Assessment of irreducible aspects in developmental hip dysplasia by magnetic resonance imaging

doi:10.21203/rs.3.rs-39006/v2

Background: The developmental dysplasia of the hip (DDH) can cause a wide range of pathological changes, and often requires surgical treatment. Preoperative evaluation is very important for DDH. We aimed to assess the diagnostic capability of magnetic resonance imaging (MRI) for irreducible aspects preventing hip reduction in DDH.

Methods: A total of 39 pediatric patients who received DDH evaluation in pediatric orthopedics from January 2015 to December 2019 were included. The samples included 4 cases of bilateral DDH and 35 cases of unilateral DDH, a total of 43 hip joint samples. All patients underwent surgical treatment, pathological examination and MRI of hip joint.

Results: With pathological results or intraoperative findings as the gold standard, the sensitivity and specificity of MRI were 90.3% and 83.3% for the affected labrum, 92% and 83.3% for thickening of the round ligament, 90.0% and 91.3% for atrophy of the iliopsoas muscle, and 100% and 100% for fibrofatty pulvinar tissue and joint effusion, respectively.

Conclutions: The MRI showed an extraordinary capability of detecting these irreducible factors and helped surgeon choose the appropriate treatment strategies.

Nuclear Medicine & Medical Imaging

Pediatrics

Orthopedics

Irreducible factors

Developmental dysplasia of the hip

MR imaging

Developmental dysplasia of the hip (DDH) encompasses a wide spectrum of pathology, ranging from complete fixed dislocation at birth to asymptomatic acetabular dysplasia in adulthood [1], which can negatively affect hip development and can lead to isolated acetabular dysplasia, subluxation, complete dislocation of the hip joint, or permanent abnormal gait [2,3]. The children with untreated persistent DDH may suffer from pain due to a series of anatomical changes such as increased abnormal articular pressure or increased tension on a smaller contact area during the process of growth and development. With the development of DDH, the degeneration of the articular cartilage, early coxarthrosis, and ischemic necrosis of the femoral head would likely happen in children [4].

Result from less invasive and more effective, early diagnosis and treatment plays important roles in restoring the normal relationship between the acetabulum and femoral head and avoiding further complications that come with growth [5]. According to the American College of Radiology (ACR) guides, the most important diagnosis method of DDH is on the basis of the results of physical examination using the Ortolani’s sign and Barlow’s test, though in 1977, Jones [6] reported that preliminary physical examination did not satisfy the clinical needs of DDH diagnosis due to low sensitivity. Several imaging techniques were also emerged in clinical, including ultrasonography (US), digital radiography (DR), and magnetic resonance imaging (MRI), which improved the diagnostic sensitivity of DDH. US is the preferred imaging modality for evaluating infants younger than 4 months [7]. However, US is not so reliable in assessing the depth of femoral head coverage due to the measurements of acetabular angles depend on the image readers and are highly variable, and limited in identifying intrinsic obstacles to reduction such as the hypertrophied pulvinar after capital femoral epiphyseal ossification. Therefore, high rates of late diagnosis in DDH persist in the context of selective ultrasound screening [8,9]. DR was commonly applied for diagnosing DDH in patients older than 6 months of age, and the cons is it’s not helpful in identifying secondary intra-articular changes and is associated with the inevitable risk of radiation [10]. Moreover, both US and DR are difficult to diagnose preoperatively inverted labrum, hypertrophied ligamentum teres, and shortened iliopsoas muscle.

With the rapid development of imaging technologies, MRI has been shown to be advantageous in the detection of bony structures as well as cartilaginous and soft-tissue structures. Although there are significant individual differences in the location and degree of acetabular dysplasia [11], MRI can provide superior soft tissue resolution in cross-sectional imaging profiles without ionizing radiation and has been advocated for the assessment of acetabular morphology and growth disturbance or deficiencies of the capital femoral epiphysis, the discrimination of ossified and unossified components, especially the identification of joint congruity and obstacles to prevent the reduction of hip dislocation, and the detection of unexpected complications after surgical reduction [12]. Benefit from MRI, it’s convenient for clinicians, regardless of experience level, subspecialty, or geographic origin, to assess the quality of hip reduction and predict surgical reduction of avascular necrosis (AVN). Magnetic resonance imaging provides a more reliable interpretation than standard X-rays and reduces radiation exposure [13,14].

