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Drennan VM, Halter M, Brearley S, et al. Investigating the contribution of physician assistants to primary care in England: a mixed-methods study. Southampton (UK): NIHR Journals Library; 2014 May. (Health Services and Delivery Research, No. 2.16.)

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Investigating the contribution of physician assistants to primary care in England: a mixed-methods study.

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Chapter 2Methods

This investigation employed an evaluative framework suggested by Maxwell73 to examine the contribution that PAs make to the effectiveness, appropriateness, equity, efficiency, acceptability and costs of primary health care. The study had two phases of enquiry. The first investigated the research questions at the macro and meso level of health-care systems through (a) a review of evidence, (b) a scoping survey74 of key informants at national and regional levels and (c) a survey of the current work deployment of PAs in UK general practice. The second phase used a comparative case study design75 of 12 general practices to investigate the research questions at the micro level of the health-care system. Each of these phases is described in detail below. The evidence from each of these elements was then synthesised by the research team and brought to a wider consultative group of people who had participated in the study, including the advisory group and public and patient involvement group.

Phase 1: investigating at the macro and meso levels of health systems

This phase had three elements: (1) a review of evidence, (2) a scoping survey74 of key informants at a national and regional level and (3) a survey of current work deployment of PAs in UK general practice.

The review of evidence

In this element we undertook three review activities. The first was a review of empirical evidence using a rapid review methodology76 for empirical evidence of the deployment and impact of PAs (research questions 1 and 2; see Chapter 1, Study aims and objectives). The second was a narrative review77 of published commentaries and opinions of the PA role in the UK setting. The third was a narrative review77 of national and international policy and developments on health-care workforce planning in relation to PAs and primary care. The last two activities addressed the question as to factors supporting or inhibiting the presence of PAs in the primary care workforce.

The review of empirical evidence

A review78 was conducted to investigate the evidence of the contribution of PAs to primary care as applicable to a European model. The European model of general practice/family medicine was that given by the European region of the World Organization of Family Doctors79 (WONCA Europe). Seven databases [British Nursing Index, Cumulative Index to Nursing and Allied Health Literature (CINAHL), EMBASE, MEDLINE, PsycINFO, Social Sciences Citation Index (SSCI) and Scopus] were searched from 1967 (or start date if later) to September 2010. A broad range of search terms was used singly and in combination: physician assistant, primary health care, family practice, general practice, family physician, general practitioner (see Appendix 3).

The inclusion criteria were defined as follows:

  • The PA role was one with a recognised PA qualification.
  • The setting was of general practice/family medicine (including community paediatrics in the USA) or the data were identified as pertaining to ‘family medicine’ within other findings from broader ‘primary care’.

The exclusion criteria were defined as follows:

  • Settings of secondary care, in-patient care ambulatory or outpatient care.
  • Health care provided by primary care specialists in the USA (obstetrics, gynaecology, internists or primary care physicians) that would be regarded as secondary care in the UK.
  • The personnel were student PAs or nurses/others who had received special training as medical assistants (that is, without a recognised PA course) for a particular disease condition.
  • The data presented did not distinguish either between PAs and other professionals or between the general practice/family medicine setting from ‘primary care’ overall in its presentation of results.

Retrieved abstracts were screened and full papers, where available, were obtained. Each full paper was assessed for inclusion by two researchers independently and a third (HG, SdeL, VMD, and MH) in cases of indecision or disagreement. A data extraction framework was developed which included categories of PA activities, study methods and key findings. Study outcome measures were categorised using Donabedian’s80 framework of structure, process and outcome. Owing to the wide range of methods used in the retrieved studies, a broad quality assessment of the studies was undertaken using critical appraisal tools81 appropriate to the papers’ methods (e.g. qualitative, cohort, health economic) with additional questions derived from the British Medical Journal’s guidance for peer reviewers.82 The heterogeneity of the retrieved studies precluded any pooling of data and a narrative synthesis was undertaken using the Donabedian80 framework.

