Christine F. Mcdonald

Christine F. Mcdonald

PhD, MBBS (Hons), FRACP, FCCP

Pulmonologist

Over 20 years of experience in respiratory and sleep medicine

Female📍 Heidelberg

About of Christine F. Mcdonald

Christine F. Mcdonald is a pulmonologist based at 145 Studley Road, Heidelberg, VIC 3084, Australia. She also looks after sleep-related breathing problems, so her work often spans both lungs and sleep health.


Over the past 20+ years, Christine has worked in respiratory and sleep medicine. In day-to-day practice, that can mean supporting people with ongoing lung conditions as well as helping when things suddenly get worse. At times, this includes families and carers, because breathing problems can be stressful and tiring to deal with.


Christine treats a wide range of respiratory issues. This can include asthma, chronic obstructive pulmonary disease (COPD), bronchiectasis, and lung infections like pneumonia. She also helps manage long-term scarring and stiffness of the lungs, including interstitial lung disease and pulmonary fibrosis. People with pleurisy or lung nodules may also be referred to her for careful assessment and follow-up.


Sleep is another big part of the job. Christine works with people who have obstructive sleep apnoea and other breathing issues that show up during sleep. Getting the right diagnosis and ongoing support can make a real difference to day-time energy, sleep quality, and overall health.


Some patients she sees have more complex needs, such as breathing issues after serious viral illnesses, including COVID-19 or long COVID. Others may be dealing with reduced breathing efficiency linked to neurological conditions, where oxygen levels and breathing control need extra attention. At times, she also helps manage problems around the lungs related to cancers, including lung cancer, and makes sure treatment plans are practical and well coordinated.


Christine’s training includes an MBBS (Hons) and a PhD, as well as specialist qualifications through the Royal Australasian College of Physicians. She also holds FRACP and FCCP. That mix of clinical work and research helps her keep up with new evidence without losing the simple, hands-on focus patients need.


She has also been involved in medical publications and clinical trials. This means she stays across better ways to assess lung and sleep conditions, and she can talk through options clearly when new treatments are being studied.


If you’re looking for a pulmonologist who takes respiratory and sleep care seriously, Christine brings a calm, grounded approach that aims to keep things understandable, step by step.

Education

  • MBBS (Hons); University of Melbourne
  • FRACP; Royal Australasian College of Physicians
  • PhD

Services & Conditions Treated

Brain TumorChronic Obstructive Pulmonary Disease (COPD)Acute Interstitial PneumoniaInterstitial Lung DiseaseAsthmaCerebral HypoxiaCOVID-19Cystic FibrosisIdiopathic Pulmonary FibrosisLung CancerPleurisyPneumoniaPulmonary FibrosisSilicosisAcute Respiratory Distress Syndrome (ARDS)Allergic RhinitisAsbestosisAstrocytomaBronchiectasisColitisCramp-Fasciculation SyndromeCrohn's DiseaseGlioblastomaGliomaGliomatosis CerebriHypertensionLong Haul COVIDLung AdenocarcinomaLung NodulesLymphofollicular HyperplasiaMeaslesNon-Small Cell Lung Cancer (NSCLC)Obesity Hypoventilation Syndrome (OHS)Obstructive Sleep ApneaParainfluenzaPneumomediastinumPulmonary EmbolismRadiation EnteritisRelapsing PolychondritisRuvalcaba SyndromeSevere Acute Respiratory Syndrome (SARS)Subacute Sclerosing PanencephalitisViral Gastroenteritis

Publications

5 total
Factors Associated with Seeking and Receiving Home Antiviral Therapy During the COVID-19 Pandemic.

