2003
DOI: 10.1097/00004872-200305000-00026
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Quantification of leg oedema in postmenopausal hypertensive patients treated with lercanidipine or amlodipine

Abstract: In postmenopausal females with mild to moderate hypertension the oedema formation of Lercanidipine was significantly less than that of Amlodipine, despite no significant differences in the antihypertensive effect.

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Cited by 60 publications
(44 citation statements)
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“…Lercanidipine was well tolerated both when administered alone 15,16 and when given in combination with enalapril. The improved efficacy of combination therapy was therefore not associated with a worse tolerability of the treatment.…”
Section: Discussionmentioning
confidence: 98%
“…Lercanidipine was well tolerated both when administered alone 15,16 and when given in combination with enalapril. The improved efficacy of combination therapy was therefore not associated with a worse tolerability of the treatment.…”
Section: Discussionmentioning
confidence: 98%
“…However, when reported by patients as 'leg swelling', one of these thirdgeneration CCBs has been associated with an oedema incidence of 22%. 26 Thus, although differences among CCBs in oedema incidence rates have been reported in a number of studies, 10,[27][28][29][30] it is evident that dose-dependent peripheral oedema remains a common side effect in patients receiving both established and newer CCBs. 10,31 Factors that may influence oedema Several factors can predispose the patient to an increased risk of oedema.…”
Section: Mechanism Of Ccb-induced Oedemamentioning
confidence: 99%
“…28 In a second example, physical examination of CCB-treated patients by the investigator led to a reported oedema incidence of 10%. 26 However, when patient reports of 'leg swelling' were used as the assessment criterion for oedema in the same study, the incidence was 22%. There is also evidence that patients do not report all symptoms that they suspect to be related to drug administration to their doctor, and that physicians do not always record symptoms reported to them by patients.…”
mentioning
confidence: 94%
“…In clinical studies, peripheral edema, as a pharmacologically-mediated adverse event, has typically been captured through water-displacement volumetry, patient self-report, or other, often non-validated, investigator assessments. [20][21][22][23][24][25] Water-displacement volumetry is widely considered to be the reference method of edema assessment; 26 however, it is also considered to be time-consuming, difficult to perform, and inappropriate in some clinical situations (e.g., postoperative), limiting the use of this method. 12,27 Documentation of the accuracy and reliability of other methods of measuring peripheral edema vary.…”
Section: Assessment Of Peripheral Edemamentioning
confidence: 99%