Review of commentaries

A documentary analysis83 was undertaken of published commentaries and opinion pieces about PAs in the UK health-care system or addressed to UK audiences. The published material was identified in two ways: first, through the electronic database search described in the previous section and, second, by an internet search using the Google™ (Mountain View, CA, USA) search engine. The internet search used a combination of terms: physician assistant, physician assistants, National Health Service (NHS), primary care, secondary care, England, Scotland, Wales, Northern Ireland, pilots and workforce, and was repeated at intervals by WC from April 2011 until December 2012. ‘Published’ was defined as in print and electronic formats including online forums between 1980 and 2012. The lower date was determined by our previous knowledge of the first paper published on the experience of a PA in UK primary care.58 A data extraction framework was developed which included a categorisation of the author (journalists, doctors, nurses, health service managers, etc.), the intended audience, any catalyst for the item (e.g. another published item), inclusion of any empirical evidence and from which country, evidence of support, resistance or neutrality in the publication. The items were recorded chronologically with the data extraction in a Microsoft Excel (Microsoft Corporation, Redmond, WA, USA) spreadsheet. A narrative synthesis was drawn from the data.

Review of workforce policy and developments

The purpose of this review was both to identify policy and developments pertaining to PAs in the primary health-care workforce in the UK and internationally in order to both help the research team contextualise the study and to identify supporting or hindering factors in the development of the PA profession in the English health-care workforce. The review drew on the methods of the documentary review.83 Publications were identified through the searches described above. Additional searches were performed to identify polices and reports on health-care workforce planning and development relevant to, primarily, the education and employment of PAs and, secondarily, primary care. The time period covered was from the mid-1990s to the present day. The searches were conducted by:

  • visiting key websites in the UK, for example government health departments in each of the four countries, the Centre for Workforce Intelligence (CfWI) and Strategic Health Authority (SHA) websites
  • using keyword searches in the Google search engine for open source materials related to the topics of interest, for example ‘primary care workforce’, ‘physician assistant/s’ (and other titles to describe this profession, such as medical care practitioners) and ‘health care workforce’
  • snowballing techniques of references and website links.

The documents identified in this way were screened to include only those with relevance to health-care workforce in primary care. Research team alerts of new policy or reports relevant to the study were generated by one researcher (WC). A data extraction framework was developed to classify the document by country, type of author, type of document (e.g. policy, analysis of primary data, opinion and evaluative reports), any reference or absence of reference to PAs and key points from or about the document. The information was saved on an electronic database with full references, any URLs and electronic copies of the original. A narrative synthesis was undertaken addressing the questions of interest.

Scoping survey

A scoping survey74 was undertaken to address research question 3: what supports or inhibits the use and development of PAs in the primary care? (See Chapter 1, Study aims and objectives.) The method is one element of a scoping review74 and allows for data to be gathered from those knowledgeable in the issue of interest, providing a range of perspectives to ensure breadth in the analysis.84 It is an approach that has been widely used, most recently in exploring European perspectives on human health resource issues.85 A purposive sample of key informants at national and regional levels in England and Wales was approached to participate. These were individuals at a senior level from central departments of health, professional organisations, regulatory organisations, patient organisations, and commissioning bodies who are concerned with the development of primary care services, workforce development and health professional regulation. At the point of the design of the study (2009) the Department of Health and Social Services (Wales), unlike the Departments of Health for England and Scotland, had not explored the use of PAs. In order to consider diversity in national environments, individuals were approached to participate in England and Wales. Individuals were identified for approach through an internet search of public domain organisational sites, suggestions of the study advisory group and members of the research team, and snowball techniques from participants. An aide-memoire was developed of topic areas, based on the issues of interest, to be used in semi-structured interviews83 which were offered either face to face or by telephone, dependent on participant preference. The aide-memoire explored knowledge of mid-level practitioners, PAs and perceptions of the factors that currently and will in the future support or inhibit their use and development in the UK settings. Notes were taken during the interview and, with permission, digitally recorded. These were transcribed, anonymised and the recordings deleted. The transcriptions and notes were analysed using the constant comparison method86 by two researchers (WC and VMD) independently, compared and further analysis confirmed with a third researcher (JG). The analysis of the early interviews assisted in identifying further stakeholder groups from whom views were sought. This element of the study was deemed service evaluation by the NHS ethics query service and as such not for research ethics review. It conformed to all university requirements.

