scholarly journals The role of telephone consultations in psychiatry

BJPsych Open ◽  
2021 ◽  
Vol 7 (S1) ◽  
pp. S339-S339
Author(s):  
Jonathan Packer ◽  
Emma Fisher ◽  
Anne-Marie Simons ◽  
Kirsty Bolochowecki ◽  
Benita Roff ◽  
...  
Keyword(s):  
Patient Experience ◽  
Time Management ◽  
Medical Practitioner ◽  
Patient Survey ◽  
Signal Interference ◽  
Initial Assessment ◽  
Service Users ◽  
Treatment Team ◽  
Open Questions ◽  
Patient Assessments

AimsTelephone consultations have been in clinical use since the early 1960s and are increasing in frequency and importance in many areas of medicine. With the advent of the COVID-19 pandemic in 2020, the use of telemedicine consultations increased dramatically alongside utilization of other digital technologies. Despite promise and potential advantages for clinicians (including remote working, improved time management and safety) there are known drawbacks to telephone consultations for psychiatrists. This includes limitations to assessments of mental state and risk, with loss of non-verbal communication often cited as a point in favour of more sophisticated technologies such as video calling. By adopting telephone consultations to a greater extent during the initial months of the COVID-19 pandemic in the Coventry Crisis Resolution and Home Treatment Team (CRHTT), we aimed to assess the patient experience in telehealth, through a patient survey.MethodAfter an initial assessment or follow-up consultation with a medical practitioner from the crisis team, patients were invited to take part in a short questionnaire with a member of the administration staff. This consisted of eight questions on a Likert scale and three open questions for comments. Results were collated and analyzed via Microsoft Excel.ResultMost patients found the telephone consultations satisfactory, with more than 90% returning positive scores in understanding, convenience and overall satisfaction. All patients felt listened to and that their confidentiality was maintained; with all but one respondent willing to engage in further consultations via the telephone. Negative scores were typically returned for practical telephonic problems including poor signal, interference and background noise. In their comments patients expressed largely positive views about their experience with their clinician; analysis revealed key insights into the patient experience, demonstrating the convenience, comfort and flexibility possible with ‘telepsychiatry’.ConclusionPatient experience of telemedicine in a UK psychiatric crisis team is mostly positive, with clear advantages for both patients and clinicians. Our results show telephone consultations can be expanded to new patient assessments alongside follow-ups, enabling the team to reach a greater number of service users. This includes service users who are housebound due to infirmity, required to shield or have significant anxiety about the pandemic.

scholarly journals Producing a new website for a paediatric liaison mental health team with our service users

2020 ◽  
Vol 9 (4) ◽  
pp. e001128
Author(s):  
Alexander Adams ◽  
Virginia Davies ◽  
Bethany Stubbs
Keyword(s):  
Mental Health ◽  
Focus Groups ◽  
Patient Experience ◽  
Service Users ◽  
Health Issues ◽  
Web Page ◽  
Mental Health Team ◽  
Children And Young People ◽  
Specific Feedback ◽  
Source Of Information

IntroductionOnline resources are an important source of information about mental health issues and services for children and young people. Our service’s website had an out-of-date appearance and was aimed at professionals. More importantly, comments in our routinely collected patient experience data indicated that service users did not know what to expect when coming to our service.MethodsWe followed the model for improvement by testing out changes in plan, do, study and act cycles that included a review of recently updated child and adolescent mental health services’ and youth charities’ websites, designing a new web page for our service and then testing out the website in focus groups. We used routinely collected patient experience data to assess impact on wider patient satisfaction.ResultsFocus groups involving patients, parents and professionals judged the new website to be clearer, more attractive and easier to understand. Routine patient experience data did not reveal any website-specific feedback.ConclusionThis study demonstrates that it is easy and possible to create an attractive and accessible website for a mental health service using quality improvement methodology. In order to capture and integrate ongoing feedback about a service’s website from service users, routinely collected patient experience measures would need to ask specific questions related to this area. In this study, preproject and postproject patient experience data did not generate any specific comments.

