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5 things COPD patients want their doctors to know, according to real patients and caregivers

MDlinx Oct 11, 2024

Chronic obstructive pulmonary disease (COPD) patients face complex challenges in their care, from difficulties accessing healthcare to inadequate education about managing their condition. These patients have three primary domains of unmet needs: First, a lack of sufficient information about the disease; second, inadequate physical, emotional, social, financial, and spiritual support; and third, gaps in overall care provision.

Rajnoveanu RM, Rajnoveanu AG, Fildan AP, et al. Palliative care initiation in chronic obstructive pulmonary disease: prognosis-based, symptoms-based or needs-based? Int J Chron Obstruct Pulmon Dis. 2020;15:1591-1600.

 

 

 

Many of these gaps lead to frustration and make managing COPD even more difficult for physicians and patients alike. Based on patient feedback and recent studies, here are the top-five things COPD patients want their doctors to know.

 

Breathlessness dominates daily life

 

Breathlessness is more than just a symptom; it permeates nearly every aspect of a COPD patient's life, with many patients living in a constant state of anxiety about their breathing. As one described it, “The breathlessness when I’m really unwell makes everything such an effort, and it’s scary.”

Early F, Lettis M, Winders SJ, et al. What matters to people with COPD: outputs from Working Together for Change. NPJ Prim Care Respir Med. 2019;29(1):11.

 

I put off doing things because of fear of attacks of breathlessness.

This debilitating symptom affects routine activities such as cooking, dressing, and household chores, as noted in a report from BCM Pulmonary Medicine.

Sumner J, Bundele A, Shankar R, et al. Living with COPD: understanding patient experiences through the lens of photovoice. BMC Pulm Med. 2023;23(1):433.

 

 

The mental and emotional toll is overwhelming

 

COPD patients endure emotional distress, including anxiety, depression, and fear—especially surrounding exacerbations and breathlessness.

Early F, Lettis M, Winders SJ, et al. What matters to people with COPD: outputs from Working Together for Change. NPJ Prim Care Respir Med. 2019;29(1):11.

 

In a research study using one-to-one discussions with patients, some expressed the feeling that they are not treated on a personal level by the healthcare system.

Early F, Lettis M, Winders SJ, et al. What matters to people with COPD: outputs from Working Together for Change. NPJ Prim Care Respir Med. 2019;29(1):11.

They feel they are “pre-judged” owing to their symptoms, and a lack of personal connection with healthcare providers compounds these feelings.

 

As one patient indicated, “I get COPD treated, not my COPD; look at me, not the computer when I come to see you—I want you to listen.”

Early F, Lettis M, Winders SJ, et al. What matters to people with COPD: outputs from Working Together for Change. NPJ Prim Care Respir Med. 2019;29(1):11.

 

Another said, “[My] nurses and the doctors are too busy, and they do not seem to have time to talk to me about my worries. In a way, I think the doctors and nurses are tired of me because I have been hospitalised so many times.”

COPD Athlete. Melodie Burnett – COPD Patient. March 20, 2017.

 

Carrying medical equipment everywhere can also make some COPD patients feel embarrassed. As one patient shared on the website COPD Athlete: “I was diagnosed with COPD at the age of 47 and had never smoked a day in my life. I spent several months carrying a nebulizer machine with me wherever I went. I carried the machine to work with me, going to isolated places to take my treatments because I was embarrassed.”

COPD Athlete. Melodie Burnett – COPD Patient. March 20, 2017.

 

 

Patients want better education and resources

 

COPD patients frequently report that they lack sufficient education on managing exacerbations and self-care strategies. 

 

In the words of COPD patient John Linnell, “Exacerbation is at first a seemingly complicated word for a patient, which physicians should realize.” Many times, patients find it difficult to distinguish between a "bad day" and a true exacerbation.

Linnell J, Hurst JR. COPD exacerbations: a patient and physician’s perspective. Adv Ther. 2020;37:10–16.

 

A caregiver for a COPD patient, Kristen Willard, shared with the COPD Foundation, “I wish perhaps most strongly that we had known there were so many things you could do to manage COPD successfully, steps we could take to set my father up for success. These included pulmonary rehabilitation, getting regular vaccinations, avoiding infections, using inhalers and nebulizers as intended, and approaching life in a way that allowed him to expend his remaining energy on things that were most important to him.”

Willard K. When a New Diagnosis Takes Your Breath Away. COPD Foundation. June 24, 2021.

 

 

 

Post-hospitalization care is often inadequate

 

After discharge, COPD patients frequently feel abandoned by the healthcare system. Effective post-hospitalization care is critical, yet many patients lack regular follow-up appointments and preventive measures.

Ghamari S, Mohebi F, Peiman S, et al. Patient experience with chronic obstructive pulmonary disease: a nationally representative demonstration study on quality and cost of healthcare services. Front Public Health. 2023;11:1112072.

 

 

One patient expressed frustration with the fragmented healthcare system, stating, “‘I was supposed to have my own personal training programme, but then suddenly I was moved [to another hospital]...so it came to nothing...I’m just sitting and waiting...”

Andersen IC, Thomsen TG, Bruun P, et al. Between hope and hopelessness: COPD patients' and their family members' experiences of interacting with healthcare providers - a qualitative longitudinal study. Scand J Caring Sci. 2018;32(3):1197-1206.

 

 

There are too many barriers

 

COPD patients also struggle to access timely care and specialist consultations. In a focus group conducted by the American Lung Association, COPD patients expressed frustration with the lack of coordination and communication among their healthcare providers.

American Lung Association. What’s it Like Living with COPD? April 22, 2024.

They felt that no one was overseeing their comprehensive care, leaving them to piece together their treatment plans.

 

I do sort of feel like it's down to me to figure it out and put the pieces together.

Patients also felt inadequately educated about managing their disease and its progression. Furthermore, despite the availability of newer treatments, many were not informed about these options. 

 

Many live far from their healthcare providers or suffer financial and movement constraints, making regular visits challenging. While telemedicine can provide an avenue for quick consultations, it is not the norm for most patients. 

Additionally, despite the proven benefits of pulmonary rehabilitation—such as improved exercise tolerance and reduced dyspnea—fewer than 4% of Medicare beneficiaries with COPD access this care. Moreover, less than 2% of patients hospitalized for COPD exacerbations participate in pulmonary rehabilitation within 6 months of discharge.

Holland AE, Cox NS, Houchen-Wolloff L, et al. Defining Modern Pulmonary Rehabilitation. An Official American Thoracic Society Workshop Report. Ann Am Thorac Soc. 2021;18(5):e12-e29.

Bhatt SP, Westra J, Kuo YF, et al. Pulmonary rehabilitation utilization in older adults with chronic obstructive pulmonary disease, 2013-2019. Ann Am Thorac Soc. 2024;21(5):740-747.

 

 

Clearly, we need a better patient-centered approach that combines physical, emotional, and educational support for effective COPD management. To improve the care experience, physicians and pulmonologists can provide better education about rehabilitation programs, conduct regular mental health assessments, promote effective communication, and consider telemedicine for patients who have mobility issues.

What this means for you

COPD patients want more than just medical treatment—they need personalized care that addresses the full scope of their physical and emotional needs. Proactively engaging with patients on these critical issues improves individual outcomes and eases the strain on healthcare systems through reduced exacerbations and hospitalizations.

 

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