Usefulness of combined handheld ultrasound and fluoroscopy-guided injection in adhesive capsulitis of the shoulder: A prospective, randomized single blind-pilot study
Abstract
BACKGROUND:
Ultrasound is increasingly being utilized in the diagnosis and treatment of adhesive capsulitis.
OBJECTIVE:
To compare the therapeutic effects and advantages of combined handheld ultrasound and fluoroscopy-guided intra-articular corticosteroid injection with those of conventional ultrasound-guided corticosteroid injection in adhesive capsulitis of the shoulder.
METHODS:
A total of 39 patients diagnosed with adhesive capsulitis of the shoulder were randomly assigned into two groups. Group A patients (
RESULTS:
Both injection methods were effective in the treatment of adhesive capsulitis. No significant differences in treatment efficacy and injection accuracy were observed between the two groups (
CONCLUSIONS:
This study showed no statistical differences in treatment efficacy between 2 groups. However, the combined use of ultrasound and fluoroscopy can increase the accuracy of injection compared with conventional ultrasound alone.
1.Introduction
Adhesive capsulitis is one of the most common causes of shoulder pain and disabilities [1]. This condition is characterized by a hypertrophic synovial capsule, adhesions and contracture of the glenohumeral capsule, fibrosis, and inflammatory processes [2, 3]. Painful shoulder stiffness can adversely affect daily life activities and ultimately reduce the quality of life [3].
Several treatment methods, such as corticosteroid injection, use of nonsteroidal anti-inflammatory drugs, and physical therapy, can be applied for treating adhesive capsulitis of the shoulder [2]. Intra-articular (IA) injection was reported to be effective in decreasing pain and increasing the shoulder range of motion (ROM) in patients with adhesive capsulitis [4, 5, 6, 7].
Ultrasound (US) is increasingly being utilized in the diagnosis and treatment of musculoskeletal diseases. A previous study has shown that US-guided IA corticosteroid injection has advantages over fluoroscopy (FL)-guided capsular distension, including lack of radiation exposure, increased accuracy by viewing the expansion of joint spaces, and better convenience of use with similar therapeutic effects [8]. Although US has more advantages than FL, the US device is still bulky and difficult to transport and handle in health-care facilities.
Previous studies have reported the accuracy of US-guided IA injection in the glenohumeral joint to be 90–93.3% [9, 10, 11]. Extra-articular corticosteroid injections can lead to complications including soft-tissue atrophy, tendon degeneration or ruptures, and skin depigmentation [12]. Several studies have reported on combined FL and US-guided interventions for musculoskeletal pain treatment [13, 14, 15]. This combined method allows avoiding critical structures in the needle path while checking the progress of the needle in real time under US. In addition, by injecting a contrast media, it is possible to confirm whether the injection was performed at the correct site through the fluoroscopic image. Therefore, this combined method enables injecting with safety and accuracy. However, studies on this method with respect to musculoskeletal treatment are still lacking. Furthermore, using US and FL simultaneously requires a large space; mastering both methods can be difficult; and cost-effectiveness problems may exist.
A portable US device was developed in 1975, and a handheld US device was developed in the late 1990s. With continuous technological advancements, smaller and lighter devices that provide high-quality images became recently available [16]. A handheld device enables physicians to make instant assessments in or outside the hospital. It can reduce the patients’ waiting time and enhance the clinicians’ workflow [16]. Moreover, previous studies have shown the efficacy and convenience of use of handheld US systems, as well as their capability to detect some diseases [17].
The aim of this study was to compare the therapeutic effects and advantages of that combined FL and handheld US-guided and the conventional US-guided IA injection in order to verify the usefulness of that combined FL and handheld US-guided IA injection in the treatment of frozen shoulders.
2.Materials and methods
2.1Participants
After obtaining institutional review board approval and clinical trial registration (GDIRB2017-113), 40 patients with frozen shoulder were enrolled into this a prospective, randomized single blind-pilot study. This study included patients who complained of shoulder pain and showed limitation of shoulder ROM from April to December 2017.
Figure 1.
