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{{Heparin-induced thrombocytopenia}}
{{Heparin-induced thrombocytopenia}}
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com]
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.B.B.S.]] [mailto:psingh13579@gmail.com] {{shyam}}
==Overview==
==Overview==
[[Heparin-induced thrombocytopenia]] is diagnosed when the [[platelet]] count falls by > 50% typically after 5-10 days of [[heparin]] therapy. It is a clinicopathologic diagnosis and early diagnosis and management may be life saving. Unlike other [[immune mediated thrombocytopenia]] (idiopathic thrombocytopenic purpura), the levels of platelet stays > 20,000 microl, thus frank clinical bleeding is less common in HIT when compared to other conditions, where the platelet may fall below 10,000/ microl.
The history of HIT always involves exposure to heparin. Typical features of a patient's history depend on the type and location of thrombosis and whether the platelet count is sufficiently low to result in bleeding. Venous and arterial thromboses can result in variable symptoms. Symptoms of [[deep vein thrombosis]] include leg pain, swelling, and/or erythema. Symptoms of [[pulmonary embolism]] include [[dyspnea]], [[Pleuritic chest pain|pleuritic chest]], and/or [[hypotension]]. Symptoms of arterial occlusion of a limb include limb pain and necrosis. Bleeding can occur spontaneously when the platelet count reaches very low levels, such as less than 10000 per microliter, though this is rare in HIT.


==History==
==History==
===Heparin therapy===
===Heparin therapy===
* Occurs commonly after 5-10 days of initiation of heparin therapy. Onset of [[HIT]] after 2 weeks of heparin therapy is uncommon. Earlier onset of HIT is usually seen in patients who have been previously treated with heparin (1-3 months back) and have circulating HIT antibodies in them. In these patients the median time of platelet fall is less than 12 hours after the start of heparin administration
The history of HIT always includes exposure to heparin or heparinoids.
* Delayed onset HIT:
 
** Occurs after heparin has been withdrawn (median time of '''14 days''' after heparin withdrawl)
* Classic HIT: This occurs typically after 5-10 days of initiation of heparin or heparin-like therapy. Onset of [[HIT]] after 2 weeks of heparin therapy is uncommon. Earlier onset of HIT is usually seen in patients who have been previously treated with heparin (1-3 months prior) and have circulating HIT antibodies. In these patients the median time of platelet fall is less than 12 hours after the start of heparin administration. Patients will typically have low platelet counts and possibly thrombosis.
** High titer platelet-activating antibodies that have both increased heparin-dependent and heparin independent platelet activation
 
** The phenomena is sometimes explained by the fact that unusually high antibody levels react with platelet-associated Platelet Factor 4 (PF4) bound to non-heparin [[glycosaminoglycans]] like [[chondroitin sulfate]] and not to heparin.  
* Delayed onset HIT: This occurs after heparin has been withdrawn (median time of 14 days after heparin withdrawal). Patients will typically have low platelet counts and possibly thrombosis.
* The incidence of delayed onset [[HIT]] are less compared to other forms of HIT.
 
===Cardiac surgery===
===Recent surgery===
* In cardiac surgery patients, decrease in the [[platelet]] count by > 50 % can occur within 3 days of surgery. This may be attributed to prolonged contact of platelets with the artificial surface and administration of large amount of [[unfractionated heparin]] ([[UFH]]). However, a diagnosis of HIT is more probable if a fall in the [[platelet]] counts ≥50 % is seen after 5-10 days of [[heparin]] therapy.
Patients with HIT often have a history of a recent cardiac or orthopedic surgery. They may develop low platelet count and [[deep vein thrombosis]] or other thrombotic manifestation.
* In cardiac surgery patients, decrease in the [[platelet]] count by > 50 % can occur within 3 days of surgery. This may be attributed to prolonged contact of platelets with the artificial surface and administration of large amount of [[unfractionated heparin]] ([[UFH]]). However, a diagnosis of HIT is more probable if a fall in the [[platelet]] count exceeds 50% is seen after 5-10 days of [[heparin]] therapy. Note that a history of surgery is not required as part of the history of HIT. Some patients with no surgical history will develop HIT.
 