However, there is few studies to systematically explore the abilities of MRI in DDH to detect the various obstacles, including thickened fibrofatty pulvinar tissue, joint effusion, thickened ligamentum teres, inversion of the labrum, hypertrophy of the cartilage of the acetabular roof, and iliopsoas muscle atrophy, to concentric reductions, which is the treatment goal of DDH and critical for better prognosis [15, 16].

The present study aimed to evaluate the capability of MRI for precisely detecting the irreducible mechanisms preventing concentric hip reduction in DDH before surgery, and its applicability in guiding clinical treatment.

Subjects

From January 2015 to May 2019, 168 children with DDH were treated at Children’s Hospital, Suzhou, China. 44 of them received the open reductions and related MR images were collected.

Three patients, who had been previously treated in other hospitals were excluded from this study, as well as one due to poor quality of MR images and another one with teratologic dislocations. A total of 39 primary patients (9 boys and 30 girls) were included in this study with a mean age of 26.4 ± 5.3 months (range, 18–48 months). Among these patients, 4 had bilateral DDH and 35 had unilateral involvement, giving a total of 43 affected hips. Although the severities of these patients were different, the imaging and pathological features are similar. Informed consents were obtained from the parents of each patient. Ethics committee approval was obtained from the Institutional Review Board of Children’s Hospital of Soochow University (Suzhou, China), and was performed in accordance with the ethical guidelines of the Declaration of Helsinki (Ethical batch number:2015KS006).

Inclusion criteria

① Patients with DDH were diagnosed clinically, and MRI scan was performed before the operation; ②no abnormal findings were found in physical examination of neuromuscular system; ③no previous treatment was performed; ④the operation was open reduction of hip joint. The above four points need to be met at the same time.

Exclusion criteria:

① Patients with DHH who have received non-surgical or surgical treatment (secondary dislocation of hip joint); ②patients with history of hip infection or suppurative hip arthritis in neonates or infants; ③patients with other diseases; ④patients with nonstandard clinical data, MRI, operation records or incomplete results. The case would be excluded when any of the exclusion criteria was satisfied.

MRI data acquisition

The MRI examinations were performed before the open reduction on a 3.0T scanner (Siemens AG, Magnet, Germany) using a baby array coil placed anterior and posterior to the hips. All children were sedated before the MR examination. The children were then positioned supine inside the scanner with both legs in a symmetrical neutral position. Then, localizer T1-weighted (T1-W) spin-echo (SE) images (repetition time [TR], 796ms; echo time [TE], 9.43 ms; time of acquisition, 3 min 55 s) were obtained in the coronal and axial planes. The coronal sequence in T2-weighted fast-spin-echo (TR/TE, 4000/103 ms; time of acquisition, 2 min 40 s) and short inversion time inversion recovery (STIR; TR/TE, 5400/42 ms; time of acquisition, 2 min 20 s) were obtained. Slice thickness was 3.0 mm for all the sequences, and the interslice gap was 1.0 mm. The field of view was 300 × 300 mm² and matrix was 256 × 256 for all images [17].

MRI image analysis

All the MR images were uploaded to the Picture Archiving and Communication Systems (PACS; Neusoft, Shenyang, China) and sent to the AW 4.6 workstation (GE Healthcare, Waukesha, WI, USA). The films were read independently by two radiologists who were with the same seniority and both unknown about the subjects’ clinical diagnosis and progress as the attending physician. Pathological changes such as fibrofatty pulvinar tissue, joint effusion, thickening of ligamentum teres, inversion of labrum, hypertrophy of the cartilage of the acetabular proof and atrophy of the iliopsoas muscle were analyzed on the AW4.6 workstation. According to the corresponding image manifestations and applying the pathological examination results or intraoperative findings as the gold standards, the sensitivities, specificities, positive predictive values (PPV), negative predictive values (NPV), and accuracies to assess the diagnostic capabilities of MRI for the pathological changes were obtained. The width of the iliopsoas muscle at the level of femoral neck was used as a criterion for muscle atrophy.

Diagnostic criteria

The severity of DDH was classified into grade I, II and III by observing the location of the femoral head on the coronal plane of MRI according to Dunn’s criteria [18] .In grade I, only the femoral head moves outward, and the center is still at the level of acetabulum; in grade II, the femoral head moves outward, but the center is beyond the upper edge of acetabulum; in grade III, the femoral head completely dislocates from the acetabulum.

Statistical analysis

Statistical analysis was performed using SPSS 22 package (SPSS, Chicago, Illinois). A Kappa test was used to assess the consistency of MRI manifestations with the results of the pathological analysis or intraoperative findings. The interobserver variability was assessed by intra-class correlation coefficient (ICC). For results of both the ICC and the Kappa test, a value of >0.75 was regarded as excellent, a value of 0.40–0.75 was regarded as fair to good, while a value<0.40 was poor.

