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Sharing personalised clinical information with diabetes patients prior to their consultation: results of a pilot study and future work Presented by Dr Máire O’ Donnell on behalf of Dr YY Hong, Dr YY Lim, Dr SY Lim and Dr SF Dinneen Diabetes Centre, University Hospital Galway Department of Medicine, NUIG Outline of talk • Present results from pilot study conducted in 2007 • Outline some thoughts on how we can progress this work Background (1) • Patient centredness – Patient involvement in decisions about their health care – Consideration of individual patient preferences and circumstances Mead N, Bower P. Patient Educ Counselling 2002;48:51-61 Background (2) • Patient centredness and chronic diseases – Diabetes requires active patient involvement in self management for improved clinical outcomes – Effective communication during the clinical consultation essential in enabling the patient to self manage Person with diabetes Diamond Primary Care Specialist care Aim To measure the impact of sharing personalised clinical information in written format with patients on the clinical consultation Intervention • Already in Use: Diamond-generated proforma (for doctors) • New: A Clinical Information Sheet was developed (for patients) – Standardised format – Personalised information – Brief explanation regarding medical terms – Prompt question Topics • • • • • • • • • Weight BMI BP Blood sugar range Exercise Diet HbA1c ACR Creatinine • • • • • • • • Cholesterol LDL TG HDL Diabetic medication Diabetic complication Other problems Other medications Clinical Information Sheet (1) The following is a brief summary of information on your diabetes. Please take the time to read it. All members of our team will be happy to answer any of your questions. Below are explanations of the medical terms used in this form. If you need further clarification, please ask a member of the healthcare team. HbA1C is a blood test used to monitor long term blood sugar control. ACR (Albumin Creatinine Ratio) and creatinine are indicators of your kidney function. Cholesterol is the main type of fat that we worry about in the blood. LDL and TG (triglyceride) are the bad cholesterol. HDL is the good cholesterol. ‘Onsets’ refer to date of onset of complications of your diabetes, if you have any. Please consider the following question: What do I wish to get out of today’s visit to the Diabetes clinic? Clinical Information Sheet (2) Patient name: Address: Date of clinic: Date of pre-assessment: Board number Date of birth: Type of diabetes Duration: Consultant: Seen by Clinic type: Alcohol: Height: Smoking status: Postcode: GP name: Address: Postcode: Phone: To be seen by: Date: DSN: Yes/No Weight BMI Targets 31/07/2007 08/09/1950 Type 2 3 years Diabetes clinic 1.76 Past smoker Dietitian Yes/No HbA1c 7.5 BP sys 130 BP dia 80 AER Male Sex Podiatrist Yes/No ACR 3.5 Creat 106 Chol 4.5 LDL HDL TG 2.5 1.0 2.0 68 5.1 3.1 1.2 .1.3 5.0 3.0 1.1 2.0 Current 23/07/2007 15/05/2007 23/04/2007 23/01/2007 16/01/2007 Treatment: 95.70 97.10 30.90 31.30 143/77 152/81 6.9 95.90 31.00 130/80 7.0 Type 2 Blood sugar range: No onsets: Problem list: Non-Diabetic Drugs: Tablets Metformin Hypos: Break Lunch 850 850 Frequency: Tea 850 Rheumatic fever (13 years), Hypertension Aspirin 75 mg od, Atenolol 100mgs od, Irbesartan 150/125, Pravastatin 20 mgs nocte Supper Methods • Subjects – Patients attending Diabetes Clinics in Galway University Hospitals • Recruitment over a 5 week period • 6 intervention clinics and 3 control clinics • Total patients = 106 (65 males and 41 females) Patient check-in Intervention (n = 63) Clinical information sheet and a brief explanation is given to patient when in waiting room Control (n = 43) No clinical information sheet is given to the patient Investigators sit in the consultation observing and measuring the doctorpatient interaction Methods Data were recorded in 3 ways – The percent of patients initiating each individual topic – The number of topics initiated by each individual patient – The patients’ conversation time vs. total consultation time Table 1 Baseline characteristics of patients in control and intervention groups Control group %(n) Intervention group (n ═ 63) 65(28) 35(15) 59 (37) 41(26) 14 (6) 42(18) 44(19) 14(9) 44(28) 41(26) Diabetes type Type 1 19 (8) 27(17) Type 2 Other 79 (34) 2 (1) 73 (46) 0(0) Diabetes duration Under 1 year 1 −5 years >5−10 yrs 10 yrs+ 7(3) 35 (15) 23 (10) 35(15) 11(7) 22 (14) 32(20) 35 (22) Male Female Age ≤39 yrs 40−64yrs 65+ yrs od t AC R LD L ea ti Ch nine ol es te ro l Cr Hb A1 C et Di Su BP ga rR an ge Ex er cis e BM I eig h ab e Di HD Tr igl L yc t e i Di rid ab c M e e et di ic c at Co io m n pli ca Ot ti he r P on Ot ro he r M ble m ed s ic a tio ns Bl o W Percent of Patients Initiating Individual Topics 60% 50% 40% 30% 20% Intervention Control 10% 0% Patient score Mean patient score Control group = 1 (range 0-4) Intervention group = 5 (range 0-14) No topics raised Control group (49%) Intervention group (16%) Patient Conversation Time vs. Total Consultation Time 20 18 Time (Minutes) 16 14 12 P>0.05 Total Consultation Time 10 Patient Conversation Time 8 6 4 2 P<0.05 0 Intervention Control Summary A personalised clinical information sheet in routine clinical practice is associated with: – Increase in number of patients initiating individual topics – Increase in number of topics being initiated by individual patients – Increase in patient conversation time – No significant lengthening of consultation Conclusion The clinical information sheet facilitates patient involvement in the consultation Study Limitations • Not a randomised controlled trial • No data collected on patients clinical or psychosocial outcomes • No control for possible confounding factors – Patients demographic, clinical, psychosocial factors – Doctors characteristics • Doctors not blinded to patients in the intervention group • Risk of observer bias Further questions • Does the type of clinical information shared with patients influence their involvement in the consultation (personalised clinical information V general information on topics)? • How does such involvement impact on clinician behaviour? Proposed research Quantitative study Aim – To explore the impact of sharing different types of clinical information with Type 2 diabetes patients on patient involvement in the consultation and patient-related outcomes Hypotheses 1. Patients receiving an information intervention will be more involved in the consultation and have better outcomes than those in the control group 2. Patients who receive personalised clinical data will be more involved in the consultation than those that receiving general clinical information only. Study design (1) Randomisation Control group Standard Care No written clinical information General clinical information just prior to consultation General plus personalised clinical information just prior to consultation Study design (2) Historical control Pre-intervention Randomisation General clinical information just prior to consultation General plus personalised clinical information just prior to consultation Outcome measures Quantitative study • Primary outcome – Patient involvement in the consultation • Patient outcomes – Patient satisfaction with the consultation – Quality of life measure – Self care behaviour (e.g. adherence to medication, blood glucose testing, exercise, diet) – Diabetes self efficacy measure – Depression/Anxiety • Secondary outcome measures – HbA1c – Cholesterol (?) – Body mass index(?) Data collection • Audiotaping of consultations • Patient questionnaires • Medical record data extraction Audiotaping of consultations • The percent of patients initiating each individual topic • The number of topics initiated by each individual patient • The patients’ conversation time vs. total consultation time Baseline questionnaire Baseline • Demographics (Age, Gender, education) • Psychosocial measures • Quality of life • Self care behaviour • Diabetes self efficacy • Depression/anxiety • Preference for involvement in the consultation Patient questionnaire straight after consultation • Patient perceived involvement in the consultation • Patient satisfaction with the consultation • Patient perception of facilitation of involvement Patient questionnaire 6 weeks post consultation Psychosocial measures • Quality of life • Self care/self management • Diabetes self efficacy • Depression/anxiety • Preference for involvement in the consultation Medical record data (1) Baseline data • Number of previous visits • Duration of Diabetes • On insulin or medication • Co morbidities Medical record data (2) Post intervention • At 6 months(?) or whenever patients next visit to clinic is? – HbA1c – Cholesterol – BMI Qualitative study Aim To explore the nature of patient engagement in the consultation and how this impacts on clinician behaviour Methods • Data analyses In-depth analyses of the nature of patients involvement in the consultation and how doctors respond to such involvement Thanks Any thoughts/comments?