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Safety and efficacy of low dose naltrexone in a long covid cohort; an interventional pre-post study, 2022, O'Kelly et al

Discussion in 'Long Covid research' started by LarsSG, Jul 8, 2022.

  1. LarsSG

    LarsSG Senior Member (Voting Rights)

    Messages:
    370
    Highlights
    • Low dose naltrexone (LDN) is safe to use in patients with long covid (LC).
    • In patients with LC for a median 11 months, LDN reduced symptoms at 2 months.
    • In this cohort, LDN also improved well-being in 6 of 7 parameters at 2 months.
    Abstract
    Background
    Up to 37.7% of patients experience symptoms beyond 12 weeks after infection with SARS-CoV-2. To date care for people with long covid has centred around multidisciplinary rehabilitation, self care and self pacing. No pharmacotherapy has been shown to be beneficial.

    Methods
    In this single centre interventional pre post study, the safety of Low Dose Naltrexone (LDN) was explored in patients with Post COVID-19 Syndrome (PCS), defined by NICE as patients with ongoing symptoms 12 or more weeks after initial infections with SARS-CoV-2 where alternative explanation for symptoms cannot be found. Patients were recruited through a Post COVID clinic, had a baseline quality of life questionnaire in symmetrical Likert format, were prescribed 2 months (1 mg month one, 2 mg month two) of LDN and repeated the same questionnaire at the end of the second month. Patients were monitored to adverse events.

    Findings
    In total 52 patients participated of whom 40(76.9%) were female. The median age was 43.5 years(IQR 33.2–49). Healthcare workers represented the largest occupational cohort n = 16(34.8%). The median time from diagnosis of COVID-19 until enrolment was 333 days (IQR 171–396.5). Thirty-eight participants (73.1%) were known to commence LDN, two of whom (5.3%) stopped taking LDN post commencement due to new onset diarrhoea and also described fatigue. In total 36(69.2%) participants completed the questionnaire at the end of the two-month period. Improvement was seen in 6 of 7 parameters measured; recovery from COVID-19, limitation in activities of daily living, energy levels, pain levels, levels of concentration and sleep disturbance (p ≤ 0.001), improvement in mood approached but was not significant (p = 0.054).

    Conclusions
    LDN is safe in patients with PCS and may improve well-being and reduce symptomatology in this cohort. Randomised control trials are needed to further explore this.

    https://www.sciencedirect.com/science/article/pii/S2666354622000758
     
    Last edited by a moderator: Jul 9, 2022
  2. LarsSG

    LarsSG Senior Member (Voting Rights)

    Messages:
    370
    Not much to take from this one, I don't think. Small N, no controls, very low naltrexone dose, vague questionnaire.
     
  3. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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    5,255
    Not liking the positive spin in the abstract. The questionnaire results don't look impressive and are uninterpretable due to lack of controls. I suppose the purpose of the study is to show LDN isn't causing any obvious serious harm so that a proper clinical trial becomes easier to get funding for.
     
    MEMarge, Ariel, Art Vandelay and 6 others like this.
  4. rvallee

    rvallee Senior Member (Voting Rights)

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    Location:
    Canada
    The more I look at how it's structured, the more I am convinced that evidence-based medicine is a useless process here. It simply cannot yield anything useful without a valid starting point for what to test, it fully depends on understanding the underlying process as otherwise it's nothing but a very limited brute force approach. It's just too expensive. The idea works, but not at the scale we need. It's like trying to brute force a password where you can only make one guess per second. If the encryption key is high enough it would take billions of years.

    How much more would we learn from a larger trial, for example? Still safe, still mildly effective for a few. So what? Trivial benefits for some, stalled progress for everyone else.

    The entire paradigm is wrong, a failure, and probably explains why so few new effective treatments are found anymore. The million monkeys on typewriters approach to things leads mostly to feces on the wall, along with people employed to decipher any meaning out of it.
     
    alktipping and Peter Trewhitt like this.
  5. Amw66

    Amw66 Senior Member (Voting Rights)

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    Oh for a better process.
    I know many who have put down their improvements to LDN.
    It would be good to have some meaningful data.
     
    MEMarge and Ariel like this.
  6. Hutan

    Hutan Moderator Staff Member

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    Location:
    Aotearoa New Zealand
    Hmm. 'Psychological' gets thrown in there, even though no evidence for that view is specifically cited.
    Hmm



    Given what we know about the problems of some antidepressants, the suggestion that they are potential therapies is concerning. Note mention of a UK study of LDN that is currently underway.

    It seems a stretch to say that LDN has been shown to be beneficial for CFS.


    I thought it was interesting that none of the 14 people tested for fibrinogen had results that were within reference range. The tests however were allocated according to 'clinical indications', so it's hard to know what it tells us.

    Perhaps this group will seek to do such a study. If they do, they could use some help e.g. in how they assess changes in symptoms.
     
    MEMarge, Ariel, Andy and 6 others like this.
  7. rvallee

    rvallee Senior Member (Voting Rights)

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    12,464
    Location:
    Canada
    That's what's called saying the quiet part out loud. So much for "evidence"-based medicine. I mean technically evidence to the contrary is evidence, all you have to do is not care what it says because you always meant your cruise ship to get to the destination it planned to get to.
     
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  8. Hutan

    Hutan Moderator Staff Member

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    Location:
    Aotearoa New Zealand
    Yes, it's something that could legitimately be said about a treatment that hasn't been researched well yet. But to say that for something like CBT or exercise aiming to improve ME/CFS, things that have been researched again and again for years, in all sorts of permutations, is a just a triumph of bias over logic.
     
    MEMarge, rvallee, Trish and 1 other person like this.

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