International Journal of Environmental Research and Public Health (MDPI)

2004 | 525,942,120 words

The International Journal of Environmental Research and Public Health (IJERPH) is a peer-reviewed, open-access, transdisciplinary journal published by MDPI. It publishes monthly research covering various areas including global health, behavioral and mental health, environmental science, disease prevention, and health-related quality of life. Affili...

Author(s):

James Rufus John
Translational Health Research Institute, Western Sydney University, New South Wales 2560, Australia
Amanda Jones
Sonic Clinical Services, Level 21, 225 George Street, Sydney, New South Wales 2000, Australia
A. Munro Neville
AusTrials, Queensland 4068, Australia
Shima Ghassempour
Research Implementation Science and eHealth Group, Faculty of Health Science, The University of Sydney, New South Wales 2006, Australia
Federico Girosi
Translational Health Research Institute, Western Sydney University, New South Wales 2560, Australia
W. Kathy Tannous
Translational Health Research Institute, Western Sydney University, New South Wales 2560, Australia


Download the PDF file of the original publication


Year: 2020 | Doi: 10.3390/ijerph17062164

Copyright (license): Creative Commons Attribution 4.0 International (CC BY 4.0) license.


[Full title: Cohort Profile: Effectiveness of a 12-Month Patient-Centred Medical Home Model Versus Standard Care for Chronic Disease Management among Primary Care Patients in Sydney, Australia]

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International Journal of Environmental Research and Public Health Article Cohort Profile: E ff ectiveness of a 12-Month Patient-Centred Medical Home Model Versus Standard Care for Chronic Disease Management among Primary Care Patients in Sydney, Australia James Rufus John 1,2, *, Amanda Jones 3 , A. Munro Neville 4 , Shima Ghassempour 5 , Federico Girosi 1,2 and W. Kathy Tannous 1,6 1 Translational Health Research Institute, Western Sydney University, New South Wales 2560, Australia; F.Girosi@westernsydney.edu.au (F.G.); k.tannous@westernsydney.edu.au (W.K.T.) 2 Rozetta Institute, Level 4, 55 Harrington Street, Sydney, New South Wales 2000, Australia 3 Sonic Clinical Services, Level 21, 225 George Street, Sydney, New South Wales 2000, Australia; amanda.jones@scs.com.au 4 AusTrials, Queensland 4068, Australia; munro.neville@austrials.com.au 5 Research Implementation Science and eHealth Group, Faculty of Health Science, The University of Sydney, New South Wales 2006, Australia; shima.ghassempour@sydney.edu.au 6 School of Business, Western Sydney University, New South Wales 2150, Australia * Correspondence: 18314234@student.westernsydney.edu.au Received: 21 February 2020; Accepted: 22 March 2020; Published: 24 March 2020 Abstract: Evidence suggests that patient-centred medical home (PCMH) is more e ff ective than standard general practitioner care in improving patient outcomes in primary care. This paper reports on the design, early implementation experiences, and early findings of the 12-month PCMH model called ‘WellNet’ delivered across six primary care practices in Sydney, Australia. The WellNet study sample comprises 589 consented participants in the intervention group receiving enhanced primary care in the form of patient-tailored chronic disease management plan, improved self-management support, and regular monitoring by general practitioners (GPs) and trained clinical coordinators The comparison group consisted of 7750 patients who were matched based on age, gender, type and number of chronic diseases who received standard GP care. Data collected include sociodemographic characteristics, clinical measures, and self-reported health assessments at baseline and 12 months. Early study findings show the mean age of the study participants was 70 years with nearly even gender distribution of males (49.7%) and females (50.3%). The most prevalent chronic diseases in descending order were circulatory system disorders (69.8%), diabetes (47.4%), musculoskeletal disorders (43.5%), respiratory diseases (28.7%), mental illness (18.8%), and cancer (13.6%). To our knowledge, the WellNet study is the first study in Australia to generate evidence on the feasibility of design, recruitment, and implementation of a comprehensive PCMH model. Lessons learned from WellNet study may inform other medical home models in Australian primary care settings Keywords: Patient-centred medical home; enhanced primary care; general practices; integrated care; chronic care model 1. Introduction The growing burden of non-communicable diseases including cardiovascular diseases (CVD), diabetes, chronic obstructive pulmonary disease (COPD), mental illnesses, lung cancer, and musculoskeletal disorders is a major cause of disability and death [ 1 , 2 ]. In Australia, chronic diseases contributed towards 61% of the total disease (fatal and non-fatal) burden and 87% of all Int. J. Environ. Res. Public Health 2020 , 17 , 2164; doi:10.3390 / ijerph 17062164 www.mdpi.com / journal / ijerph

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[Find the meaning and references behind the names: Meet, Cdm, Aim, Better, Delivery, Life, Vary, Single, Body, Poor, Long, Hospital, Multi, Part, High, Span, Last, Given, Due, Small, Quality, Rising]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 2 of 21 deaths in 2015 [ 3 , 4 ]. Furthermore, the burden of multiple chronic conditions (‘multimorbidity’) is a major public health issue with recent findings reporting that the prevalence of Australians with two or more and three or more conditions is 26% and 16%, respectively [ 5 ]. Studies show that patients with multimorbidity often experience poor health-rated quality of life (HR-QOL) [ 6 ], psychological distress [ 7 ], and increased mortality [ 8 ]. Multimorbidity is also associated with increased hospital admissions [ 9 ], health care expenditure [ 10 ], and inappropriate polypharmacy [ 11 ]. Furthermore, evidence suggests that the health burden of chronic diseases is projected to increase in the future, thereby challenging health systems worldwide to revisit strategies towards e ff ective management and prevention [ 12 , 13 ]. Over the last few decades, advancements in public health policies and evidence-based medical treatments have contributed to increased life expectancy [ 14 ]. Consequently, the higher life span has resulted in a greater number of patients with comorbidities and, subsequently, a greater demand for health services [ 15 , 16 ]. Health care systems in high-income countries, including Australia, are primarily focused on the ‘single-disease framework’, where care delivery for the management of multimorbidity is often fragmented, lacking integration and continuity of care [ 17 ]. Conversely, studies show that coordinated and collaborative approaches in primary care with strong emphasis on self-management of chronic diseases are e ff ective in managing complex multimorbidity [ 18 , 19 ]. Therefore, the rising demand for e ff ective management of complex multimorbidity requires enhanced models of primary care for better patient and health service delivery outcomes [ 20 ]. Primary health care is the cornerstone of Australia’s health care system, providing continual, comprehensive and coordinated care that is targeted towards patients’ healthcare needs [ 21 , 22 ]. The country’s current primary health care system is built around a strong general practice foundation and it is estimated that 85 percent of Australians consulted a GP at least once annually [ 3 ]. A number of initiatives have recently been undertaken to integrate primary care for the management chronic diseases by government and primary care organisations, including the ‘Australian Better Health Initiative’, ‘National Primary Health Care Strategy Framework’, and ‘Australian Primary Care Collaboratives Program’ [ 23 , 24 ]. Though encouraging, primary care-based data and research on the e ff ectiveness and feasibility of these initiatives providing a coordinated, multi-disciplinary team (MDT) care for long-term chronic disease management remains limited and not definitive [ 25 , 26 ]. The patient-centred medical home (PCMH) model has been lauded as providing the best model of primary care for patients with one or more chronic diseases. This is due to provision of continuous, comprehensive, and MDT care for collaborating services to meet patients’ health care needs [ 27 ]. Although definitions vary [ 28 , 29 ], the PCMH model typically includes a general practitioner (GP) as part of a MDT, working in conjunction with patients to provide coordinated and focussed care that promotes long-term patient engagement using a long-term chronic disease approach. There is a small but growing body of evidence, primarily from the United States, suggesting that various models of PCMH primary care are more e ff ective than standard care in improving clinical outcomes in patients with one or more chronic diseases [ 30 , 31 ], increasing the quality of care delivered [ 32 , 33 ] and reducing hospital admissions [ 34 , 35 ]. However, in Australia, PCMH models have not been evaluated given the country’s health care setting and funding models. Therefore, the aim of this article is to report on the design, implementation, and early findings of the 12-month PCMH model called ‘WellNet’ delivered across six primary care practices in Sydney, Australia. Additionally, this article will also detail the overall aims and objectives of the WellNet study and the ongoing research activities conducted to evaluate the study outcomes 2. Materials and Methods 2.1. Design of the WellNet Chronic Disease Management (CDM) Program Sonic Clinical Services (SCS) developed the 12-month WellNet chronic disease management (‘WellNet’) program in 2016. This is closely aligned to the principles of the PCMH primary care model

