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General Practitioners

General Pratitioners (GPs) are primary care physicians who provide comprehensive medical care to patients of all ages.
They diagnose and treat a wide range of acute and chronic conditions, and play a crucial role in disease prevention and health promotion.
GPs serve as the first point of contact for patients, coordinating referrals to specialists and maintaining continuity of care.
Their practice encompasses a broad scope, from managing common illnesses to addressing complex medical and social needs.
As the backbone of the healthcare system, GPs are essential in ensuring accessible, high-quality, and patient-centered care for individuals and communities.

Most cited protocols related to «General Practitioners»

The EstBB is a population-based biobank at the Institute of Genomics, University of Tartu. The current cohort size is 200,000 individuals (aged ≥18 years), reflecting the age, sex and geographical distribution of the adult Estonian population. Overall, 83% of the samples are from Estonian individuals, 14% from Russian people and 3% from other ethnicities. All participants were recruited by general practitioners, physicians in hospitals and during promotional events. After recruitment, all participants completed a questionnaire about their health status, lifestyle and diet. Specifically, the questionnaire included personal data (place of birth, place(s) of living, nationality, among others), genealogical data (family history of medical conditions spanning four generations), educational and occupational history, and lifestyle data (physical activity, dietary habits (food frequency questionnaires), smoking status, alcohol consumption, women’s health and quality of life). The EstBB database is linked with national registries (such as the Cancer Registry and Causes of Death Registry), hospital databases and the database of the national health insurance fund, which holds treatment and procedure service bills. Diseases and health problems are recorded as ICD-10 codes and prescribed medicine according to the ATC classification. These health data are continuously updated through periodical linking to national electronic databases and registries. All participants were genotyped with genome-wide chip arrays and further imputed with a population-specific imputation panel consisting of 2,244 high-coverage (30 times) whole-genome sequence data from individuals and 16,271,975 high-quality variants57 (link). Researchers at the EstBB ran an association analysis of the 15 phenotypes (Supplementary Table 8) used in this study in 136,724 individuals. The association analysis was conducted with SAIGE52 mixed models with age, sex and ten PCs used as covariates.
We used the Pan UKBB (https://pan.ukbb.broadinstitute.org/) project European subset association analysis summary statistics in the UKBB replication58 (Supplementary Table 7).
As both the EstBB and the UKBB are on human genome build 37, we lifted over the coordinates to build 38 to match FinnGen. Variants were then matched on the basis of chromosome, position, reference and alternative alleles.
Inverse variance weighted meta-analysis was used to perform a meta-analysis on the three cohorts (code available at https://github.com/FINNGEN/META_ANALYSIS).
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Publication 2023
Adult Alleles Chromosomes Diet DNA Chips Ethnicity Europeans Food General Practitioners Genome Genome, Human Malignant Neoplasms National Health Insurance Pharmaceutical Preparations Phenotype Physicians Population Group Woman
The mixed methods project utilised both survey and interview techniques to extrapolate data from the two participant groups (acupuncturists and general practitioners). The research aimed to evaluate and define current practice in order to develop effective strategies to connect the two groups. The tools and strategies allow clinical utility and transferability to other similar clinical groups. Ethics approval for this study was obtained from the The University of Otago Ethics Committee, and additionally the Ngai Tahu Research Consultation Committee approved the research and considered it of importance to Maori health.
The case study example within this article was part of a mixed method project which contained a qualitative approach to interpreting interview data using thematic analysis. It is the analysis of the qualitative component of this study that forms the basis of the discussion contained herewith. These types of qualitative analyses posit that reality consists of people’s subjective experiences or interpretations of the world. Therefore, there is no singular correct pathway to knowledge. This mode of analysis suggests a way to understand meaning or try to make sense out of textual data which may be somewhat unclear. Knowledge is derived from the field through a semi-structured examination of the phenomenon being explored. Thus there is no objective knowledge which is independent of thinking [16 ].
The case example utilised a codebook as part of the thematic analysis. A codebook is a tool to assist analysis of large qualitative data sets. It defines codes and themes by giving detailed descriptions and restrictions on what can be included within a code, and provides concrete examples of each code. A code is often a word or short phrase that symbolically assigns a summative, salient, essence-capturing, or attribute for a portion of data [17 ]. The use of a codebook was deemed appropriate to allow for the testing of interpretations of the data, and to allow for demonstration of rigour within the project.