Combined fluoroscopy (FL) and handheld ultrasound (US)-guided intra-articular (IA) injection technique. (A) Combined FL and handheld US equipment set. (B) Handheld US equipment set. (C) Image of the handheld US on the shoulder. D, deltoid; IS, infraspinatus; G, glenoid; HH, humeral head. Arrows indicate the needle. (D) Image of the FL with the handheld US equipment on the shoulder.
The diagnosis of adhesive capsulitis was made by two physiatrists based on history taking, physical examination, radiologic evaluation, and musculoskeletal US findings. The inclusion criteria were as follows: disease duration of 3–9 months and a
The exclusion criteria were as follows: US finding of a full-thickness tear of rotator cuff; hospitalization over the previous 6 months for a shoulder joint-related incident; a severe psychiatric problem; age
2.2Randomization of participants
After the eligibility assessment, initial evaluation was performed. Participants were randomly assigned into one of 2 groups using a computer-generated randomization table.
For group A, portable US (SONON 300L
The frequencies of the linear probes were between 5 and 15 MHz. Patients in groups A and B were administered the same mixture containing 0.5% lidocaine (7 ml), triamcinolone 20 mg (1 ml), and nonionic contrast medium (Omnipaque 300; GE Healthcare, Shanghai, USA; 2 mL).
2.3Combined FL and handheld US-guided IA injection technique
All US examinations of the shoulder and combined FL and handheld US-guided IA injection procedures were performed by one physician (K.D. Park) with
During the injection, the patients were placed on the C-arm table in the prone position with their upper arm adducted and internally rotated. The posterior of the acromion was palpated, and the injection site was 1 cm inferior and 1 cm medial to the acromion. Under FL and handheld US guidance, injection with a posterolateral approach was performed using a 25-gauge, 2.5 inch needle (Fig. 1) [12, 18]. All injections were made after ensuring with US that the needle tip was properly located in the IA space and finally checking the contrast medium in the joint cavity with FL.
Figure 2.
Ultrasound (US)-guided intra-articular (IA) injection techniques. (A) US-guided IA injection with the posterolateral approach. (B) Image of the US on the shoulder. D, deltoid; IS, infraspinatus; G, glenoid; HH, humeral head. Arrows indicate the needle and arrowhead indicates the needle tip in the IA space.
Figure 3.
Shoulder posterior-anterior view. (A) Before intra-articular (IA) steroid injection. (B) After IA corticosteroid injection. (C) Leakage of contrast medium to outside the articular space. Arrows indicate the contrast medium.
2.4US-guided IA injection techniques
During the injection, the patients were in a sitting position with their arm adducted and internally rotated. The posterior of the acromion was palpated, and the injection site was 1 cm inferior and 1 cm medial to the acromion. After needle entry, injection was performed toward the coracoid process. Under US guidance, injection with a posterolateral approach was performed using a 25-gauge, 2.5 inch needle. All injections were made after ensuring with US that the needle tip was properly located in the IA space. The accuracy of injection into the IA space was checked during the procedure, and joint capsule distension was assessed in appropriate cases (Fig. 2) [18].
The participants in both groups were asked to limit shoulder motion for at least 10 min after injection to allow the localization of the injected drugs in the articular capsule. All participants were prescribed a simple exercise program comprising pendulum exercise and scapular setting (isometric scapular retraction). Additionally, acetaminophen or ice massage was permitted in patients with pain at the injection site. The first IA injection was immediately performed after the diagnosis of adhesive capsulitis. After 2 weeks, a second IA injection was performed. The injection frequency was identical for groups A and B.
2.5Evaluation of accuracy, treatment effect and procedure time
The accuracy of combined US and FL-guided injection can be immediately confirmed on the C-arm image after contrast injection. For US-guided injection into the IA space, the accuracy was assessed using shoulder radiography after the injection. If contrast medium was observed in the glenohumeral joint space, the injection was considered to be accurate (Fig. 3).
The evaluation of the treatment effects of IA injection was completed a total of three times: before the first injection and at 2 and 6 weeks after the second injection. Verbal numeric pain scale (VNS), Shoulder Pain and Disability Index (SPADI), and pROM were assessed during treatment efficacy evaluation. All assessments were performed by one evaluator who was unaware of patient grouping under supervision.