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[Find the meaning and references behind the names: Range, Change, Royal, Resources, Print, Broad, Key, Links, Active, Risk, Apps, Aimed, Tools, Heart, Coaching, Play, Role, Goal]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 3 of 21 as it aims to deliver a coordinated and MDT model of care tailored directly to the needs of patients according to the level of risk and complexity of their chronic conditions. This includes health coaching, care navigation, education, self-management and regular review (Figure 1 ). Int. J. Environ. Res. Public Health 2020 , 17 , x 3 of 22 according to the level of risk and complexity of their chronic conditions. This includes health coaching, care navigation, education, self-management and regular review (Figure 1). Figure 1. Patient-centred medical home (PCMH) components used in the WellNet model. The WellNet program combined face-to-face and telephone consultations with care coordinators and GPs to provide optimal health outcomes through the delivery of patient-tailored healthcare interventions. The interventions are based on the key pillars of: • Patient identification and enrolment; • Patient centred integrated care; • Outcomes-based program philosophy; • Data analytics, risk assessment and patient stratification; • Evidence-based interventions; • Shared electronic health records; and • Patient education and teaching self-management skills. The WellNet program structured interventions are based on the best available models of care applicable to the primary care setting. The program is authored by Australian and international institutes, including the Royal Australian College of General Practitioners (RACGP), Diabetes Australia, Australian Lung Foundation, Therapeutic Guidelines Expert Groups and the National Heart Foundation [36–51]. As patients’ clinical presentations and needs are heterogeneous, the structured interventions are adapted to meet an individual patient’s needs within the IT platform, cdmNET, and with the guidance of the patients’ usual GP A key component of the program is the involvement of specialised chronic disease management (CDM) care coordinators at the medical centres. This was identified as key to successful integration of a CDM program by the literature [52,53]. Supporting the care coordinators were a wide range of services and structured interventions. These included online and print educational materials directed at encouraging behavioural change and a technology platform that facilitates the delivery of interventions across a broad healthcare delivery team In addition, patients were provided access to a user-friendly application called ‘GoShare’ which enables sharing of a range of health resources including video series, links to credible websites, apps, and tools tailored to patients’ information needs. This program is aimed to improve self-efficacy, selfmanagement behaviours, and empower patients to play a more active role in their health care decisions [54]. The WellNet program consisted of 7 in-practice visits and 3 telephone contacts with the care coordinator (2 contacts linked with GP appointments on commencement of the program) and Patienttailored goal setting Health coaching and education Care navigation Regular review Selfmanagement support Figure 1. Patient-centred medical home (PCMH) components used in the WellNet model The WellNet program combined face-to-face and telephone consultations with care coordinators and GPs to provide optimal health outcomes through the delivery of patient-tailored healthcare interventions. The interventions are based on the key pillars of: • Patient identification and enrolment; • Patient centred integrated care; • Outcomes-based program philosophy; • Data analytics, risk assessment and patient stratification; • Evidence-based interventions; • Shared electronic health records; and • Patient education and teaching self-management skills The WellNet program structured interventions are based on the best available models of care applicable to the primary care setting. The program is authored by Australian and international institutes, including the Royal Australian College of General Practitioners (RACGP), Diabetes Australia, Australian Lung Foundation, Therapeutic Guidelines Expert Groups and the National Heart Foundation [ 36 – 51 ]. As patients’ clinical presentations and needs are heterogeneous, the structured interventions are adapted to meet an individual patient’s needs within the IT platform, cdmNET, and with the guidance of the patients’ usual GP A key component of the program is the involvement of specialised chronic disease management (CDM) care coordinators at the medical centres. This was identified as key to successful integration of a CDM program by the literature [ 52 , 53 ]. Supporting the care coordinators were a wide range of services and structured interventions. These included online and print educational materials directed at encouraging behavioural change and a technology platform that facilitates the delivery of interventions across a broad healthcare delivery team In addition, patients were provided access to a user-friendly application called ‘GoShare’ which enables sharing of a range of health resources including video series, links to credible websites, apps, and tools tailored to patients’ information needs. This program is aimed to improve self-e ffi cacy, self-management behaviours, and empower patients to play a more active role in their health care decisions [ 54 ].

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[Find the meaning and references behind the names: Four, Northern, Plus, Low, October, Cases, Harp, December, Turn, Held, Case, Target, Factor, Good]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 4 of 21 The WellNet program consisted of 7 in-practice visits and 3 telephone contacts with the care coordinator (2 contacts linked with GP appointments on commencement of the program) and quarterly GP reviews (4 visits) making up to a total of 14 contacts. Flexibility with the number of contacts was also provided according to patient’s needs and availability. Therefore, patients’ clinical and self-reported outcomes were collected over 12 months plus or minus 3 months 2.2. Specific and Broader Aims and Rationale of Study Design This article aims to describe the design, implementation, and early findings of the 12-month PCMH model called ‘WellNet’ delivered across six primary care practices in Sydney, Australia The broader aim of the WellNet study is to evaluate the e ff ectiveness of a PCMH model for improving clinical outcomes in primary care patients. The specific objectives of this study are to: (1) evaluate changes in clinical outcomes in study participants compared to patients receiving standard care between baseline and 12 months; (2) assess changes in participants’ self-reported health-related quality of life (HR-QoL) and level of activation; (3) determine changes in the risk of hospital admissions; (4) evaluate changes in disease-specific risk assessments; and (5) explore predictors of treatment uptake, response, and compliance A cohort study design with a comparison group (aim (1)) and a case-series study design (aims (1) to (5)) was used to evaluate WellNet’s ‘between group’ and ‘within group’ e ff ectiveness. This was for the WellNet program delivered in six general practices in Northern Sydney, New South Wales, Australia. The rationale for using a synthetic comparison group was to have a sample that would be similar to the WellNet treatment cohort at baseline, which in turn would be used to test the hypothesis that WellNet group will have better clinical outcomes at 12 months compared to standard care 2.3. Patient Characteristics 2.3.1. Treatment Group—Enrolment Methods and Outcome The WellNet study’s treatment group constituted 636 patients from six primary care practices in Northern Sydney who met the eligibility criteria to participate in the 12-month program and provided written consent to have their data shared for evaluation The recruitment period for the study was between December 2016 and October 2017. SCS developed and executed a computerised algorithm to identity from electronic medical records those patients who met the diagnosis and risk factor criteria shown in Figure 2 . The WellNet risk algorithm categorised patients into four groups of complexity based on the number of chronic conditions and presence of risk factors. Patients in groups C and D (the more complex cases) were the target groups for the intervention, however eligibility was confirmed at initial assessment by Hospital Admission Risk Profile (HARP) score Patients were eligible if they satisfied either criteria: Criteria 1: Patients aged 40 years or above and who had seen a GP at least three times in the last two years; had been diagnosed with one to three chronic diseases and had presented with one or more elevated clinical risk factors; and held a HARP score of greater than 10 (medium risk or greater) OR Criteria 2: Patients aged 40 years or above and who had seen a GP at least three times in the last two years and had been diagnosed with four or more chronic diseases with or without one or more risk factors; and held a HARP score of greater than 10 (medium risk or greater) Additionally, patients with low HARP score ( < 10) but with at least one or more chronic diseases and one or more consistently elevated risk factors were also included in the study through direct GP referrals as GPs deemed them as good candidates that could benefit from the WellNet care.

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[Find the meaning and references behind the names: List, Chosen, Liver, Mass, Lft, Homes, Living, Rate, Hba]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 5 of 21 Int. J. Environ. Res. Public Health 2020 , 17 , x 5 of 22 Figure 2. Eligibility criteria for the WellNet study . Dx – Diagnosis of chronic condition; BMI – Body Mass Index; HbA 1 c – Glycated Haemoglobin; eGFR – estimated Glomerular Filtration Rate; UACR – Urine Albumin Creatinine Ratio; LFT – Liver function test. ** Additionally, patients with low Hospital Admission Risk Profile (HARP) score (<10) but with at least one or more chronic diseases and one or more consistently elevated risk factors were also included in the study through general practitioner (GP) referrals Patients were eligible if they satisfied either criteria: Criteria 1 : Patients aged 40 years or above and who had seen a GP at least three times in the last two years; had been diagnosed with one to three chronic diseases and had presented with one or more elevated clinical risk factors; and held a HARP score of greater than 10 (medium risk or greater) OR Criteria 2 : Patients aged 40 years or above and who had seen a GP at least three times in the last two years and had been diagnosed with four or more chronic diseases with or without one or more risk factors; and held a HARP score of greater than 10 (medium risk or greater) Additionally, patients with low HARP score (<10) but with at least one or more chronic diseases and one or more consistently elevated risk factors were also included in the study through direct GP referrals as GPs deemed them as good candidates that could benefit from the WellNet care The care coordinators eliminated unsuitable patients, such as those living in nursing homes or with significant cognitive impairment, before presenting a list of potentially eligible patients to GPs for their review and selection. Potentially eligible patients were then contacted either through an invitation letter (n = 1431) or by GP referrals during routine visits (n = 359). A minimum of three Figure 2. Eligibility criteria for the WellNet study. Dx–Diagnosis of chronic condition; BMI–Body Mass Index; HbA 1 c–Glycated Haemoglobin; eGFR–estimated Glomerular Filtration Rate; UACR–Urine Albumin Creatinine Ratio; LFT–Liver function test. ** Additionally, patients with low Hospital Admission Risk Profile (HARP) score ( < 10) but with at least one or more chronic diseases and one or more consistently elevated risk factors were also included in the study through general practitioner (GP) referrals The care coordinators eliminated unsuitable patients, such as those living in nursing homes or with significant cognitive impairment, before presenting a list of potentially eligible patients to GPs for their review and selection. Potentially eligible patients were then contacted either through an invitation letter (n = 1431) or by GP referrals during routine visits (n = 359). A minimum of three follow-up phone calls were made by the care coordinator for each patient invited by letter who did not respond directly to the letter Out of the total 1790 patients contacted, 698 (38.9%) attended the initial assessment. From the initial assessment, 688 patients were found to be eligible for the program based on their HARP score. Of these, 52 declined to participate in the WellNet Program or the cohort study, resulting in 636 (92.4%) consenting eligible participants enrolled into the study 2.3.2. Comparison Group—Matching Iterations and Outcomes For matching purposes, four general practices with similar geographical proximity as WellNet practices that did not provide PCMH care were chosen. In order to be concurrent with the enrolment

