This paper describes pathological and clinical investigations of glomerular lesions in bucillamine-induced nephropathy by analyzing biopsy materials from 9 patients with rheumatoid arthritis (RA). There was no specific predisposition for nephrotic syndrome induced by bucillamine in clinical profiles related to age, onset, duration of disease, sex, activity and dose of bucillamine. In light-microscopic, electron-microscopic and immunofluorescent findings, the characteristic changes were similar to those of idiopathic membranous glomerulonephritis (MGN). After discontinuance of bucillamine, the nephrotic syndrome improved slowly with or without corticosteroid therapy. Results confirmed that the most common lesion of nephrotic syndrome associated with bucillamine therapy in RA is MGN. We recommend that corticosteroid therapy should be restricted to cases with severe proteinuria.

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1 Comparison of measured trough serum digoxin concentrations (SDC) with those predicted at steady-state by forty sets of previously described pharmacokinetic equations in conjunction with either measured or estimated creatinine clearance (Clcr) was made in an elderly group of patients with varying Clcr (25-89 ml/min) who received maintenance digoxin therapy. 2 Mean values of day-to-day variation (% coefficient of variation) for serum creatinine and measured Clcr examined three times within a week in 7 of 40 elderly patients were 6.42 and 8.36% respectively, while this value for SDC was 12.46%. 3 There was a statistically significant correlation (r = 0.72 to 0.79, P < 0.001, n = 40) between measured Clcr and that estimated from three different methods. Siersbaek-Nielsen's nomogram approach gave the best correlation. 4 The calculated correlation coefficient values between measured and predicted SDC lay within a relatively narrow range but were weak (r = 0.443-0.628). Prediction error analysis, however, allowed us to determine the best set of pharmacokinetic equations for a first approximation to appropriate digoxin maintenance dosage requirements, namely Gault-estimated elimination rate constant, measured Clcr, and Jusko-estimated volume of distribution.

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