Guest guest Posted May 23, 2006 Report Share Posted May 23, 2006 , Thank you, Once again you came through with great info. I really appreciate you efforts. I went to my rheumy today, he took one look at me and knew I was in a huge flare up. He does believe that my flare-up is related to my sinsus infection. Sed rate was way high...and my white blood cells were elevated, not to high, but high enough to indicate that I am fighting an infection... He increased my prednisone to 10 mg for a short period of time. He also prescribed motrin 600mg 3 times per day and told me to stay on the MTX unless the ENT(ear nose and throat specialist) tells me to stop. I told him how long I have had this infection and all of the anti-biotics that I have been on. He insisted that I see an ENT specialist asap. and couldn't understand why my reg doc had not referred me. My reg doc is right next door and my rheumy talked to him while I waited, and lo and behold I got the referral. Called the ENT specialist office with great hope of a quick appt. only to be told that the earliest appt. was June 8th. I told them it was not acceptable for me to wait as I have RA and I'm having a huge flare up and that my sinus infection has been going on for over 3 mths and that I need to get treatment asap. They were not real concerned, but said to call Thursday am and ask for any cancellations. Wish me luck... I am going to be very pro-active in getting an appt asap. At least I'm going to try.....Because the way I see it, the sooner I get over this infection the sooner my flare up goes away which means the sooner I am mobile and hopefully in less pain. These past 3 months have been terrible. Every joint is inflamed and painful.....losing a lot of sleep because I wake up in the middle on the night in such pain. Torture getting out of bed....I am fatiqued because of the loss of sleep and fighting this infection....well you all know what its like...I'm sure you have all been there....I do appreciate the ear you all give me to vent....sometimes I just need to share my frustration and I thank you for the opportunity and support of this web site. <Matsumura_Clan@...> wrote: Introduction Sinus problems, whose symptoms are primarily associated with fatigue and increased pain (1;2), are common in the general population and may be increased in persons with immune disorders (3;4). In addition, clinical trials suggest an increase in sinus symptoms in anti-TNF treated persons with RA (5). In the current study we had several aims: 1) to determine that rate of sinus problems and whether they occurred more frequently in persons with RA; 2) to determine which clinical symptoms were associated with sinus problems; 3) to determine if anti-TNF therapy or other DMARD therapy was associated with sinus problems; and 4) to determine the incidence rate of hospitalization for sinus disease in persons with RA. Sinus Disorders in Rheumatoid Arthritis: Prevalence and Treatment Effects Kaleb Michaud and Fred Wolfe -- National Data Bank for Rheumatic Diseases, Wichita, KS, USA Abstract PURPOSE: Sinus problems are common in the population. In rheumatoid arthritis randomized clinical trials (RCT) the incidence of sinus infection was increased among patients receiving anti-TNF therapies compared with persons not on such therapies. Patients with RA might be at increased risk for sinus disorders because of rheumatoid arthritis (RA) or because of immuno-modulatory therapies. The purpose of this study is to determine if rates of sinus disease are increased in RA and whether RA treatments alter the risk of sinus disease. METHODS: As part of a longitudinal study of rheumatic disease outcomes, 7,243 patients with RA, 1,667 with osteoarthritis (OA) and 447 with fibromyalgia were evaluated in 2003 as to sinus problems. We determined medical visits and prescription medication use for sinus problems, and defined an important sinus problem as one that required a physician visit. RESULTS: The lifetime prevalence of sinus disorders diagnosed by a physician was 42.9%. During the previous 6 months 22.4% of RA patients, 24.0% of OA patients and 25.1 % of fibromyalgia patients visited a physician for a sinus problem (p = 0.181) and 22.3%, 24.0% and 25.1% received a prescription medication for a sinus problem (p = 0.184). After adjustment for age and sex, the rate of physician visits was significantly lower for RA patients (22.1%) compared with OA patients (24.8%), p = 0.021. We developed a predictive multivariable model for sinus problem physician visits in RA patients (Table 1). The strongest predictor of sinus problems was a history of allergies and younger age. Sinus problems were also more common in whites and among those with an asthma history. Etanercept (odds ratio 1.2 (95% C.I.: 1.0 to 1.4) increased the risk of sinus problems while leflunomide (OR 0.8 (0.8 to 1.0)) and sulfasalazine (OR 0.7 (0.5 to 0.9)) were associated with reduced risk. Other (non-significant) variables are omitted from Table 1. In contradistinction to the modest associations of treatment with outpatient medical visits, a strong association was seen for hospitalization for sinus disease with prior (lagged) prednisone therapy (OR 10.7 (95% C.I.: 3.1 to 36.4)) but not with lagged DMARD or biologic therapy, after controlling for age, sex and allergies. CONCLUSIONS: Medical visits for sinus problems are not increased in RA compared to OA and fibromyalgia. Among RA patients etanercept is a modest risk factor for sinus problems, and sulfasalazine and leflunomide appear to reduce the risk. Antecedent prednisone substantially increases the risk of hospitalization for sinus surgery. However, as prednisone may have been used as a sinus treatment, it is not possible to say if prednisone is causally linked to sinus surgery. Discussion (cont.) Upper respiratory and sinus infections are more common in anti-TNF treated patients than in control subjects in clinical trials (5), with very slight increases in those treated with adalimumab and for sinusitis in those treated with infliximab (12% vs. 6%) (5). In clinical trials, upper respiratory infections and sinusitis were the most frequently reported infections in patients receiving etanercept or placebo, and the rate of upper respiratory tract infections was 17% in placebo group and 22% in etanercept group. There were no increases in the rates of serious infections (requiring hospitalization) (19). However, the data of the current study indicate that sinus problems are not increased in persons with RA, and after adjustment for age and sex are even slightly reduced compared with OA, although the difference, though statistically significant, is small (24.8% vs. 22.1%). We found that sulfasalazine, although use by few patients (5.8%) has a protective effect on sinus problems, OR 0.62 (95% C.I.: 0.47-0.82). This reduction might be related to its anti-bacterial effect (20;21). We also found that leflunomide had a reduced association with sinus problems (OR 0.83 (95% C.I.: 0.77-0.99). Persons receiving etanercept had an increased risk of sinus infections in age and sex adjusted analyses of Table 2 (OR 1.21 (95% C.I.: 1.04-1.41)). The effect was decreased in multivariate analyses of Table 3 (OR 1.16 (95% C.I.: 0.99-1.36). However, compared with infliximab the increased risk remained: OR 1.23 (95% C.I.: 1.03-1.48). In summary, sinus problems are not increased in RA compared with patients with OA and fibromyalgia. Slight protective effects on sinus problems are noted with sulfasalazine and leflunomide, and a slight increase in risk of sinus problems is noted with etanercept. http://72.14.203.104/search?q=cache:stJqa8WL384J:www.arthritis-research.org/Docu\ ments/sinus_poster_20043.ppt+rhinosinusitis+etanercept & hl=en & gl=us & ct=clnk & cd=10 Not an MD I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org Quote Link to comment Share on other sites More sharing options...
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