This study included 55 patients with the diagnosis of
cervical MPS (mean age: 36.2±12.2 years). Patients with
pathological findings in routine blood tests (complete
blood count, serum glucose, renal and liver function tests,
calcium, phosphorus, alkaline phosphatase, erythrocyte
sedimentation rate, C-reactive protein) or on cervical X-ray
radiographs were excluded from the study. Patients who
had received physical therapy and trigger point injections
within the previous six months were also excluded. MPS
diagnosis was made according to Simons criteria, which
include five major and three minor criteria
6.
Major criteria:
1. Regional pain complaint in the neck.
2. Pain complaint or altered sensation in the expected
distribution of referred pain from a myofascial trigger
point.
3. Taut band palpable in an accessible muscle.
4. Excruciating spot tenderness at one point along the
length of the taut band.
5. Some degree of restricted range of motion (ROM),
when measurable.
Minor criteria:
1. Reproduction of clinical pain complaint, or altered
sensation, by pressure on the tender spot.
2. Elicitation of a local twitch response by transverse
snapping palpation at the tender spot or by needle
insertion into the tender spot in the taut band.
3. Pain alleviated by elongating (stretching) the muscle
or by injecting the tender spot (trigger point).
Cervical MPS was diagnosed with five major criteria
and at least one minor criterion. All the patients included
in the study were asked not to take any analgesic
medication during the follow-up. Patients were divided
randomly into two treatment groups. Random sampling
method was performed using numbered envelopes.
Ultrasound (US) treatment was performed with Enraf-
Nonius Sonopuls 590 device. In Group 1 (n=28), US was
performed every three trigger points bilaterally to cover
the trapezius muscle over 8 minutes (mins) (1.5 watt/cm²
dose, 1 MHz frequency, continuous mode US) during a
session every day, for a total of 15 sessions (in a 3-week
period). In Group 2 (n=27), the same treatment protocol
was given, but the US instrument was switched off during
applications. All patients in both groups performed daily
isometric exercise and stretching exercises for the cervical
region under the supervision of the physiotherapist. All
US applications were carried out by the same
physiotherapist.
One of the doctors evaluated the clinical parameters
before the initiation of treatment. After the treatment,
results were evaluated by the other doctors. All physicians
were blinded to the treatment. Only physiotherapists (not
included in the study) knew the treatment and applied
this treatment to the patient. Evaluation parameters
were measured at the beginning of the study and after 4
and 12 weeks.
Pain at rest and at movement was evaluated with
visual analog scale (VAS). Joint ROM measurements were
performed using inclinometer and goniometer (cervical
flexion-extension, lateral flexion and rotation). Neck
Disability Index (NDI) was used to measure changes in
functional disability. Quality of life was measured with
Nottingham Health Profile (NHP).
The NHP consists of two parts, but only the first part
was utilized in this study. The first part includes six fields
(pain, physical abilities, emotional reactions, energy,
social isolation and sleep) and 38 yes/no questions. NHP
scores range from zero (no problem) to 100 (presence of
all the problems in an area). The NHP Turkish version was
used in this study7.
The NDI consists of 10 items and each item is scored
between 0-5. The maximum score is 50. The obtained
score can be multiplied by 2 to produce a percentage
score. The obtained score was also multiplied by 2 in this
study8.
Informed consent was obtained before the
examination and the study received approval from the
local ethics committees of the Kocatepe University.
Statistical Analysis
A value of p<0.05 was considered significant for the
study. The average percentage changes in values of both
groups were compared using the Mann-Whitney U test.
Paired t-test was used for comparison of values within
groups before and after treatment. The chi-square test
and Fisher's exact test were used for comparison of
categorical variables. All analyses were performed using
the SPSS 13.0 for Windows.