SPADI is a self-administered assessment tool that measures pain and disability related to shoulder disease [8]. It consists of five pain and eight disability items, each measured on a visual analogue scale. The pain and disability subscales are calculated as the mean of the corresponding items on a 0–100 scale, with the highest score indicating the most severe pain and disability. The total score is calculated by summing the pain and disability subscale scores. SPADI has been used in previous randomized trials investigating treatment effects in populations with frozen shoulder [19, 20, 21]. The psychometric properties of the index have been tested in patients with shoulder problems, and the index has been shown to have acceptable validity for group comparisons [8].
The VNS is an 11-point scale ranging from 0 (“no pain”) to 10 (“the worst pain possible) [8]. For the VNS evaluation, the patients were asked to rate their pain on a scale from 0 to 10 (0 and 10 represented “no pain” and “the worst pain possible,” respectively), in whole numbers with 11 integers including zero [8].
ROM was measured by physicians with the patient in the supine position. A physician assisted the patient to achieve maximum passive motion, and another physician measured pROM values in three directions (forward flexion and abduction from neutral position and external rotation from 45
Procedure time was defined as the time interval between the point of contact of the US probe with the patient’s skin and the completion of injection.
2.6Statistical analysis
The purpose of this pilot study is to compare the therapeutic effects, advantages, and the feasibility for a further large-scale clinical trial of combined handheld ultrasound and fluoroscopy-guided intra-articular corticosteroid injection with those of conventional ultrasound guided steroid injection in adhesive capsulitis of the shoulder We did not find a suitable reference to calculate the sample size, but a minimum sample size of the clinical trial with 20 patients per group is used instead [22].
An independent t-test was used to compare differences in participant characteristics and procedure time between the two groups. Data acquired at the initial diagnosis of adhesive capsulitis, and those obtained at 2 and 6 weeks after the second injection, were used for comparisons between the two groups. Comparison of VNS score, ROM, and SPADI between the two groups was performed using a normality test of the Shapiro-Wilk test and a two-way repeated-measures analysis of variance. A p-value of
Table 1
Characteristics of the participants
| Group A | Group B | ||
|---|---|---|---|
| Number | 19 | 20 | |
| Sex | M2/F17 | M4/F16 | |
| Age (years) | 57.90 | 55.65 | 0.418 |
| Duration (months) | 6.48 | 7.85 | 0.148 |
| BMI (kg/m | 23.30 | 22.06 | 0.093 |
| Lesion side (R/L) | 8/11 | 11/9 | 0.434 |
Values are mean
Table 2
Comparison of the effect of intra-articular corticosteroid injections on VNS, SPADI, and pROM
| Group | Before steroid injections | 2 wks. after 2 | 6 wks. after 2 | ||||
|---|---|---|---|---|---|---|---|
| VNS | A | 7.08 | 2.41 | 2.47 | |||
| B | 6.96 | 2.88 | 2.52 | ||||
| SPADI | A | 60.23 | 27.24 | 26.42 | |||
| B | 64.52 | 30.23 | 28.35 | ||||
| pROM | |||||||
| FL | A | 131.58 | 150.79 | 154.74 | |||
| B | 126.25 | 148.25 | 151.50 | ||||
| AB | A | 106.32 | 138.16 | 139.74 | |||
| B | 100.25 | 131.75 | 133.25 | ||||
| ER | A | 48.95 | 69.21 | 70.53 | |||
| B | 43.50 | 64.00 | 65.25 | ||||
Values are mean
Figure 4.
Design and flow of participants in the study. FL, fluoroscopy; IA, intra-articular; US, ultrasound; VNS, verbal numeric pain scale; SPADI, shoulder pain and disability index; pROM, passive range of motion.