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[Find the meaning and references behind the names: Choice, Bias, Final, Cem, Pam, Blood, Year, Place, Post, Table, Close, Past, Match]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 6 of 21 period, patients who visited any one of the four general practices between December 2016 and October 2017 were identified (n = 20,478) The Coarsened Exact Matching (CEM) was used to match treatment participants with the comparison group. CEM is a Monotonoic Imbalance Bounding (MIB) matching method that temporarily coarsens the data according to the researchers’ choice and then finds exact matches so that adjusting the imbalance on one variable has no e ff ect on the maximum imbalance of any other [ 55 ]. Using ‘Coarsened Exact Matching’ analysis in R, five di ff erent matching iterations were conducted. Several variables including age (continuous and categorical), gender, chronic disease type (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer), number of chronic diseases, systolic blood pressure (continuous and categorical), and total cholesterol: HDL-C ratio were considered to determine the best possible matching outcome, and from that, the best model was chosen Subclass or strata groups without at least 1 treatment to 1 comparison patient were excluded CEM in turn returns ‘weights’ to compensate for di ff erential strata sizes to be used in the subsequent analyses [ 55 ]. This matching procedure has shown to e ff ectively limit selection bias and variance between the groups, thereby minimising bias in the final model showing treatment e ff ects [ 55 ]. Table 1 provides the matching iteration numbers by the variables and their outcomes. Matching iteration number 1 was chosen as the best model as it produced the highest number of matched patients in both treatment and comparison groups whilst closely matching the two groups based on age and gender, along with the same type and number of chronic diseases. Of the WellNet program group of 636 patients, 589 were matched to the comparison group (Figure 3 ). Int. J. Environ. Res. Public Health 2020 , 17 , x 8 of 22 Figure 3. Flowchart of patient enrolment . 2.4. Provider Characteristics A total of 66 GPs were invited to participate in a Likert scale survey on their perspectives on 1) chronic disease management; 2) WellNet program; and 3) PCMH model of care. In addition, some sociodemographic characteristics on age, gender, place of graduation and years of general practice experience were also collected 2.5. Follow-Up There are two phases of follow-up in the WellNet program. Phase 1 involved follow-up at 12 months to evaluate changes in clinical outcomes, HARP, Patient Activation Measure (PAM), selfreported EuroQol 5 Dimensions 5 Levels (EQ-5 D-5 L), and other disease-specific risk assessments [49,56–65]. Phase 2 of the evaluation is planned as a two-year post intervention follow-up that will study changes in health services utilisation and medication prescription with the use of hospitallinked administrative datasets 2.6. Data Collection Data collected at various stages of baseline and follow-up from participants included sociodemographic information, private health insurance membership status, lifestyle risk factors, chronic disease diagnoses, clinical measures (as clinically relevant), and several validated healthrelated surveys that participants were asked to complete upon enrolment (Table 2). These surveys involved information regarding: (a) health-related quality of life, (b) level of health engagement and activation, (c) self-management of their health, (d) other disease-specific risk assessments Primary care practices 4 Primary care practices providing standard care (Comparison group) 6 Primary care practices providing PCMH care (Intervention group) Matching criteria - Age - Gender - Type and number of chronic condition 688 Patients found eligible 20,476 Patients who visited the practice at least 2 times in the past year (close geographical proximity and concurrent timeline) 636 Consented patients in the WellNet program 52 Patients who declined to participate in the evaluation 589 Matched patients in the WellNet program 7750 Matched comparison group patients Figure 3. Flowchart of patient enrolment.

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[Find the meaning and references behind the names: Reading]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 7 of 21 Table 1. Matching iterations and outcomes Matching Iteration Number Matching Variables Treatment (Overall n = 636) Comparison (overall n = 20478) N (Matched Treatment: Comparison) N (Unmatched Treatment: Comparison) 1 Age (continuous), gender, type of chronic disease (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer) and number of chronic diseases 617 * 20478 * 589:7750 28:12728 2 Age (continuous), gender, type of chronic disease (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer), systolic, and total cholesterol: HDL-C ratio 447 ** 3899 ** 228:604 219:3205 3 Age categories (breaks = 10 years), gender, (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer), systolic, and total cholesterol: HDL-C ratio 447 ** 3899 ** 260:749 260:749 4 Age (continuous), gender, type of chronic disease (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer), systolic (breaks = 2 mmHg), and total cholesterol: HDL-C ratio 447 ** 3899 ** 202:517 245:3292 5 Age categories (breaks = 10 years), gender, (cardiovascular disease, respiratory disease, diabetes, musculoskeletal disease, mental illness, and cancer), systolic (breaks = 2 mmHg), and total cholesterol: HDL-C ratio 447 ** 3899 ** 242:735 205:3074 HDL-C–High Density Lipoprotein Cholesterol; * Of the 636 WellNet participants, 19 did not have a chronic disease and were not included in the matching analysis, resulting in 617 participants; ** Out of 636 WellNet participants, 19 did not have a chronic disease, 15 did not have a systolic reading and 166 did not have a TC: HDL reading, and they were automatically removed during matching. Similarly, out of 20478 comparison patients, 9176 did not have a chronic disease, 3169 did not have a systolic reading and 4234 did not have a TC: HDL reading, and they were automatically removed during matching.

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[Find the meaning and references behind the names: Pain, Time, Back, Heath]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 8 of 21 2.4. Provider Characteristics A total of 66 GPs were invited to participate in a Likert scale survey on their perspectives on (1) chronic disease management; (2) WellNet program; and (3) PCMH model of care. In addition, some sociodemographic characteristics on age, gender, place of graduation and years of general practice experience were also collected 2.5. Follow-Up There are two phases of follow-up in the WellNet program. Phase 1 involved follow-up at 12 months to evaluate changes in clinical outcomes, HARP, Patient Activation Measure (PAM), self-reported EuroQol 5 Dimensions 5 Levels (EQ-5 D-5 L), and other disease-specific risk assessments [ 49 , 56 – 65 ]. Phase 2 of the evaluation is planned as a two-year post intervention follow-up that will study changes in health services utilisation and medication prescription with the use of hospital-linked administrative datasets 2.6. Data Collection Data collected at various stages of baseline and follow-up from participants included sociodemographic information, private health insurance membership status, lifestyle risk factors, chronic disease diagnoses, clinical measures (as clinically relevant), and several validated health-related surveys that participants were asked to complete upon enrolment (Table 2 ). These surveys involved information regarding: (a) health-related quality of life, (b) level of health engagement and activation, (c) self-management of their health, (d) other disease-specific risk assessments Table 2. Summary of data collected in the WellNet Study Type of Data Time of Data Collection Variables Measured Socio-demographic data Baseline Age and gender Private health insurance membership Baseline Private insurance status and name of the insurance provider Diagnosis of chronic condition Baseline Diagnosis of arthritis, asthma, back pain, cancer, cardiovascular diseases (CVD), chronic obstructive pulmonary disease (COPD), diabetes, mental illness and kidney diseases Clinical assessments Baseline 6-month 12-month Height, weight, waist circumference, Body Mass Index (BMI), blood pressure (BP), blood sample - cholesterol [serum total cholesterol, high density lipoprotein cholesterol (HDL-C) and low-density lipoprotein cholesterol (LDL-C)], triglycerides, glycated haemoglobin (HbA 1 c), estimated glomerular filtration rate (eGFR), and urine albumin-creatinine ratio (UACR) Risk of hospital admission Baseline 12-month Hospital Admission Risk Profile (HARP) score to estimate the risk of hospitalisation in the next 12 months Health utility data Baseline 12-month Medication–drug name, dosage and frequency of use and number of prescriptions Patient activation, engagement and readiness to change Baseline 12-month Patient Activation Measure (PAM) scores to evaluate patient self-e ffi cacy and self-management behaviours Patient self-reported health-related quality of life Baseline 12-month EuroQol 5 Dimensions 5 Levels (EQ-5 D-5 L) to assess patient’s heath related quality of life

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[Find the meaning and references behind the names: Human, Date, Cont, Set, Koos, Tool, Hoos, Cat, Hip, Track, Kessler, Redi, Dass, Chi, Pre, Short]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 9 of 21 Table 2. Cont Type of Data Time of Data Collection Variables Measured Disease-specific risk assessments Baseline 12-month Absolute Cardiovascular Disease Risk (CVDR), Australian Type 2 Diabetes Risk Tool (AusDrisk) scores, UK Prospective Diabetes Risk Engine (UKPDS), Chronic Obstructive Pulmonary Disease Assessment Test (CAT) scores, Kessler Psychological Distress scale (K 10) scale, Depression Anxiety Stress Scale (DASS 21), short versions of Knee Injury and Osteoarthritis Outcome Score (KOOS), Hip Disability and Osteoarthritis Outcome Score (HOOS) Patient experience survey 12-month Patient satisfaction survey on quality of care outcomes; patient-provider relationship, communication, and empowerment outcomes; and access to information technology outcomes Feasibility outcomes 12-month Recruitment: number of patients’ who potentially met the program’s inclusion criteria; Retention rates: number of completed and dropouts; Treatment compliance: rates of adherence to overall protocol 2.7. Statistical Analyses Data extraction on the WellNet program group and the comparison group were provided by SCS to the researchers. The data were provided in de-identified form and the patient’s cdmNET number was used to track patients over time 2.7.1. Analysis Conducted to Date Descriptive statistics are presented as mean and standard deviation (SD) for continuous variables whereas frequency counts and percentages are used for reporting categorical variables. Independent samples t-test was conducted to determine significant di ff erences between treatment and comparison group at baseline 2.7.2. Ongoing Analysis To assess changes over time between baseline and 12 months, significant within-group mean di ff erences (pre-test / post-test) from baseline to 12 months will be determined by using Paired samples t-test. In addition, between-group analyses (treatment and comparison group) will be conducted to determine significant mean di ff erences using independent samples t-tests and chi-squared tests for continuous and categorical variables, respectively. Furthermore, analysis of covariance (ANCOVA) and repeated measures ANCOVA will be used to determine any significant between-group and within-group di ff erences in the clinical measures and assessments after adjusting for covariates such as age, gender and baseline values. Finally, multivariate regression analyses using the backward stepwise method will be used to determine predictors of several clinical endpoints at 12-month follow-up All analyses will be performed using R statistical software. Significance level is set as 0.05 and all statistical tests will be two-sided 2.8. Ethical Considerations The study was reviewed by the Western Sydney University Human Research Ethics Committee (REDI Reference: H 12215). Written informed consent was obtained from the study participants 3. Results and Discussion Since the WellNet study is ongoing, the baseline findings on recruitment outcomes, baseline clinical and health assessment surveys along with provider level experiences at baseline are described We have also discussed the strengths and limitations of the WellNet study along with potential determinants a ff ecting study reproducibility.