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Publication 2019
Ethics Committees General Practitioners Maori Maritally Unattached Muscle Rigidity
Following a review of the literature, existing awareness questionnaires were examined and relevant items extracted. This was supplemented with a review of the ‘grey’ literature (i.e. unpublished surveys carried out by cancer charities and other organisations) to include items not published in academic journals. Following this review, an item pool consisting of 137 items was created. These covered a range of topics including awareness of warning signs and risk factors, cancer incidence and awareness of national screening programmes. Items were then excluded if they were poorly worded, used terminology not frequently used in the United Kingdom (e.g. Pap test) or were attitudinal in nature (e.g. ‘I believe there are no early symptoms of cancer’). Items relating to awareness of the purpose of screening, the benefits of early detection and cancer survival rates were also omitted from the measure because the primary focus was symptom recognition. In addition, the research team generated several items specifically for the instrument that had not been used in previous questionnaires.
Once consensus over the items had been reached, a first version of the cancer awareness measure (CAM) was circulated to a panel of experts (n=16) including academic researchers, cancer charity representatives, general practitioners, oncologists and experts in the field of questionnaire design, to ensure content validity and face validity. In addition, cognitive interviews were conducted with the general public. These encourage respondents to verbalise their cognitions, making it possible to identify areas where interpretation of the questions is ambiguous (Collins, 2003 (link)). Cognitive interviews were conducted with a small sample of participants (n=6) aged between 23 and 70 years. Minor modifications were made to the phrasing of several items as a result.
The final version of the CAM consisted of the following: (i) 10 items on awareness of warning signs (one open-ended question and nine recognition items); (ii) nine items on anticipated time to seek medical advice (asking about each of the warning signs); (iii) 10 items on barriers to seeking medical advice (covering a range of practical, service delivery and emotional barriers); (iv) 13 items on awareness of risk factors (one open-ended question, 11 recognition items and one asking participants to rank the importance of different types of risk factor); (v) seven items on cancer incidence (one asking about overall cancer incidence and six asking about the three most common cancers for men and women) and (vi) six items on awareness of NHS screening programmes (asking about awareness of the cervical, breast and bowel screening programmes and the age from which screening is offered for each).
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Publication 2009
Awareness Breast Cognition Early Diagnosis Emotions General Practitioners Intestines Malignant Neoplasms Neck Obstetric Delivery Oncologists Vaginal Smears Woman
Starting from the conceptual model of health literacy,9 (link) a Delphi process among the HLS-EU Consortium members was conducted to generate items for assessing health literacy: the way people access, understand, appraise and apply information to make decisions regarding health care, disease prevention and health promotion. The resulting draft questionnaire was pre-tested for face validity in three focus groups (in Greece, Ireland and the Netherlands) and field-tested with 50 computer-assisted face-to-face interviews in two countries (n = 99 in Ireland and the Netherlands). Following the results of a principal component analysis and reliability analysis of the data, as well as inputs from consultations with external experts, a pre-final version of the questionnaire was achieved through a consensus-based item selection process. The pre-final version was subjected to a ‘plain language’ assessment by literacy experts to obtain the final version, which is known as HLS-EU-Q47 because it includes 47 items across 12 subdomains. For each item, respondents rated the perceived difficulty of a given task on a four-category Likert scale (i.e. very easy, easy, difficult and very difficult). This kind of operationalisation follows the tradition of subjective assessments of health literacy13 (link) and reflects the interactive or relational nature of health literacy by measuring the fit of personal competences with contextual or situational demands of social systems.14 (link) More details about the questionnaire’s development and the specific items of the HLS-EU-Q47 are presented in Sorensen et al.11 (link)
For the purpose of the HLS-EU survey the HLS-EU-Q47 was supplemented with an additional section, which contained 39 items referring to antecedents and precedents outlined in the conceptual model.9 (link) They included inter alia indicators for the respondents’ health service use, health behaviour, subjective health status and socio-demographic and socio-economic situations supplemented with the Newest Vital Sign, which is a quick assessment of literacy.15 (link) Examples of items include gender, age, education (using score cards and answers were transformed to international standard classification of education (ISCED) levels, social status, financial deprivation, self-assessed health (SF-36), long term illness, visit to general practitioner, hospital admission, alcohol consumption, smoking, exercise, work experience in health sector and insurance coverage. The final version of the questionnaire for the HLS-EU survey included the 47 health literacy items and the additional 39 items and was named the HLS-EU-Q86.