==Symptoms==
==Symptoms==
* Presents with symptoms suggestive of arterial and venous thrombosis. The increased incidences of thrombosis may be attributed to:
Patients can present with symptoms suggestive of arterial and venous thrombosis. The increased incidences of thrombosis may be attributed to:
** Release of procoagulants by activated [[platelets]]
* Release of procoagulants by activated [[platelets]]
** Release of platelet membranes that in turn activates coagulation pathways
* Release of platelet membranes that in turn activates coagulation pathways
** HIT antibodies bind and activate endothelial cells resulting in release of tissue factor and thrombin
* Binding and activation of HIT antibodies to [[endothelial cells]] resulting in release of tissue factor and thrombin
 
===Venous thrombosis===
===Venous thrombosis===
==== [[Deep vein thrombosis]] ([[DVT]])====
* Leg pain: This is a common manifestation of [[deep vein thrombosis]]. It typically occurs in the calf muscles. Homan's sign is pain on dorsiflexion of the calf.
* (The classical symptoms of DVT include: Pain, redness and [[swelling]] of the affected area, dilation of the surface veins.
* Leg swelling: This is a common manifestation of [[deep vein thrombosis]]. Swelling is due to obstruction of venous return and dilation of the surface veins.<ref name="pmid22315270">{{cite journal |vauthors=Linkins LA, Dans AL, Moores LK, Bona R, Davidson BL, Schulman S, Crowther M |title=Treatment and prevention of heparin-induced thrombocytopenia: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines |journal=Chest |volume=141 |issue=2 Suppl |pages=e495S–e530S |date=February 2012 |pmid=22315270 |pmc=3278058 |doi=10.1378/chest.11-2303 |url=}}</ref>
====[[Pulmonary embolism]]====
* Leg erythema: This is a common manifestation of [[deep vein thrombosis]].
* Three major clinical presentations can exist: difficulty in breathing with or without pleuritic [[chest pain]] and blood stained sputum, [[syncope]] (associated with massive pulmonary embolism). In the elderly, it may mimick as indolent [[pneumonia]] or [[heart failure]]. Pulmonary embolism should be suspected<ref name="pmid20592294">{{cite journal| author=Agnelli G, Becattini C| title=Acute pulmonary embolism. | journal=N Engl J Med | year= 2010 | volume= 363 | issue= 3 | pages= 266-74 | pmid=20592294 | doi=10.1056/NEJMra0907731 |pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20592294  }} </ref> in all patients who present with the following symptoms, without an alternative obvious cause.
* [[Dyspnea]] (new or worsening): This is a common manifestation of pulmonary embolism.
* [[Dyspnea]] (new or worsening)
* Pleuritic [[chest pain]]: This can be a manifestation of pulmonary embolism.<ref name="pmid20592294">{{cite journal| author=Agnelli G, Becattini C| title=Acute pulmonary embolism. | journal=N Engl J Med | year= 2010 | volume= 363 | issue= 3 | pages= 266-74 | pmid=20592294 | doi=10.1056/NEJMra0907731 |pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20592294  }} </ref>
* [[Chest pain]]
* Sustained [[hypotension]]: This can be a manifestation of a massive [[pulmonary embolism]].
* Sustained [[Hypotension]]
====Limb gangrene====
* Can be seen in both upper and lower extremities. However, lower extremities are commoner compared to upper.


