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  1. #1
    chp4211
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    HBLA27 Inflammatory Spondyloarthritis

    Must have Kinesiology Taping DVD
    Hi all - I have recently picked up a patient who has been Dx'd as having a "type" of Ankylosing Spondylitis - ie: he has an inflammatory spondyloarthritis believed to be associated with the HBLA27 gene. This is a new one on me and the info I can find is limited but basically states that it is Mx'd the same as AS. Has anyone come across this before and found anything to be particularly useful? Thanks & regards..

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  2. #2
    minniemau
    Guest

    Re: Ankylosying Spond

    I know someone very close who suffers from AS. You are correct the mgmt is similar to AS. As in AS you need to address pain relief, ROM maintanence, strengthening and importantly stress on breathing exs since the chest is likely to be affected. Massage helps in pain relief and relaxing muscles thereby improving ROM if limited by muscle spasms which occur in most patients. Swimming is also very helpful as a general ROM and endurance improving exs. Tai Chi I have found helps this person I know. Hope this helps.


  3. #3
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    Here's an extract from a paper on NSAIDs and AS with reference to the HLA-27 gene. It is from the website www.hopkins-arthritis.som

    Ankylosing Spondylitis
    Abstract 518 Inhibition of Radiographic Progression in Ankylosing Spondylitis (AS) by Continuous Use of NSAIDs
    Wanders, van der Heijde, Dougados
    summarized by Jon Giles, M.D. and Joan Bathon, M.D.

    NSAIDs remain first line therapy for AS and are associated with rapid improvement in axial signs and symptoms. The potential for this class of drugs to modify/slow disease has never been shown, though few rigorous evaluations have been performed. Here, Wanders et al hypothesize that continuous use of NSAIDs will reduce progression of structural damage in AS compared to intermittent, on-demand use.

    Methods: This was a two-year treatment study in which subjects fulfilling modified New York criteria for AS were randomized into one of two treatment groups. Group 1 (continuous NSAID use) was assigned to receive celecoxib 100 mg BID. The dosage could be increased to 200 mg BID or an alternative NSAID could be used for severe symptoms. Group 2 (on-demand use) was assigned to receive celecoxib per patient demand for symptoms. A change to an alternate NSAID was allowed for severe symptoms. Participants underwent lateral plain radiographs of the cervical and lumbar spine at baseline and after two years. Radiographs were scored using the modified Stoke Ankylosing Spondylitis Spine Score (SASSS) by a blinded observer. The primary endpoint was change in SASSS at two years.

    Results: 215 patients were randomized, 111 into the continuous NSAID group and 104 into the on-demand NSAID group. Mean age in both groups was approximately 40 years. 70% were male. 80% were HLA B-27 positive. Groups were well matched to baseline characteristics, except for disease activity, which was slightly higher in the on-demand NSAID group.

    96 participants in the continuous NSAID group completed the study. At two years, 68 were using celecoxib while 28 had changed to an alternate NSAID. The average dose of celecoxib in this group was 243 mg/day. 86 participants in the on-demand NSAID group completed the study. At two years, 67 were using celecoxib while 19 had changed to an alternate NSAID. The average dose of celecoxib in this group was 201 mg/day.

    Efficacy Endpoints — For subjects with complete radiographs (n=76 in the continuous NSAID group, n=74 in the on-demand NSAID group), the mean change in SASSS was 0.4 and 1.5 for the continuous NSAID and on-demand NSAID groups, respectively. BASDAI scores were similar in both groups over two years.

    Safety Endpoint — GI symptoms were equivalent in both groups. Hypertension was higher in the continuous NSAID group.

    Conclusions: Continuous NSAID use in AS is superior to intermittent, on-demand NSAID use in slowing radiographic progression over two years. Continuous NSAID is as safe as intermittent NSAID.

    Editorial Comments: These results are quite surprising since most rheumatologists have assumed that NSAIDs do not slow progression of any inflammatory joint disease. Well designed treatment and radiologic studies of NSAIDs or most DMARDs in AS have been few and far between. However, the current findings are even more surprising given that the mean doses of celecoxib taken by the two groups are only modestly different. Cox-2 has been shown to regulate differentiation of mesenchymal cells to osteoblasts. Thus, slowing syndesmophyte formation via Cox-2 inhibition with NSAIDs is the proposed mechanism of action.

    A critical question, as in RA, is whether these radiographic differences in progression will be associated, in the long-term, with better functional and quality-of-life outcomes. It is unlikely that monotherapy with an NSAID or Cox-2 inhibitor (without concurrent DMARD therapy) will be endorsed by most rheumatologists except in the mildest cases of AS.

    hope this is of use

    8o


  4. #4
    chp4211
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    Thank you for the responses it is essentially the direction I've taken with this patient. Appreciate the comments

    Regards
    Ray


  5. #5
    nickhedonia
    Guest
    sounds like yet another medical euphemism for " I don't know"


  6. #6
    1234nale
    Guest

    Re:HLA B 27 Iflammatory Spondyloarthritis

    Is also known as"morbus Bechterew" is inflammation rheumatoid disease witch attack whole organism. Its attack more often men then women(according to some statistics 10 times more). The most significant sign is ossification of soft-tissue around the spine, ligaments, vertebral discus, so at the end spine takes the position of one stiff stick, like "bamboos stick".Disease starts slowely, usualy at age 18-35.First sign that alert to this disease is morning siffness in lumbar spine with around pain in erly morning hours.As disease slowly progresses pain is lokalized and permanently present day and night.It's more and more difficult for patient to flex the spine, espetially lateral flexion.Spine change its normal position wich change postural status: lumbar lordossis is flattend, thoracic kyphosis is bigger, and the head is protruded to the front.Sometimes disease attack two big joint, shoulder and hip, witch then have restriction of motion in them and characteristic status of"skiing man", with hips and knees in flexion.
    In treatment, first step is education of patient for right position in seating, wlking, standing and sleeping. Its necessary for patient to lie on relatively hard bed without pillow(not even for day rest), and to know that the best position for sleeping is on the stomach, for sitting the best is cheer with high support, and in wlking to protrude chest and put back the shoulder.Generally, it's advised more moving and changin body position in work but avoiding of physical overloading.The most important is kinesytherapy with exercises for greeter motion of spine, exercises for greeter motion of hip and knee, and breathing exercises(witch is especially important because fo tendency of disease to restrict volume capacity of the chest), with excluing of abdominal breathing and forcing toracic breathing( you may use sme forme of games etc.)
    Its complex disease, and if you still have some questions feel free to ask, I'll be glad to help!
    Best regards Natasha.



 
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