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New Treatment For Hepatitis

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Before we discuss the exciting new ways of managing chronic tendonitis, let's talk about what tendonitis is… and what it isn't.

Tendons are thick cords of fibrous tissue that connect muscles to bones. It is this connection that allows joint motion. When muscles contract, they pull on the tendons which cause the bones to move.

In order for tendons to glide they move inside a lubricated sheath of tissue that is lined with synovial tissue. This synovial tissue is the same type of tissue that lines the inside of joints. Tendonitis occurs when the sheath through which a tendon glides becomes inflamed. This leads to severe pain. The pain usually gets worse with use of the affected joint. However, when tendonitis becomes severe, there may be pain at rest, particularly at night.

Since muscles and tendons surround most joints, tendonitis is rather common. The diagnosis of tendonitis is relatively simple for the experienced clinician. Generally, the diagnosis is made by history and physical examination. In difficult diagnostic cases, diagnostic ultrasound or magnetic resonance imaging is helpful in confirming the diagnosis.

Some of the more common types of tendonitis are:

Shoulder tendonitis. The tendons in the shoulder that are most often affected are the rotator cuff and biceps tendons.

The rotator cuff consists of four tendons that sit on top of the upper arm bone. They are the supraspinatus, infraspinatus, subscapularis, and teres minor tendons. The location of these tendons and the muscles they attach to are what give the shoulder such a great range of motion.

Rotator cuff tendonitis may occur as a result of repetitive activity or tendon degeneration. Pain is felt with most movements and is usually located on the outside part of the shoulder. Certain movements such as reaching behind or to the side may be uncomfortable.

The biceps tendon permits the arm to be flexed at the elbow. Biceps tendonitis also occurs due to repetitive activity and pain is felt in the front of the shoulder.

Shoulder tendonitis can sometimes be treated successfully with anti-inflammatory medication, physical therapy, and occasionally glucocorticoid (cortisone) injection. These methods are most useful for acute tendonitis.

Tendonitis in the elbow is usually located either on the outside and is called lateral epicondylitis or tennis elbow. It may also occur along the inside part of the elbow- medial epicondylitis. This is called golfer's elbow.

Treatment for this condition consists of physical therapy, stretching and strengthening exercises, splints, and injections. While surgery is sometimes recommended for chronic case, I will discuss why that is inadvisable.

Tendonitis in the wrist arises because of repetitive motion. A peculiar form of tendonitis, called Dequervain's tendonitis, is felt on the outside of the thumb.

Tendonitis in this area is managed with glucorticoid injections and immobilization with a splint. Physical therapy modalities may be helpful. Rarely, if ever, is surgery required. Tendonitis in the fingers can lead to catching of the fingers. This is termed “trigger finger.” Trigger finger usually responds to injection.

Tendonitis in the knee may affect the patellar tendon. This is the tendon that connects the knee cap to the tibia (lower leg bone). Patellar tendonitis usually occurs because of excessive jumping and is actually called “jumpers knee.” This is treated with rest, anti-inflammatory medications, and physical therapy.

Tendonitis in the ankle can occur along the outside of the ankle (peroneal tendonitis), the inside of the ankle (posterior tibial tendonitis), or at the back of the ankle (Achilles tendonitis). The tendonitis that occurs along the outside or inside of the ankle can occur because of trauma or because of mechanical instability. Another potential cause is an underlying arthritis condition.

Achilles tendonitis often occurs as a result of excessive stress and loading of the tendon as well as repetitive motion. The Achilles tendon is the thick cord at the back of the ankle that connects the heel bone to the calf muscle. Treatment involves rest, elevation of the heel to take the tension off the Achilles tendon, and physical therapy. Glucocorticoid injection should be avoided because of the danger of Achilles tendon rupture. Anti-inflammatory medication may be helpful.

So what can be done to treat chronic tendonitis? What can you do if you've tried all of the above treatments and still have a problem?

The first new approach, particularly with tendons that are balky is to use hydrodissection. This is a form of treatment where a small gauge needle is introduced into the tendon sheath and a large volume of saline, glucocorticoid, and lidocaine are used to dissect the sheath away from the tendon. Often chronic inflammation causes the sheath and tendon to stick together and this can cause pain as well as loss of function. This type of therapy is particularly effective for the small tendons in the hand.

