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Is being able to walk to the letterbox life-changing? A qualitative assessment of measures of improvement in persistent breathlessness

Diana H. Ferreira, Magnus Ekström, Cornelia Verberkt, Daisy J.A. Janssen, David C. Currow
ERJ Open Research 2023 9: 00530-2022; DOI: 10.1183/23120541.00530-2022
Diana H. Ferreira
1Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, NSW, Australia
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  • For correspondence: diana.mbhf@gmail.com
Magnus Ekström
2Department of Clinical Sciences, Division of Respiratory Medicine & Allergology, Lund University, Lund, Sweden
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Cornelia Verberkt
3Department of Health Services Research, Care and Public Health Research Institute, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands
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Daisy J.A. Janssen
3Department of Health Services Research, Care and Public Health Research Institute, Faculty of Health Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands
4Department of Research & Development, Ciro, Haelen, The Netherlands
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David C. Currow
1Faculty of Science, Medicine and Health, University of Wollongong, Wollongong, NSW, Australia
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Abstract

Exploring clinically meaningful measures of improvement for people with persisting breathlessness https://bit.ly/3WaCzFh

To the Editor:

Persistent breathlessness is a prevalent cause of disability in COPD [1]. Many people with COPD do not achieve acceptable symptom control despite optimisation of disease-specific and nonpharmacological treatments [2]. Regular, low-dose, sustained-release morphine may reduce persistent breathlessness in some people, noting wide interindividual variation in benefits and harms. Ideally, sustained-release morphine should only be prescribed to people who are likely to experience a net benefit. To date, the clinicodemographic characteristics of people most likely to benefit from sustained-release morphine for persistent breathlessness have not been defined. Benefits quantified need to reflect people's perceptions [3].

This study aimed to explore how experiences of large perceived qualitative benefits from regular, low-dose, sustained-release morphine for persistent breathlessness may be reflected in changes in clinical, quantitative measures of efficacy and safety.

This was an exploratory analysis of qualitative and quantitative data from a phase III, double-blind, dose-increment, randomised, placebo-controlled trial (RCT) of regular, low-dose, sustained-release morphine for persistent breathlessness [4]. The trial and the qualitative substudy were approved by the Hunter New England Human Research Ethics Committee (ref. 15/12/16/3.06).

Participants had COPD and a modified Medical Research Council (mMRC) breathlessness scale score ≥3 at baseline despite optimal treatment of the underlying disease(s) [4]. The study included three sequential randomisations (weeks 1, 2 and 3) to final doses of sustained-release morphine (0 (i.e. placebo), 8, 16, 24 or 32 mg). There was an optional 6-month blinded extension using the dose prescribed in week 3. 13 patients and, separately, their caregivers were interviewed about their experiences of persistent breathlessness before and after initiating the study medication as part of a pre-planned qualitative study [5]. Interviews were conducted at participants’ homes, while the participants and interviewer were still blinded. Quotes were taken directly from participants’ transcripts.

Two participants used the term “life-changing” to describe their experiences with the study medication and were identified as “super-responders” (both on sustained-release morphine). None had psychological comorbidities (Hospital Anxiety and Depression Scale score ≤7 for both anxiety and depression). Quantitative measures obtained in the RCT were explored for changes meaningful to participants including: breathlessness and functional impairment due to breathlessness (0–10 Numerical Rating Scale (NRS), mMRC, Chronic Respiratory Disease Questionnaire (CRQ) – dyspnoea and mastery); activity measures collected from FitBits; performance status (Australia-modified Karnofsky performance status (AKPS)); quality of life (EQ-5D-5L questionnaire); perceived sleep quality and daytime sleepiness (Leeds Sleep Questionnaire and Epworth Sleepiness Scale); harms (constipation, nausea and drowsiness); global impression of change (GIC) (7-point Likert scale); and caregiver's burden (Zarit Burden Interview (ZBI-12)).

Super-responders’ final doses of morphine were 16 and 24 mg, and both continued in the 6-month blinded extension. Neither had unplanned hospital presentations throughout the study. Participant 1 highlighted, “Climbing a set of stairs was difficult. There were steps up from [location A] to [location B], three flights… I would try going up those, but it took at least three stops to get from the bottom to the top, and then I was panting… […] About a month ago I walked up all three flights and continued walking without a pause. And that is more or less across the board. I can do things now that I haven't been able to do for a long, long time.”

