| Study characteristic | First author/publication yeara | ||
|---|---|---|---|
| Bing 1981 | Zacharias 1981 | Milia 2006 | |
| Population d | Hospital (hypertension clinic) | No information | Cerebrovascular clinic |
| Inclusion criteria | Mild essential hypertension (defined as diastolic BP ≥95 mmHg) | Patients treated with atenolol 100 mg day–1 or 200 mg day–1 as their sole antihypertensive therapy for at least 8 weeks | Ambulant patients with first‐ever minor hemispheric ischaemic stroke or transient ischaemic attack with or without hypertension status |
| Exclusion criteria | Clinical gout, abnormal renal function (judged by blood urea and serum creatinine) | Cardiac, renal or hepatic failure, known sensitivity to thiazide diuretics or pregnant | Significant poststroke disability (Barthel score <70), comorbidity or contraindication to antihypertensive treatment; pre‐existing moderate to severe renal impairment (serum creatinine >200 mmol l–1) or with ≥50% stenosis of either carotid artery, BP >180/100 mmHg |
| Definition of hypertension | Mild essential hypertension (DBP ≥95 mmHg) | Hypertension not adequately controlled on atenolol alone | No information |
| How BP was measured | Auscultatory method; supine and upright position | Hawksley random zero sphygmomanometer; supine and upright position | Critikon Dinamap equipment (mean of three measurements); supine position |
| Sponsorship | Servier Laboratories | No information | No information |
| Follow‐up | 16 weeks on single drug, followed by 16 weeks of combined therapy (indapamide + bendroflumethiazide) | 12 weeks | 28 days |
| Age (years) | 32–64 | No information | 68.8 ± 10.6 |
| Sex N (%) females | 10 (50) | 9 (53) | 13 (50) |
| Indapamide | 2.5 mg daily | 2.5 mg + placebo–bendroflumethiazide 5 mg | 2.5 mg daily |
| Bendroflumethiazide | 5.0 mg daily | 5 mg + placebo–indapamide 2.5 mg | 2.5 mg daily |
| Study size | 20 | 17 | 26 |
| Indapamide | 10 | No information | 13 |
| Bendroflumethiazide | 10 | No information | 13 |
BP, blood pressure; DBP, diastolic BP
All studies were conducted in the UK