Survey of current use of physician assistants in general practices in England

An online, anonymous, self-completion survey was developed and piloted with two PAs who had previously worked in general practice in England. It posed questions of career history, work environment, work activities and estimates of volumes of work. PAs known to working in primary care were invited to participate in 2010 through e-mails sent out by the UK Association of Physician Assistants (UKAPA), course leaders of PA courses in English universities and practices identified as employing PAs in previous research.72 All invitation e-mails included a link to the survey website and requested forward distribution to any other PAs thought to be working in primary care. UKAPA estimated that there were about 25 of their member PAs employed in primary care. The electronic survey was open for responses for 7 weeks (7 October to 30 November 2010). It addressed three areas: the activities and role of PAs in the primary care team, their primary care setting and their qualifications. Those interested in volunteering for the second phase of the study were given an opportunity to give their contact details at the end of the survey. The survey did not require NHS ethical review and fulfilled all university requirements for the ethical conduct of research. Descriptive analysis of the data was undertaken using Statistical Product and Service Solutions (SPSS) (IBM Corporation, Armonk, NY, USA).

Phase 2: the micro level

A comparative case study design75 was used to address the three overarching research questions at the micro level of analysis through examination of 12 case studies: six general practices currently employing PAs and six matched practices not including PAs in their staffing. A mixed-methods approach87 allowed for both description and the quantification of the impact of PAs in the context of general practice. This element of the study addressed specific additional questions:

  1. How are PAs deployed and supervised in general practice and how do their roles and responsibilities compare with those of the doctors, NPs and practice nurses?
  2. How do PA outcomes of care differ from those of GPs, specifically with respect to prescriptions rates, referrals, investigations, reattendances for the same problem within 2 weeks, patient safety, and patient satisfaction?
  3. How do patients understand the role of PAs and what is the experience of patients when consulting PAs?
  4. How does employment of PAs affect practice organisation, staffing configurations and costs?
  5. What are the factors that support or inhibit the employment of PAs?

The six practices employing PAs were identified either by the PAs initially volunteering through the survey (see Survey of current use of physician assistants in general practices in England) or by an expression of interest from a practice. The volunteering PA practices achieved diversity in features such as general practice size, practice population sociodemographic characteristics, rural and urban coverage, and in the country in which the PAs had qualified. The comparative that was designed required some similarity between PA and comparator GP practices. Following the agreement to participate from PA employing practices, comparison practices were sought in the same health economy and with similar characteristics and patient population size. After the adoption of the study by the UK Clinical Research Network (UKCRN) Primary Care Research Network (PCRN), officers in five local PCRNs made the initial approaches and requests for comparison general practices. Practices expressing interest were then contacted and provided with information, and an initial meeting was set up between the researchers (VMD and MH) and the GP, the practice manager and, in those employing practices, the PA. A summary description of the practices is provided at the end of Chapter 2 (see Table 5).

TABLE 5

TABLE 5

Summary of the practice settings

The general practices and staff likely to be included in the study were provided with full participant information sheets for all research activities. Written agreement and consent for the practice to participate was obtained from the senior partner GP. Procedures for obtaining individual informed consent for each of the research activities are described below.

Data were gathered through the activities detailed in the following sections in this chapter. The analysis is described in each section and the economic analysis in Economic analysis. Analyses were then combined and synthesised to address the research questions as outlined in Table 2.