Participant 2 emphasised, “Breathing became easier. […] I used to battle to walk down to the letter box and back. Now I can walk down to the letter box with no problem. It has improved to that degree.”

Quantitatively, functional changes reported by participants were accompanied by reductions in mMRC and CRQ-dyspnoea scores, and an improvement in GIC (table 1). The number of active minutes and active calories (i.e. triggered by activity of ≥10 min, burning three times as many calories as those spent at rest) improved in both participants. After 6 months of sustained-release morphine, these quantitative improvements persisted.

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TABLE 1

Daily doses of sustained-release morphine and quantitative study measures across study stages for the two super-responders identified through the semistructured interviews

Participant 1 experienced a reduction in the breathlessness NRS intensity scores (i.e. “worst” and “average” breathlessness in the previous 24 h), and an improvement in CRQ-mastery, AKPS and EQ-5D-5L scores. These were mostly unchanged for participant 2. Daily steps and daily calories were relatively stable (participant 1) or decreased (participant 2).

Both participants reported better sleep and higher energy levels during the day. Participant 1 said: “My wife particularly noticed a significant increase, I would say within a week, with my energy levels, my ability to hyper exertion without gasping. I think you also notice a difference in my breathing at night that I was not gasping. I had been subjected to significant coughing fits on a regular basis. This came down to almost to nil. And there is a feeling of wellbeing.”

Participant 2 reported: “[Before taking morphine] I'd wake up probably a couple of times a night to go to the toilet and then when I come back from the toilet it takes me a while to go back to sleep because of the breathing. […] [After taking morphine] Breathing became easier, I slept quite a lot more you know? I go to bed at 10 o'clock at night and sleep until 8:00 am in the morning. Quite honestly, I don't think I could manage without it [morphine].”

Most quantitative measures of perceived sleep quality improved consistently throughout the study, except for daytime sleepiness (increased for participant 1).

Constipation was the only harm reported in the first few days of therapy, which required adjustment of the participants’ medication or trying new interventions. However, the participants never considered stopping the study medication because the perceived benefits outweighed perceived harms, findings reflected in quantitative assessments. Participant 1 reported: “Constipation was the downside and that was really the only downside. They give you the pills [laxatives] but they should issue bottles of prune juice because they would be a lot more effective.”

Participant 2 said: “Constipation is also a problem with the drug [morphine]. And it wasn't anything that you couldn't adapt to. […] So OK, you mightn't go to the toilet twice a day and use your bowels and you might miss a day. But it does not matter, you know?”

At interview, caregiver 1 reported: “My life changed. I am not worried every minute of every day; I don't sit up in bed and listen to him breathing. And we can go out and enjoy life more.” Caregiver 2 reported not being involved in hands-on care, living her life fairly detached from the patient. These experiences translated into a significant reduction in the ZBI-12 score for caregiver 1, sustained for 6 months. The absence of burden for caregiver 2 was reflected in the ZBI-12.

This analysis explored the relationship between subjective qualitative experiences of breathlessness and changes in multiple quantitative measures of benefits and harms, while sustained-release morphine was being introduced and continued in two men with COPD. The results suggest functional improvement is a key driver of perceived benefit, which seems to be accompanied by clinically meaningful reductions in CRQ-dyspnoea [6], appreciable improvements in mMRC scores and an increase in active steps per day.

Compared to participants reporting small or no benefit, super-responders reported that they could perform more meaningful activities [5]. More importantly, they actually engaged in such activities, which is not always the case for people who increase their functional capacity [7]. Possibly, a quick functional adjustment to a new threshold of breathlessness is one of the key characteristics of super-responders. Super-responders may also be less vulnerable to anticipatory anxiety before breathlessness-inducing activities, as suggested by low baseline anxiety scores. Adjustments to new levels of physical activity are unlikely to be translated into changes in unidimensional breathlessness measures but may be captured by appropriate assessment tools covering function [8, 9].

