Appropriate Depth of Needle Insertion During Rhomboid Major Trigger Point Block

Seung Jun Seol; Hyungpil Cho; Do Hyun Yoon; Seong Ho Jang

doi:10.5535/arm.2014.38.1.72

Abstract

Objective

To investigate an appropriate depth of needle insertion during trigger point injection into the rhomboid major muscle.

Methods

Sixty-two patients who visited our department with shoulder or upper back pain participated in this study. The distance between the skin and the rhomboid major muscle (SM) and the distance between the skin and rib (SB) were measured using ultrasonography. The subjects were divided into 3 groups according to BMI: BMI less than 23 kg/m² (underweight or normal group); 23 kg/m² or more to less than 25 kg/m² (overweight group); and 25 kg/m² or more (obese group). The mean±standard deviation (SD) of SM and SB of each group were calculated. A range between mean+1 SD of SM and the mean-1 SD of SB was defined as a safe margin.

Results

The underweight or normal group's SM, SB, and the safe margin were 1.2±0.2, 2.1±0.4, and 1.4 to 1.7 cm, respectively. The overweight group's SM and SB were 1.4±0.2 and 2.4±0.9 cm, respectively. The safe margin could not be calculated for this group. The obese group's SM, SB, and the safe margin were 1.8±0.3, 2.7±0.5, and 2.1 to 2.2 cm, respectively.

Conclusion

This study will help us to set the standard depth of safe needle insertion into the rhomboid major muscle in an effective manner without causing any complications.

INTRODUCTION

Myofascial pain syndrome is a painful musculoskeletal condition produced by myofascial trigger points [1]. Trigger point injection is one of the treatment methods for this condition and is known to provide temporary or long-term relief [2]. When a skilled operator performs an injection, the procedure is generally very safe, but some side effects have been reported [3]. The reported side effects include pain, nerve injury, bleeding, infection, and some serious complications, such as pneumothorax [4,5].

Iatrogenic pneumothorax can occur when patients are treated with trigger point injection on their shoulder and neck region, such as the trapezius muscle, rhomboid major or minor muscles. Among these muscles, the rhomboid major muscle is very thin, and the thicknesses of the skin, subcutaneous fat layer and other soft tissues around the muscle vary between individuals. Furthermore, in the deep part of the muscles, there are intercostal nerves, blood vessels, and pleura. Thus, the determination of an appropriate injection depth becomes one of the most important factors when performing injections into these muscles. However, there is no research with clear criteria regarding the depth of needle insertion that allows safe and effective alleviation of pain. With this in mind, we carried out this study to provide some reference for safe and effective treatment through determining an appropriate injection depth according to the body type of patients using body mass index (BMI) during trigger point injection into the rhomboid major muscle.

MATERIALS AND METHODS

Subjects

Our subjects were 62 outpatients and hospitalized patients who had visited the rehabilitation medicine department of our hospital for pain in their upper back or shoulder. Patients with a history of fractures or surgery around the shoulder were excluded from the study because of the potential of anatomical changes around their shoulders. Also, patients who could not maintain their posture for more than 5 minutes because of serious pain or limited range of motion were excluded. Age, sex, weight, and BMI of the patients are described in Table 1.

Measurements

We measured the depth and thickness of the rhomboid major muscle by ultrasonography. During the study, patients put their hand of the affected side on the opposite shoulder to relax the rhomboid major muscle (Fig. 1). A transducer was then placed at point 1 cm medial to the midpoint of the medial border of the scapula of the affected side, parallel to the medial border, and perpendicular to the skin surface (Fig. 2). Great care was taken not to exert excessive pressure with the transducer. Participants were required to inspire fully and hold their breath during measurement. Following this, two values were measured; the distance from the skin to the surface of the rhomboid major muscle was named SM (skin-muscle distance), indicating the minimal depth for the needle tip needle during trigger point injection into the rhomboid major muscle. The distance between the skin and the surface of the rib was named SB (skin-bone distance) (Fig. 3). The SB indicated the maximum depth of the needle tip that can be inserted safely with no danger of pneumothorax or injury of to intercostal nerves and vessels. The difference between SB and SM was the thickness of the rhomboid major muscle. When the tip of the needle was in this range, it indicated that the needle tip was safely located within the rhomboid major muscle. We also defined a range between mean+1 SD of SM and the mean-1 SD of SB as a safe margin of needle depth in each group.

This study was carried out by a skillful medical specialist of rehabilitation medicine, using Accuvix V10 (Medison, Seoul, Korea) and linear probes with a frequency between 5 and 13 MHz. The subjects were divided into 3 groups according to BMI: 1) BMI less than 23 kg/m² (underweight or normal group); 2) 23 kg/m² or more to less than 25 kg/m² (overweight group); and 3) 25 kg/m² or more (obese group).

Statistical analysis

SPSS ver. 18.0 (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. The independent t-test was used to compare the measured values between males and females. Statistical difference of the measured values between the groups according to the BMI was analyzed using the one-way analysis of variance (ANOVA) test.