[[[ p. 10 ]]]

[Find the meaning and references behind the names: North, Male, Present, Success, Female, Phi]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 10 of 21 3.1. Recruitment Outcomes Almost 98% of the patients enrolled in the WellNet program were over 40 years of age and with 93% having one to three chronic conditions with one or more risk factors present, and 98% of participants had a HARP score in the > 10 range (medium or greater risk). Thereby, it can be observed that the patient identification algorithm used was e ff ective in identifying those patients who potentially met the program’s inclusion criteria (Table 3 ). Table 3. Feasibility outcomes Criteria Success Rate Age 40 years and above 97.5% Number of chronic diseases Number of patients with 1 to 3 chronic diseases 93.4% Number of patients with 4 or more chronic diseases 6.6% Risk factors Patients with 1 chronic disease (n = 227) 1 risk factor 47.6% > 1 risk factor 31.7% Patients with 2 chronic diseases (n = 237) 1 risk factor 42.6% > 1 risk factor 27.4% Patients with 3 chronic diseases (n = 115) 1 risk factor 40% > 1 risk factor 35.7% Patients with 4 or more chronic diseases (n = 38) 1 risk factor 44.7% > 1 risk factor 26.3% HARP score > 10 97.7% 3.2. Sociodemographic Characteristics The key demographic findings are presented in Table 4 . The mean (SD) age of the study participants was 70.05 (11.6) years with nearly even gender distribution of males (49.7%) and females (50.3%). A majority of participants (68.7%) in the WellNet treatment group had private health insurance. There is higher than usual patients with private health insurance (PHI) because of higher socioeconomic status of North Sydney region and the PHI members targeted for intervention Table 4. Sociodemographic characteristics and prevalence of chronic conditions in the treatment and comparison group Determinants WellNet Treatment Group (N = 589) WellNet Comparison Group (N = 7750) p -Value N (%) N (%) Age groups 0.798 40–44 years 7 (1.2) 141 (1.8) 45–54 years 57 (9.7) 722 (9.3) 55–64 years 118 (20.0) 1580 (20.4) 65–74 years 188 (31.9) 2360 (30.4) 75–84 years 156 (26.5) 2029 (26.2) ≥ 85 years 63 (10.7) 918 (11.8) Mean (SD) 70.05 (11.59) 69.95 (11.86) Sex 0.936 Male 293 (49.7) 3842 (49.6) Female 296 (50.3) 3908 (50.4)

[[[ p. 11 ]]]

[Find the meaning and references behind the names: Smoker, Missing, Acr]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 11 of 21 Table 4. Cont Determinants WellNet Treatment Group (N = 589) WellNet Comparison Group (N = 7750) p -Value N (%) N (%) Smoking status Ex–smoker 237 (42.1) 2274 (36.4) < 0.001 Non–smoker 280 (49.7) 3655 (58.6) Smoker 46 (8.2) 309 (5.0) Unknown 26 (4.4) 1512 (19.5) Drinking status Drinker 256 (43.5) 1465 (18.9) < 0.001 Non–drinker 176 (29.9) 147 (1.9) Unknown 156 (26.5) 6138 (79.2) Private insurance status Yes 404 (68.7) NA – No 184 (31.3) Missing 1 (0.2) Prevalence of chronic conditions 1.000 Diseases of the circulatory system 411 (69.8) 5408 (69.8) Respiratory diseases 169 (28.7) 2224 (28.7) Musculoskeletal disorders 256 (43.5) 3368 (43.5) Diabetes 279 (47.4) 3671 (47.4) Mental illness 111 (18.8) 1461 (18.8) Cancer 80 (13.6) 1053 (13.6) Number of chronic conditions 1.000 1 disease 133 (22.6) 1750 (22.6) 2 diseases 249 (42.3) 3276 (42.3) 3 diseases 159 (27.0) 2092 (27.0) 4 diseases 42 (7.1) 553 (7.1) ≥ 5 diseases 6 (1.0) 79 (1.0) SD-Standard Deviation; NA—not available 3.3. Chronic Disease Diagnosis and Clinical Indicators The prevalence of chronic disease among the treatment and comparison group was similar The most prevalent chronic diseases in descending order were: circulatory system disorders (69.8%), diabetes (47.4%), musculoskeletal disorders (43.5%), respiratory diseases (28.7%), mental illness (18.8%), and cancer (13.6%). Consistent with other Australian studies [ 66 , 67 ], the distribution of chronic diseases significantly di ff ered across age groups as the number of chronic diseases generally increased with age (Figure 4 ). In terms of gender distribution, diabetes (54.8%) was significantly more prevalent amongst males than females (40.1%), whilst considerably more females had musculoskeletal disorders (54.3% vs. 31.3%), respiratory (34.1% vs. 23.8%), and mental illness (23.7% vs. 16.9%) than males Descriptive statistics of clinical measures for the treatment and comparison group are present in Table 5 . Although treatment and comparison groups were e ff ectively matched based on the type and number of chronic conditions, findings of the independent t-tests show significant di ff erences in blood pressure, glycated haemoglobin (HbA 1 c), Low Density Lipoprotein Cholesterol (LDL-C), total cholesterol, and waist circumference (females only) between the treatment and comparison group. However, there were no statistically significant di ff erences between treatment and comparison group for clinical measures like Body Mass Index (BMI), weight, waist circumference (males only), High Density Lipoprotein Cholesterol (HDL-C), estimated Glomerular Filtration Rate (e-GFR), and Albumin Creatinine Ratio (ACR) at baseline. In order to e ff ectively manage baseline di ff erences, ANCOVA will be used to determine any significant between-group di ff erences in the clinical measures after adjusting for covariates such as age, gender and baseline values.

[[[ p. 12 ]]]

[Find the meaning and references behind the names: Square, Cut, Mor, Min]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 12 of 21 Int. J. Environ. Res. Public Health 2020 , 17 , x 12 of 22 Mental illness 111 (18.8) 1461 (18.8) Cancer 80 (13.6) 1053 (13.6) Number of chronic conditions 1.000 1 disease 133 (22.6) 1750 (22.6) 2 diseases 249 (42.3) 3276 (42.3) 3 diseases 159 (27.0) 2092 (27.0) 4 diseases 42 (7.1) 553 (7.1) ≥ 5 diseases 6 (1.0) 79 (1.0) SD-Standard Deviation; NA—not available 3.3. Chronic Disease Diagnosis and Clinical Indicators The prevalence of chronic disease among the treatment and comparison group was similar. The most prevalent chronic diseases in descending order were: circulatory system disorders (69.8%), diabetes (47.4%), musculoskeletal disorders (43.5%), respiratory diseases (28.7%), mental illness (18.8%), and cancer (13.6%). Consistent with other Australian studies [66,67], the distribution of chronic diseases significantly differed across age groups as the number of chronic diseases generally increased with age (Figure 4). In terms of gender distribution, diabetes (54.8%) was significantly more prevalent amongst males than females (40.1%), whilst considerably more females had musculoskeletal disorders (54.3% vs. 31.3%), respiratory (34.1% vs. 23.8%), and mental illness (23.7% vs. 16.9%) than males Figure 4. Distribution of chronic disease prevalence by age groups among WellNet patients. Chisquared test between age group and number of chronic conditions returned a p < 0.001. Descriptive statistics of clinical measures for the treatment and comparison group are present in Table 5. Although treatment and comparison groups were effectively matched based on the type and number of chronic conditions, findings of the independent t-tests show significant differences in blood pressure, glycated haemoglobin (HbA 1 c), Low Density Lipoprotein Cholesterol (LDL-C), total cholesterol, and waist circumference (females only) between the treatment and comparison group. However, there were no statistically significant differences between treatment and comparison group for clinical measures like Body Mass Index (BMI), weight, waist circumference (males only), High Density Lipoprotein Cholesterol (HDL-C), estimated Glomerular Filtration Rate (e-GFR), and Albumin Creatinine Ratio (ACR) at baseline. In order to effectively manage baseline differences, ANCOVA will be used to determine any significant between-group differences in the clinical measures after adjusting for covariates such as age, gender and baseline values. 11 ( 68.8% ) 18 (50 0 % ) 45 (44.1% ) 50 ( 3 2 9 % ) 59 ( 31.7% ) 16 ( 12.8% ) 4 (25.0%) 13 ( 36 1% ) 25 ( 24.5 % ) 42 (27.6% ) 52 (28.0% ) 36 (28.8% ) 1 (6 .3% ) 5 ( 13.9% ) 22 ( 21.6% ) 39 (25.7% ) 38 (20.4% ) 30 (24.0%) 0 ( 0 .0% ) 0 ( 0 .0% ) 6 (5 .9% ) 16 ( 10.5% ) 24 ( 12.9% ) 21 ( 1 6 8 % ) 0 ( 0 .0% ) 0 ( 0 .0% ) 4 (3 .9% ) 5 (3 .3 % ) 13 ( 7.0% ) 22 ( 1 7 6% ) L E S S T H A N 4 0 Y E A R S 4 0 T O 4 9 Y E A R S 5 0 T O 5 9 Y E A R S 6 0 T O 6 9 Y E A R S 7 0 T O 7 9 Y E A R S 8 0 Y E A R S A N D A B O V E 1 disease 2 diseases 3 diseases 4 diseases 5 or mor e diseases N=617 Figure 4. Distribution of chronic disease prevalence by age groups among WellNet patients. Chi-squared test between age group and number of chronic conditions returned a p < 0.001 Table 5. Clinical measures among treatment and comparison group collected at baseline Clinical Measures WellNet Treatment Group (N = 589) WellNet Comparison Group (N = 7750) p -Value N (%) N (%) Systolic blood pressure (mmHg), Mean (SD) 139.37 (19.30) 135.96 (16.51) < 0.001 Diastolic blood pressure (mmHg), Mean (SD) 79.27 (10.32) 76.02 (11.31) < 0.001 Body Mass Index, Mean (SD) 29.54 (6.36) 29.12 (5.63) 0.151 Weight (kg)–Mean (SD) 81.81 (20.72) 81.73 (19.70) 0.930 Waist Circumference* (Males) (cm), Mean (SD) 106.09 (15.63) 104.30 (14.30) 0.120 Waist Circumference* (Females) (cm), Mean (SD) 98.82 (14.62) 93.15 (12.47) < 0.001 HbA 1 c (%), Mean (SD) 7.16 (1.41) 6.71 (1.24) < 0.001 HDL-C (mmol / L), Mean (SD) 1.37 (0.40) 1.40 (0.42) 0.147 LDL-C (mmol / L), Mean (SD) 2.71 (1.08) 2.52 (0.98) < 0.001 Serum total cholesterol (mmol / L), Mean (SD) 4.81 (1.38) 4.60 (1.13) < 0.001 Estimated Glomerular Filtration Rate (mL / min / 1.73 m 2 ) > 90 mL / min / 1.73 m 2 109 (24.9) 1467 (24.8) 0.868 60–89 mL / min / 1.73 m 2 247 (56.5) 3436 (58.2) 45–59 mL / min / 1.73 m 2 46 (10.5) 622 (10.5) 30–44 mL / min / 1.73 m 2 26 (5.9) 274 (4.6) < 30 mL / min / 1.73 m 2 9 (2.0) 106 (1.8) Missing 152 (25.8) 1845 (23.8) Albumin-Creatinine Ratio* (mg / mmol) (Males), Mean (SD) 15.52 (67.54) 13.08 (53.18) 0.653 Albumin-Creatinine Ratio* (mg / mmol) (Females), Mean (SD) 7.53 (22.31) 8.07 (32.12) 0.878 SD - Standard deviation; HbA 1 c–Glycated Haemoglobin; HDL-C - High Density Lipoprotein Cholesterol; LDL-C - Low Density Lipoprotein Cholesterol; p-value by Chi-square test (categorical) or independent samples t-test (continuous) between treatment and control group; *Variables with gender-specific cut-o ff points.

