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Conditions > Rheumatoid Arthritis > Rheumatoid Arthritis Treatment > Arthritis Treatment: Early is Best
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Arthritis Treatment: Early is Best

Receiving rheumatoid arthritis treatment sooner rather than later may be your key to remission

A hot topic among rheumatologists lately is whether when you treat rheumatoid arthritis (RA) matters as much as how you treat it. Some believe strongly in early arthritis treatment, prescribing an aggressive regimen of RA drugs during what is called "the window of opportunity." Doing so, they maintain, just may stop the disease in its tracks.

"I am a strong believer in the window of opportunity, which probably spans two years after symptom onset," says Salahuddin Kazi, MD, associate professor of internal medicine and chief of rheumatology at the Dallas VA Medical Center. "If RA goes untreated for two years, the majority of people with RA will develop joint erosion, indicating disease progression."

"The debate over whether a window of opportunity exists is semantics to some extent," says Arthur Kavanaugh, MD, rheumatologist and director of the Center for Innovative Therapy at the University of California, San Diego. "Some people don't like the term because people with active disease can – and should – always be treated, even beyond the two-year mark."

Treating RA as early as possible is not a new concept. In 1989, a study published in The Lancet emphasized the importance of starting a regimen of antirheumatic drugs early. The drugs commonly used then were hydroxychloroquine (Plaquenil) and sulfasalazine (Azulfidine); methotrexate wasn't yet an option, and biologics were not yet developed. The main difference between discussions of early arthritis treatment 15 to 20 years ago and today are the drugs available for aggressive treatment, says Dr. Kavanaugh.

Early, aggressive treatment is particularly important for those who will develop a more serious disease. Figuring out who those patients are is quite a challenge, but guiding principles exist. "I think it's pretty clear right now that if a patient has antibodies to rheumatoid factor (RF) or cyclic citrullinated proteins (anti-CCP) at any time during the course of disease -- from day one to 12 weeks or 12 years – then he has a greater risk for persistent disease that is worse and more destructive," says Stephen Paget, MD, rheumatologist and physician-in-chief of the Hospital for Special Surgery in New York City. "Those patients need aggressive therapy that's constantly monitored."

A recent study of adalimumab (Humira) plus methotrexate showed one in two people with early RA – diagnosed less than three years earlier – achieved a clinical remission at two years. More than 60 percent of the patients showed at least a 50-percent improvement in symptoms. The effect with combination therapy was observed as early as two weeks, and these differences were sustained throughout the two-year study.

Another study, the Definitive Intervention in New-Onset Rheumatoid Arthritis (DINORA) trial, is reviewing the use of infliximab (Remicade) in people with very early inflammatory RA (those who had it fewer than 14 weeks) to see if it can prevent the development of destructive disease.

While it's ideal to initiate treatment as early as possible, aggressive treatment throughout the course of the disease is essential, say the experts.

"If you're past that two-year mark with no treatment or treatment that wasn't aggressive enough, all is not lost," says Dr. Kavanaugh. 