RESULTS

The study population consisted of 19 men and 43 women with an age range of 53.6±13.2 years (from 23 to 78). In terms of BMI, there was no statistical difference between men and women (p=0.09). The baseline characteristics of the subjects are provided in Table 1. SM, SB, and the difference between SM and SB did not differ significantly by gender (Table 2).

The number of subjects in each group divided by the BMI was 29 for the underweight or normal weight group, 14 in the overweight group, and 19 in the obese group (Table 3). Both SM and SB were deeper in the group with higher BMI (p<0.001) although the difference between the underweight or normal group and the overweight group were not statistically significant (p=0.07 for SM, p=0.19 for SB). The thickness of the rhomboid major muscle (the difference between SM and SB) was not significantly difference between the groups divided by BMI. The safe margin was 1.4 to 1.7 cm in the underweight or normal group and 2.1 to 2.2 cm in the obese group. In the overweight group, the safe margin of needle depth could not be calculated because SB-1 SD was larger than SM+1 SD in this group (Table 3).

DISCUSSION

The purpose of this study was to provide the standard depth of needle insertion during trigger point injection into the rhomboid major muscle. According to our results, the depth of needle insertion was dependent on the patient's BMI, but gender did not influence SM and SB in our study. However, the number of male participants was small, thus there should be an additional study to compare the values between men and women. Although both SM and SB were deeper in the group with higher BMI, the difference between SM and SB (the thickness of rhomboid major muscle) was not significantly different between the groups divided by BMI. This suggests that the main factor influencing the depth of insertion is the thickness of fat tissue, not muscle. In addition, we set a range between the mean+1 SD of SM and mean-1 SD of SB as a safe margin of needle depth in each group divided by BMI. This was done to assure that the needle tip is placed safely in the rhomboid major muscle without any possibility of pneumothorax, which was achieved in 71% of all patients. However, even if the needle tip is inserted deeper than SB, pneumothorax does not occur until the needle tip reaches the pleura. According to Mohr et al. [6], the average width of the rib around the rhomboid major muscle is 7.5±1.8 mm, and this value is the difference between the depth to the rib and to the pleura. Therefore, safety is guaranteed in much more than 71% of patients because of this width of the rib.

To our knowledge, this is the first trial that uses ultrasonography to set the standard depth of safe needle insertion according to the patient's body type during trigger point injection. According to Dupont et al. [7], it is widely acknowledged that real-time ultrasonography is accurate in precisely measuring muscle thickness, and for being time-efficient. Ultrasonography has also been reported to be as accurate as magnetic resonance imaging when measuring the cross-sectional area of low back muscles [8]. Also, there have been some previous studies using ultrasonography to measure the depth or cross-sectional area of a muscle. For example, Yang et al. [5] used ultrasonography to measure the thickness of the interscapular soft-tissue. However, they did not divide their participants into subgroups by the BMI. They also enrolled normal young adults, but the present study was conducted with elderly patients with shoulder pain.

On the other hand, there is a controversy about the appropriate depth of needle insertion during trigger point injection. Ceccherelli et al. [9] revealed that when injecting into a trigger point in the low back muscle, there were no significant differences regarding their short-term pain relief between the superficially inserted group and deeply inserted group. Another study compared the effects on 35 older adults with chronic low back pain by injecting into a trigger point with 3-mm depth and 2-cm depth [10]. The study revealed that the group with deep insertion showed greater effects of pain relief as well as improvement in quality of life, although the results were not statistically significant.

In contrast, Baldry [11] reported that more deeply inserted needles cause more pain than superficially inserted needles. Kalichman and Vulfsons [12] also suggested superficial injection.

The best outcome wtihout complications may be expected by injecting a needle precisely into the exact location of the trigger point.

There are a few limitations to consider in our study. Although we calculated the standard depth of insertion in each group, there may be some variations because the depth from the skin to the rhomboid major muscle or its thickness may be different according to the patient's posture. Also, even if we measured the vertical distance from the skin to the rhomboid major muscle or rib, the needle is not always inserted into the skin vertically in clinical practice, so there may be some errors in applying the values we measured in all situations. Moreover, even if we specify a certain point as the standard location in order to maintain consistency of measurement, for a real patient, the trigger point may exist at another place.

However, at present, since the criteria of needle depth at the trigger point injection of the rhomboid major muscle have not been elucidated, we expect that the values measured by this study would be useful reference values ensuring safer and more effective practice by physicians.

Even though the total number of subjects of this study may be too small to give statistical meaning, if we conduct further research with a larger number of subjects in the future, we would be able to formulate more accurate standard values.

In conclusion, we measured the values that can help us predict an appropriate depth of needle insertion during a trigger point injection. If we inject a needle at the trigger point of the rhomboid major muscle with these values in mind, we are more likely to deliver a safer and more efficient procedure.