scholarly journals P-150 Insights into the gastric and oesophageal cancer patient experience: Results of a pan-European patient survey

2021 ◽  
Vol 32 ◽  
pp. S150
Author(s):  
Z. Maravic ◽  
V. Fotaki ◽  
O. Mesalles Naranjo ◽  
E. Gasenko ◽  
I. Rawicka ◽  
...  
Keyword(s):  
Cancer Patient ◽  
Patient Experience ◽  
Oesophageal Cancer ◽  
Patient Survey

scholarly journals The Patient Survey Programme: Transforming the patient experience in Irish healthcare

2017 ◽  
Vol 65 (4) ◽  
pp. 83-99 ◽  
Author(s):  
Vivienne Byers ◽  
Daragh Fahey ◽  
Carol Mullins ◽  
Carol Roe
Keyword(s):  
Patient Experience ◽  
Patient Survey

scholarly journals Test–retest stability of patient experience items derived from the national GP patient survey

SpringerPlus ◽  
2016 ◽  
Vol 5 (1) ◽  
Author(s):  
Antoinette F. Davey ◽  
Martin J. Roberts ◽  
Luke Mounce ◽  
Inocencio Maramba ◽  
John L. Campbell
Keyword(s):  
Patient Experience ◽  
Patient Survey

Intravenous versus subcutaneous trastuzumab: an economic and patient perspective

2019 ◽  
Vol 28 (10) ◽  
pp. S15-S20 ◽  
Author(s):  
Helen Mitchell ◽  
Diane Morrissey
Keyword(s):  
Clinical Trial ◽  
Patient Experience ◽  
Patient Perspective ◽  
Subcutaneous Administration ◽  
Patient Survey ◽  
Patient Choice ◽  
Intravenous Route ◽  
Treatment Delivery ◽  
Treatment Pathway ◽  
Number Of Patients

Since 2005, when the first patients outside of a clinical trial were treated with trastuzumab at The Christie NHS Foundation Trust, a nurse-led service has been developed to facilitate and support a safe treatment pathway for patients. There have been significant developments in the number of patients treated, the mode of administration of the drug and patient choice regarding the location of treatment delivery. This article focuses on the change from intravenous to subcutaneous administration, considering patient experience and choice, particularly in light of the advent of biosimilar drugs, which will necessitate a return to the intravenous route. The relative costs of intravenous and subcutaneous administration are illustrated and the results of a patient survey presented, indicating a strong preference for subcutaneous trastuzumab.

scholarly journals What happens to patient experience when you want to see a doctor and you get to speak to a nurse? Observational study using data from the English General Practice Patient Survey

BMJ Open ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. e018690 ◽  
Author(s):  
Charlotte A M Paddison ◽  
Gary A Abel ◽  
Jenni Burt ◽  
John L Campbell ◽  
Marc N Elliott ◽  
...  
Keyword(s):  
General Practice ◽  
Patient Experience ◽  
Secondary Analysis ◽  
Patient Survey ◽  
Models Of Care ◽  
Unintended Consequences ◽  
Multidisciplinary Teams ◽  
Face To Face ◽  
Patient Reported ◽  
Practice Patient

ObjectivesTo examine patient consultation preferences for seeing or speaking to a general practitioner (GP) or nurse; to estimate associations between patient-reported experiences and the type of consultation patients actually received (phone or face-to-face, GP or nurse).DesignSecondary analysis of data from the 2013 to 2014 General Practice Patient Survey.Setting and participants870 085 patients from 8005 English general practices.OutcomesPatient ratings of communication and ‘trust and confidence’ with the clinician they saw.Results77.7% of patients reported wanting to see or speak to a GP, while 14.5% reported asking to see or speak to a nurse the last time they tried to make an appointment (weighted percentages). Being unable to see or speak to the practitioner type of the patients’ choice was associated with lower ratings of trust and confidence and patient-rated communication. Smaller differences were found if patients wanted a face-to-face consultation and received a phone consultation instead. The greatest difference was for patients who asked to see a GP and instead spoke to a nurse for whom the adjusted mean difference in confidence and trust compared with those who wanted to see a nurse and did see a nurse was −15.8 points (95% CI −17.6 to −14.0) for confidence and trust in the practitioner and −10.5 points (95% CI −11.7 to −9.3) for net communication score, both on a 0–100 scale.ConclusionsPatients’ evaluation of their care is worse if they do not receive the type of consultation they expect, especially if they prefer a doctor but are unable to see one. New models of care should consider the potential unintended consequences for patient experience of the widespread introduction of multidisciplinary teams in general practice.