JOY
17 Nov 2009, 17:37
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Several people have told me they had good results after treating RA symptoms with minocycline or other cycline drugs. Anyone have experience with either of these?
Tonya
15 Oct 2009, 21:46
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I was diagnosed with Lupus 2.5 years ago. I was in and out of the ER monthly for the first year. To Brenda: I was covered in sores all over my hands and elbows at every joint. Some were even open. My symptoms have been controled since late last year. I take methotrexate once a week. Watch that you have blood tests monthly. I went from 8-6 a week when a small problem arose. It has not shown up again. I take placquinal twice a day, I am down to 3 prednisone a day. For the sores I was put on Nebumetone twice a day. So far they have not returned. You can get low iron levels so I take 1 folic acid a day. When you look at it all it sound like a lot of medicine but except for a small flare up after taking the flu shot I have been fine for most of this year. It just took a while to get used to remembering all of it. When I look at where I started and where I am now I can live with it.
joyce
28 Sep 2009, 21:38
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My PCP thought I was a drug seeker when he first met me, because I complained of such bad pain, and aparently I didn't "look like" I was in pain. I wasn't having a flare but I was truly in pain. He decided he would prove there was nothing wrong with me by ordering blood tests, well he had egg all over his face! When he had me return to go over my results I was shocked because he actually told me he thought I was just looking for drugs! And quickly apologized, and told me I need to see a Rhum.
Noella Willier
24 Jun 2009, 01:27
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I was diagnosed with R.A. in 2000 and kept it in remission with natural remedies for 5 yrs when I ran out of money and the R.A. went full blown I went on Metrotrexate in at end of 2006 and have been on Metrotrexate and celbrex combo and Metro and Naproxen which went well for about 6 months and now I am on Metro and predisone which has given me the best results as a combo. After reading side affects of people in their 60's, its risky business. I lost a bro of lupus and I am T.B. positive and my rheumatologist is pushing Enbrel on me and after reading the enbrel side affect experiences, it does not sound too promising, does anyone have any suggestions for me please. Noella
Lou
05 Jun 2009, 22:11
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I was diagnosed with RA two months ago.
Started on Prednisone,Meloxicam and Mesothraxate 4 pills once a week.
After the forth week of Mesothraxate I developed a lung infection and my Rheumatologist took me off of it. Went to see him two weeks later after I was better and he decided to put me back on the Mesothraxate because he is not sure if the infection was caused by the medication.
Honestly I am afraid to take Mesothraxate again, but I am also afraid to start on biologics.
I am so confused when it comes to making the right decision on the course of treatment.
I think I just want to call and tell the Dr. that I don't want to try Mesothrexate again but feel that he is the doctor and that I should do what he says.
A confused patient.
Dawn Masterson
05 Jun 2009, 20:52
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I thought I had a high resistance for pain. But nothing prepared me for RA. It started in my feet, then knees. My doctor ordered water pills to get rid of the swelling. This probably brought my RA out of hiding. Then all of a sudden I was an invalid. I called the doctor crying I was hyperventilating ready to call an ambulance. They finally gave me steroids. I have relief now for 2 days but oh my God I guess I have something very horrible.
Dawn Masterson
05 Jun 2009, 20:51
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I thought I had a high resistance for pain. But nothing prepared me for RA. It started in my feet, then knees. My doctor ordered water pills to get rid of the swelling. This probably brought my RA out of hiding. Then all of a sudden I was an invalid. I called the doctor crying I was hyperventilating ready to call an ambulance. They finally gave me steroids. I have relief now for 2 days but oh my God I guess I have something very horrible.
brenda
02 Jun 2009, 15:50
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I have been recently Dx with RA. My Rheumatologist Rx Placquinil / and steroids. The steroids masked the side effects of the Placquinil x 2 weeks.When the steroids wore off I broke out in a rash all over my body with open sores,in my hair and in my mouth. I itched like crazy for 4 days, could not sleep and was sent to a Dermatologist he Rx steriods high dose x 2 days - I continued to break out and itch/ no sleep still, I was exhausted.He(dermatologist) Rx cyclosporin x 4 days.After 2 days I finally went to sleep. It has been 2 months since this happened I still have dry itchy skin and still have RA. Makes me wonder(what did this medicine do to my vital organs) I am apprehensive about going back to see my Rheumatologist.I know there are other medicines out there that are used.I ask myself (am I?) brave enough to jump in for another round of hell? It Will take some time for me to decide, I suppose I am doomed for RA.
Kay Teague
26 Apr 2009, 20:54
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I have been diagnosed for the 2nd time with RA.
I was diagnosed with Fibromyalgia in August 2001 by a Rheumatologist. I followed her instructions, went to physical therapy, am being followed by a psychariatist, and told the medicine she prescribed. After about 2 years I started having bad joint pains.She said it was just the fibro and she started prescribed really strong narcotics. I have always had a slightly elevated Rheumatoid factor, but the other tests have been normal until about 3 years ago when my WBC, RBC, and platelets started being elevated. I wasn't able to get an appointment with my Rheumatologist when both of my knees almost doubled in size with increased pain, warmth, and redness. My primary care doctor stated I had rheumatoid arthritis-he was aware of the fibro history and joint pain history-he started me on low dose of Methotrexate and
Prednisone. I responded quickly and felt much better. At my next appointment with the Rheumatologist, she asked why I was taking methotrexate I told her my PCP put on it because of my knees. She was quite agitated and said "YOU ONLY HAVE FIBROMYALGIA, YOU DO NOT HAVE RHEUMATOID ARTHRITIS!!!" and told me to stop the prednisone and methotrexate.
My insurance changed and I wasn't able to she her any longer. My primary care doctor retired. My pain and fatigue became so bad I had to quit work. I waited almost 3 years to be declared " disabled" in December 2008. In Greenville County SC there are not many rheumatologists. Most of them want to review a patient's records before they accept them into their practice. The wait for a new patient appointment is about 4 months. Most of them will turn down a patient with fibromyalgia. Last fall, I started having problems with my feet and ankles, so I went to see my orthopaedic doctor that did surgery on my feet. He looked at me and said I think you have more going on with you that fibromyalgia and he ordered some lab. MY non cardiac CRP was elevated so he referred me to a new hospital based rheumatology group. I was seen as a new patient within 2 weeks. My new rheumatologist is wonderful. I have been seeing her since Dec 1, 2008. After knee xrays (never ordered before), several medication trails, wrist MRI, and follow up wrist x-ray to verify fluid accummulation, she has restarted me on methotrexate 2.5 mg take 4 one day a week and Folic acid 1gm daily. I can't say I'm feeling much better yet because I've just started these meds but I know that she is concerned about me. She admitted to me that I don't really look like I have RA unless you review all my symptoms,
elevated CRP, slightly elevated Rh factor, elevated WBC and platelets, positive MRI and x ray results, strong family history of RA on both sides of the family, osteopenia, DDD, entrapment syndromes-carpal and tarsal tunnel, it all adds up. I don't know what it takes to get a doctor to recognize other symptoms other than labs. But this new doctor was able to piece together several symptoms because she was willing to listen to her patient and doesn't depend on labwork results. Early detection of RA is critical to prevent joint destruction and early symptoms may be different. Unfortunately, I feel that my RA has not been caught early and I think it is likely I will need to move beyond methotrexate to the next line of RA drugs. To all doctors, RNs, PAs, ,and rheumatologists, please please please listen to your patients, listen to what they are saying, ask questions, don't rely only on the standard lab results. It is possible to have more than one medical problem. Just because I have fibromyalgia, it doesn't rule out any other diseases. In fact, I read a report that states patients with RA have an increased chance of also having fibromyalgia.
Angela
19 Apr 2009, 19:35
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What I find seriously concerning is seeing so many people that experienced what I personally had to go through with general MDs.
Should the Professional RA community consider better education in early symptoms recognition for PCPs?
I went through 6 months of hell to get diagnosed and start treatment, and I'm severe category RA, age 32 at diagnosis. I also "finally found a doctor" to take me seriously, but by that time I could barely move so they didn't have much choice. I was so severe that I was hospitalized 1 day later after finding my new PCP.