The daily number of active minutes and active calories seem to better reflect perceived changes in function, compared to number of calories or number of daily steps. Possibly, super-responders are strategic in engaging in daily activities that are meaningful to them and that were previously out of scope. Even small gains in function create a greater sense of worth and wellbeing [10]. These moments of targeted and calculated exertion are unlikely to be captured by the total number of daily steps but may be reflected in measures of more strenuous activity.

People with persistent breathlessness report better subjective sleep quality after initiating sustained-release morphine [11]. This study suggests that subjective sleep improvements may be critical to improve people's perceived energy levels during the following day and, perhaps, facilitate functional gains. Better subjective sleep quality for patients may also translate into decreased burden for caregivers, for whom breathlessness is distressing to witness (including during the night) [12].

Gains in function outweighed the transient harms of constipation, despite its troubling nature. Prevention and ongoing management of constipation is important to achieve a net benefit from sustained-release morphine [3].

This study may have a critical role in informing the design of large-scale studies assessing value-based therapy for people with persistent breathlessness and their caregivers, in which self-reporting measures ought to be central [13]. It is not intended that these results be generalised but that they inform a discussion of outcomes that should be used subsequently. While symptom reduction needs to be a priority in the short term, it is critical to ensure patients remain physically active in the medium-to-long term, which may reduce deconditioning and social isolation.

Future research needs to focus on identifying the best outcome measures for people with persistent breathlessness, which may include the use of multidimensional assessment tools [14] and measures of daily function. In particular, the daily numbers of active minutes and active calories need to be investigated as primary outcome measures in future studies.

In conclusion, perceived improvements in meaningful activity and sleep may be key drivers of benefit for patients with persistent breathlessness and their caregivers. The best outcome measures for these populations need to be investigated in future qualitative and quantitative studies.

Footnotes

  • Provenance: Submitted article, peer reviewed.

  • Conflict of interest: C. Verberkt reports grant from Radboudumc. D. Janssen reports grants from the Netherlands Organisation for Health Research and Development (ZonMw), Stichting Astmabestrijding and NRS Award. D.C. Currow reports advisory board membership and consultancy for Helsinn Pharmaceuticals; consultancy and receives payment for intellectual property with Mayne Pharma International Pty Ltd.; subcontracting to Nous Group Pty Ltd; board membership for icare Dust Diseases Care NSW; and board membership/directorship for Chris O'Brien Lifehouse. The remaining authors have nothing to disclose.

  • Received October 13, 2022.
  • Accepted December 12, 2022.
  • Copyright ©The authors 2023
http://creativecommons.org/licenses/by-nc/4.0/

This version is distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. For commercial reproduction rights and permissions contact permissions{at}ersnet.org