[[[ p. 13 ]]]

[Find the meaning and references behind the names: Walk, Lack, Severe, Confidence, Take]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 13 of 21 3.4. Self-Reported Health Assessments General health and disease-specific risk assessments were recorded only among the WellNet treatment group (Table 6 ). As targeted, around 98% of participants had medium risk or greater HARP scores. The majority of study participants self-rated their health positively with mean EQ-5 D-5 L index score of 0.79 out of 1. Consistent with other studies [ 68 , 69 ], the mean EQ-5 D-5 L score significantly decreased with increased number of chronic diseases ( p < 0.001). In terms of patient activation and self-management, only 21% reported having actively changed their health-related behaviour, with 22% beginning to take actions at baseline. However, 19% believed that action was not important, with a majority of participants (38%) reporting that the biggest di ffi culty in attempting to change behaviour was a lack of confidence or knowledge in managing and improving their condition Table 6. General and disease-specific assessments among WellNet treatment group only at baseline Patient Survey Questionnaires WellNet Treatment Group (N = 635) n (%) Hospital Admission risk profile (N = 628) Low risk (1–10) 14 (2.2) Medium risk (11–23) 581 (92.5) High risk (24–38) 33 (5.3) Missing 7 (1.1) Patient Activation Measure scores (N = 626) Not believing that activation is important ( < 47) 121 (19.3) A lack of knowledge and confidence to take action (47.1–55.1) 236 (37.7) Beginning to take action (55.2–67) 138 (22.0) Taking action ( > 67.1) 131 (20.9) Missing 9 (1.4) Mean EQ-5 D-5 L score (overall)–Mean (SD) 0.79 (0.19) EQ-5 D-5 L score percentage EQ-5 D-5 L mobility (N = 626) No problem 298 (47.6) Slight problem 171 (27.3) Moderate problem 108 (17.3) Severe problem 47 (7.5) Unable to walk 2 (0.3) Missing 9 (1.4) EQ-5 D-5 L self-care (N = 623) No problem 521 (83.6) Slight problem 79 (12.7) Moderate problem 19 (3.0) Severe problem 4 (0.6) Unable 0 (0.0) Missing 12 (1.9) EQ-5 D-5 L usual activities (N = 626) No problem 312 (49.8) Slight problem 187 (29.9) Moderate problem 98 (15.7) Severe problem 26 (4.2) Unable 3 (0.5) Missing 9 (1.4) EQ-5 D-5 L pain / discomfort (N = 627) No problem 156 (24.9) Slight problem 246 (39.2) Moderate problem 165 (26.3) Severe problem 55 (8.8) Extreme 5 (0.8) Missing 8 (1.3)

[[[ p. 14 ]]]

[Find the meaning and references behind the names: Normal, Mild]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 14 of 21 Table 6. Cont Patient Survey Questionnaires WellNet Treatment Group (N = 635) n (%) EQ-5 D-5 L anxiety / depression (N = 629) No problem 321 (51.0) Slight problem 190 (30.2) Moderate problem 94 (14.9) Severe problem 16 (2.5) Extreme 8 (1.3) Missing 6 (0.9) DASS 21 Scores (N = 331) DASS 21–Depression scale Normal 230 (69.5) Mild 26 (7.9) Moderate 40 (12.1) Severe 12 (3.6) Extremely severe 23 (6.9) DASS 21–Anxiety scale Normal 211 (63.7) Mild 32 (9.7) Moderate 53 (16.0) Severe 14 (4.2) Extremely severe 21 (6.3) DASS 21–Stress scale Normal 260 (78.5) Mild 29 (8.8) Moderate 20 (6.0) Severe 15 (4.5) Extremely severe 7 (2.1) K 10 scores (N = 302) Low level of psychological distress 137 (45.4) Moderate level of psychological distress 88 (29.1) High level of psychological distress 49 (16.2) Very high level of psychological distress 28 (9.3) UKPDS risk profile (N = 140) Coronary Heart Disease risk - mean percentage (SD) 18.98 (14.11) Fatal Coronary Heart Disease risk - mean percentage (SD) 14.94 (16.14) Stroke risk - mean percentage (SD) 14.37 (15.10) Fatal stroke risk - mean percentage (SD) 2.33 (2.60) Missing 53 (27.5) AusDRisk scores (N = 220) Low risk 5 (2.3) Intermediate risk 34 (15.5) High risk 181 (82.3) Missing 137 (38.4) Absolute cardiovascular risk (N = 370) Low risk 167 (45.1) Moderate risk 84 (22.7) High risk 119 (32.2) Missing 48 (11.5) COPD impact scores (N = 26) Normal 2 (7.7) Low 4 (15.4) Medium 12 (46.2) High 3 (11.5) Very high 5 (19.2) Missing 38 (59.4)

[[[ p. 15 ]]]

[Find the meaning and references behind the names: Just, Euro, Excellent, Optimistic, Ness, Believe, Sti, Reason, Positive, Seven, Common]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 15 of 21 Table 6. Cont Patient Survey Questionnaires WellNet Treatment Group (N = 635) n (%) HOOS score (N = 31) HOOS pain score - Mean (SD) 64.92 (23.37) HOOS function score - Mean (SD) 68.95 (19.80) HOOS symptoms score - Mean (SD) 66.15 (17.23) Missing 168 (84.4) KOOS score (N = 59) KOOS sti ff ness score - Mean (SD) 61.86 (28.37) KOOS pain score - Mean (SD) 64.72 (22.01) KOOS function score - Mean (SD) 63.13 (25.58) KOOS symptoms score - Mean (SD) 63.09 (18.14) Missing 140 (70.3) SD—Standard Deviation; EQ-5 D-5 L—Euro-Qol Five dimensions and Five levels; DASS 21—Depression Anxiety Stress Scale 21 questions version; K 10—Kessler’s Psychological Distress scale; AusDRisk—Australian Type-2 Diabetes Risk score; COPD—Chronic Obstructive Pulmonary Disease; HOOS—Hip Disability and Osteoarthritis Outcome Score; KOOS—Knee Injury and Osteoarthritis Outcome Score 3.5. Provider-Level Findings 3.5.1. Provider-Level Baseline Characteristics Of 66 eligible GPs, 49 (74%) responded to the self-reported survey. 62.5% of GPs were aged 55 and above and almost two-thirds (63.3%) had graduated in Australia. More than 63% reported more than 20 years of experience working in general practice 3.5.2. GPs Perspectives on Chronic Disease Management At baseline, GPs were largely of the opinion (67% strongly agreed or agreed) that they had systematic approaches toward patients with chronic disease. Likewise, 70% of GPs reported using the skills and support of their practice nurses and primary care team. Around 90% stated that they routinely prepared chronic disease management plans for their patients and liaised with patients’ care teams. However, only 50% reported regularly reviewing and updating their disease management plans. How the latter number changes over the course of the twelve months of Phase 1 is of especial interest to the program 3.5.3. GPs Perspectives on WellNet Study On the whole, GPs held positive perspectives toward the WellNet program. The majority of clinicians ( > 70%) agreed or strongly agreed that they were familiar with the concept of the program GPs also reported to have excellent relationships with their primary care team (85% agreed or strongly agreed) as well as had confidence that clinical teams were providing highly coordinated care (77%) Thirty-seven GPs identified and referred patients to the WellNet program and were confident that patients would benefit from the program. However, eleven stated that they had not. Of these, the most common reason was that the doctors in question did not know how to identify and refer patients to the program (n = 5). If these numbers have not changed after twelve months, greater clinician engagement may be necessary. One clinician stated that they did not believe the program had benefits to their patients, whilst one GP each stated that they had not identified any patients yet, had just started the program, or did not have any eligible patients 3.5.4. GPs Perspectives on PCMH Model On the whole, it seems that clinicians were relatively aware of the PCMH concept (61% strongly agreed or agreed). These numbers should be expected to improve over twelve months. The majority of GPs were also optimistic that voluntary patient enrolment can enhance patient care (79%) and that

