ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2025
[Chinese expert consensus on the diagnosis and treatment of high-altitude polycythemia(2025)].
Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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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.
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Who cites it
2 citing papers in PubMed.
- High-altitude polycythemia: State-of-the-art review.Therapeutic advances in hematology · 2026Review
- Association of residential altitude with pure-tone hearing thresholds in plateau residents aged ≤50 years: a cross-sectional study.Frontiers in neurologyArticle
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Authors and funding
2 authors.
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Abstract
High-altitude polycythemia (HAPC) is defined as a secondary excessive erythrocytosis caused by prolonged exposure to hypoxic environments at altitudes above 2,500 meters, characterized primarily by significantly elevated hemoglobin levels (≥210 g/L in males and ≥190 g/L in females). Clinically, HAPC manifests as headache, fatigue, sleep disturbances, and is prone to complications such as thrombosis and organ damages. China encompasses extensive high-altitude regions of critical strategic significance, with a growing population of residents and travelers relocating or temporarily staying in these areas. However, there has been a lack of systematic and standardized clinical guidelines for the diagnosis and management of high-altitude-related diseases. To standardize the diagnosis and treatment of HAPC in China, the Red Blood Cell Disease Group, Chinese Society of Hematology, Chinese Medical Association and Chinese Hospital Association Hematology Branch formulated this consensus based on extensive expert consultation, integrating the latest evidence-based findings and practical experience in high-altitude medicine. The consensus defines a stratified diagnostic and therapeutic strategy to guide the clinical management of HAPC: mild cases are managed with low-flow oxygen therapy; moderate cases require combined pharmacological and oxygen therapy; and severe cases are recommended for erythrocytapheresis as the primary intervention, supplemented by pharmacotherapy and oxygen support.
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