ArticleCureus2026
Efficacy of Plasma Exchange in Secondary Thrombotic Microangiopathy: A Case Report and Literature Review.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
- Complement-amplified thrombotic microangiopathy in systemic lupus erythematosus and lupus nephritis: a systematic review of 78 reported patients.Frontiers in immunology · 2026Pooled it
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Thrombotic microangiopathy (TMA) is a severe syndrome characterized by thrombocytopenia, microangiopathic hemolytic anemia, and organ damage. It includes primary forms such as thrombotic thrombocytopenic purpura (TTP) and atypical hemolytic uremic syndrome, as well as secondary TMA, which can result from conditions such as autoimmune diseases, infections, and malignancies. While plasma exchange (PE) is a well-established treatment for thrombocytopenic purpura, its effectiveness against secondary TMA is debated, primarily because of the varying etiologies and pathomechanisms. There is a lack of comprehensive studies on the effectiveness of PE based on the underlying causes of secondary TMA. Herein, we report a woman in her 60s who was undergoing treatment for systemic lupus erythematosus (SLE). She presented with lower back pain and altered consciousness. The patient was diagnosed with a urinary tract infection and severe thrombocytopenia (1,000/μL). A PLASMIC score of 6 indicated a high likelihood of TTP, prompting the initiation of PE, which improved her platelet count. Her A disintegrin and metalloproteinase with thrombospondin motif 13 activity was 16%, confirming secondary TMA. The efficacy of PE for secondary TMA remains debated, with its effectiveness likely varying depending on the underlying cause. Case reports suggest poor outcomes for TMA caused by malignancies, whereas other causes tend to be associated with more favorable prognoses. However, no study has specifically examined the effectiveness of PE based on the primary underlying condition, highlighting the need for further research.
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Registered trials
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