MedRxiv : The Preprint Server For Health Sciences • June 10, 2025

Stuart Quan, Matthew Weaver, Mark Czeisler, Lauren Booker, Mark Howard, Melinda Jackson, Christine Mcdonald, Anna Ridgers, Rebecca Robbins, Prerna Varma, Shantha M Rajaratnam, Charles Czeisler

Home antiviral treatment (HAVT: nirmatrelvir/ritonavir [Paxlovid] and molnupiravir [Lagevrio]) for COVID-19 was approved in December 2021 by the U.S. Food and Drug Administration, but ensuing utilization during the COVID-19 pandemic was low. Factors associated with seeking HAVT treatment have not been fully explored. Cross-sectional survey of 9,944 U.S. adults to identify factors associated with seeking and receiving HAVT in persons with confirmed or suspected COVID-19. COVID-19 infection was confirmed or suspected in 4,355 (43.8%) participants. HAVT was sought by 1,331 (26.3%) and medication was received by 928 (20.7%). In comparison to those who were COVID-19 test negative and had no loss of taste or smell (aOR: 1.856, 95% C.I.: 1.262-2.728), the factor most associated with seeking HAVT was a loss of taste or smell irrespective of a positive (aOR: 3.823, 95% C.I.: 2.626-5.567) or negative COVID-19 test (aOR: 3.306; 95% C.I.: 2.086-5.241). Loss of taste or smell was similarly associated with receiving HAVT. Male sex, younger age, Black race, Hispanic ethnicity, conservative or liberal political preference, and medical discrimination were some of the other factors associated with a greater likelihood of seeking HAVT. Barriers to obtaining treatment included feeling uncomfortable obtaining HAVT while sick and lack of transportation; 14.7% of those seeking treatment reported at least one barrier. In a general population, HAVT was an underutilized resource during the COVID-19 pandemic. Loss of taste or smell was the most important factor among several others associated with seeking HAVT irrespective of COVID-19 test status.

Thoracic Society of Australia and New Zealand (TSANZ) Is Abrogating Its Leadership Role in Asia-Pacific.

Respirology (Carlton, Vic.) • January 05, 2025

Philip Bardin, Christine Mcdonald, Debra Sandford, Gregory King, Christine Jenkins, Paul Reynolds

Lately, as numerous world events with life-changing consequences across the globe unfold, we have been reflecting upon relationships and how they can guide, and enhance, but also destroy. Relationships can be tricky to navigate and should never be assumed to be immutable. This topic has been especially at the forefront as the tenure of the Co-editors in Chief of Respirology draws to a close and after the recent 2024 Asia-Pacific Society of Respirology (APSR) Congress in Hong Kong. Since 2023/2024, the Board of the Thoracic Society of Australia and New Zealand (TSANZ) decided to pause en bloc membership of APSR. We believe this to be a regrettable ‘own goal’ and a decision that is not supported by members of the society. If this decision is not reversed, the leadership role and hard-won influence of TSANZ in this key geographic area are likely to be permanently damaged and may ultimately be squandered. The history of APSR bears reviewing. It was started in the late 1980s by Professors Ann Woolcock, an icon of Australian Respiratory Medicine, and Yoshi Fukuchi from Japan. They anticipated the rise of the Asia-Pacific as a major geographical region able to compete with the Americas and Europe. That has indeed been the case and the Asia-Pacific is now an economic (and political) powerhouse that is predicted to account for > 50% of global economic output by 2050. Ann believed that Australia was geographically linked closely to Asia-Pacific and had a key educational, scientific and leadership role to play in the region. She also understood that Australia had to wean from our colonial origins in Europe to become active contributors in the Asia-Pacific. Since the APSR's inception, the members of TSANZ have made large contributions to the APSR including Norbert Berend, Phil Thompson, Jane Bourke, Kwun Fong, Cheryl Salome, Guy Marks along with numerous other members who were involved in APSR activities. Importantly, the APSR journal, Respirology, has played an important role to raise the level of scientific publishing in the region. Joining the editorial team at Respirology has provided opportunity for junior TSANZ members and faculty to get involved in the world of publishing and to upskill in this field. By not continuing with en bloc membership of the APSR, TSANZ members risk losing these and other benefits. TSANZ disengagement with APSR will likely have other unforeseen detrimental effects. TSANZ members will be unable to hold APSR executive positions or to lead APSR interest groups and will lose access to the expedited peer review process afforded to en-bloc society position papers. TSANZ will also be unable to host the APSR Annual Scientific Meeting. It is clearly incumbent on TSANZ to negotiate the best financial and membership arrangements with APSR for its members. However, change is more easily achieved from within, than from without. TSANZ has an opportunity to advance its aims (e.g., to facilitate diversity and inclusivity in the region) within APSR, but such influence and actions are more challenging when TSANZ members are no longer part of the APSR. Ultimately it is up to individual TSANZ members to take advantage of en bloc membership. Like joining a gym, members might not take advantage of all the gym has to offer, all the time, but it is there for members to utilize if they so choose. Importantly, the APSR is in a phase of modernization and advancement, and there is much goodwill towards Australia despite the recent decision to halt en bloc membership. When en bloc membership is again reviewed by the TSANZ Board, the wider TSANZ membership should be consulted if continued disengagement, a momentous step, is to be further contemplated. It is our view—and we believe likely shared by many TSANZ members—that en bloc membership should not have been cancelled without wider consultation. We urgently request that TSANZ reconsiders this decision at the earliest possible time. We believe TSANZ has an important leadership role to play in the Asia-Pacific via our membership of APSR. This is ‘our place’ and our involvement will have a large impact by way of educational, clinical and scientific contributions from TSANZ members. We urge TSANZ and the membership not to miss this opportunity to continue to facilitate the advancement of respiratory and sleep medicine in our region.

