Tranexamic acid in life threatening haematuria

Date First Published:
August 15, 2014
Last Updated:
March 11, 2015
Report by:
Dr Peter Hulme, ST6 (Manchester Royal Infirmary, Manchester, UK)
Search checked by:
Katharine Wylie, Manchester Royal Infirmary, Manchester, UK
Three-Part Question:
In [patients with life threatening haematuria] does [tranexamic acid] [improve outcomes]
Clinical Scenario:
A 70yr old man is rushed into resus with a BP of 60/30. He has been passing blood and clots in the urine for the last 24 hours. As you commence fluid resuscitation you wonder whether tranexamic acid may have a role in his manageemnt
Search Strategy:
Medline using NHS evidence date of searching 20 November 2014: [exp tranexamic acid/OR tranexamic AND acid.ti,ab OR txa.ti,ab] AND [exp hematuria/ OR haematuria. ti, ab].

Embase using NHS evidence SAFETY SEARCH: [*tranexamic acid/] AND [*hematuria/OR haematuria. ti, ab].

The Cochrane Library Issue 11 of 12, November 2014: MeSH descriptor: [Tranexamic Acid] explode all trees AND MeSH descriptor: [Hematuria] explode all trees.
Outcome:
Sixteen papers were found, of which four provided the best evidence to answer the question
Relevant Paper(s):
Study Title Patient Group Study type (level of evidence) Outcomes Key results Study Weaknesses
A successful treatment of life-threatening bleeding from polycystic kidneys with antifibrinolytic agent tranexamic acid. Vujkovac B.,Sabovic M. 2006 Slovenia One patient with autosomal dominant polycystic kidney disease (ADPKD) Case report Nephrectomy Bilateral Nephrectomies avoided Case report.
Thromboembolism Ureters obstructed by clots requiring J stents
Mortality Patient survived
Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuria. Peces R, Aguilar A, Vega C, et al. 2012 Spain 8 patients with autosomal dominant polycystic kidney disease (ADPKD) Prospective observational study Cessation of haematuria Stopped within 2-5 days in all patients Only 8 patients. All patients had ADPKD.
Renal function Remained stable
Haemoglobin Remained stable
Mortality All patients survived
Thromboembolism No cases of thromboemblism
Tranexamic Acid Treatment of Life-Threatening Hematuria in Polycystic Kidney Disease. AlAmeel T, West M. 2011 Canada One patient with autosomal dominant polycyctic kidney disease (ADPKD) with recurrent episodes of life threatening haematuria. Case report Haematuria Stopped within 24-36hrs Case report.
Renal function Improved to baseline
Thromboembolism No incidence of thromboembolism
Mortality Patient survived
Oral tranexamic acid as a novel treatment option for persistent haematuria in patients with sickle cell disease. Davies NF, McGuire BB, Lawlor L, et al. 2010 Ireland Female patient with sickle cell anaemia and haematuria requiring blood transfusion Case report Haematuria Stopped within 4 days of treatment Case report.
Haemoglobin Remained stable
Mortality Patient survived
Thromboembolism No incidence of thromboembolism
Author Commentary:
The evidence for the use of tranexamic acid in life-threatening haematuria is weak and predominantly in patients with autosomal-dominant polycystic kidney disease. The case reports do suggest a benefit, but larger studies are needed to prove this benefit and exclude the increased risk of thromboembolic complications.
Bottom Line:
The evidence is limited, but there may be a role for tranexamic acid in life-threatening haematuria, particularly in patients with autosomal-dominant polycystic kidney disease.
References:
  1. Vujkovac B.,Sabovic M.. A successful treatment of life-threatening bleeding from polycystic kidneys with antifibrinolytic agent tranexamic acid.
  2. Peces R, Aguilar A, Vega C, et al.. Medical therapy with tranexamic acid in autosomal dominant polycystic kidney disease patients with severe haematuria.
  3. AlAmeel T, West M.. Tranexamic Acid Treatment of Life-Threatening Hematuria in Polycystic Kidney Disease.
  4. Davies NF, McGuire BB, Lawlor L, et al.. Oral tranexamic acid as a novel treatment option for persistent haematuria in patients with sickle cell disease.