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Publication 2015
Diagnostic Self Evaluation Face Gender Health Literacy Health Promotion Signs, Vital
The primary outcome measure was mental well-being as measured using the self-completion Warwick-Edinburgh Mental Well-being Scale (WEMWBS) [19 (link)]. This 14-item instrument has been validated for the UK population and adopted by the Scottish Health Survey and the Health Survey for England. It asks respondents to read statements about feelings and thoughts and to choose the response (a 5-point scale ranging from none of the time to all of the time) that best describes their experience over the previous two weeks. Example items are “I’ve been feeling optimistic about the future” and “I’ve been thinking clearly.” It has been shown to have good content validity and shows high correlations with other scales of mental health and well-being. It has a near-normal population distribution, with no ceiling effects.
Secondary outcomes were self-completed Center for Epidemiologic Studies Depression scale (CES-D) depression scores, Generalized Anxiety Disorder 7-item (GAD-7) anxiety scores, EuroQol Group 5-Dimension Self-Report Questionnaire (EQ-5D) quality of life scores, physical activity (self-reported frequency of exercise), and use of health services (self-reported general practitioner consultations or hospital visits). All outcomes were measured at the start of the trial (baseline before the intervention), immediately following the intervention (6 weeks after baseline), and 6 weeks after the intervention was finished (12 weeks after baseline).
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Publication 2013
Anxiety Disorders Melancholia Mental Health Optimism

Most recents protocols related to «General Practitioners»

The Capital Region of Denmark has a population of 1.6 million people. Patients in the Capital Region of Denmark are referred by their general practitioner (GP) or other treatment providers to a central diagnostic and referral centre within the mental health services that yearly assesses 20.000 referrals. About 4000 patients are further evaluated in person and diagnosed by the centre.
Five mental health centres in the region provide treatment packages for first-episode depression and will include participants in the study. The Mental Health Centre Amager and the Copenhagen centre consisting of two clinics located in the City of Copenhagen and treat approximately half of all patients, whereas Ballerup and Glostrup treat approximately a third of patients in the surrounding suburb (Sup. Figure 2). The Psychiatric Centre Northern Zealand treats approximately 16% of patients and is located north of Copenhagen, in a region of intermediate urbanisation with individual municipalities classified as rural.
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Publication 2023
Chin Mental Health Patients Urbanization
Two pairs in the research team (one neonatologist and one paediatrician in the first pair, one paediatrician and one general physician in the other pair) analysed the relevance of the identified problems and actions taken based on facilitators’ diaries from the 52 facilities. The independent scoring of each analyst was discussed to reach a consensus. A maximum score of 22 points could be obtained in the knowledge assessment (1 point for each correctly answered question). Baseline and endline results were compared across levels of the health systems (commune health centres and hospitals) and categories of health workers (physician, midwife and nurse). Data from the antenatal care observations were compared before and after the 12 months of PeriKIP intervention. Data from knowledge assessment and observations were entered using EpiData (version 3.1) and analysed in SAS (version 9.4). Descriptive statistics included proportions, means with 95% confidence intervals and t-tests with p-values.
The qualitative data were transcribed verbatim, translated into English and analysed by content analysis with both inductive and deductive features [45 (link)]. First, each interview of each type (midwives, village health workers, PeriKIP groups at hospitals, facilitators) was read several times to get a naïve understanding. This step informed the decision to approach the material as one data set. After that, open coding was undertaken. Codes were written in the margin of each interview describing aspects of the content. Codes were sorted into sub-categories; thereafter, sub-categories were sorted under categories, and finally, categories were placed under four main categories, i.e. the i-PARIHS dimensions (Innovation, Recipients, Facilitation and Context). One relevant category, Gaining knowledge and insights, as identified in the qualitative analysis, could not be sorted under the i-PARIHS dimensions. This category is presented together with the study outcomes.