===Arterial thrombosis===
===Arterial thrombosis===
It can present itself with one of these diseases like [[stroke]], [[myocardial infarction]], peripheral arterial occlusion, or end organ infarction (renal).
The symptoms of arterial thrombosis are variable and depend on the organ involved. It can present itself as [[stroke]], [[myocardial infarction]], peripheral arterial occlusion, or end organ infarction (for example, renal dysfunction from renal artery occlusion).<ref name="pmid9627146">{{cite journal |vauthors=Tietge UJ, Schmidt HH, Jäckel E, Trautwein C, Manns MP |title=Low molecular weight heparin-induced skin necrosis occurring distant from injection sites and without thrombocytopenia |journal=J. Intern. Med. |volume=243 |issue=4 |pages=313–5 |date=April 1998 |pmid=9627146 |doi= |url=}}</ref>
 
===Limb gangrene===
This can be seen in both upper and lower extremities. However, lower extremities are more common compared to upper.<ref name="pmid9382401">{{cite journal |vauthors=Warkentin TE, Elavathil LJ, Hayward CP, Johnston MA, Russett JI, Kelton JG |title=The pathogenesis of venous limb gangrene associated with heparin-induced thrombocytopenia |journal=Ann. Intern. Med. |volume=127 |issue=9 |pages=804–12 |date=November 1997 |pmid=9382401 |doi= |url=}}</ref>
 
===Skin necrosis===
===Skin necrosis===
* Redness of skin, purpura, bleeding from the area
Skin [[necrosis]] is commonly seen in the abdomen, distal [[extremities]], and nose.<ref name="pmid8603024">{{cite journal |vauthors=Warkentin TE |title=Heparin-induced skin lesions |journal=Br. J. Haematol. |volume=92 |issue=2 |pages=494–7 |date=February 1996 |pmid=8603024 |doi= |url=}}</ref>
* Commonly seen in abdomen, distal extremities and nose.
* Redness of skin
* [[Purpura]]
* Bleeding from the skin
 
===Bleeding===
[[Bleeding]] can occur in the setting of [[thrombocytopenia]]. Spontaneous [[bleeding]] usually does not occur unless the platelet count is less than 10000 per microliter. Bleeding can occur at platelet counts below 50000 per microliter if a patient is undergoing an invasive procedure or experiences trauma.<ref name="pmid25629757">{{cite journal |vauthors=Warkentin TE, Safyan EL, Linkins LA |title=Heparin-induced thrombocytopenia presenting as bilateral adrenal hemorrhages |journal=N. Engl. J. Med. |volume=372 |issue=5 |pages=492–4 |date=January 2015 |pmid=25629757 |doi=10.1056/NEJMc1414161 |url=}}</ref>


==Reference==
==Reference==
{{Reflist|2}}
{{Reflist|2}}


[[Category:Drugs]]
[[Category:Hematology]]
[[Category:Hematology]]
[[Category:Up-To-Date]]


{{WS}}
{{WH}}
{{WH}}
{{WS}}

Latest revision as of 16:02, 8 August 2018

Heparin-induced thrombocytopenia

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Priyamvada Singh, M.B.B.S. [2] Shyam Patel [3]

Overview

The history of HIT always involves exposure to heparin. Typical features of a patient's history depend on the type and location of thrombosis and whether the platelet count is sufficiently low to result in bleeding. Venous and arterial thromboses can result in variable symptoms. Symptoms of deep vein thrombosis include leg pain, swelling, and/or erythema. Symptoms of pulmonary embolism include dyspnea, pleuritic chest, and/or hypotension. Symptoms of arterial occlusion of a limb include limb pain and necrosis. Bleeding can occur spontaneously when the platelet count reaches very low levels, such as less than 10000 per microliter, though this is rare in HIT.

History

Heparin therapy

The history of HIT always includes exposure to heparin or heparinoids.

  • Classic HIT: This occurs typically after 5-10 days of initiation of heparin or heparin-like therapy. Onset of HIT after 2 weeks of heparin therapy is uncommon. Earlier onset of HIT is usually seen in patients who have been previously treated with heparin (1-3 months prior) and have circulating HIT antibodies. In these patients the median time of platelet fall is less than 12 hours after the start of heparin administration. Patients will typically have low platelet counts and possibly thrombosis.
  • Delayed onset HIT: This occurs after heparin has been withdrawn (median time of 14 days after heparin withdrawal). Patients will typically have low platelet counts and possibly thrombosis.

