Shum 2000.
Methods | Randomised trial | |
Participants | 1815 patients (total group), mean age 27.5 years, 40% male 5 nurses 19 doctors | |
Interventions |
Intervention: patients allocated to nurse
Control: patients allocated to doctor Detailed description of the intervention: Compared acceptability and effectiveness of a practice‐based minor illness service led by nurses versus routine care offered by general practitioners. Nurses managed patient care and took the history, performed a physical examination, offered advice and treatment, issued prescriptions (which required a doctor's signature), and referred the patient to the doctor when appropriate. Supervision, oversight: Patients seen by a nurse were referred to a general practitioner when appropriate. |
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Outcomes |
Patient outcomes:
Process of care:
Resource utilisation:
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Notes |
Country: UK Study period: 2 weeks Nurse role: first contact care for patients with urgent problems Nurse title: practice nurse Nurse educational background: EQF level unknown Nurse years of experience: average of 8.4 (3.8) years of experience in practice nursing Nurse additional training: 3‐month academically accredited degree level course on managing minor illnesses. Nurses attended one half‐day a week of formal group teaching by a nurse practitioner and were taught twice a week by general practitioners during routine surgeries in the practice where the nurses worked. |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Sequence was generated by non‐resealable opaque envelopes. "Allocation to being seen by a doctor or nurse was determined using random permuted blocks of four with sequentially numbered, non‐resealable opaque envelopes". |
Allocation concealment (selection bias) | Low risk | Allocation was concealed by sequentially numbered, non‐resealable opaque envelopes. "Allocation to being seen by a doctor or nurse was determined using random permuted blocks of four with sequentially numbered, non‐resealable opaque envelopes". |
Baseline characteristics | Low risk | Baseline characteristics were reported and were similar for both groups. "The two groups of patients were comparable in terms of age, sex, the number who usually preferred to see a female doctor rather than a male, and their reported rates of consultation in the previous 12 months (table 1)". Baseline outcome measures were not relevant. |
Baseline outcome measurement | Unclear risk | Primary outcomes were not assessed before the intervention. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | It is unclear whether the outcome was influenced by lack of blinding of patients and care providers. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No information |
Incomplete outcome data (attrition bias) All outcomes | Low risk | For most outcomes, follow‐up was > 80%. Follow‐up for satisfaction questionnaire was > 75%, for mailed questionnaire 76%. |
Selective reporting (reporting bias) | Unclear risk | The protocol was not available. |
Contamination | Unclear risk | No information |
Bias due to lack of power | Low risk | Sufficient power "It was calculated that 1060 valid responses would be sufficient to detect an effect size of 0.2 SD at the 95% confidence level with a power of 90% using two tailed tests". |