References

  1. ↵
    1. Johnson MJ,
    2. Yorke J,
    3. Hansen-Flaschen J, et al.
    Towards an expert consensus to delineate a clinical syndrome of chronic breathlessness. Eur Respir J 2017; 49: 1602277. doi:10.1183/13993003.02277-2016
    OpenUrlAbstract/FREE Full Text
  2. ↵
    1. Marciniuk DD,
    2. Goodridge D,
    3. Hernandez P, et al.
    Managing dyspnea in patients with advanced chronic obstructive pulmonary disease: a Canadian Thoracic Society clinical practice guideline. Can Respir J 2011; 18: 69–78. doi:10.1155/2011/745047
    OpenUrlCrossRefPubMed
  3. ↵
    1. Ferreira DH,
    2. Silva JP,
    3. Quinn S, et al.
    Blinded patient preference for morphine compared to placebo in the setting of chronic refractory breathlessness – an exploratory study. J Pain Symptom Manage 2016; 51: 247–254. doi:10.1016/j.jpainsymman.2015.10.005
    OpenUrlPubMed
  4. ↵
    1. Ekström M,
    2. Ferreira D,
    3. Chang S, et al.
    Effect of regular, low-dose, extended-release morphine on chronic breathlessness in chronic obstructive pulmonary disease: the BEAMS randomized clinical trial. JAMA 2022; 328: 2022–2032. doi:10.1001/jama.2022.20206
    OpenUrl
  5. ↵
    1. Ferreira D,
    2. Kochovska S,
    3. Honson A, et al.
    Patients’ and their caregivers’ experiences with regular, low-dose, sustained-release morphine for chronic breathlessness associated with COPD: a qualitative study. BMJ Open Respir Res 2022; 9: e001210. doi:10.1136/bmjresp-2022-001210
    OpenUrlAbstract/FREE Full Text
  6. ↵
    1. Wyrwich KW,
    2. Fihn SD,
    3. Tierney WM, et al.
    Clinically important changes in health-related quality of life for patients with chronic obstructive pulmonary disease: an expert consensus panel report. J Gen Intern Med 2003; 18: 196–202. doi:10.1046/j.1525-1497.2003.20203.x
    OpenUrlCrossRefPubMed
  7. ↵
    1. Carl J,
    2. Schultz K,
    3. Janssens T, et al.
    The “can do, do do” concept in individuals with chronic obstructive pulmonary disease: an exploration of psychological mechanisms. Respir Res 2021; 22: 1–10. doi:10.1186/s12931-021-01854-1
    OpenUrlCrossRef
  8. ↵
    1. Ekström M,
    2. Elmberg V,
    3. Lindow T, et al.
    Breathlessness measurement should be standardised for the level of exertion. Eur Respir J 2018; 51: 1800486. doi:10.1183/13993003.00486-2018
    OpenUrlAbstract/FREE Full Text
  9. ↵
    1. Verberkt CA,
    2. van den Beuken-van Everdingen MHJ,
    3. Schols J, et al.
    Effect of sustained-release morphine for refractory breathlessness in chronic obstructive pulmonary disease on health status: a randomized clinical trial. JAMA Intern Med 2020; 180: 1306–1314. doi:10.1001/jamainternmed.2020.3134
    OpenUrl
  10. ↵
    1. Spathis A,
    2. Booth S,
    3. Moffat C, et al.
    The Breathing, Thinking, Functioning clinical model: a proposal to facilitate evidence-based breathlessness management in chronic respiratory disease. NPJ Prim Care Respir Med 2017; 27: 27. doi:10.1038/s41533-017-0024-z
    OpenUrlPubMed
  11. ↵
    1. Martins RT,
    2. Currow DC,
    3. Abernethy AP, et al.
    Effects of low-dose morphine on perceived sleep quality in patients with refractory breathlessness: A hypothesis generating study. Respirology 2016; 21: 386–391. doi:10.1111/resp.12681
    OpenUrlPubMed
  12. ↵
    1. Ferreira DH,
    2. Kochovska S,
    3. Honson A, et al.
    Two faces of the same coin: a qualitative study of patients’ and carers’ coexistence with chronic breathlessness associated with chronic obstructive pulmonary disease (COPD). BMC Palliat Care 2020; 19: 64. doi:10.1186/s12904-020-00572-7
    OpenUrl
  13. ↵
    1. Bae J-M
    . Value-based medicine: concepts and application. Epidemiol Health 2015; 37: e2015014. doi:10.4178/epih/e2015014
    OpenUrlPubMed
  14. ↵
    1. Ekström M,
    2. Currow DC,
    3. Johnson MJ
    . Outcome measurement of refractory breathlessness: endpoints and important differences. Curr Opin Support Palliat Care 2015; 9: 238–243. doi:10.1097/SPC.0000000000000147
    OpenUrl
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Is being able to walk to the letterbox life-changing? A qualitative assessment of measures of improvement in persistent breathlessness
Diana H. Ferreira, Magnus Ekström, Cornelia Verberkt, Daisy J.A. Janssen, David C. Currow
ERJ Open Research Mar 2023, 9 (2) 00530-2022; DOI: 10.1183/23120541.00530-2022

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Is being able to walk to the letterbox life-changing? A qualitative assessment of measures of improvement in persistent breathlessness
Diana H. Ferreira, Magnus Ekström, Cornelia Verberkt, Daisy J.A. Janssen, David C. Currow
ERJ Open Research Mar 2023, 9 (2) 00530-2022; DOI: 10.1183/23120541.00530-2022
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