Recent surgery

Patients with HIT often have a history of a recent cardiac or orthopedic surgery. They may develop low platelet count and deep vein thrombosis or other thrombotic manifestation.

  • In cardiac surgery patients, decrease in the platelet count by > 50 % can occur within 3 days of surgery. This may be attributed to prolonged contact of platelets with the artificial surface and administration of large amount of unfractionated heparin (UFH). However, a diagnosis of HIT is more probable if a fall in the platelet count exceeds 50% is seen after 5-10 days of heparin therapy. Note that a history of surgery is not required as part of the history of HIT. Some patients with no surgical history will develop HIT.

Symptoms

Patients can present with symptoms suggestive of arterial and venous thrombosis. The increased incidences of thrombosis may be attributed to:

  • Release of procoagulants by activated platelets
  • Release of platelet membranes that in turn activates coagulation pathways
  • Binding and activation of HIT antibodies to endothelial cells resulting in release of tissue factor and thrombin

Venous thrombosis

  • Leg pain: This is a common manifestation of deep vein thrombosis. It typically occurs in the calf muscles. Homan's sign is pain on dorsiflexion of the calf.
  • Leg swelling: This is a common manifestation of deep vein thrombosis. Swelling is due to obstruction of venous return and dilation of the surface veins.[1]
  • Leg erythema: This is a common manifestation of deep vein thrombosis.
  • Dyspnea (new or worsening): This is a common manifestation of pulmonary embolism.
  • Pleuritic chest pain: This can be a manifestation of pulmonary embolism.[2]
  • Sustained hypotension: This can be a manifestation of a massive pulmonary embolism.

Arterial thrombosis

The symptoms of arterial thrombosis are variable and depend on the organ involved. It can present itself as stroke, myocardial infarction, peripheral arterial occlusion, or end organ infarction (for example, renal dysfunction from renal artery occlusion).[3]

Limb gangrene

This can be seen in both upper and lower extremities. However, lower extremities are more common compared to upper.[4]

Skin necrosis

Skin necrosis is commonly seen in the abdomen, distal extremities, and nose.[5]

  • Redness of skin
  • Purpura
  • Bleeding from the skin

Bleeding

Bleeding can occur in the setting of thrombocytopenia. Spontaneous bleeding usually does not occur unless the platelet count is less than 10000 per microliter. Bleeding can occur at platelet counts below 50000 per microliter if a patient is undergoing an invasive procedure or experiences trauma.[6]

Reference

  1. Linkins LA, Dans AL, Moores LK, Bona R, Davidson BL, Schulman S, Crowther M (February 2012). "Treatment and prevention of heparin-induced thrombocytopenia: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines". Chest. 141 (2 Suppl): e495S–e530S. doi:10.1378/chest.11-2303. PMC 3278058. PMID 22315270.
  2. Agnelli G, Becattini C (2010). "Acute pulmonary embolism". N Engl J Med. 363 (3): 266–74. doi:10.1056/NEJMra0907731. PMID 20592294.
  3. Tietge UJ, Schmidt HH, Jäckel E, Trautwein C, Manns MP (April 1998). "Low molecular weight heparin-induced skin necrosis occurring distant from injection sites and without thrombocytopenia". J. Intern. Med. 243 (4): 313–5. PMID 9627146.
  4. Warkentin TE, Elavathil LJ, Hayward CP, Johnston MA, Russett JI, Kelton JG (November 1997). "The pathogenesis of venous limb gangrene associated with heparin-induced thrombocytopenia". Ann. Intern. Med. 127 (9): 804–12. PMID 9382401.
  5. Warkentin TE (February 1996). "Heparin-induced skin lesions". Br. J. Haematol. 92 (2): 494–7. PMID 8603024.
  6. Warkentin TE, Safyan EL, Linkins LA (January 2015). "Heparin-induced thrombocytopenia presenting as bilateral adrenal hemorrhages". N. Engl. J. Med. 372 (5): 492–4. doi:10.1056/NEJMc1414161. PMID 25629757.

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