot to stop bleeding at the site of injury is known as haemostasis. The blood vessel, platelets, and different proteins called coagulation factors help in haemostasis. Prolonged bleeding will occur due to any abnormality of blood vessels or deficiency in the number or function of platelets and/or coagulation factors.

Common inherited blood disorders

The most common inherited bleeding disorders are ‘haemophilia A’ due to ‘FVIII’ deficiency, which can affect one in 5000 males and Von Willebrand Disease (VWD), which can affect 1% of the population. ‘Factor IX’ deficiency causes ‘haemophilia B’.

Bleeding disorders may have variable presentations. It may include nose bleed, red to bluish patches on the skin, mouth, swelling of joints, excessive bleeding from the umbilical cord, spontaneous swelling below the skin, excessive bleeding from a cut, dental extraction, childbirth or surgeries, heavy menstrual cycles etc. Early age of presentation with a repeated similar history of bleeding manifestations indicate a possible bleeding disorder of genetic origin. If similar history has been noted in the family members, then there is a high probability of inherited bleeding disorder.

Bleeding disorders can be of three types based on their presentation. Mild bleeding disorders may not present with spontaneous bleeding or bleeding with minor trauma or trivial injury. But there may be life-threatening bleeding following major trauma, surgery or childbirth.

Severe bleeding disorders may present with bleeding manifestation from an early age and have multiple episodes. They may have bleeding manifestation to trivial trauma. Sometimes, the bleeding is so severe that it requires blood transfusion, or surgical suturing etc. But whatever may be the nature, we cannot take bleeding disorders lightly whether mild or severe. We need to remember that even a mild bleeding disorder may present with severe bleeding during surgery or trauma, costing precious life. Positive family history may be a sufficient reason to screen for it at an early age to avoid any serious consequences. A known foe is better than an unknown friend.

Anything that bleeds is a bleeding disorder! No. It’s a myth. Many times, bleeding is acquired or local in nature. Inherited bleeding disorders are rare. A black stool may indicate gastrointestinal bleeding. A bleed while coughing may be because of some respiratory cause. Blood in the urine may be related to kidney-related abnormality, stone in the urinary tract, or a tumour in the bladder etc. So, patients presenting with bleeding from one site with a late age of onset are usually suffering from some other disease leading to bleeding manifestation.

Awareness is must

But we must be aware of certain seminal facts about bleeding disorders. Heavy menstrual bleeding can be due to inherited bleeding disorders like VWD or some platelet functional disorders. But the majority of patients may not have an inherited bleeding disorder. All patients with heavy menstrual bleed without a definite cause being identified should be evaluated for bleeding disorders.

Do you know that a habitual abortion can indicate bleeding disorders? All patients with a history of repeated abortion should be evaluated for bleeding disorder too because ‘Factor XIII’ deficiency and afibrinogenemia present as repeated abortion. Even patients with a history of delayed wound healing since childhood, delayed bleeding from a wound, umbilical cord bleeding or delay in healing of the umbilical cord should be evaluated for ‘Factor XIII’ or fibrinogen tests.

Many times, a childhood joint swelling can be misdiagnosed as arthritis which is actually joint bleeding and the child may be suffering from ‘haemophilia A’, ‘haemophilia B’ or a severe type of VWD. One should not neglect it as repeated bleeding leads to swelling of joints and in long run can lead to deformity.

These bleeding disorders are diagnosed based on a battery of tests, which include basic screening tests like bleeding time, clotting time, prothrombin time, activated partial thromboplastin time, platelet counts and morphology to highly specialized tests like specific factor assay, platelet function tests, VWD factor assay, molecular studies etc.

The most commonly performed tests are bleeding time and clotting time (BT & CT). But we need to know that a normal BT & CT can’t exclude all types of bleeding disorders. One cannot neglect the subjective and methodological variations involved in BT & CT and its drawback being highly error-prone. A good history of bleeding, positive family history, platelet count, PT, aPTT can be the best way to screen for bleeding disorders and are widely available in many centres across the state. A person found to have a bleeding disorder can be referred to higher centres for a definitive diagnosis.

The bigger question remains – Can an inherited bleeding disorder be cured? Research is on to get a cure for these disorders. But in the current scenario, there is no definite cure available as it involves an abnormality of the gene. But different treatment modalities are available like factor replacement therapy, which can treat bleeding manifestation and avoid any life-threatening events.

Even prophylactic therapies are available. The treatment may be expensive sometimes. Many global NGOs like the World Federation of Haemophilia (WFH) are committed to bringing society, which is involved in helping patients. The tertiary care centres in the states including medical colleges are also actively engaged in treating these special cases. We should realise that with the currently available treatments, haemophilia or VWD patients can have a near-normal life.

It’s a sincere request to all, let’s get aware of any abnormal bleeding, get screened and diagnosed before it’s too late.

As a concluding remark, I would like to quote from Charles Dickens’s ‘A Tale of Two Cities, 1859’:

“It was the best of times, it was the worst of times, it was the age of wisdom, it was the age of foolishness, it was the epoch of belief, it was the epoch of incredulity, it was the season of Light, it was the season of Darkness, it was the spring of hope, it was the winter of despair, we had everything before us, we had nothing before us, we were all going direct to Heaven, we were all going direct the other way.”

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