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Eculizumab for paroxysmal nocturnal haemoglobinuria: catastrophic health expenditure in Nepalese patients.

Authors :
Adhikari, Sugat
Sapkota, Surendra
Shrestha, Suraj
Karki, Kshitiz
Shrestha, Anjan
Source :
Orphanet Journal of Rare Diseases; 6/30/2023, Vol. 18 Issue 1, p1-4, 4p
Publication Year :
2023

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) results from a mutation in the phosphatidylinositol glycan class-A gene which causes uncontrolled complement activation with resultant intravascular hemolysis and its sequelae. Eculizumab is a terminal complement inhibitor that blocks this complement activation and has revolutionized the treatment of PNH but comes with an enormous price which can have catastrophic health expenditure in low-middle income countries (LMIC) like Nepal. Here, we discuss the potential way forwards in the treatment of PNH in Nepal and other LMICs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17501172
Volume :
18
Issue :
1
Database :
Complementary Index
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
164659412
Full Text :
https://doi.org/10.1186/s13023-023-02779-2