[[[ p. 16 ]]]

[Find the meaning and references behind the names: Real, Renders, Large, Point, Rather, Sta]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 16 of 21 they involved clinicians in the design of health service delivery (83%), while most also believed that they worked collaboratively in their practices and that clearly defined roles and responsibilities existed amongst sta ff It should also be noted that clinicians strongly valued patient feedback: nearly 40% strongly agreed, while 55% agreed. That said, only 71% agreed or strongly agreed that they had su ffi cient data for evaluating and improving their practices, and 81% believed that they were encouraged or supported to improve care quality and safety—indicating that there may be gaps in the collection or utilisation of patient outcome and experience data or insu ffi cient structures in place that could support quality improvement 3.6. Factors A ff ecting Reproducibility of Study Findings Similar to other studies based on an originally developed program, reproducibility of study findings is constrained by the uniqueness of the data and also by several patient and provider-level determinants. Patients’ levels of education, social gradient, and health behaviour and practices would have di ff erent levels of impact towards improved health coaching and self-management practices leading subsequently to varying levels of management. For instance, patients with a higher level of education will better perceive the importance of self-management and would be more likely to adhere to health coaching provided by the GPs and care coordinators in the WellNet program. In terms of provider-level determinants, varying levels of experience and training among GPs and care coordinators will impact quality of care in terms of e ff ectively delivering PCMH care 3.7. Study Strengths Despite general practices being the first point of health-related interactions among the predominant percentage of Australians, research based on GP data is disproportionately low [ 25 ]. To our knowledge, the WellNet program is the first study in Australia to generate the first real-world evidence on the feasibility and e ff ectiveness of a comprehensive PCMH model with the use of primary care-based data The study comprises a large, e ff ectively targeted sample with wide range of GP-based data on chronic disease diagnosis as well as self-reported risk assessments. The use of general and disease-specific self-reported health assessments recorded among study participants helps understand patients’ quality of life, self-management practices, and severity of diseases in addition to routine clinical metrics. Furthermore, use of validated questionnaires renders better quality of data with improved credibility as well as higher comparability with other sample populations. In addition, the study also includes standardised clinical measurements that are collected by trained health care professionals as opposed to self-reported information, thereby eliminating any potential self-reporting bias 3.8. Study Limitations The WellNet program has some limitations in terms of the evaluation study design and data The WellNet study was based on the case series study design for the treatment group only and did not include a control group. Therefore, analyses of self-reported assessments were limited to ‘within group’ comparisons rather than ‘between groups’. Although the treatment group was closely matched with the comparison group based on age, gender, type and number of chronic diseases, there were statistically significant di ff erences observed across some clinical measures between the two groups at baseline. To minimize this, ANCOVA techniques will be used to control for baseline di ff erences In terms of data limitations, the reason why 52 patients declined from participation was not recorded The impact of each component of PCMH contributing to primary and secondary outcomes was not explored. In addition, facilitators or barriers that contributed to early implementation experiences were also not recorded.

[[[ p. 17 ]]]

[Find the meaning and references behind the names: Capital, June, Start, Work, Aus, Afshin, File, Wang, Abd, Cda, Gov, Read, Bureau, Works, Abdulle, Abbas, Abd-Allah, Original, Abate, Cer, Abera, Sanderson, Abdulkader, Cocker, Palmer, Agrawal, Abs, Centre, Hay, Dalys, Hale, Author, Allah, Cee, Focus]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 17 of 21 4. Conclusions There has been increased advocacy to implement PCMH models for e ff ective management at the primary care level worldwide. The WellNet study is one of the few studies in Australia to generate evidence on the feasibility of design, recruitment, and implementation of a comprehensive PCMH model. To date, the recruitment outcomes of WellNet study indicate that the patient algorithm was e ff ective in identifying eligible patients for enrolment Lessons learnt from the baseline findings include understanding of the characteristics of the sample participants not only in terms of their chronic disease diagnosis, but also to assess their level of self-management behaviours, quality of life and other disease-specific surveys at baseline. As the PCMH model aims to provide a structured patient-tailored chronic disease management with focus on self-management behaviours, the baseline lifestyle and other health behaviours of the sample participants recorded at the start of the program enables GPs to better understand individual needs and provide better quality of care However, upon completion, we expect that the findings of WellNet study will inform patients on the benefits of the PCMH model in terms of improved clinical outcomes and quality of care, as well as reduced risk of hospitalisation Author Contributions: Conceptualization, A.M.N.; methodology, F.G., A.M.N.; formal analysis, J.R.J., W.K.T., S.G., A.M.N., A.J.; investigation, A.M.N., A.J., F.G., J.R.J.; data curation, A.J., J.R.J., S.G.; writing—original draft preparation, J.R.J., W.K.T.; writing—review and editing, J.R.J., W.K.T., A.J., A.M.N.; supervision, W.K.T., F.G.; project administration, A.J.; funding acquisition, F.G. All authors have read and agreed to the published version of the manuscript Funding: J.R.J.’s PhD scholarship was provided by Capital Markets Cooperative Research Centre (Now Rozetta Institute). The funders did not have any role in the design, methods, analysis, or preparation of this manuscript Acknowledgments: We are particularly grateful to the WellNet participants for their active involvement and to the participating health care team from di ff erent primary care practices for their high-quality work Conflicts of Interest: J.R.J., W.K.T., S.G. and F.G. have no competing interests. A.M.N. works for AusTrials, which has received funds from the sponsor for the design and evaluation of the WellNet program. Previously, he was the Chief Medical O ffi cer of SCS. A.J. is employed by SCS as the Operational Manager Integrated Care and is responsible for the implementation of WellNet. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results References 1 Hay, S.I.; Abajobir, A.A.; Abate, K.H.; Abbafati, C.; Abbas, K.M.; Abd-Allah, F.; Abdulkader, R.S.; Abdulle, A.M.; Abebo, T.A.; Abera, S.F. Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016 Lancet 2017 , 390 , 1260–1344. [ CrossRef ] 2 Naghavi, M.; Abajobir, A.A.; Abbafati, C.; Abbas, K.M.; Abd-Allah, F.; Abera, S.F.; Aboyans, V.; Adetokunboh, O.; Afshin, A.; Agrawal, A. Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: A systematic analysis for the Global Burden of Disease Study 2016 Lancet 2017 , 390 , 1151–1210. [ CrossRef ] 3 Australian Institute of Health and Welfare: Australia’s health 2018. Available online: https: // www.aihw. gov.au / getmedia / fe 037 cf 1-0 cd 0-4663-a 8 c 0-67 cd 09 b 1 f 30 c / aihw-aus-222.pdf.aspx?inline = true (accessed on 10 June 2019) 4 Australian Bureau of Statistics: Causes of Death, Australia 2017. Available online: https: // www.abs.gov.au / ausstats / abs@.nsf / mf / 3303.0 (accessed on 22 June 2019) 5 Australian Bureau of Statistics: National Health Survey: First results 2014–15 2015. Available online: https: // www.ausstats.abs.gov.au / ausstats / subscriber.nsf / 0 / CDA 852 A 349 B 4 CEE 6 CA 257 F 150009 FC 53 / $File / national%20 health%20 survey%20 first%20 results,%202014-15.pdf (accessed on 15 June 2019) 6 Wang, L.; Palmer, A.J.; Cocker, F.; Sanderson, K. Multimorbidity and health-related quality of life (HRQoL) in a nationally representative population sample: Implications of count versus cluster method for defining multimorbidity on HRQoL Health Qual. Life Outcomes 2017 , 15 , 7. [ CrossRef ] [ PubMed ]

[[[ p. 18 ]]]

