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[Nephrological aspects of complement-mediated thrombotic microangiopathy]
A V Smirnov1, A V Karunnaya1, V A Dobronravov1
1I.P. Pavlov Saint Petersburg State Medical University, Ministry of Health of Russia, Saint Petersburg, Russia.
Insights
Early diagnosis and treatment of complement-mediated thrombotic microangiopathy (C-TMA) are crucial for better kidney outcomes. Prompt intervention improves prognosis and reduces the risk of end-stage renal failure in C-TMA patients.
Area of Science:
- Nephrology
- Hematology
- Internal Medicine
Background:
- Complement-mediated thrombotic microangiopathy (C-TMA) is a severe condition.
- Delayed diagnosis of C-TMA is associated with significant morbidity and organ damage.
Purpose of the Study:
- To analyze complement-mediated thrombotic microangiopathy (C-TMA) cases in a hospital nephrology department.
- To evaluate the clinical course, treatment, and short-term outcomes of C-TMA.
Main Methods:
- Prospective study of 10 newly diagnosed C-TMA patients over one year.
- Collected demographic data, clinical severity, organ involvement, and treatment outcomes (plasma therapy, eculizumab).
- Assessed hematological remission and need for renal replacement therapy (RRT).
Main Results:
- Median diagnostic delay was 5 months; incidence was 6.4/1000 inpatients.
- All patients had renal dysfunction, 80% required RRT.
- No fatal outcomes; all achieved hematological remission. 30% recovered kidney function and stopped dialysis.
Conclusions:
- C-TMA is severe, causing multi-organ dysfunction and high risk of end-stage renal failure if diagnosed late.
- Early detection and treatment are key to improving renal prognosis in C-TMA.
- Prompt intervention can lead to recovery of kidney function and cessation of dialysis.
Aim:
To analyze cases of complement-mediated thrombotic microangiopathy (C-TMA) in the daily practice of a hospital nephrology department, relative to the general aspects of the clinical course, therapy, and short-term outcomes.
Subjects And Methods:
The prospective study conducted in the period June 1, 2015 to June 1, 2016 included 10 patients with C-TMA newly diagnosed during hospitalization. Standard demographic parameters, generally accepted clinical data showing the severity of TMA and the involvement of vital organs were recorded at admission. Short-term outcomes of therapy (plasma therapy and/or eculizumab therapy), such as achievement of hematological remission and the need for maintenance therapy and renal replacement therapy (RRT), were evaluate.
Results:
The median time from the onset of symptoms of the disease to diagnosis in the analyzed cases was 5 months (range 1 week to 26 months). The incidence of C-TMA among the inpatients of nephrology departments was 6.4 per 1,000 patients per year. Five patients were admitted to a clinic with symptoms of obvious extrarenal organ disorders; 4 of them had multiple organ dysfunction. Evident clinical symptoms of renal dysfunction were detected in all the patients, which necessitated RRT in 8 out of the 10 patients. Renal biopsy was performed in 7 patients. All were found to have typical morphological manifestations of acute and chronic TMA. All the patients received plasma therapy; most of them had plasma exchanges; 4 patients took eculizumab. There were no fatal outcomes. All achieved hematological remission. Three of the 8 cases could achieve varying recovery of kidney function and stop dialysis.
Conclusion:
Analysis of this series of cases confirms the idea about the severity of TMA due to multiple organ dysfunction and the high risk of end-stage renal failure at late diagnosis. The key points of better renal prognosis are the earliest detection and treatment of the disease.
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