Literature DB >> 18271838

Hemodialysis: a therapeutic option for severe attacks of acute intermittent porphyria in developing countries.

Murugesan R Prabahar1, Rajendran Manorajan, Devasahayam Sathiyakumar, Periyasamy Soundararajan, Matcha Jayakumar.   

Abstract

Acute intermittent prophyria (AIP) is an autosomal dominant disease that results from a defect in the enzyme porphobilinogen deaminase. Acute intermittent porphyria is the most common of hepatic porphyrias and can tax the therapeutic capabilities of the physician to the limit. Motor weakness is a major feature of an acute attack, and flaccid paralysis of all extremities can occur rapidly, within a matter of days. The acute attacks may be life threatening. Hematin (Heme Arginate) should be given early during an acute attack to prevent neurologic sequel. Hemodialysis and hemoperfusion have been tried in the treatment of acute attacks of AIP with success. As hematin is not available in India, a severe acute attack of AIP in a patient was managed with hemodialysis successfully. Later, hematin was imported and provided to the patient. An 18-year-old girl was admitted to our hospital with recurrent abdominal pain and 2 episodes of convulsions. She had undergone an appendectomy earlier at another hospital for abdominal pain. On evaluation, she had hyponatremia, episodic abnormal behavior, generalized muscle pain, hypertension, and sinus tachycardia. In view of the above clinical picture, a clinical diagnosis of acute intermittent porphyria was made. Her 24-hr urinary porphobilinogen was 90.8 mg/day (<2 mg-normal) and alpha amino levalunic acid was 108.8 mg/day (1-7 mg-normal), consistent with the diagnosis. Her hyponatremia was corrected. Arrangements were made to import hematin and she was managed with dextrose infusion. Meanwhile, she developed flaccid quardriparesis with urinary incontinence and bulbar palsy. Her brain MRI was normal. Her nerve conduction study was suggestive of motor radiculoneuropathy. Specific treatment for severe porphyric crisis was planned. She failed to improve with dextrose infusion alone. As hematin was not readily available in the country, other therapeutic options were considered. As few case reports of AIP being successfully treated with hemodialysis were available, the option of dialytic support was explained to the family. After procuring informed consent, she was subjected to hemodialysis for 4 hr in the first day, increasing to 6 hr a day for the next 6 days. Her abdominal pain and myalgia subsided on the third day of dialysis. Her lower limb muscle power improved and she became ambulant by the fourth day. Urinary retention improved within 4 days. Hematin was imported by then from the United States. Later, 2 doses of hematin (4 mg/kg-160 mg in 20% albumin) were given via a central vein. She was maintained on physiotherapy. Repeat nerve conduction study revealed recovery. She has been provided with a list of drugs that have to be avoided. Currently, she is on outpatient follow-up with occasional abdominal pain, which subsides with intravenous dextrose therapy.

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Year:  2008        PMID: 18271838     DOI: 10.1111/j.1542-4758.2008.00237.x

Source DB:  PubMed          Journal:  Hemodial Int        ISSN: 1492-7535            Impact factor:   1.812


  4 in total

1.  Effects of hemin and hemodialysis in a patient with acute intermittent porphyria and renal failure.

Authors:  Shirin Attarian; Chunli Yu; Karl E Anderson; Ellen W Friedman
Journal:  Blood Adv       Date:  2017-06-05

2.  Paediatric porphyria and human hemin: a treatment challenge in a lower middle income country.

Authors:  Syeda Anum Fatima; Humaira Jurair; Qalab Abbas; Arshalooz Jamila Rehman
Journal:  BMJ Case Rep       Date:  2020-01-08

3.  Acute intermittent porphyria: A critical diagnosis for favorable outcome.

Authors:  Chhaya Divecha; Milind S Tullu; Akanksha Gandhi; Chandrahas T Deshmukh
Journal:  Indian J Crit Care Med       Date:  2016-07

4.  Acute intermittent porphyria: Diagnostic dilemma and treatment options.

Authors:  Mohan Deep Kaur; Nita Hazarika; Namita Saraswat; Rajesh Sood
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2015 Jul-Sep
  4 in total

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