Kabir 2007.
Methods | Study design: ITS | |
Participants | Physicians Clinical speciality: not clear Level of training: fully trained Setting/country: not clear/Ireland |
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Interventions | 3 PEMs were studied in this report: 1. the LIFE (2002), 2. the ALLHAT (18 December 2002), and 3. the VALUE (2004). The LIFE study showed that for a similar level of BP reduction losartan reduced events more than atenolol, a β‐adrenoceptor blocker. The ALLHAT trial confirmed that thiazides (chlorthalidone) controlled systolic BP as well as, and in elected subgroups better than both ACE inhibitors (lisinopril) and calcium channel blockers (amlodipine). However, the VALUE trial showed that the amlodipine‐based regimen significantly reduced BP further than valsartan, especially in the early period. Another feature common to all studies was a demonstration of the need for polypharmacy to achieve BP control | |
Outcomes | 7 process outcomes:
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Notes | ‐ | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Intervention independent of other changes ‐ ITS | Unclear risk | No information was provided |
Shape of Intervention effect pre‐specified ‐ ITS | Unclear risk | Quote, pg. 382: "studies in Canada and the US have shown that such publications have influenced prescribing patterns. This study assesses such prescribing patterns in Ireland from January 2001 to July 2005, 12 months before and after the publication of the three major hypertension trials: LIFE, ALLHAT and VALUE" |
Intervention unlikely to affect data collection ‐ ITS | Low risk | The interventions (LIFE, ALLHAT, and VALUE studies) did not affect either the source or method of data collection |
Blinding of outcome assessors (detection bias) ‐ ITS All outcomes | Low risk | The outcome was objective |
Incomplete outcome data (attrition bias) ‐ ITS All outcomes | Low risk | Data were collected from a regional database |
Selective reporting (reporting bias) ‐ ITS | Low risk | All relevant outcomes in the methods section were reported in results section |
Other bias ‐ ITS | Low risk | There was no evidence of other risks of bias |