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Publication 2023
Care, Prenatal General Practitioners Health Personnel Midwife Neonatologists Nurses Pediatricians Physicians Village Health Workers
A cross-sectional quantitative survey was performed in Harghita County (Transylvania, Romania). The patients were recruited from three randomly chosen settlements (Joseni, Ciumani and Lăzarea) with the help of general practitioners of these villages. All of the patients were informed about the purpose of the study and the voluntary nature of the participation. Participants gave written informed consent before taking part in the study. The protocol of the study was approved by the Ethics Committee of the University of Babeș-Bolyai (RO) and by the Code of Deontology for the professions of psychologists, elaborated by the Romanian College of Psychologists. Cognitive functions were assessed independently for each participant by accredited clinical psychologists. Inclusion criteria were: 1) ages between 35 and 65 years [8 (link), 9 ], 2) diagnosed with T2D or hypertension or both (comorbid T2D and hypertension) according to the standards of the American Diabetes Association (2020) [10 (link)] and according to the standards of the American College of Cardiology and American Heart Association guidelines [11 ], respectively, and 3) diabetes and/or hypertension duration at least 5 years. From this study, patients were excluded with 1) any medical illnesses other than T2D, dyslipidemia, hypertension and obesity, 2) a history of hypoglycemic coma or complications of diabetes, 3) primary neurological condition as history of transient ischemic attacks, cerebrovascular stroke or epilepsy or psychiatric disease, 4) previous serious head injury, 5) any sensory or motor disorder that would preclude psychological testing (including blindness), 6) regular treatment with any medications known to have psychoactive effect, and 7) drug or alcohol abuse. The control group was made up of people who applied at the invitation of the municipality's management and did not have a chronic illness. Their health status was checked at the health clinic of the municipality.
The patients were divided into three groups: a group with T2D, a group with hypertension and a group with both diseases. The control group was specifically recruited from the settlement where the patients were registered.
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Publication 2023
Abuse, Alcohol Blindness Cardiovascular System Cerebrovascular Accident Cognition Comatose Complications of Diabetes Mellitus Craniocerebral Trauma Diabetes Mellitus Disease, Chronic Dyslipidemias Epilepsy Ethics Committees General Practitioners High Blood Pressures Hypoglycemic Agents Mental Disorders Motor Disorders Nervous System Disorder Obesity Patients Pharmaceutical Preparations Pharmacotherapy Transient Ischemic Attack
Cognitive functions were assessed using the Wechsler Memory Scale – Revised (WMS-R) [12 ]. The test was administered during a routine visit to the general practitioner and it required around 1 h to complete. The WMS-R is a neuropsychological test designed to measure different memory functions such as verbal, visual memory, attention/concentration and delayed memory. The psychometric characteristics of the WMS-R are evaluated and related to its clinical utility in the Romanian population [13 , 14 (link)]. The weighted scores (weighted raw score summaries) were calculated according to the scoring system from in the WMS-R administrative and scoring manual, with a higher score indicating better functioning.
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Publication 2023
Attention Cognition Delayed Memory Memory Neuropsychological Tests Psychometrics Vision
This paper draws on interview-based research conducted from May to June 2022, as part of a broader project investigating how information about medicines moves between patients, pharmacists, and general practitioners. To explore how GP’s approached prescribing decisions and understood their relationships with patients and pharmacists around medicines, we elected to use an interview methodology. Interview methodologies are well-suited to research that investigates people’s thoughts and experiences, and the semi-structured format accommodates emergent findings that might not be anticipated in the original research design. The project received ethics approval from the Victoria University of Wellington Human Ethics Committee (#28324).
Given our aim to solicit general practitioners’ views specifically, we followed a purposive sampling strategy and recruited from a national pool, so as to gain cross-sectional insights from different geographic, socioeconomic, and institutional settings. Using the Medidata database of general practitioners, we issued an invitation for interview participants that reached 1,331 recipients. Of these, 25 people registered their interest via the supplied link, and 16 followed through to an interview. Our only selection criterion was that participants must be currently practicing general practitioners, as all 25 initial respondents were. Recruitment stopped when participants stopped opting in to the study.