Why do so many general MD's not even consider RA?
Chassity
08 Apr 2009, 13:41
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Nevermind...:]
Chassity
08 Apr 2009, 13:39
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Hello, and excuse me. But I have a question which I not seem to find on here for some reason I'm in mi health class right now, and unfortunatly. I cannot find this question.
" For arthritis pain. What are the cures, symptoms, injuries,and cares for such thing?
Thank you,
Chassity Schenally
Jim
06 Apr 2009, 21:03
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I'd like to second Dr. Deb's notion regarding follow-up. It would serve the audience well if the comments left by the community were followed up by the author of the source article. As community, we can respond to each other...but I know I'd benefit from the expertise of the Arthritis Today panel. This really is a great source of information. Of course there is always room for improvement.
Peggy
06 Apr 2009, 08:46
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Diagnosed 6 weeks ago with RA; from what I read it is moderate to severe (I thought it was h...) and I see from comments I was very lucky to have an MD who didn't believe the negative lab work and sent me to a rheumatologist after my 2nd visit about roaming, crippling pain in multiple joints; he thought RA even though labs neg.; also very lucky to have a rheumatologist who chose to treat aggresively. No severe flares for 3 weeks, minor flares less frequent. I'm hoping for no flares soon.
I love this site, so full of good info, tips etc.. Thanks
deborah konietzko, md
24 Mar 2009, 00:06
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I'd be interested to hear comments from the Rheumatologists quoted in the above article, after they've seen the comments.
The ones I've seen don't want to discuss current research, or (or "have time" to) have a real discussion about issues such as those many of the the people commenting above have raised.
I didn't have access to last year's European Rheumatology Conference concensus paper on RA, but have been told i should consider going to Europe because they are ahead of us in RA treatment! If i were well, had money and support people, that would be conceivable, but even then, it shouldn't be necessary!
US Rheumatologists: "we need help (here)!"
Please ask yourselves: "If it were my daughter, wife or mother, what would I recommend?"