TABLE 2

TABLE 2

Summary of data to address research questions

Semi-structured interviews with practice staff

Semi-structured interviews83 were undertaken with PAs, GPs, practice managers, receptionists and practice nursing staff. A purposive sample in each practice was approached, provided with information and invited to participate. Aide-memoires for each professional group were developed addressing the questions (a), (b), (d) and (e), above, but allowing flexibility to explore new issues or ideas raised in the interview. GPs, PAs and nurses were also asked to describe their responsibilities and activities within the practice. In addition, practice managers and GPs were invited to provide any practice documents that would provide the research team with information about the practice, its working practices, services provided, staffing and planning. If documents on staffing were not available, the practice managers were asked to provide this information verbally. The interviews were conducted face to face or by telephone as preferred by the participant, digitally recorded with consent, transcribed and erased after analysis. Thematic analysis was undertaken88 initially by one researcher (RL), with further analysis by two other researchers (VMD and MH) and interpretative discussion with the wider research team. Documentary evidence on staffing was read and data extracted as relevant to providing contextual information for each practice.

Consultation record review and linked patient survey

The consultation record review and linked patient survey, which addressed question (b) above, was of patients presenting in urgent or same-day surgeries. This was the type of surgery that PAs were predominately working in as identified from the national survey (p. 9). Each practice identified time periods in summer and winter periods (known as reference periods) during 2011 and 2012 in which they were able to assist the research team in data gathering. The length of time periods were based on the practice’s estimation as to the number of surgeries required to reach the sample size. Each practice made staff and patients aware of the research during the reference periods in keeping with their usual practice, for example via notices at the reception desk.

The patient surveys

The validated General Practice Assessment Survey (GPAS)89 focuses on patient outcomes and consultation experience and was used with permission (Paula Metcalfe, GP Patient Survey Team, 12 October 2010, personal communication). During a meeting of the study’s public and patient participation group (see Chapter 1, Study aims and objectives) the GPAS was scrutinised and amendments suggested to improve the clarity of the wording and to specifically address the experience of a consultation with a PA. The amended, self-completion GPAS (see Appendix 4) was then to be offered to adult patients in each designated surgery during the reference periods. The method of distribution and collection varied in each practice, according to their working practices. In some practices, the GP or PA handed the patient a sticker to return to the receptionist, following the consultation, to collect a survey pack (containing a questionnaire, participant information sheet, and business reply envelope). In other practices, the survey pack was sent by post either the same day or the next. All completed questionnaires could be returned in a sealed envelope to a collection box in the practice reception or by post to the research team. The questionnaire did not include any information that could identify the person. Each questionnaire had a unique study identifier (study ID). Practice staff kept a log of the dates of survey administration (the index event) and recorded the unique practice identifier of the patient against the study ID. Practice staff were asked to send out a research team prepared reminder and duplicate survey pack to all those who had taken or been sent a questionnaire who had not responded. The practice staff did not have any access to any of the completed questionnaires, ensuring that anonymity was protected. Data were entered onto a SPSS spreadsheet and descriptively analysed. The data were then also added to the data drawn from the consultation record review as described below.

In the PA-employing practices, the survey pack included additional material inviting patients to participate in a face-to-face or telephone interview. A separate consent form and business reply envelope were provided to respond to the invitation.

Consultation record review

This review addressed the primary outcome of the study: the rate of reattendance in general practice or an urgent care facility defined for the study as GP out-of-hours care, emergency department, walk-in centre, minor injury unit or other direct entry emergency unit (e.g. early pregnancy assessment unit) within 2 weeks of the initial consultation (the index consultation) with a PA or GP, and questions of whether or not the initial consultation activity by the PA or GP was appropriate in the light of the subsequent reattendance. The consultation records also provided the data for the process measures of advice, investigations, treatments, referrals and prescriptions.