Another new form of therapy called tenotomy is now being used. This almost always negates the need for an open surgical procedure. With tenotomy, a small gauge needle is introduced with local anesthetic and used to “irritate” the insertion of the tendon where the site of inflammation is located. The needle is inserted using direct ultrasound visualization. After the needling, injection of a small amount of platelet rich plasma (PRP) is performed at the site of needling, again using direct ultrasound visualization. PRP is rich in growth factors that stimulate healing. The process of healing takes only a few days to weeks as opposed to the several weeks to months that an open surgical procedure takes.

Tenotomy can be performed at almost any site where there is chronic tendon inflammation. Results are usually excellent.

Both of these procedures are excellent for the aging athlete who wants to keep going.

For more information about hydrodissection and tenotomy, contact the Arthritis and Osteoporosis Center of Maryland at (301) 694-5800
New Treatment For Hepatitis
Suboxone consists of two drugs; buprenorphine and naloxone. The naloxone is irrelevant if the addict uses the medication properly, but if the tablet is dissolved in water and injected the naloxone will cause instant withdrawal. When suboxone is used correctly, the naloxone is destroyed in the liver shortly after uptake from the intestines and has no therapeutic effect. Buprenorphine is the active substance; it is absorbed under the tongue (and throughout the mouth) but destroyed by the liver if swallowed. There is a formulation of buprenorphine without naloxone called subutex; I have used this formulation when the patient has apparent problems from naloxone, including headaches after dosing with suboxone. I have also treated addicts who have had gastric bypass, where the first part of the intestine is bypassed and the stomach contents empty into a more distal part of the small intestine. In such cases the naloxone escapes ?first pass metabolism', the process with normal anatomy where the drug is taken up by the duodenum and transferred directly to the liver by the portal vein, where it is quickly and completely destroyed. The changes in anatomy with gastric bypass allow naloxone to pass from the distal small intestine to the bloodstream, bypassing the liver and resulting in mild symptoms of withdrawal.

Buprenorphine has a ?ceiling effect'-the narcotic effect of the drug increases with increasing dose up to about one or two mg, but then the effect plateaus and higher amounts of buprenorphine do not increase narcosis. The average patient usually takes 12-24 mg of suboxone per day, and quickly becomes tolerant to the effects of buprenorphine (buprenorphine does have significant narcotic potency, but the potency usually pales in comparison to the degree of tolerance found in active opiate addicts).. The opiate receptors in the brain of the addict become completely bound up with buprenorphine, and the effects of any other opiate medication are blocked. Once the addict is tolerant to the correct dose of suboxone, the buprenorphine that is bound to their opiate receptors reduces cravings and prevents the effects-and so the use--of other opiates. Suboxone is very effective in preventing relapse; the ?choose to use' issue is effectively removed by the fact that use would require the addict to go through several days of withdrawal in order to remove the receptor blockade and allow other opiates to have an effect. Given addicts' attitudes toward withdrawal, the appeal of this ?choice' is quite low. The only real problem with suboxone treatment relates to specificity. With suboxone, the addict stays off opiates, but there is nothing to prevent the substitution of alcohol. On the other hand, naltrexone reduces alcohol cravings by blocking opiate receptors, and it is quite likely that suboxone, through its similar mechanism, will reduce alcohol cravings as well. Such an effect has been reported to me by a number of suboxone patients, but has not been reported in the literature at this point. The suboxone patients who move from one substance to another will likely require an approach that demands total sobriety. But in the case of pure opiate addiction, suboxone allows treatment without the misery of protracted withdrawal, without the high cost of residential centers, without the stigma and limitations imposed by methadone programs.

As I stated in part one of this article, I predict that suboxone will eventually be the standard treatment for opiate addiction, and will change the treatment approach for other substance addictions as well. My only reservation with this statement is that it is unclear how the current recovering community will respond to patients treated with suboxone. If suboxone patients are rejected by the recovering community, what will be the long-term outcome of their addictions when the substance is removed but the personalities and issues remain untreated? Is it a given that all addicts have a disease that requires group therapy? As things stand now, addicts maintained on suboxone are often referred for addiction counseling. But the exact message to deliver with counseling is debatable. In many ways, a patient maintained with suboxone becomes similar to a patient with hypertension treated for life with medication-the underlying problem persists, but the active disease is held in remission. If the uncontrolled use of opiates is effectively treated, is that enough? Should counseling be focused on removing the shame of having the disease of addiction, and on encouraging the treated addicts to get on with their normal lives? Or should we continue to see addiction as a consequence of a deeper problem or faulty character structure, which requires groups and meetings if one hopes to become ?normal'? Unfortunately the use of suboxone runs counter to successful adoption of sobriety through 12-step programs, which in the first step require acceptance of the fact that the addict is powerless over the substance-that there is no amount of will power that will allow the addict to control the deadly effects of the drug. By using suboxone the addict may develop the impression that he/she has control, particularly if suboxone becomes popular on the street for self-medication of withdrawal.