Home-Based Exercise and Self-Management After Lung Cancer Resection: A Randomized Clinical Trial.

JAMA Network Open • December 02, 2024

Catherine Granger, Lara Edbrooke, Phillip Antippa, Gavin Wright, Christine Mcdonald, Diana Zannino, Shaza Abo, Meinir Krishnasamy, Louis Irving, Karen Lamb, Georgina Whish Wilson, Linda Denehy, Selina Parry

Importance: Patients with lung cancer have poor physical functioning and quality of life. Despite promising outcomes for those who undertake exercise programs, implementation into practice of previously tested hospital-based programs is rare. Objective: To evaluate a home-based exercise and self-management program for patients after lung resection. Design, setting, and participants: A randomized clinical trial with assessor blinding was conducted among 116 patients undergoing surgery for non-small cell lung cancer from November 23, 2017, to July 31, 2023, at tertiary hospitals in Australia. Patients were followed up for 12 months postoperatively. Intervention: Patients randomized to the intervention group received a postoperative 3-month home-based exercise and self-management program, supported by weekly physiotherapist-led telephone consultations. Patients randomized to the control group received usual care. Main outcomes and measures: The primary outcome was self-reported physical function (30-item European Organization for the Research and Treatment of Cancer Core Quality of Life Questionnaire [EORTC QLQ-C30] score) at 3 months. Secondary outcomes included objective measures of physical function and exercise capacity (at 3 and 6 months) and patient-reported outcomes including quality of life (at 3 and 6 months, with some questionnaires completed at 12 months). Analysis was performed on an intent-to-treat basis. Results: A total of 1370 patients were screened, with 177 eligible and 116 consented (mean [SD] age, 66.4 [9.6] years; 68 women [58.6%]). Of these 116 patients, 58 were randomized to the intervention and 58 to the control. A total of 103 patients (88.8%) completed assessments at 3 months, 95 (81.9%) at 6 months, and 95 (81.9%) at 12 months. There were no statistically significant differences between the intervention and control groups for self-reported physical function (EORTC QLQ-C30 physical functioning domain score) at the 3-month primary end point (mean [SD] score, 77.3 [20.9] vs 76.3 [18.8]; mean difference, 1.0 point [95% CI, -6.0 to 8.0 points]). Patients in the intervention group, compared with the control group, had significantly greater exercise capacity (6-minute walk distance: mean difference, 39.7 m [95% CI, 6.8-72.6 m]), global quality of life (mean difference, 7.1 points [95% CI, 0.4-13.8 points]), and exercise self-efficacy (mean difference, 16.0 points [95% CI, 7.0-24.9 points]) at 3 months as well as greater objectively measured physical function (Short Physical Performance Battery score: mean difference, 0.8 points [95% CI, 0.1-1.6 points]), exercise capacity (6-minute walk distance: mean difference, 50.9 m [95% CI, 6.7-95.1 m]), and exercise self-efficacy (mean difference, 10.1 points [95% CI, 1.9-18.2 points]) at 6 months. One minor adverse event and no serious adverse events occurred. Conclusions and relevance: In this randomized clinical trial, a postoperative home-based exercise and self-management program did not improve self-reported physical function in patients with lung cancer. However, it did improve other important clinical outcomes. Implementation of this program into lung cancer care should be considered. Trial registration: http://anzctr.org.au Identifier: ACTRN12617001283369.

