Literature DB >> 11766630

[Drug therapy of arthrosis].

J Steinmeyer1.   

Abstract

Osteoarthritis is one of the most common and economically important chronic diseases amongst adults, especially those of a senior age. There now exists a range of effective medications, which either alone or in combination can alleviate the symptoms of the disease and improve the quality of life. Because these medications are not always sufficiently effective and must sometimes be interrupted due to side effects, a large arsenal of active agents is necessary. Alleviation of pain and inhibition of inflammation are the primary goals of pharmacotherapy, whereby the objective is to return an active or transiently painful, decompensated osteoarthritis to a latent (silent, pain-free) condition. This therapeutic goal can almost always be accomplished by using analgesics, nonsteroidal anti-inflammatory drugs (NSAIDs), or intraarticular injection of glucocorticoids. The main problem in administering NSAIDs is their gastrointestinal toxicity,for which a prophylactic medication (e.g., simultaneous application of misoprostol or switching to a COX-2 selective NSAID) should be considered especially with risk groups. The newly developed COX-2 selective NSAIDs represent a true enrichment of our therapeutic options. The spectrum of indications for COX-2 selective NSAIDs should in the future correspond to that of older NSAID preparations, providing that no as yet unknown and serious side effects come to light from their use. Pharmacological results published until now confirm that a clinically relevant analgesic and/or anti-inflammatory effect is associated with the use of SYSA-DOAs (symptomatic slow acting drugs in osteoarthritis). However, no clinical studies exist which can positively confirm prevention of morphologically recognizable cartilage defects in man, or a slowing down or reversal of any progressively developing joint cartilage destruction by any individual medication. Neither the benefits, risks, pharmaceutical quality, nor composition of Orthokin are known, and for this reason its use can not be recommended. Pharmacotherapy should only be considered as one of the three pillars of a long-term,stage-adjusted, and individually customized therapy, the other two of which are represented by nonpharmacological measures and surgical treatment.

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Year:  2001        PMID: 11766630     DOI: 10.1007/s001320170022

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  5 in total

1.  [Reduction of arthrosis associated knee pain through a single intra-articular injection of synthetic hyaluronic acid].

Authors:  D Krocker; G Matziolis; J Tuischer; J Funk; S Tohtz; F Buttgereit; C Perka
Journal:  Z Rheumatol       Date:  2006-07       Impact factor: 1.372

2.  Whole body vibration compared to conventional physiotherapy in patients with gonarthrosis: a protocol for a randomized, controlled study.

Authors:  Gregor Stein; Peter Knoell; Christoph Faymonville; Thomas Kaulhausen; Jan Siewe; Christina Otto; Peer Eysel; Kourosh Zarghooni
Journal:  BMC Musculoskelet Disord       Date:  2010-06-21       Impact factor: 2.362

Review 3.  [Conservative therapy of cartilage defects of the upper ankle joint].

Authors:  U C Smolenski; N Best; B Bocker
Journal:  Orthopade       Date:  2008-03       Impact factor: 1.087

4.  Evaluation of long-term antinociceptive properties of stabilized hyaluronic acid preparation (NASHA) in an animal model of repetitive joint pain.

Authors:  Michael Karl Boettger; Diana Kümmel; Andrew Harrison; Hans-Georg Schaible
Journal:  Arthritis Res Ther       Date:  2011-07-07       Impact factor: 5.156

5.  Dexamethasone Does not Compensate for Local Anesthetic Cytotoxic Effects on Tenocytes: Morphine or Morphine Plus Dexamethasone May Be a Safe Alternative.

Authors:  Anne Lene Oeyen; Jörn Kircher; Melanie Vogl; Irina Ickert; Nani Osada; Rüdiger Krauspe; Bernd Bittersohl; Monika Herten
Journal:  Arthrosc Sports Med Rehabil       Date:  2021-12-23
  5 in total

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