Plasma exchange (PLEX) is capable of removing significant amounts of circulating antibodies. In anti-neutrophil cytoplasmic antibody-associated vasculitis, PLEX was reserved for patients with severe presentation forms such as rapidly progressive glomerulonephritis and pulmonary haemorrhage. The Plasma Exchange and Glucocorticoids in Severe ANCA-Associated Vasculitis (PEXIVAS) trial included all comers with a glomerular filtration rate <50 mL/min/1.73 m2 and thus aimed to answer the question of whether PLEX is an option for patients with no relevant kidney function impairment or not. PEXIVAS revealed that after a follow-up of almost 3 years, routine administration of PLEX does not provide an additional benefit to reduce the rate of a composite comprising end-stage kidney disease or death. In the absence of histological parameters, it is tempting to speculate whether PLEX is effective or not in those with a potential for renal recovery. A subset of patients presented with alveolar haemorrhage, and there was a trend towards a better outcome of such cases receiving PLEX. This would be in line with observational studies reporting a recovery of alveolar haemorrhage following extracorporeal treatment. In this PRO part of the debate, we highlight the shortcomings of the PEXIVAS trial and stimulate further research paths, which in our eyes are necessary before abandoning PLEX from the therapeutic armamentarium.
Andreas Kronbichler, Keum Hwa Lee, Sara Denicolò, Daeun Choi, Hyojeong Lee, Dong-Hyun Ahn, Kang Hyun Kim, Ji-Han Lee, Hyungtae Kim, M. Hwang, Sun Wook Jung, Changjun Lee, Ho‐June Lee, Haejune Sung, Dongkyu Lee, Jae-Hyuk Hwang, Sohee Kim, Injae Hwang, Do Young Kim, Hyung Jun Kim, Geonjae Cho, Yunryoung Cho, Dong‐Il Kim, Min Choi, Junhye Park, Junseong Park, Kalthoum Tizaoui, Han Li, Lee Smith, Ai Koyanagi, Louis Jacob, Philipp Gauckler, Jae Il Shin
Sergey Moiseev, Jiwon Lee, Anastasiia Zykova, N. Bulanov, Pavel Novikov, Eugeniy Gitel, Mayra Bulanova, E. S. Safonova, Jae Il Shin, Andreas Kronbichler, David Jayne
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