Age-related lymphoma patient experience: Results from the Lymphoma Coalition 2018 Global Patient Survey.

2020 ◽  
Vol 38 (15_suppl) ◽  
pp. e20071-e20071
Author(s):  
Raul Cordoba ◽  
Natacha Bolanos ◽  
Lorna Warwick ◽  
Natalie Dren
Keyword(s):  
Patient Experience ◽  
Age Groups ◽  
Well Being ◽  
Patient Survey ◽  
Activity Level ◽  
Age Group ◽  
Lymphoma Patient ◽  
Medical Issues ◽  
Age Related ◽  
Patient Reported

e20071 Background: Over the past two decades, the incidence of lymphoma has increased by 8-10% per year in older adults. Despite the growing population of older cancer patients, there are a limited number of studies that focus on the experience of these patients. Lymphoma Coalition (LC) saw the need in the 2019 Report Card on Lymphomas to examine the age-related lymphoma patient experience. The objectives of this study were to identify: 1) informational needs and understanding levels, 2) physical conditions and medical issues, 3) psychosocial issues, and 4) barriers in patient-doctor communication. Methods: Using a subset of data from the LC 2018 Global Patient Survey on Lymphomas and CLL (LC 2018 GPS), this study will specifically examine the experiences of newly diagnosed lymphoma patients within the following age categories: 1) Young (18-59) (n = 1473); Mid (60-69) (n = 371); Old (70+) (n = 162). Results: From January to March 2018, 2,006 participants were included in this analysis from 47 countries. The majority of all three patient groups wanted additional medical information beyond what was provided at their diagnosis meeting with the doctor, with the greatest need for information in the young patient group (73%). The highest proportion of poor understanding was reported by the mid-age group (14%) and the highest proportion of very good understanding was reported by the old age group (53%). Across all three age groups, fatigue was the top reported physical condition affecting well-being. Regarding older patients, hair loss was reported in 36% vs 54% in younger patients (p = 0.01), and muscle weakness was reported in 40%. A greater proportion of those in the old group reported that their lifestyle (86%) and general activity level (87%) had been affected. The reported prevalence of medical issues was highest in the young group and lowest in the old group, both during and after treatment. Fear of relapse was the top reported psychosocial issue following treatment for patients in all three age groups. Of those who discussed their fear of relapse with their doctor (young 42% vs old 21%, p = 0.0022), less than one third of patients felt their discussion helped alleviate the fear. Conclusions: This study emphasizes that lymphoma patients in all age groups need more information and support beyond what is currently being provided. While certain age-specific trends were identified, the majority of patient-reported issues span across all three of the age groups examined.

scholarly journals Reasons of Diagnostic Errors and the Ways to Overcome among Medical Residents

2019 ◽  
Vol 09 (04) ◽  
pp. 324-325
Author(s):  
Shafaq Sultana ◽  
Farhat Fatima
Keyword(s):  
Patient Safety ◽  
Diagnostic Tests ◽  
Diagnostic Errors ◽  
Medical Practitioner ◽  
Accurate Diagnosis ◽  
Medical Residents ◽  
Initial Assessment ◽  
Diagnostic Process ◽  
Global Precedence

Arriving at an accurate diagnosis is one of the competencies prime of the medical practitioner. Errors may occur in the diagnostic process anywhere from the point of patient’s initial assessment and interpretation of diagnostic tests, and even during follow-up and patient referral. Patient safety is gaining global precedence and in this context diagnostic errors are speculate as an important cause of harm to the patients.1 An awareness of the possible underlying factors leading to diagnostic errors, along with a repertoire of strategies to improve can be of great help to both junior and senior medical residents

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