The sources of

The sources of information that inhibitor Dovitinib should be used to access accurate information about a patient’s

medication were described in 35 policies and the timeframe over which this should be done in 30 (within 1day in 10 Trusts, 2days in 2 Trusts, 3days in 8 Trusts, 7days in 1 Trust, and other timeframes in 8 Trusts). There were 32 policies that stated where in a patient’s clinical record information pertaining to medicines reconciliation should be recorded. Only 10 (22%) policies could be considered comprehensive in that they covered all of the following: who was responsible, in what timeframe and where medicines reconciliation should be documented in the clinical records. Audits of clinical practice Inhibitors,research,lifescience,medical Patient samples At baseline, 42 Trusts submitted data for 1790 patients under the care of 375 clinical teams. At re-audit, 43 Trusts submitted data for 2296 patients under the care of 455 clinical teams. Five Trusts Inhibitors,research,lifescience,medical that participated at baseline did not participate at re-audit and six Trusts participated for the first time at re-audit. The characteristics of patients in the baseline and re-audit samples, including demographics, diagnostic groupings, Mental Health Act status and types of admitting service, are shown in Table 2. With respect to the time of admission, Inhibitors,research,lifescience,medical in the baseline audit, 44% were admitted between 9 a.m. and 5p.m. Monday

to Friday, 33% between 5p.m. and 9a.m. on weekday nights, and 16% at the weekend, between 5p.m. Friday and 9a.m. Monday. For the remaining

7%, the time of admission Inhibitors,research,lifescience,medical was unknown. The respective figures at re-audit were 45%, 33%, 17% and 5%. Table 2. EPZ-5676 IC50 Demographic and clinical characteristics of the patient samples at baseline (n=1790) and re-audit (n=2296). Clinical teams’ accounts of medicines reconciliation The sources of information that were checked by members of the clinical team within 24h, 3days Inhibitors,research,lifescience,medical and 7days of admission at baseline and re-audit are shown in Table 3. At baseline, within 7days of admission, patients who were admitted to adult settings were more likely to have been asked about the medication they were taking (736/1055, 70%) than those admitted to elderly settings (209/614, 34%) (χ2=201.6, p<0.001). Those patients in elderly settings (371/614, 60%) were more likely to have had particular sources of information checked compared with those in adult care settings: consultation with their GP Anacetrapib (488/1055, 46%) (χ2=31.2, p<0.001); examination of their medication (258/614, 42% versus 179/1055, 17%; χ2=126.0, p<0.001); and enquiry of their carer (171/614, 28% versus 148/1055, 14%; χ2=61.3, p<0.001) or residential or care home (97/614, 16% versus 29/1055, 3%; χ2=94.6, p<0.001). Table 3. Sources of information about medicines, used during the reconciliation process, in acute adult inpatient settings at baseline and re-audit.

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