The sample

The sample size required for the primary outcome was based upon randomised controlled trial data which compared the rate of reattendance in general practice within 2 weeks and outcomes of care delivered by NPs and GPs in the UK for patients attending ‘same-day appointments’. These studies reported figures ranging from a self-reported 18.2%90 through to extracted medical records 28.4%91 and 29%92 for patients seeing GPs and 20.4%, 31% and 37.2% for NPs, respectively. Taking Venning et al.’s91 analysis as the most robustly adjusted of these, the reattendance rate within 2 weeks of the consultation for this sample size calculation was taken as 28.4% for GPs and 37.2% for NPs. Assuming an OR of 1.5 and adjusting for slight multicollinearity as reported by Venning et al.,91 we estimated that a sample size of 205 in each group (consultations with a PA or a GP) was needed to give 80% power at a significance level of 5% for a logistic regression using the covariates of age, gender and general practice. We estimated that anonymised clinical records data might be required for up to approximately 600 patients each attended by PAs and GPs in the 12 practices in the data collection periods in order to meet the required sample size, assuming a response rate of 30% to the patient survey. However, in conducting the study, two problems arose. The first was that a condition of the research ethics approval was that child consultations were excluded from the survey element but could be included in the review of clinical records. We therefore included all child consultations in the designated surgeries in the reference periods as our review and survey had shown that PAs were consulted by children and their parents. The second problem arose through inaccurate research team and practice staff estimates of patient survey return rates in their practice (i.e. lower than our assumptions) resulting in more surgeries being designated for survey distribution. In some practices, clinical records were passed to the research team some months after the designated surgeries and only then did it become apparent to the research team that these had much greater numbers than anticipated. In addition, in some practices, there was a lack of fidelity to the protocol in that not all eligible patients were offered the survey (in some instances only 30% were offered). This was apparent to the research team staff only when they returned to discuss the participant numbers and check that the reference periods were similar to those of the preceding weeks for the practice. As the possibility of selection bias could not be eliminated, the research team decided to include all of the clinical records sent by the practices. This resulted in a larger sample than in the study design.

The data

Data from the electronic records of those patients who consulted in the designated surgeries during the reference periods were extracted and all patient identifiers removed in the practice. These data were then passed to the research team using the unique study ID number only. The data extraction occurred at a time point more than 2 weeks after the end of the reference period. The data extracted by the practice staff for the index event included the consultation date, person consulted (PA or GP) and length of consultation; the patient’s age, gender, ethnicity and postcode; the patient’s presenting conditions; number of prescriptions from the consultation; the number and type of Quality and Outcome Framework93 chronic conditions registers the patient was entered on; the number of repeat prescriptions; and the number of times the patient had contact with the practice in the three months preceding the index event. For any consultations in the following 2-week period, the location of consultation, the professional consulted, presenting condition(s) and number of prescriptions issued were recorded. The research team used the postcode on each record to assign the Index of Multiple Deprivation (IMD)94 and then deleted the postcode. The practice records varied in the extent to which Read codes95 were used for the presenting problem or diagnosis. The research team subsequently reviewed each record and assigned Read codes95 to presenting problems that were documented but not coded by practice staff and assigned study codes for groups of diagnostic tests, referrals, procedures, certificates, medicine management and advice given (see Appendix 5). Each consultation record was coded by one member of the research team and then checked by a second. Uncertainties were discussed and resolved with a third member of the team. A categorisation of the presenting problems in the index consultation was also assigned to each patient record in order to examine the case mix of the consulting patients. This classification of acute, chronic, minor/symptoms, prevention and processes was an adaptation of that used by de Jong et al.,96 developed by the research team in which the GP in the research team (SdeL) made the final decisions on categorisation and assignment. The method of assignment of a condition category to each patient is presented in Appendix 6.

Each index consultation that had subsequent consultations was identified. Each subsequent consultation was coded by two research team members to identify whether it was for exactly the same, a linked or a different problem to that of the index consultation. The method for designation was developed and refined with the GP research team member (SdeL).

All data were entered into a SPSS spreadsheet, to which the data from the patient survey (where available) could be matched by the study unique identifying number.

The data were then analysed descriptively, involving summary measures of location (e.g. means /medians/proportions) and dispersion [standard deviations (SDs)/percentiles] appropriate for the type and distribution of the individual variables. Differences in processes and outcome between those practices with and without PAs were assessed by generalised estimating equation models.97 The resulting ORs or rate ratios were adjusted for the case mix and IMD variables where they were significant predictors or notably confounded the relationship between practice type and the dependent variable. The correlation matrix was set to be exchangeable, that is to say patients were assumed to have some shared characteristics within each practice, whether from demographics or organisation of the practice.

