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Drug-induced peripheral oedema: An aetiology-based review

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BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
卷 87, 期 8, 页码 3043-3055

出版社

WILEY
DOI: 10.1111/bcp.14752

关键词

capillary permeability; oedema; lymphedema; microcirculation; pharmacovigilance; renal reabsorption

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Drug-induced peripheral edema can occur through various mechanisms, such as vasodilatory edema, renal edema, lymphedema, and permeability edema. Different drugs may cause different types of peripheral edema, which may be underestimated and misdiagnosed, leading to inappropriate prescribing.
Many drugs are responsible, through different mechanisms, for peripheral oedema. Severity is highly variable, ranging from slight oedema of the lower limbs to anasarca pictures as in the capillary leak syndrome. Although most often noninflammatory and bilateral, some drugs are associated with peripheral oedema that is readily erythematous (eg, pemetrexed) or unilateral (eg, sirolimus). Thus, drug-induced peripheral oedema is underrecognized and misdiagnosed, frequently leading to a prescribing cascade. Four main mechanisms are involved, namely precapillary arteriolar vasodilation (vasodilatory oedema), sodium/water retention (renal oedema), lymphatic insufficiency (lymphedema) and increased capillary permeability (permeability oedema). The underlying mechanism has significant impact on treatment efficacy. The purpose of this review is to provide a comprehensive analysis of the main causative drugs by illustrating each pathophysiological mechanism and their management through an example of a drug.

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