Out of exasperation, I'm thinking of developing a pilot study; i am requesting input.

When doctors and nurses (3 out of the 5 of us commenting above) can't get good guidance from their colleagues, this indicates there are serious problems which need resolution.
Thanks.
Please forward this so we may be responded to.
sick n tired of being sick n tired
23 Mar 2009, 17:57
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I was diagnosed with Psoriatic Arthritis/Rheumatoid Arthritis and probable spondylitis, 3 years ago. I am on my way to a pain management Dr at the suggestion on Rheumatologist. Humira worked good but exceeded my annual prescription benefits and got a serious infection on Remicade.

Currently I on Placquinil, NSAIDS no longer work, on my 6+ month of Orencia infusions, and on the maximum dosage of injectible methotrexate. What options are left for me?

I just turned 39 and take 14 meds a day (3 are vitamin/supplements-to ward off side effects the other 11 Rx)-which equats to 24 PILLS A DAY, on top of monthly B-12 shots, Orencia infusions and weekly methotrexate injections. Did I forget to mention, thyroid, kidney disease, hypertension, latent TB, fibromyalgia, chronic cough, IBS and osteopenia....



Leigh Ann
19 Mar 2009, 15:44
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I recently have met w/rheumatologist who thinks I have RA and suggested methotrexate soon. I have a one year old and was planning on getting pregnant again at the time of this diagnosis. I'm unsure of where to plan my next pregnancy. I'm a 35 years old and do not want to wait too long to get pregnant again. Also, had flares last spring while pregnant, which they tell me is unusual.Also, do not want the disease to continue/start damage..Any suggestions?
amy
12 Mar 2009, 23:29
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I was finally diagnosed last monday. Thanks to a doctor that actually listened to my concerns. I have been complaining of problems for years but to no avail. Looking back on my symptoms,I have probably had this at least 10 years but in a latent phase. General pain, easily dismissed skin pigmentation and OB complications that were written off as pregnancy induced hypertention (with acute renal failure of unknown origin). My doctor is suggesting celebrex only. I am not sure what to do even though I am an RN. I have exprience with RA but it is so different when you are the patient. I have been treating my symptoms with OTC's and massage for years but now my hips are involved. I am having difficulty walking even though i'm only 33. My doctor doesnt feel I need agressive treatment, mainly due to my age. Truthfully I am afraid of the drugs available. I had severe renal complications with both of my pregnancies. I don't want to end up on dialysis but at the same time, relief of the constant pain and fatigue would be nice.I am out of space!
mary alexander lpn
11 Mar 2009, 19:21
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Ihavejust been diagnosed with RA but being an educated medical proffessional I have known for about two years I had the signs/symptoms of the disease.My Dr seems to think waiting on agressive treatment will be more benefical concerning my renal status.I am concerned with the benefits of early vs later treatment.I love my job as a Hospice nurse and do not want the disability to jeporadize that.Im only 46 and hope to continue working for several years.So which is more benefical with less side effects?
deborah konietzko, md
06 Mar 2009, 19:34
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I find that, having RA myself, still "early" (one year out), the clinical skills of rheumatologists are very variable when signs are subtle. Some seem to think that if they can't see it from across the room, then you've got no problem... Maybe symptoms, but not worth treating...
There is still a great reticence to treat at the subtle early stage, even when there are blood markers (RF and anti-CCP) unless they include CRP. Also there is a lack of LISTENING to the patient.
And as for use of ultrasound or extremity MRI, these are barely utilized. Since it's hard to predict how much progression which patients will have, and since MRI findings (not plain films) can show occurrence of abnormalities within the first 6 months, it would seem eminently reasonable to get some kind of baseline to track those you are lucky enough to reach early on.
But there's no interest...
Is it all about the money?
sign me,
A frustrated doc

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