3.Results
3.1General characteristics of patients
Initially, 40 participants were randomly assigned and divided into two groups. A total of 20 participants were assigned into group A and the other 20 participants were assigned into group B. However, one of the participants in group A had a failed follow-up (Fig. 4). Finally, group A was composed of 19 patients (2 men, 17 women) with a mean age of 57.90 years. The mean duration of disease among group A patients was 6.48 months. Group B was composed of 20 patients (4 men, 16 women) with a mean age of 55.65 years. Among the patients of this group, the mean disease duration was 7.85 months. No significant differences in the general patient characteristics were observed between the two groups (
3.2Change in pain severity according to VNS, SPADI and ROM in passive movements
The VNS score before IA corticosteroid injection was 7.08
The SPADI scores before injection were 60.23
After the procedure, pROM showed improvements in both groups. Significant improvements in ROM for three types of movements were observed in both groups at 2 and 6 weeks after the procedure (
3.3Accuracy and procedure time
In all patients of group A, contrast medium was completely injected into the articular cavity, while three cases of leakage and injection outside the articular space were confirmed in group B (Fig. 3). No statistically significant difference in injection accuracy was observed between groups (19/19 (100%) vs. 17/20 (85%),
3.4Complications
No severe complications, such as vasovagal syncope, allergic reactions, steroid-associated infection, adipose tissue atrophy, or toxic reactions including dizziness, were observed after injections in both groups.
4.Discussion
Adhesive capsulitis commonly affects about 2–3% of the general population and up to 5% in certain populations [4, 23, 24]. Adhesive capsulitis can occur as a primary or secondary disorder. Primary adhesive capsulitis can occur spontaneously. Secondary adhesive capsulitis is often observed after shoulder joint fracture-dislocation, arm fracture, or other severe joint trauma [25].
IA corticosteroid injection has been reported to have greater efficacy than oral administration of steroids in the treatment of adhesive capsulitis [5]. Hettrich et al. [4] showed that IA corticosteroid injection is effective in decreasing fibromatosis and myofibroblast numbers in capsular tissue. Other studies have also reported improvements in pain and ROM after IA corticosteroid injection [6, 7]. In IA corticosteroid injection, the accuracy of the injection is the key factor that determines the inflammation-reducing effect [26, 27]. As accurate injection into the desired site is crucial for ensuring the therapeutic effect, guidance using several modalities can enhance the efficacy of corticosteroid injection treatment. US guidance is one of the modalities that can be utilized in IA corticosteroid injection. Previous studies have shown that US guidance can be utilized in the treatment of adhesive capsulitis of the shoulder [1, 8].
US is an excellent visualization tool that avoids vulnerable structures such as nerves and vessels during injection, whereas contrast FL can only detect when the tip of the needle is at the target point. It should be kept in mind that FL may not be able to detect that the needle has already traversed a vessel on its way to the target, whereas US can avoid this problem [28]. Therefore, if both methods are used simultaneously, patient safety and more accurate injection can be guaranteed than by injection with each method alone. Some studies on the use of the combined US and FL-guided injection method for detecting renal abscess, for kidney biopsy, and for the treatment of musculoskeletal disorders have been recently; however, data are still insufficient [29, 30, 31, 32].
In US-guided IA shoulder injection with a posterior approach, the direction of the needle tip can be checked in real time. After the needle is positioned at the target point, the drug can be injected into the IA space; however, because a contrast agent is not used, it is difficult to directly check the accuracy of the injection into the joint cavity. Moreover, obese patients have a disadvantage in that it is difficult to check the needle tip position on the US image, and, when injected, the drug may flow out of the joint cavity, causing some adverse effects. The FL-guided injection method has the advantage of using a contrast agent to ensure the accurate injection of the drug into the joint cavity; however, it is costly, bulky, and exposes the patient and clinician to ionizing radiation. A risk of damage to the major structures in the path of needle progression also exist.
If the two methods are used simultaneously, critical structures can be avoided in the injection process, needles can be placed at the target point, and the accurate injection of the drug can be detected with contrast medium use. Furthermore, despite the risk of radiation exposure, the amount of irradiation may be smaller than when using FL alone. The disadvantages of using both methods simultaneously are that both the FL and US equipment are bulky. Thus, in this study, the spatial constraints were reduced through the use of handheld US.
Cases of injection failure in group B included not only a direct extra-articular space injection but also cases in which the nonionic contrast medium was visible in bursal layers because of drug leakage after an IA injection. In total, there were three failed cases: In all three cases, all injections were accurately performed on the targeted site, joint capsular distension was confirmed during injection and capsular rupture was not observed. These failures were primarily attributed to technical problems, not to patient factors. The causes of such failures were the following: (1) potential cases in which the position of needle in the course of injection could not be identified, such that the needle used for the procedure could be easily misaligned because of the narrow beam of US to the extent of 1 mm, and (2) the needles may not have been fixed correctly because a freehand technique was used in this study.