The clinical review of reconsultations records

All records in which a patient had reconsulted within 2 weeks for the same or a linked problem were assigned to clinical record review. The review of medical records, or ‘chart review’, is a longstanding method of assessing the consultation98 used in assessing overall quality99 and considered reliable in detecting prescribing errors.100

An anonymised printout of the computerised medical record system was reviewed to assess the quality of the record and to assess the appropriateness and safety. The data on whether it had been a GP or PA who had conducted the index consultation were removed, as well as any other references that might identify the practice or its geographical area (e.g. hospital name). A clinical review process, which addressed the question as to whether or not, in the light of the subsequent consultation(s), the first consultation had been appropriate, was developed by the GP member of the research team (SdeL) in consultation with the clinical review team of four GPs. The four GPs all had experience of assessing the quality of the consultation and, to a more limited extent, of the medical record. They were all active in education: one was a trainer while the other three took medical students in their practices; two were research active; two were male, two were female. They were trained in two 2-hour training sessions led by SdeL.

Based on the problem-orientated medical record format,101 the experienced GP reviewers were asked to judge each element of the consultation, the overall appropriateness and whether a GP or a PA had been consulted. Weed’s taxonomy,101,102 for the elements of a problem-orientated medical record, was used as an measure of quality of the record, and the opinion of experienced GPs about appropriateness of the content of each part was used for the problem presented. The GP raters also gave an overall assessment. Weed’s101,102 approach was to suggest that there were four key elements of the record, described by the acronym SOAP:

  • Subjective: what the patient complains of, the problem from the patient’s perspective.
  • Objective findings from the consultation (e.g. blood pressure measurement).
  • Analysis by the clinician of the problem.
  • Plan for future action, including follow-up.

We modified this by making it explicit that the plan could have different elements: investigations, prescriptions and other aspects of the plan, such as referral or follow-up (Table 3).

TABLE 3

TABLE 3

Modification of Weed’s SOAP to judge the appropriateness of the medical record

Each record was assessed by a GP and 20% by two GPs independently using a study-designed form (see Appendix 7). Data were entered into a SPSS spreadsheet, analysed descriptively and inter-rater reliability was assessed. Inter-rater reliability is a measure of the extent to which the reviewers agreed with each other in their responses. Fleiss’s kappa103 is a simple measure of this inter-rater reliability. A kappa score of 0 indicates no more agreement than one would expect to occur simply by chance, and a score of 1 indicates complete agreement on all the data that were rated. Negative scores indicate agreement that is worse than chance. It is often said that a kappa score of 0.0–0.2 is ‘poor’, one of 0.21–0.4 is ‘fair’, 0.41–0.6 is ‘moderate’, 0.61–0.8 is ‘good’, and 0.81–1.0 is ‘very good’.104 The raters assessed one case/medical record as a group. Next, they analysed three cases on their own and checked back afterwards. They then did a further 10 cases, which were assessed for inter-rater reliability.

Patient interviews

Patients who had consulted PAs and received a survey were also invited to participate in telephone or face-to-face interviews. This was designed to address question (c): how do patients understand the role of PAs and what is the experience of patients when consulting PAs? An aide-memoire was developed to explore issues not captured by the patient survey such as patient choice, understanding of the role of the PA, perceptions of the consultation with regard to communication and perceived expertise. A researcher (WC) contacted those who responded to the invitation as soon after the index consultation as possible. With consent, the interviews were digitally recorded, transcribed and analysed thematically88 by three researchers (LJ, MH, WC) using the NVivo software programme (QSR International Pty Ltd, Doncaster, Australia) (LJ, MH).

Observation of physician assistants and general practitioners

Patient consultations were video recorded, with consent of the practitioner and the patients, during one surgery per PA and GP. This element addressed questions (a), (b) and (e). We recorded GPs and PAs using two video channels, and assessed competence at consulting using the validated Leicester Assessment Package (LAP) rating scale.105 Video recording is an established method of assessing the consultation106 and the use of two channels was a compromise between the multichannel recording we planned106 and what we could gain the NHS REC permission for.