Before suboxone, the only option for opiate addicts was to lose a sufficient number of things-family, employment, freedom, health-to cause them to accept treatment and recovery. Only a small fraction of addicts recovered, and only after significant losses-and relapse rates were high. Suboxone is an amazing breakthrough; one that for the first time allows treatment of addicts early in the course of their illness, and that reliably induces remission in most patients. But there are some things to be concerned about, that have the potential to reduce the effectiveness of this amazing new drug and treatment approach. First, some insurers demand that the drug be used only short-term, in some cases for only three weeks! This requirement totally misses the nature of addiction, and ignores the known high relapse rate after short-term use of suboxone (and why wouldn't it be high?). Some physicians use the medication in this short-term way; hopefully the motivations for this ineffective treatment method are not related to the limits placed on the numbers of maintenance patients per physician. Other physicians will transfer their attitudes toward opiate agonists to the use of suboxone, and place constant downward pressure on the daily dose of suboxone. This approach is not appropriate with suboxone; the value of the drug requires adequate dosing to achieve the long half-life and repression of cravings. At doses of less than 8 mg, suboxone becomes more similar to a pure agonist; one might as well be giving small doses of hydrocodone to prevent withdrawal. There is no reason beyond drug cost to reduce the dose, as tolerance is limited by the ceiling effect that occurs with relatively low doses. In other words, higher doses of suboxone do not result in eventual higher degrees of withdrawal. Another issue is that the medication is sometimes prescribed carelessly, without emphasizing the need to dose once per day. Patients left to their own devices will start using the medication multiple times per day as a ?prn' medication, and will remain in the same addiction behavior that brought them to treatment. Once per day dosing is important because it allows the addictive behavior to be extinguished over time. The frequent dosing does provide a distraction and placebo effect, and so initially patients will have an increase in anxiety when the dosing obsession is removed. But over time the anxiety will fade, and the huge void left by the removal of addictive obsession will allow the development of relationships and other positive character traits that were forced out by their addiction.

Given the time pressures and payment structures of modern medicine, suboxone may eventually replace residential treatment as a more reliable, less costly alternative. I believe that the time has come to replace the ?recovery' model with a new ?remission' model, which allows treatment of a much higher percentage of users at an earlier stage of disease. With time, will we find analogous agents that provide a low level of intoxication in return for receptor blockade? While not likely with alcohol, such an outcome is certainly within the bounds of imagination for cocaine, benzodiazepines, and barbiturates. While it is true that daily use of a partial agonist would represent a reversal from our current approach where all intoxicating substances are to be avoided, it is also true that the current approach has no bragging rights based on outcome. Finally, perhaps the adoption of a remission model will lessen the time until opiate and other addictions carry as much moral stigma as hypertension or diabetes-two other diseases that are generally treatable, but that require long-term use of medications.
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Both Nathan Wei & Jeffrey T. Junig are contributors for EditorialToday. The above articles have been edited for relevancy and timeliness. All write-ups, reviews, tips and guides published by EditorialToday.com and its partners or affiliates are for informational purposes only. They should not be used for any legal or any other type of advice. We do not endorse any author, contributor, writer or article posted by our team.

Nathan Wei has sinced written about articles on various topics from Arthritis Pain, Health and Arthritis Signs. Nathan Wei, MD FACP FACR is a board-certified rheumatologist. For more info: and. Nathan Wei's top article generates over 550000 views. to your Favourites.

Jeffrey T. Junig has sinced written about articles on various topics from . Jeffrey Junig MD PhD can be contacted through his addiction and pain practice, , or through his psychiatry practice,. Jeffrey T. Junig's top article . to your Favourites.
Baby Car Seat Safety Ratings
The safest place is the center of the back seat. This is because studies show that air bags in the front seat may cause injuries to children. So if possible, never allow a child to be seated in front
 
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