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Role of splenectomy for immune thrombocytopenic purpura (ITP) in the era of new second-line therapies and in the setting of a high prevalence of HIV-associated ITP

Katherine Rae Antel, Eugenio Panieri, Nicolas Novitzky

Abstract


Background. New agents are being used as second-line treatment for immune thrombocytopenia (ITP) and have brought into question the relevance of splenectomy for steroid-resistant ITP.

Methods. We retrospectively analysed 73 patients who underwent splenectomy for ITP at our institution over an 11-year period. The median follow-up period was 25 months; patients with follow-up of <1 month were excluded. The outcomes of splenectomy were compared in HIV-positive v. HIV-negative patients.

Results. The rate of complete response was 83%, and response was sustained for at least 1 year or until latest follow-up in 80% of patients. Twelve patients were HIV-positive. Splenectomy was laparoscopic in 43 patients (62%) with an overall 16% complication rate. The 90-day mortality rate was 1.38%. There was no statistically significant difference in response or complication rate in the HIV-positive patients. There was a statistically significant (p=0.017) poorer response to splenectomy in the patients with steroid-resistant ITP.

Conclusion. Splenectomy is effective and safe irrespective of HIV status and remains an appropriate second-line treatment for ITP. Further research is needed to corroborate our finding of lower response in patients who are steroid-resistant, as this might be a subgroup of patients who may benefit from thrombopoietin agonists as second-line therapy.


Authors' affiliations

Katherine Rae Antel, Department of Internal Medicine, Faculty of Health Sciences, University of Cape Town, South Africa

Eugenio Panieri, Department of Surgery, Faculty of Health Sciences, University of Cape Town, South Africa

Nicolas Novitzky, Department of Surgery, Faculty of Health Sciences, University of Cape Town, South Africa

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Keywords

Splenectomy; Immune thrombocytopenic purpura; ITP; HIV; Second-line therapies

Cite this article

South African Medical Journal 2015;105(5):408-412. DOI:10.7196/SAMJ.8987

Article History

Date submitted: 2015-09-17
Date published: 2015-09-17

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