Patients in the designated surgeries were provided with information and consent was sought in writing by a researcher in the waiting room before recording commenced. Recording was stopped at the end of each consultation. Patients were then asked whether they continued to give consent or would prefer that it was withdrawn and the recording deleted. Practitioners also reconsented to the inclusion of each recording or could ask for a recording to be withdrawn at the end of the surgery. The recordings were made using ALFA: a computer-mediated consultation observation technique developed to provide an analysable overview of the consultation.107 Each consultation was assessed by two GPs independently using the LAP105 for assessing competence in general practice on dimensions of interviewing and history taking, patient management, problem solving and behaviour and relationship with patients.

The LAP for video consultation is a tool for measuring competence by direct observation. It was initially developed in the 1990s and demonstrated to have validity108110 and reliability across levels of clinical competence.107 Testing of reliability found a range of mean scores between 51.3% and 70.2% in one study, depending on levels of experience,110 and between 45% and 75% in another looking at the effect of interruption.109 Although it has been criticised, no better package has been developed.111,112 The LAP has also been used in a range of clinical contexts – assessment of cancer patients,112 the needs of caregivers113 and in the assessment of psychosexual problems.114 This package has also been used in an international setting, where a 50% pass mark was included,115 for assessing practice nurses116 and medical students.117

Grades were given by the four raters, using the seven main categories of the assessment package, and the results were then analysed. The seventh element of the package, the record, could not be rated as it could not be properly observed from the two-camera set-up used. Record keeping referred to how the health-care professional (HCP) interacted with the computer. It was not possible to view the detail of the individual record being collected by the HCP owing to the fact that only two channels of video were being recorded, and an additional channel is required for recording video directly from the HCP’s computer screen. Three of the seven categories – interview/history taking, patient management and problem solving – are given a double weighting, and count for 20% of overall marks (Table 4). When combined, this means that the LAP scale total is 100, allowing final results to be expressed as a mean score (out of 5 for each category) or be expressed as a total percentage score.

TABLE 4. Components of the LAP (adapted from Fraser et al.

TABLE 4

Components of the LAP (adapted from Fraser et al.)

A workshop was held to discuss the findings with the raters (unblinded) which was video recorded and transcribed.

Observation was also undertaken in a sample of practice clinical meetings in which PAs and GPs were both present to understand more broadly how the PAs interact with the GPs in clinical decision-making in the practice. Permission and invitations was sought from the practice manager, the GPs and the PA. Permission and consent to observe was sought at each meeting that the research team was invited to. Field notes were made of only the activity and interaction of the team members. Analysis of these notes was used to complement data from the staff interviews (see Semistructured interviews with practice staff) and consultation video observations.

Work activities of physician assistants and general practitioners

Work activity diaries, using the 2006–7 general practice workload survey,118 were offered to PAs to complete for 1 week in the summer and winter. This addressed question (a), above. Early discussions with GPs made it evident that these diaries were unlikely to be completed by practice professionals other than the PAs and the data were therefore sought through interviews (see Semi-structured interviews with practice staff) and administrative systems. Data were entered onto a SPSS spreadsheet and analysed descriptively.

Economic analysis

The economic analysis was conducted at two levels:

  1. The resource implications and costs of different team configurations were explored using practice-level data on staffing. Skill mixes, and the relative contribution of different practitioners, were compared within and between practices that do and do not employ PAs, after consideration of case mix differences. Nationally validated scales119 were used to calculate total human resource costs and costs per patient.
  2. The impact of PAs, compared with GPs, on consultation processes (e.g. prescribing, referral and investigations), consultation outcomes (e.g. reattending, consultation satisfaction) and length, at individual patient level, as analysed in the clinical record element were incorporated in a high-level analysis of costs and effectiveness.

Practice level

Data

Each of the 12 practices (six with and six without a PA) was asked in November 2012 to provide information about their staffing configurations – headcounts and whole-time equivalents (WTEs) of:

  1. clinical personnel
    • – GPs (partners and salaried/other)
    • – mid-level professionals – PAs and NPs
    • – nursing and other staff engaged in direct patient care – practice nurses (PNs), HCAs, phlebotomists
  2. support staff
    • – managers and professionals [e.g. for information technology (IT), finance]
    • – secretarial, reception, clerical.