[Find the meaning and references behind the names: Foreman, Davies, Lee, Bower, Hallberg, Clark, Wol, Coventry, Mannino, Almeida, Barnett, Lovell, Arch, Aust, Hann, Hocking, Chew, Mercer, Emery, Clin, Prim, Sullivan, Loughlin, Mair, Htm, Nicholl, Attack, View, Jakobsson, Annu, Stratton, Main, Marquez, Bell, August, Mills, Jani, Martinez, Vyas, Ford, Dickens, Joc, Garrett, Divo, Cross, Cost, Camacho, Gibbons, Graham, Pan, Med, Mcdermott, Lange, Anderson, Gunn, Boyle, Guthrie, Watt, Clarke, Gallacher]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 18 of 21 7 Atlantis, E.; Sullivan, T.; Sartorius, N.; Almeida, O.P. Changes in the prevalence of psychological distress and use of antidepressants or anti-anxiety medications associated with comorbid chronic diseases in the adult Australian population, 2001–2008 Aust. NZJ Psychiatry 2012 , 46 , 445–456. [ CrossRef ] [ PubMed ] 8 Gallacher, K.I.; McQueenie, R.; Nicholl, B.; Jani, B.D.; Lee, D.; Mair, F.S. Risk factors and mortality associated with multimorbidity in people with stroke or transient ischaemic attack: A study of 8,751 UK Biobank participants JOC 2018 , 8 , 1–8. [ CrossRef ] [ PubMed ] 9 Condelius, A.; Edberg, A.-K.; Jakobsson, U.; Hallberg, I.R. Hospital admissions among people 65 + related to multimorbidity, municipal and outpatient care Arch. Gerontol. Geriat 2008 , 46 , 41–55. [ CrossRef ] [ PubMed ] 10 Wol ff , J.L.; Starfield, B.; Anderson, G. Prevalence, expenditures, and complications of multiple chronic conditions in the elderly Arch. Int. Med 2002 , 162 , 2269–2276. [ CrossRef ] 11 Vyas, A.; Pan, X.; Sambamoorthi, U. Chronic condition clusters and polypharmacy among adults Int. J Famiy. Med 2012 , 193168 , 1–8. [ CrossRef ] 12 Atlantis, E.; Lange, K.; Wittert, G.A. Chronic disease trends due to excess body weight in Australia Obes Rev 2009 , 10 , 543–553. [ CrossRef ] 13 Foreman, K.J.; Marquez, N.; Dolgert, A.; Fukutaki, K.; McGaughey, M.; Pletcher, M.A. Forecasting life expectancy, years of life lost, and all-cause and cause-specific mortality for 250 causes of death: Reference and alternative scenarios for 2016–40 for 195 countries and territories using data from the Global Burden of Disease Study 2016 Lancet 2018 , 392 , 2052–2090. [ CrossRef ] 14 Ford, E.S.; Capewell, S. Proportion of the decline in cardiovascular mortality disease due to prevention versus treatment: Public health versus clinical care Annu. Rev. Public Health 2011 , 32 , 5–22. [ CrossRef ] [ PubMed ] 15 Divo, M.J.; Martinez, C.H.; Mannino, D.M. Ageing and the epidemiology of multimorbidity Eur. Respir. J 2014 , 44 , 1055–1068. [ CrossRef ] [ PubMed ] 16 Lunenfeld, B.; Stratton, P. The clinical consequences of an ageing world and preventive strategies Best Pract Res. Clin. Obstet. Gynaecol 2013 , 27 , 643–659. [ CrossRef ] [ PubMed ] 17 Barnett, K.; Mercer, S.W.; Norbury, M.; Watt, G.; Wyke, S.; Guthrie, B. Epidemiology of multimorbidity and implications for health care, research, and medical education: A cross-sectional study Lancet 2012 , 380 , 37–43 [ CrossRef ] 18 Camacho, E.M.; Davies, L.M.; Hann, M.; Small, N.; Bower, P.; Chew-Graham, C.; Baguely, C.; Gask, L.; Dickens, C.M.; Lovell, K. Long-term clinical and cost-e ff ectiveness of collaborative care (versus usual care) for people with mental–physical multimorbidity: Cluster-randomised trial Br. J. Psychiatry 2018 , 213 , 456–463 [ CrossRef ] [ PubMed ] 19 Coventry, P.; Lovell, K.; Dickens, C.; Bower, P.; Chew-Graham, C.; McElvenny, D.; Hann, M.; Cherrington, A.; Garrett, C.; Gibbons, C.J. Integrated primary care for patients with mental and physical multimorbidity: Cluster randomised controlled trial of collaborative care for patients with depression comorbid with diabetes or cardiovascular disease BMJ 2015 , 350 , h 638. [ CrossRef ] 20 O’Loughlin, M.; Mills, J.; McDermott, R.; Harriss, L. Review of patient-reported experience within Patient-Centered Medical Homes: Insights for Australian Health Care Homes Aust. J. Prim. Health 2017 , 23 , 429–439. [ CrossRef ] 21 Australian Nursing Federation. Primary health care in Australia: A nursing and midwifery consensus view 2009. Available online: https: // anmf.org.au / documents / reports / PHC_Australia.pdf (accessed on 1 June 2019) 22 Department of Health. National Primary Health Care Strategic Framework 2013. Available online: https: // www.health.gov.au / internet / main / publishing.nsf / Content / 6084 A 04118674329 CA 257 BF 0001 A 349 E / $File / NPHCframe.pdf (accessed on 3 August 2019) 23 Commonwealth of Australia: National primary health care strategic framework 2016. Available online: https: // www 1.health.gov.au / internet / main / publishing.nsf / Content / 6084 A 04118674329 CA 257 BF 0001 A 349 E / $File / NPHCframe.pdf (accessed on 11 August 2019) 24 Department of Health: Australian Primary Care Collaboratives Programme 2014. Available online: https: // www.health.gov.au / internet / main / publishing.nsf / Content / health-pcd-programs-apccp-index.htm (accessed on 10 August 2019) 25 Canaway, R.; Boyle, D.I.; Manski-Nankervis, J.A.E.; Bell, J.; Hocking, J.S.; Clarke, K.; Clark, M.; Gunn, J.M.; Emery, J.D. Gathering data for decisions: Best practice use of primary care electronic records for research Med. J. Aust 2019 , 210 , S 12–S 16. [ CrossRef ]

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[Find the meaning and references behind the names: Excellence, Barron, Fam, Prada, Landon, Hughes, Lampe, Bitton, Bloom, Dolor, Davis, Martin, Chatterjee, Ann, Nice, Reid, Schneider, Ross, Lawrence, Gill, Doucette, Devries, Kendrick, Brown, Irvine, Hummel, Fishman, Grace, Powers, Ama, Tufano, Berk, Guide, Sridhar, Soman, Larson, Kemper, Jama, Graf, Gen, Chen, Willard, Meta, Pro, Serv, Jackson]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 19 of 21 26 Winzenberg, T.M.; Gill, G.F. Prioritising general practice research Med. J. Aust 2016 , 205 , 55–57. [ CrossRef ] [ PubMed ] 27 Jackson, G.L.; Powers, B.J.; Chatterjee, R.; Bettger, J.P.; Kemper, A.R.; Hasselblad, V.; Dolor, R.J.; Irvine, R.J.; Heidenfelder, B.L.; Kendrick, A.S. The patient-centered medical Home: A Systematic review Ann. Intern Med 2013 , 158 , 169–178. [ CrossRef ] 28 Australian Medical Association. AMA Position Statement on the Medical Home 2015. Available online: https: // ama.com.au / position-statement / ama-position-statement-medical-home (accessed on 13 June 2019) 29 Bodenheimer, T.; Ghorob, A.; Willard-Grace, R.; Grumbach, K. The 10 building blocks of high-performing primary care Ann. Fam. Med 2014 , 12 , 166–171. [ CrossRef ] [ PubMed ] 30 Berk-Clark, C.; Doucette, E.; Rottnek, F.; Manard, W.; Prada, M.A.; Hughes, R.; Lawrence, T.; Schneider, F.D. Do Patient-Centered Medical Homes Improve Health Behaviors, Outcomes, and Experiences of Low-Income Patients? A Systematic Review and Meta-Analysis Health Serv. Res 2018 , 53 , 1777–1798. [ CrossRef ] [ PubMed ] 31 Maeng, D.D.; Graf, T.R.; Davis, D.E.; Tomcavage, J.; Bloom Jr, F.J. Can a patient-centered medical home lead to better patient outcomes? The quality implications of Geisinger’s ProvenHealth Navigator Am. J. Med Qual 2012 , 27 , 210–216. [ CrossRef ] [ PubMed ] 32 Bitton, A.; Martin, C.; Landon, B.E. A Nationwide Survey of Patient Centered Medical Home Demonstration Projects J. Gen. Intern. Med 2010 , 25 , 584–592. [ CrossRef ] 33 DeVries, A.; Li, C.-H.W.; Sridhar, G.; Hummel, J.R.; Breidbart, S.; Barron, J.J. Impact of medical homes on quality, healthcare utilization, and costs Am. J. Manag. Care 2012 , 18 , 534–544 34 Peikes, D.; Chen, A.; Schore, J.; Brown, R. E ff ects of care coordination on hospitalization, quality of care, and health care expenditures among medicare beneficiaries: 15 randomized trials JAMA 2009 , 301 , 603–618 [ CrossRef ] 35 Reid, R.J.; Fishman, P.A.; Yu, O.; Ross, T.R.; Tufano, J.T.; Soman, M.P.; Larson, E.B. Patient-centered medical home demonstration: A prospective, quasi-experimental, before and after evaluation Am. J. Manag. Care 2009 , 15 , e 71–e 87. [ PubMed ] 36 Global Initiative for Chronic Obstructive Lung Disease: Global Strategy for Diagnosis, Management, and Prevention of COPD 2016. Available online: https: // goldcopd.org / global-strategy-diagnosis-managementprevention-copd-2016 / (accessed on 10 May 2019) 37 Lampe, L. Drug treatment for anxiety Aust. Prescr 2013 , 36 , 186–189. [ CrossRef ] 38 National Heart Foundation of Australia: Guide to management of hypertension (2008 updated 2010) 2010 Available online: https: // www.healthylivingnt.org.au / system / files / f / HypertensionGuidelines 2008 QRG 2010 Update.pdf (accessed on 1 May 2019) 39 National Heart Foundation of Australia: Guideline for the diagnosis and management of hypertension in adults 2016. Available online: https: // www.heartfoundation.org.au / images / uploads / publications / PRO-167_ Hypertension-guideline-2016_WEB.pdf (accessed on 11 June 2019) 40 National Heart Foundation of Australia and the Cardiac Society of Australia and New Zealand: Guidelines for the prevention, detection and management of chronic heart failure in Australia 2011 Available online: https: // www.heartfoundation.org.au / images / uploads / publications / Chronic_Heart_Failure_ Guidelines_2011.pdf (accessed on 11 June 2019) 41 National Institute for Health and Care Excellence: Hypertension in adults: Diagnosis and management 2011 Available online: https: // www.nice.org.uk / guidance / cg 127 (accessed on 13 June 2019) 42 National Institute for Health and Care Excellence: Type 1 diabetes in adults: Diagnosis and management 2015. Available online: https: // www.nice.org.uk / guidance / ng 17 (accessed on 12 June 2019) 43 National Institute for Health and Care Excellence: Chronic heart failure in adults: Diagnosis and management 2018. Available online: https: // www.nice.org.uk / guidance / ng 106 (accessed on 11 June 2019) 44 National Institute for Health and Care Excellence: Recognition, assessment and initial management of depression in adults 2018. Available online: http: // pathways.nice.org.uk / pathways / depression (accessed on 10 June 2019) 45 National Prescribing Service. Managing Blood Pressure based on Absolute Risk 2016. Available online: https: // www.nps.org.au / medical-info / clinical-topics / blood-pressure (accessed on 16 June 2019).

