Basis, indications and risk
Neroreflexotherapy (NRTI)
It consists of the stimulation of skin nerve fibers related to
the nerves involved in pain, inflammation and muscle contracture.
Surgical material -surgical staples- is implanted on the skin surface,
and kept in place for approximately three months.
Objective
To reduce pain, inflammation and muscle contracture.
Theoretical base
Pain,
neurogenie
inflammation and muscle
contracture are produced by activation of specific nerve cells.
Neuroreflexotherapy (NRTI) consists of stimulating other nerve
fiber endings on the skin - named Ab-.
Their stimulation activates medullar cells - called "layer IV neurons"-
that release a substance - called "enkephaline"-. This substance
affixes to pain nerves, inactivating them. By this mechanism nerves
stop releasing substances that trigger neurogenic inflammation,
and activation of the cells provoking muscle contracture ceases.
It is essential that the stimulated neurons of layer IV are specifically
the ones that connect with the activated pain nerves in each specific
patient.
Diverse neurologic mechanisms could explain why, if NRT intervention
has been successful, when withdrawing the implanted surgical material
pain may not reappear.
Evidence of efficacy
Available scientific studies coincide in proving the efficacy
of NRT intervention in the treatment of back pain resistant to pharmacological
treatment, including chronic cases.
Risks and contraindications
Adverse
effects derive from the surgical material implanted into the skin,
although it is performed very superficially (it penetrates about
2 mm). This may be bothersome, especially in sensitive patients.
Additionally, immediately after implantation, patients may feel
skin tightness, which may take hours to fade.
Infection of implanted material occurs very rarely -studies performed
showed occurrence in less than 2% of cases- but the skin may become
irritated and temporarily require the use of an ointment.
Finally, after extraction of the surgical material, a little scar
remains at the site of implantation. Usually, scars will vanish
within days or weeks, but may take longer in sensitive skins.
Indications
NRT intervention is not mentioned by the existing recommendations
based on scientific evidence, probably because they have only considered
scientific publications before 1996 with preference for those published
in English. Research studies performed on NRT before 1996 were published
in Spanish, and publications in English appeared afterward.
NRT intervention is indicated in patients whose:
- Back pain lasts for more than 14 days despite pharmacological
treatment.
- Pain is sufficiently intense to justify the skin discomfort
derived from implanting surgical material, and
- Medical evaluation indicates that there are no objective criteria
for urgent
surgery.
|