Thoracic Society of Australia and New Zealand (TSANZ) Guidance for the Management of Electronic Cigarette Use (Vaping) in Adolescents and Adults.

Respirology (Carlton, Vic.) • October 02, 2024

Henry Marshall, Moya Vandeleur, Emma Dean, Chris Barton, Nia Luxton, Kristin Carson Chahhoud, Andre Schultz, Janet Williams, Tahlia Grammatopoulos, Emily Stone, Smita Shah, Stuart Jones, Christine Mcdonald, Matthew Peters

Electronic cigarette (EC) use, especially among younger members of society, has grown to concerning levels in many countries, including Australia and New Zealand. Uptake in the general population, driven by technological and pharmacological innovations, and accelerated by aggressive tobacco/vaping industry marketing, has outpaced medical research. As the harms of EC use become increasingly evident, the Australian Government has introduced policies to curb recreational EC use, whilst still allowing access for smoking cessation. This highly dynamic environment presents new challenges to clinicians as the evidence to support clinical practice with respect to vaping use and its cessation remains very limited. This guidance document from the Thoracic Society of Australia and New Zealand aims to address this unmet need by offering practical advice for clinicians to help protect their patients' lung and general health by: preventing EC uptake in children, adolescents, and young adults; providing guidance for ceasing EC use in adolescents and adults who have never smoked; and providing guidance for ceasing EC use in people who currently or formerly smoked who now use EC long-term. Underpinned by a systematic review, this multidisciplinary expert consensus document summarises the current landscape of EC use, nicotine addiction, behavioural and pharmacotherapy treatments. Illustrative case vignettes are provided. The advice, largely extrapolated from the smoking cessation literature, is based on the consensus of the authors in the absence of high-quality randomised trials for vaping cessation and is applicable to all age groups. We emphasise the urgent unmet need for vaping-specific cessation research to inform future practice.

Clinical Trials

2 total

A Pragmatic, Phase III, Multi-site, Double-blind, Placebo Controlled, Parallel Arm, Dose Increment Randomised Trial of Regular, Low Dose Extended Release Morphine for Chronic Refractory Breathlessness