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[Find the meaning and references behind the names: Slade, Mcdonald, Hibbard, Badia, Jalaluddin, Soc, King, Jenkins, Parkin, Berry, Harding, East, Mitchell, Development, Tonkin, Wiklund, Janssen, Henry, Franke, Franklin, Smith, Melbourne, Mahoney, Padgett, Simple, Lyman, Full, Balance, Sager, Porro, Phillips, Kind, Andrews, Shaw, Magliano, Crawford, Lloyd, Yang, Leidy, Scales]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 20 of 21 46 National Prescribing Service Blood pressure treatment targets 2016 Available online: www.nps.org.au / conditions / heart-blood-and-blood-vessel-conditions / blood-pressure / for-health-professionals / managing-blood-pressure-based-on-absolute-risk / bp-treatment-targets (accessed on 14 June 2019) 47 National Prescribing Service. Non-pharmacological management of depression 2016. Available online: https: // www.nps.org.au / news / medicinewise-news-exploring-non-drug-options-in-depression (accessed on 11 June 2019) 48 National Prescribing Service Understanding high blood pressure 2017 Available online: www.nps.org.au / conditions / heart-blood-and-blood-vessel-conditions / blood-pressure / for-individuals / understanding-high-blood-pressure (accessed on 10 June 2019) 49 National Vascular Disease Prevention Alliance: Guidelines for the management of absolute cardiovascular disease risk 2012. Available online: https: // www.heartfoundation.org.au / images / uploads / publications / Absolute-CVD-Risk-Full-Guidelines.pdf (accessed on 18 June 2019) 50 The Royal Australian College of General Practitioners: General practice management of type 2 diabetes: 2016–18. East Melbourne 2016. Available online: https: // static.diabetesaustralia.com.au / s / fileassets / diabetesaustralia / 5 d 3298 b 2-abf 3-487 e-9 d 5 e-0558566 fc 242.pdf (accessed on 11 June 2019) 51 Yang, I.; Brown, J.; George, J.; Jenkins, S.; McDonald, C.; McDonald, V.; Smith, B.; Zwar, N.; Dabscheck, E The COPD-X Plan: Australian and New Zealand Guidelines for the management of Chronic Obstructive Pulmonary Disease Med. J. Aust 2018 , 207 , 436–442. [ CrossRef ] 52 Department of Health: Evaluation Report of the Diabetes Care Project 2015 Available online: https: // www.health.gov.au / internet / main / publishing.nsf / Content / 302 DF 0372 F 537 A 43 CA 257 E 35000138 E 8 / $File / DCP%20 Evaluation%20 Report.pdf (accessed on 17 June 2019) 53 Primary Health Care Advisory Group: Better Outcomes for People with Chronic and Complex Health Conditions 2016 Available online: https: // www.health.gov.au / internet / main / publishing.nsf / Content / 76 B 2 BDC 12 AE 54540 CA 257 F 72001102 B 9 / $File / Primary-Health-Care-Advisory-Group_Final-Report.pdf (accessed on 11 June 2019) 54 Leelani, K. Impact on diabetes management of general practice management plans, team care arrangements and reviews Med. J. Aust 2013 , 199 , 261–265 55 Lacus, S.M.; King, G.; Porro, G. Causal inference without balance checking: Coarsened exact matching Political. Anal 2012 , 20 , 1–24 56 Andrews, G.; Slade, T. Interpreting scores on the Kessler psychological distress scale (K 10) Aust. NZJ Public Health 2001 , 25 , 494–497. [ CrossRef ] [ PubMed ] 57 Chen, L.; Magliano, D.J.; Balkau, B.; Colagiuri, S.; Zimmet, P.Z.; Tonkin, A.M.; Mitchell, P.; Phillips, P.J.; Shaw, J.E. AUSDRISK: An Australian Type 2 Diabetes Risk Assessment Tool based on demographic, lifestyle and simple anthropometric measures Med. J. Aust 2010 , 192 , 197. [ CrossRef ] [ PubMed ] 58 Henry, J.D.; Crawford, J.R. The short-form version of the Depression Anxiety Stress Scales (DASS-21): Construct validity and normative data in a large non-clinical sample Br. J. Clin. Psychol 2005 , 44 , 227–239 [ CrossRef ] 59 Herdman, M.; Gudex, C.; Lloyd, A.; Janssen, M.; Kind, P.; Parkin, D.; Bonsel, G.; Badia, X. Development and preliminary testing of the new five-level version of EQ-5 D (EQ-5 D-5 L) Qual. Life Re.s 2011 , 20 , 1727–1736 [ CrossRef ] 60 Hibbard, J.H.; Stockard, J.; Mahoney, E.R.; Tusler, M. Development of the Patient Activation Measure (PAM): Conceptualizing and measuring activation in patients and consumers Health Serv. Res 2004 , 39 , 1005–1026 [ CrossRef ] 61 Jones, P.; Harding, G.; Berry, P.; Wiklund, I.; Chen, W.; Leidy, N.K. Development and first validation of the COPD Assessment Test Eur. Resp. J 2009 , 34 , 648–654. [ CrossRef ] 62 Lyman, S.; Lee, Y.-Y.; Franklin, P.D.; Li, W.; Cross, M.B.; Padgett, D.E. Validation of the KOOS, JR: A short-form knee arthroplasty outcomes survey Clin. Orthop. Relat. Res 2016 , 474 , 1461–1471. [ CrossRef ] 63 Lyman, S.; Lee, Y.-Y.; Franklin, P.D.; Li, W.; Mayman, D.J.; Padgett, D.E. Validation of the HOOS, JR: A short-form hip replacement survey Clin. Orthop. Relat. Res 2016 , 474 , 1472–1482. [ CrossRef ] 64 Sager, M.A.; Rudberg, M.A.; Jalaluddin, M.; Franke, T.; Inouye, S.K.; Landefeld, C.S.; Siebens, H.; Winograd, C.H. Hospital admission risk profile (HARP): Identifying older patients at risk for functional decline following acute medical illness and hospitalization J. Am. Geriatr. Soc 1996 , 44 , 251–257. [ CrossRef ]

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[Find the meaning and references behind the names: Liu, Hazell, Basel, Britt, Popescu, Brett, Cao, Kothari, Liang, Linehan, Sci, Holman, Moorhead, Frank, China, Arnold, Under, Knox, Reed, Open, Soliman, Adler, Miller, Harrison, Guo, Stevens, Fine]

Int. J. Environ. Res. Public Health 2020 , 17 , 2164 21 of 21 65 Stevens, R.J.; Kothari, V.; Adler, A.I.; Stratton, I.M.; Holman, R.R. The UKPDS risk engine: A model for the risk of coronary heart disease in Type II diabetes (UKPDS 56) Clin. Sci 2001 , 101 , 671–679. [ CrossRef ] [ PubMed ] 66 Brett, T.; Arnold-Reed, D.E.; Popescu, A.; Soliman, B.; Bulsara, M.K.; Fine, H.; Bovell, G.; Moorhead, R.G. Multimorbidity in Patients Attending 2 Australian Primary Care Practices Ann Fam Med 2013 , 11 , 535–542 [ CrossRef ] [ PubMed ] 67 Britt, H.C.; Harrison, C.M.; Miller, G.C.; Knox, S.A. Prevalence and patterns of multimorbidity in Australia Med. J. Aust 2008 , 189 , 72–77. [ CrossRef ] 68 Heyworth, I.T.; Hazell, M.L.; Linehan, M.F.; Frank, T.L. How do common chronic conditions a ff ect health-related quality of life? Br. J. Gen. Pract 2009 , 59 , e 353–e 358. [ CrossRef ] [ PubMed ] 69 Tan, Z.; Liang, Y.; Liu, S.; Cao, W.; Tu, H.; Guo, L.; Xu, Y. Health-related quality of life as measured with EQ-5 D among populations with and without specific chronic conditions: A population-based survey in Shaanxi Province, China PLoS One 2013 , 8 , e 65958. [ CrossRef ] [ PubMed ] © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http: // creativecommons.org / licenses / by / 4.0 / ).

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