Cervical Epidural Corticosteroid Injection In Degenerative Disease

Introduction
Epidural injections of anesthetic agents and steroids have been used for the treatment and diagnosis in low back pain for more than 40 years. White, Derby and Wynne reported in a prospective study in 1980 1 the usefulness of lumbar epidural injections in diagnosis and treatment. They reported initial relief in 82% of patients which was reduced to 7% relief at six months or longer follow up. The technique was found to be useful in restoring mobility and alleviating discomfort quickly. A similar technique has been applied to the neck as a therapeutic intervention. This paper documents the usefulness of this technique in 33 consecutive patients.

Few reports have been published on cervical epidural corticosteroid injections (CECI).2,3,4 There has been only one study on the technique as a therapeutic modality in cervical discogenic disease. Rowlingson and Kirschenbaum reported on a retrospective study on 25 patients. They noted a 24% excellent clinical result rate, with very short follow up. Of the 25 patients, 18 had an average follow up of only 1.8 months. Of the 24% excellent results of 6 patients, four patients had one-month follow up, one patient had three-month follow up, and one patient had ten-month follow up.

Materials
Thirty-three cervical epidural corticosteroid injections were performed in 30 patients. All patients had a history of neck pain and 21 patients (70%) had concurrent shoulder and/or upper extremity pain.

The mean age was 43 years, with a range of 27 to 68 years. There were 16 females and 14 males. The average duration of symptoms prior to the injection was 22 months. The diagnoses are shown in Table 1.

TABLE 1

Diagnosis

Number of
Patients
Cervical disc herniation 25
Degenerative disc disease 4
Foraminal stenosis 1

All patients had undergone extensive conservative treatment, including rest (off work), traction, nonsteroidal antiinflammatory drugs, physiotherapy, and attempts at physical conditioning and rehabilitation. Eight patients were also placed on tapering doses of oral prednisone. Transient, limited relief was obtained in only one of these patients. The average time in physical therapy and rehabilitation was 8.8 months, with a range of two to 15 months.

All patients were evaluated with cervical spine radiographs, CT and/or MRI and EMG. Two patients had myelograms and eight patients had discograms.

All patients were considered to have exhaustive conservative care, without improvement, and were stationary at an unacceptable level of symptoms or function. Patients were then referred for CECI.

METHODS
All CECI were performed by one skilled anesthestiologist, using the following procedure:

Patient was placed in the prone position on the fluoroscopy table and the exact level to be blocked was identified under fluoroscopy in the AP projection. Skin was marked, prepped and draped. Skin and subcutaneous tissue were infiltrated with local anesthetic. An 18-gauge Crawford type needle was advanced to the lower lamina. Eighty percent of the injections were at the C7-T1 level, and the remainder of injections were at the C6-7 level. The needle was then walked up the lamina until it contacted the ligamentum flavum. The needle was then carefully advanced through the ligamentum flavum, using loss of resistance to injection of fluid to gauge when the ligamentum flavum was perforated. Careful aspiration was done in all planes. .5cc of 1% Xylocaine was then injected as a test dose. After three or four minutes, 8cc of .5% Xylocaine mixed with 80mg of DepoMedrol was injected.

Patients were followed up at an average of nine months, with a range of seven to 13 months.

RESULTS
Based on standardized pain questionnaires and analog pain scales which were filled out by the patients and reviewed by an independent examiner, patient results were categorized into one of four categories:

Excellent..........100% relief of all symptoms

Good...............Greater than 80% relief of symptoms

Fair...............50% to 79% relief of symptoms

Fail...............Less than 50% relief of symptoms

Initial results are shown in Table 2. Fourteen patients had an excellent initial response to CECI. Nine of these 14 patients have continued to do well and have resumed normal daily activities, without neck pain. The remaining five patients had the following results: Two patients' symptoms returned to a dysfunctional level at three and four months. Both received a second CECI and were returned to therapy, still symptomatic but somewhat improved. At four and five months post second CECI, both patients are pain free and doing well. Two patients who had diagnoses of herniated discs had several weeks of excellent relief of symptoms with gradual return of symptoms. They then elected to have surgery. The last of the five patients received an excellent result from CECI but was lost to follow up four months later.

Five patients were categorized as having an initial good result. Three of these were able to return to their physical therapy programs with continued gradual improvement and good results at the time of last follow up. One patient had a relapse of symptoms and was treated with a second CECI. The second injection only conferred fair relief. The fifth patient had good relief for less than one week only.

Six patients had fair results from their cervical epidural corticosteroid injections. One returned to work and a pain free state after continued physical therapy. The other two patients had fair relief for 3.5 weeks, followed by return of their pre-injection symptomatology. Three of the patients with initial fair results showed continued partial improvement after injection.

Five patients received little or no benefit from the injection. Two patients went on to surgery, with only fair results. The remaining three patients had no relief from any treatment offered, including tapering doses of oral prednisone. It is of note that these last three patients all are involved in pending litigation over injuries related to their symptoms.

TABLE 2

  Initial Results Repeat Injection
Excellent 14 2
Good 5 1
Fair 5  
Fail 5  

TABLE 3

Initial Response to CECE

End Result
Excellent Good Fair Fail
Excellent 14 11 0 0 3
Good 5 3 0 1 1
Fair 6 0 1 3 2
Fail 5 0 0 0 5

CONCLUSIONS
Cervical epidural corticosteroid injection is a safe and effective therapeutic modality for cervical degenerative disease which is refractory to conservative treatment.

The study results show marked initial relief in 63% (19/30), with relief lasting an average of eight months in 50% (15/30) of all injected patients (Table 3). Seventy-six percent of injected patients who had relief initially sustained their improved state or improved further during follow up.

Although this is a preliminary retrospective study, the fact that the pre-injection treatment period was prolonged (average 22 months), with no significant clinical improvement, suggests the technique is a valid therapeutic intervention.

The technique appears to be useful in rapid control of pain in many patients, facilitates quick return to a more normal lifestyle, and makes further conservative care more feasible. When performed by an expert with resuscitation skills, we have seen no complications in over 100 cases to date.

REFERENCES

1. White AII, Derby R, Wynne G: Epidural Injections for the Diagnosis and Treatment of Low Back Pain. Spine 5:78-86, 1980. back

2. Rowlingson JC, Kirschenbaum LP: Epidural Analgesic Techniques in the Management of Cervical Psin. Anesth Analg 65:938-43, 1986. back

3. Dirksen R, Rutgers MJ, Coolen MW: Cervical Epidural Steroids in Relfex Sympathetic Dystrophy. Anesthesiology 66:71-73, 1987. back

4. Kainuma M, Shimada Y, Matsuura M: Cervical Epidural Anaesthesia in Carotid Artery Surgery. Anaesthesia 41: 1020-1023, 1986. back