The number of patients on the list of each practice and the proportions aged > 65 years and < 15 years were obtained from the Department of Health NHS Commissioning Board.120 IMD 2010 for each practice was obtained from the NHS Information Centre.121

Costs

Unit costs of clinical personnel were obtained from validated national sources.119 These unit costs provide a value, per annum, that covers remuneration, on-costs, qualifications (where relevant), training, capital and other overheads associated with each role (see Appendix 8). PAs were costed as Band 7 nurses (secretary of UK Association of PAs, 2012, personal correspondence). The same costs were applied to GP partners and salaried GPs because evidence on this was contradictory. One study suggested that partners cost less than salaried GPs122 and others argued partners cost slightly more123 or the same.124

The remuneration levels of management and other support staff were obtained by looking at several job vacancies within the NHS for each role (outside London rates) in January 2013, and inferring an average salary. The on-costs and overheads associated with each role were assumed to be equivalent to those of clinical NHS staff working in general practice with the same remuneration. For example, the salary of a NP was £38,800 and job advertisements for practice managers were around the same level, so the on-costs and overheads of the NP were used to estimate the costs of a practice manager.

Analysis

The numbers of WTE staff in each category, and numbers of patients per GP, were calculated and compared within and between practices with and without a PA. Reported vacancies were included in the calculations.

Staffing costs were calculated for each category in each practice on an annual basis by multiplying the WTE by the unit cost. Total staff costs for each practice per annum were obtained by summing across all staff categories. An average cost per patient per practice was calculated, and compared within and between practices with and without a PA.

The sample of practices included in the study in both the PA and no-PA groups were compared with national staff headcount data from the NHS Information Centre 2012125 with respect to the proportions of GPs who were salaried (vs. partners), and the numbers of administrative/clerical staff and nurses/direct patient care staff per GP.

Patient level

Analysis

The patient-level analysis used findings from the analysis of consultation records and the patient survey to compare the costs and effectiveness of consultations by PAs and GPs. The mean length of consultations in minutes for PAs and GPs was calculated from available data recorded by the ‘time enter’ and ‘time leave’ functions on practice management systems. Nationally validated unit costs119 were applied to mean consultation lengths to explore differences between PA and GP practices in the cost of consultations. Other ways in which the use of PAs may affect practice costs were also considered, such as GP time spent in supervision and training, but could not be quantified as data were not available. The relative effectiveness of PAs and GPs was judged by rates of reconsultation (primary outcome), patient satisfaction, and rates of referring, prescribing, testing, fitness to work certification, procedures and advice giving (process outcomes). Adjusted values of variables were used, after controlling for covariates.

Ethics and research governance

Phase 2 of the study required a number of types of reviews and agreements. The research ethical review was undertaken by NHS Research Ethics Committee (REC) South East Coast – Surrey who gave approval but required that child patients were not included in some elements (REC reference number: 10/H1109/28). Local NHS primary care research governance approvals were obtained using different local processes from five different bodies. The procedures for local agreement of the UKCRN NHS service support costs to research in general practice varied in each area. Agreements were obtained for each participating general practice.

The case study settings

Twelve practices participated in the study in the south-west, east and south-east of England. They were diverse in the sociodemographic features of their locale, the number of practice partners and the size of their registered patient population. These data are presented within ranges, to ensure anonymity for the practices, in Table 5.

The report now turns to presenting the findings.

Copyright © Queen’s Printer and Controller of HMSO 2014. This work was produced by Drennan et al. under the terms of a commissioning contract issued by the Secretary of State for Health. This issue may be freely reproduced for the purposes of private research and study and extracts (or indeed, the full report) may be included in professional journals provided that suitable acknowledgement is made and the reproduction is not associated with any form of advertising. Applications for commercial reproduction should be addressed to: NIHR Journals Library, National Institute for Health Research, Evaluation, Trials and Studies Coordinating Centre, Alpha House, University of Southampton Science Park, Southampton SO16 7NS, UK.

Included under terms of UK Non-commercial Government License.

Bookshelf ID: NBK259809

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