Intraarticular corticosteroid injection failure such as extraarticular space leakage can cause temporary increases in pain, skin atrophy, depigmentation, and septic arthritis as well as deleterious effects on tendon degeneration and even tendon ruptures [33]. Although there were no statistical significance, three extraarticular leakage injection cases were observed in group B. Accurate intraarticular injection is essential to ensure safety of procedure, and this can be made by use of assistant modalities such as US. Studies have been reported about advantages and safety for combined US and FL guidance injection technique for the treatment of musculoskeletal pain through complementing each method’s weakness [34, 35].
Many previous studies have reported the applicability of handheld US in diagnosing diseases in many subfields of medicine. Tse et al. [16] compared the performance of a handheld US device against the conventional US device in terms of image quality in common abdominal pathologies. In their study, the handheld US device showed satisfactory imaging quality and proved to be useful in emergency screening or general screening of abdominal organ pathologies. In the field of musculoskeletal diseases, we expect that a handheld device would not be inferior to a conventional device and would be more convenient in diagnosing and treating both outpatients and inpatients. Moreover, we were set on the idea of using a handheld device for US guidance in the treatment of adhesive capsulitis, specifically with IA corticosteroid injection.
After injections, both groups showed significant improvements in pain severity and ROM. The differences in VNS and ROM between 2 and 6 weeks after the second injection were significantly lower than when they were compared with the initial assessment. However, the efficacy of treatment showed no significant differences between group A (combined handheld US and FL) and group B (conventional US). Moreover, in group A, the effect of flexion continued until 6 weeks after the last injection and was more effective than after 2 weeks. In group B, the effect continued for 6 weeks after injection, and the SPADI and VNS score were also significantly different between 2 and 6 weeks after injection. These results imply that both groups showed attenuated symptoms of adhesive capsulitis and that the corticosteroid injection treatment was effective, which suggests that handheld US under FL is not inferior to FL
The time consumed for the whole procedure was compared between groups A and B. The whole injection procedure took about 9 min in group A and about 8 min in group B. The combined method requires additional time to check the FL image after the injection; however, no statistical differences were observed. Although the combined method may take longer than US guidance alone, it is recommended as a safe method because it can help reduce the complications caused by leakage of drugs out of joint spaces through contrast medium detection and has lower radiation exposure than with using FL alone.
4.1Limitations
One of the limitations of this study was the small sample size in each group. Only 19 and 20 patients were included in groups A and B, respectively. The short follow-up period was also a limitation. Subsequent studies with larger numbers of participants and with longer follow-up periods should be conducted to thoroughly evaluate the outcomes of US-guided IA steroid injection in the treatment of adhesive capsulitis. Moreover, operators should conduct handheld US- and conventional US-guided methods to determine which of the two devices is more convenient to use. A wide range of operators, from less skilled to well trained, should be surveyed in investigating the convenience of use of US devices and the operator satisfaction in using each device We checked whether participants were doing the prescribed exercise properly during outpatient visits but did not check the compliance by quantifying it. This could be a bias in treatment efficacy.
5.Conclusion
The results of this study showed no statistical differences in treatment efficacy between the combined use of handheld US and FL and the use of conventional US alone during shoulder IA corticosteroid injection. Furthermore, the combined use of US and FL can increase the accuracy of injection compared with conventional US alone.
Acknowledgments
The authors have not received any benefits from commercial sources for the work reported in the manuscript. This research was supported by the Technology Innovation Program (Industrial Strategic Technology Development Program-20009571, Developing AI ultrasound system and platform for intelligent intervention procedures) funded by the Ministry of Trade, Industry & Energy (MOTIE, Korea), and the Korea Medical Device Development Fund grant funded by the Korean government (the Ministry of Science and ICT, the Ministry of Trade, Industry and Energy, the Ministry of Health & Welfare, the Ministry of Food and Drug Safety) (Project Numbers: 9991006834, KMDF_PR_20200901_0164 and 9991007387, KMDF_PR_20200901_0170), and the Seoul R&D Program (BT190153) through the Research and Development for Regional Industry.
Conflict of interest
None to report.
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