CompletedPhase 3

Breathlessness is an overwhelming symptom affecting tens of thousands of Australians every day. For many people, it persists even when all the underlying causes have been optimally managed (chronic breathlessness). In these circumstances, it often occurs at rest or with minimal exertion. Evidence from a number of clinical studies suggests that a small, regular dose of morphine helps to reduce safely the sensation of breathlessness. However, it is not well established which patients derive more benefit and what is the net clinical effect of this treatment (weighing benefits and harms). This is a phase III, multi-site, randomised, double-blind, placebo-controlled trial with patients with chronic obstructive pulmonary disease (COPD) and severe chronic breathlessness which will explore several important questions: * Are regular, low doses of morphine at four possible doses over 3 weeks more effective than placebo at improving breathlessness? * Does increasing the dose in people who already are experiencing some benefit provide even greater reduction in worst breathlessness? * Does the medication have any effect on daily activity and quality of life? * What are the common or serious side effects of this intervention? * Does the benefit from the medication outweigh the side effects it produces? * Are there specific characteristics of people who are more likely to receive benefit from extended release morphine? Participants will receive once daily extended release morphine (plus laxative, docusate with senna), or placebo (placebo laxative) in addition to their usual medication for up to 3 weeks at increasing doses. Participants will have a medical interview and physical examination to collect some general health information, and baseline measurements including; daily activity, symptoms, and quality of life. A small amount of blood may be required to check eligibility. Further blood samples may be taken at week 1 and 3 to enable testing on how individuals respond to opioids, further consent will be obtained for these samples. Data on benefits, side effects, and medical care will be collected during comprehensive weekly visits. Participants will also fill out a simple diary twice daily for weeks one to three of the study, and for one day each week during an optional 6 month extension stage. The outcome of this study may enable better management of symptoms and activity in people COPD with medicines that are shown to be effective and safe.

Participants: 171

Benefits and Costs of Home-based Pulmonary Rehabilitation in Chronic Obstructive Pulmonary Disease

Completed Phase 3

Pulmonary rehabilitation is an effective treatment for people with chronic obstructive pulmonary disease (COPD) which improves symptoms, reduces hospitalisation and lowers healthcare costs. However less than 1% of Australians with COPD receive pulmonary rehabilitation each year, due to poor access to programs and high levels of disability. This randomised controlled trial will examine the benefits and costs of a novel, entirely home-based pulmonary rehabilitation program for COPD. We hypothesise that home-based pulmonary rehabilitation can deliver equivalent clinical outcomes at lower cost than the centre-based program. We will randomly allocate 144 people with COPD to undertake either standard pulmonary rehabilitation in a hospital setting, or a low-cost home-based program. Those who undertake pulmonary rehabilitation in the hospital setting will attend the hospital twice each week for eight weeks for supervised exercise training and education. People in the home pulmonary rehabilitation group will receive one home visit and weekly telephone calls for eight weeks, for supervision and mentoring of exercise and provision of education. We will compare the number of people who complete the program in each setting. We will also test whether the groups have similar results for the standard pulmonary rehabilitation outcomes of breathlessness, quality of life and exercise capacity, at the end of the program and 12 months later. We will compare health care costs and personal costs between groups after 12 months. If home-based pulmonary rehabilitation can improve uptake of this important treatment, deliver good clinical outcomes and reduce costs this will have significant and long-lasting benefits for patients, the community and the health system

Participants: 144

Frequently Asked Questions

What services does Dr Christine Mcdonald offer?
Dr Mcdonald provides expert care in respiratory and sleep medicine, covering conditions such as COPD, asthma, interstitial lung disease, idiopathic pulmonary fibrosis, lung cancer, pneumonia, pleurisy, bronchiectasis, pulmonary embolism and long haul COVID, among others.
What conditions does she treat?
She treats a range of lung and sleep-related conditions, including COPD, asthma, ILD, pulmonary fibrosis, lung nodules, lung cancer, pneumonia, ARDS, sleep apnoea and related respiratory issues.
Where is the clinic located?
The practice is at 145 Studley Road, Heidelberg, VIC 3084, Australia.
How do I book an appointment?
To book an appointment, contact the clinic directly or use the practice's booking options available at the Heidelberg location.
Does she have experience in sleep medicine?
Yes. Dr Mcdonald has extensive experience in respiratory and sleep medicine, with over 20 years in the field.
What should I bring to my first visit?
Bring any relevant medical records, tests, or imaging related to your lung or sleep concerns, and a list of current medications.

Contact Information

145 Studley Road, Heidelberg, VIC 3084, Australia

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Memberships

  • Fellow of the Royal Australasian College of Physicians (RACP)
  • Fellow of the American College of Chest Physicians (ACCP)
  • Member of the Thoracic Society of Australia and New Zealand (TSANZ)
  • Member of the Australian and New Zealand Society of Respiratory Science (ANZSRS)