Patient perceptions of barriers to effective migraine management in Aotearoa New Zealand, 2024, McInnarney et al.

Discussion in 'Other health news and research' started by SNT Gatchaman, May 22, 2024.

  1. SNT Gatchaman

    SNT Gatchaman Senior Member (Voting Rights)

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    Patient perceptions of barriers to effective migraine management in Aotearoa New Zealand
    Blair McInnarney; Fiona Imlach; Jonathan Kennedy; Susan M. Garrett

    INTRODUCTION
    Migraine is a complex neurological condition which requires evidence based treatment, tailored to the individual. International evidence shows that treatment is often sub-optimal, but the experience of people with migraine in NZ is unknown.

    AIMS
    This study aimed to describe the barriers people with migraine disease face when seeking care for their condition in Aotearoa New Zealand (NZ).

    METHODS
    The Migraine in Aotearoa New Zealand Survey (MiANZ) was delivered online via SurveyMonkey from 22 August 2022 to 7 October 2022. Questions included: sociodemographics, the Migraine Disability Assessment Scale (MIDAS), ability to access health care, perception of health professionals’ knowledge and open-ended questions. Analysis used a mixed method approach.

    RESULTS
    Five hundred and thirty people from NZ responded, of whom 82% (433/530) were female and 77% (409/530) NZ European/other. Eighty-eight percent (467/530) had accessed primary care for migraine, with 36% (167/467) finding GPs’ knowledge of migraine to be excellent or very good. Forty-two percent (222/530) reported at least one instance where they had felt judged because of migraine by a health professional. Themes from free-text data included patient perception of health professionals’ knowledge of migraine, the presence of stigma within medical practice and systemic barriers to accessing effective health care.

    DISCUSSION
    People with migraine in NZ report significant barriers when trying to access effective management. Barriers were in both primary and secondary care and impacted the ability of people with migraine to manage their condition. More current migraine continuing medical education for GPs and other health professionals, better development and communication of care plans between primary and secondary care and patients and measures to address stigma are required to improve management of this complex disease.

    Link | PDF (Journal of Primary Health Care) [Open Access]
     
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  2. SNT Gatchaman

    SNT Gatchaman Senior Member (Voting Rights)

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  3. Hutan

    Hutan Moderator Staff Member

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    From the article
     
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  4. Hutan

    Hutan Moderator Staff Member

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    Seems sensible. Perhaps she could be a useful ally. Perhaps we could let her know that the disease formerly known as chronic fatigue syndrome is also often mis-named.
     
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  5. Hutan

    Hutan Moderator Staff Member

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    These neurologists...

    They seem very picky, don't they. They don't want anyone with 'functional' symptoms, which we are repeatedly told constitutes a substantial part of their clientele. And now it seems they don't want people with migraines because they are 'emotionally draining and time-consuming'. Who would have thought that a migraine patient was more emotionally draining for a doctor than a child with terminal cancer? The poor lambs, dealing with all those time-consuming angst-causing migraine patients. It's enough to make you give up medicine and go play golf.
     
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  6. Hutan

    Hutan Moderator Staff Member

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    A comment on access.

    I didn't see any discussion about the particular challenges that people in rural areas or even outside main centres face in getting good care. Also I didn't see any discussion of the extra barriers that people who are not NZ European might face. People who are not NZ European were under-represented in this online survey. It's also likely that wealthier people and people who think their opinions are worth listening to and are more likely to be assertive about getting good care are better represented. It is noted that 45% of the respondents have health insurance, whereas only 28% of the general population does.

    The paper notes that the modern migraine medicines are not funded in New Zealand, despite evidence of effectiveness and economic benefits.

    This study suggests GPs are not adequately informed about migraines treatment. My experience with a GP educator based in the Otago medical system was that they were dismissive about the role of HealthPathways, which provides guidance to doctors for use during consultations, seemingly believing that GPs don't need such assistance. This survey and the news suggests that it is very difficult to even get a GP appointment. I don't think we can rely on GPs for much.

    It occurs to me that specialist migraine treatment (and, for that matter, ME/CFS management) is something that could be provided well and cost-effectively using a telehealth system. Sure, there have to be some physical exams along the way. I've been meaning to check out online options for primary care.
     
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  7. Hutan

    Hutan Moderator Staff Member

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    To be fair, not all neurologists. Contrast the attitude of those neurologists who find migraine patients emotionally draining and time consuming with the people in the team working to understand ALS, discussed in an article here.

     
  8. rvallee

    rvallee Senior Member (Voting Rights)

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    The same problem is found in almost all health problems. So are they going to do more training on all those conditions? No one is ever going to understand all diseases, so advising training on all conditions is delusional. This isn't the way to address this, it's not even close to be realistic. Might as well advise to have angels take up the slack.

    There are reasons why this happens. Almost always it's the same process: MDs ignore patient reports, downplay symptoms and psychologize problems, seemingly believing that their job stops at looking for deadly diseases and reassuring patients when they don't seem to have one, and more often than not don't even have the time anyway.

    Unless the underlying reasons are addressed, this makes zero sense. You have to address root causes. Why doesn't medicine do root cause analyses? This is how you solve core problems, it's highly effective in all engineering fields. But instead we have this piecemeal and wildly redundant isolated take on each individual problem, all finding the same issues and all concluding the same way: more training for this specific condition. Nothing ever connects the dots, everyone is always looking at one question and spits out one answer, regardless of whether either have anything to do with the problem.

    Medicine seems incapable of self-correcting. It's impossible to ignore it at this point. Things are so bad that I pretty much assume than in most conditions, AI models would already do better because of this alone, but there is no way to verify because the only valid comparisons would be with a system that currently fails at it. The simple fact of there being no limits on time and number of patients probably far outweighs better ability to diagnose in the best circumstances, which are usually the exception.

    Once AI medicine takes off it's going to be shocking how many systemic problems it will expose. It will be like lighting up a room that was only ever looked at with tiny flashlights.
     

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