How I Treat Thrombotic Microangiopathy in the Setting of Triggers

Complement-mediated thrombotic microangiopathy can be difficult to recognize when it presents in the setting of an apparent clinical trigger, such as pregnancy, severe hypertension, or kidney transplantation. These conditions can each cause endothelial injury directly, but may also unmask complement dysregulation in susceptible individuals. In these situations, the critical question is not whether a trigger exists but whether it fully explains the syndrome and whether urgent complement blockade is warranted to prevent irreversible kidney injury. In this How I Treat article, we use three real-world cases to illustrate how we approach this decision in practice. We emphasize the bedside features that most influence our threshold to treat, including the pattern and severity of kidney injury, tempo of disease progression, and lack of improvement with supportive or trigger-directed care. We also address the interpretation of complement genetic findings, pregnancy- and transplant-specific risk stratification, and individualization of treatment duration. Functional assays can support mechanistic assessment in selected cases but remain an adjunct to the diagnosis and should not drive management decisions.

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Publication Details

Journal
Blood
Published
2026-07-22
DOI
https://doi.org/10.1182/blood.2026033525
Primary Topic
Complement system in diseases
Type
article
Field-Weighted Citation Impact
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article

How I Treat Thrombotic Microangiopathy in the Setting of Triggers

Meera Sridharan, Spero R. Cataland, Anuja Java
Blood
Complement system in diseases
article

How I Treat Thrombotic Microangiopathy in the Setting of Triggers

Meera Sridharan, Spero R. Cataland, Anuja Java
article en

Abstract

Complement-mediated thrombotic microangiopathy can be difficult to recognize when it presents in the setting of an apparent clinical trigger, such as pregnancy, severe hypertension, or kidney transplantation. These conditions can each cause endothelial injury directly, but may also unmask complement dysregulation in susceptible individuals. In these situations, the critical question is not whether a trigger exists but whether it fully explains the syndrome and whether urgent complement blockade is warranted to prevent irreversible kidney injury. In this How I Treat article, we use three real-world cases to illustrate how we approach this decision in practice. We emphasize the bedside features that most influence our threshold to treat, including the pattern and severity of kidney injury, tempo of disease progression, and lack of improvement with supportive or trigger-directed care. We also address the interpretation of complement genetic findings, pregnancy- and transplant-specific risk stratification, and individualization of treatment duration. Functional assays can support mechanistic assessment in selected cases but remain an adjunct to the diagnosis and should not drive management decisions.

Blood
Mayo Clinic (US), Washington University in St. Louis (US), The Ohio State University (US)
Good health and well-being
Openalex Percentile: Top 14%
Complement system in diseases
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How I Treat Thrombotic Microangiopathy in the Setting of Triggers — Meera Sridharan, Spero R. Cataland, et al. · Blood (2026) | TGRS Research Map | TGRS