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Review of long‐term treatment with labetalol.

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1 Labetalol has been used to treat 163 patients at the Dunedin Hypertension Clinic for periods up to 6.5 y, and of 128 patients in a New Zealand multicentre study for 2 yr. 2 Labetalol was often effective when other anti‐hypertensive agents, including beta‐blockers, had failed. It was usually given with a diuretic. 3 Mean daily dose was 700 mg (range 100‐2400 mg). No tolerance to the anti‐hypertensive effect was seen. 4 Some postural‐induced decrease in blood pressure on labetalol was common. 5 Side‐effects led to withdrawal of labetalol in about 25% of patients, mainly during the first few months of therapy. Another 25% had minor side‐effects but could continue with the drug. 6 There were three types of side‐effects (in order of frequency): (a) non‐ specific, (b) related to alpha‐blockade and (c) related to beta‐ blockade. The latter were much less troublesome than on “pure” beta‐ blockers. 7 There was no significant evidence of renal haematological or hepatic toxicity. 8 Anti‐nuclear antibody tests became positive on labetalol in about 15%, usually at low titres but in one patient the titre increased to a high level and fell when labetalol was stopped. 9 In a subset of 25 patients who took labetalol for the longest time (up to 6.5 yr) there was a 16% incidence of anti‐mitochondrial antibodies.
Title: Review of long‐term treatment with labetalol.
Description:
1 Labetalol has been used to treat 163 patients at the Dunedin Hypertension Clinic for periods up to 6.
5 y, and of 128 patients in a New Zealand multicentre study for 2 yr.
2 Labetalol was often effective when other anti‐hypertensive agents, including beta‐blockers, had failed.
It was usually given with a diuretic.
3 Mean daily dose was 700 mg (range 100‐2400 mg).
No tolerance to the anti‐hypertensive effect was seen.
4 Some postural‐induced decrease in blood pressure on labetalol was common.
5 Side‐effects led to withdrawal of labetalol in about 25% of patients, mainly during the first few months of therapy.
Another 25% had minor side‐effects but could continue with the drug.
6 There were three types of side‐effects (in order of frequency): (a) non‐ specific, (b) related to alpha‐blockade and (c) related to beta‐ blockade.
The latter were much less troublesome than on “pure” beta‐ blockers.
7 There was no significant evidence of renal haematological or hepatic toxicity.
8 Anti‐nuclear antibody tests became positive on labetalol in about 15%, usually at low titres but in one patient the titre increased to a high level and fell when labetalol was stopped.
9 In a subset of 25 patients who took labetalol for the longest time (up to 6.
5 yr) there was a 16% incidence of anti‐mitochondrial antibodies.

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