While most of our resulting sample worked full-time in general practice, some of our interviewees worked part-time, as locums, or combined their general practice work with, e.g., working for hospice. Of our sixteen participants, 10 were female and six male. Eight were based in one of New Zealand’s three major cities, six in a smaller city or large town, and two rurally. Thus, while our sample is not representative, it does encompass a range of professional and regional experiences and clear themes were evident across the data set.
Interview guides were developed from the overall project’s aims, and included questions about participants’ professional backgrounds and contexts, prescribing practices and views on medicines, relationships to pharmacists, and perspectives on the New Zealand health system. In keeping with the semi-structured interview process, we allowed these guides to steer our conversations without dictating or unnecessarily limiting their course. The interview procedure was not adjusted in light of emergent findings, so as to ensure maximum comparability across the data set. However, the interview guide was adapted in some cases to suit individual participants’ time availability.
The authors conducted all interviews via Zoom, between May 1 and June 30 2022. Interviews lasted from 24 to 68 min, with a mean duration of 46 min 30 s. Typically, shorter interviews were those conducted during participants’ lunch breaks, and longer ones were conducted on participants’ days off or in the evenings. All interviews were audio recorded using the computer’s inbuilt recording software, then professionally transcribed verbatim. The original audio files and resulting transcripts were allocated pseudonymised alphanumeric file names (linked to identifying information in one securely stored spreadsheet) and stored in the University’s secure cloud storage system.
Although Denise Taylor training as a pharmacist could potentially be expected to influence how interviewees spoke about the pharmacists they interacted with, we did not note any discernible differences in the results collected by each interviewer, and neither had any existing relationship with any participants. It is possible that conducting interviews via Zoom also mitigated the extent to which the researchers’ positionality shaped interviews. We were known to participants’ primarily by our qualifications, professional roles, and association with a respected funder, with few cues as to our respective physical presentations beyond the shoulders-up Zoom window.
Our data analysis was conducted by (Courtney Addison) June through October 2023, and checked and discussed with Denise Taylor. Our analytic process was grounded in the constructivist tradition of Corbin and Strauss [34 ], which acknowledges the role of the analyst in meaning-making, and followed a Reflexive Thematic Analysis process [35 (link)]. This began with familiarisation with the data set (all interview transcripts), followed by iterative, open coding of the corpus. Codes were then reviewed and grouped into themes, which were themselves reviewed against the transcripts. The review process enabled refinements to the theme, so that, for example, the theme ‘Doctor/pharmacist interactions’ became ‘Sharing information about patients’, ‘Seeking medicines information’, ‘Correcting mistakes’. To check the validity of findings, the authors discussed transcripts and codes from their distinct disciplinary perspectives (Anthropology and Pharmacy, respectively) and also compared findings against the data set from the other arm of this project, which consists of interviews and observations from a community pharmacy. This confirmed, for example, that doctors were using pharmacists in the ways they described in the interviews reported on here, and that pharmacists were indeed picking up mistakes as interviewees report.
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Publication 2023
Ethics Committees General Practitioners Homo sapiens Hospice Care Interviewers Light Males Patients Pharmaceutical Preparations Physical Examination Physicians Shoulder Thinking Woman

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More about "General Practitioners"

General Practitioners (GPs), also known as family physicians or primary care doctors, play a vital role in the healthcare system.
They are the first point of contact for patients, providing comprehensive and holistic medical care to individuals of all ages.
GPs diagnose and treat a wide range of acute and chronic conditions, from common illnesses to complex medical and social needs.
They are responsible for disease prevention, health promotion, and coordinating referrals to specialists, ensuring continuity of care for their patients.
GPs utilize various research tools and statistical software to inform their clinical decision-making and improve patient outcomes.
SAS version 9.4, Stata 13, SPSS version 22.0, and their newer counterparts, SAS v9.4, Stata 14, and Stata v14, are commonly used in medical research to analyze data, conduct clinical trials, and generate insights.
Additionally, specialized equipment like the MicroMaxx and ACTA Gnosis IV ECG recorder are employed by GPs to capture and interpret patient data.
By staying up-to-date with the latest research, technologies, and best practices, GPs can provide high-quality, patient-centered care that addresses the diverse needs of individuals and communities.
As the backbone of the healthcare system, GPs play a crucial role in ensuring accessible and effective medical services for all.