Forty-three of the affected hips received open reductions after diagnosis. As a result, 31 inversed labrum, 31 fibrofatty pulvinar tissue, 25 thickened round ligament, 26 joint effusion, and 20 iliopsoas muscle atrophy were confirmed in the surgeries. It was showed that thickened fibrofatty pulvinar tissue appeared in 31 hips with intensified signal on T1-W coronal slices (Fig. 1). Ligamentum teres was voluminous in 26 hips, which produced low-intensity signals in all sequences (Fig. 2). Joint effusion was found in 26 hips with intensified signals on STIR coronal section images (Fig. 3). The labrum was inversed in the joint and intermediate-intensity signal was obtained on T1-W sequences (Fig. 1). Iliopsoas muscle atrophy appeared in 20 hips, which produced intermediate-intensity signals on T1-W axial section images and showed decreased muscle width compared with the other side (Fig. 4). Four patients with thickened round ligament were followed up for 3.5 years after DDH surgery, 2 of them developed bilateral AVN of femoral head. It’s found that femoral head had heterogenous signal intensity and non-integrality osseous morphology in MRI images (Fig. 5).

With pathological results and intraoperative findings as the gold standards, the sensitivity, specificity, PPV, NPV and accuracy for detecting affected labrum by MRI were 90.3%, 83.3%, 93.3%, 76.9%, and 88.4%, respectively (kappa = 0.718, 95% confidence interval (CI) (0.488,0.948); Table 1), 92.0%, 83.3%, 88.5%, 88.2%, and 88.4% for detecting thickened round ligament respectively (kappa = 0.759, 95% CI (0.561, 0.957); Table 1) and 90.0%, 91.3%, 90.0%, 91.3%, and 90.7% for iliopsoas muscle atrophy respectively (kappa = 0.813, 95% CI (0.639, 0.988); Table 1). The corresponding values for both fibrofatty pulvinar tissue and joint effusion were 100%, 100%, 100% and 100%.

Global interobserver consistencies between the two senior radiologists of MRI were as follows (Table 2): for fibrofatty pulvinar tissue and joint effusion (ICC = 1.00), for thickening of the ligamentum teres (ICC = 0.72, 95% CI (0.490, 0.850)), for inversion of the labrum (ICC = 0.88, 95% CI (0.777, 0.934)) and for atrophy of the iliopsoas muscle (ICC = 0.93, 95% CI (0.870, 0.962)), indicating excellent agreement.

Despite the cost and possible requirement of additional sedatives, the advantages of MR imaging are considerable in DDH assessment, including the absence of radiation, possibility of imaging in multiple planes, and higher resolution and contrast between bony and cartilaginous components [19]. The high accuracy of MRI in demonstrating the details of DDH has been described in previous literature by comparing with anatomical preparations in cadavers [20]. More recently, MRI is being used in the diagnosis of the anatomical obstructions to reduction, such as fibrofatty pulvinar tissue, joint effusion, thickened ligamentum teres, inversed and thickened labrum, and iliopsoas muscle atrophy. Most of these studies evaluated one of these characteristics and confirmed the role of MRI in the diagnosis of DDH [20-22]. In these papers, the diagnostic values of MRI are evaluated comprehensively. And the diagnostic capability of MRI was in good agreement with pathological examination or surgical findings.

In the evaluation of 43 affected hips, the fibrofatty pulvinar tissue and joint effusion were easily detected by MRI due to different signal manifestations in T1WI, T2WI and STIR fat suppression sequences for tissues with fat or liquid. T1WI and T2WI showed high signal for fat and liquid signals, while stir fat suppression sequence showed low signal intensity. T1WI and Flair showed low signal for liquid signals, while T2W showed high signal. MRI can show fat and liquid sensitively, and the coincidence rate with pathological diagnosis is 100%. However, Benjamin et al [23] reported that a small amount of adipose tissue and joint effusion can be completely absorbed once the femoral head is relocated and well covered by the acetabulum.

The labrum is one of the most important structures of the hip joint, which can improve the lateral coverage of the femoral head and deepen the joint. The labrum is typically everted with mild joint dislocation, but it may invaginate into the hip joint together with a capsular fold and inhibit reduction in the case of complete joint dislocation. In order to achieve a concentric reduction, the everted, inverted, and hypertrophied labrum require radial cuts [17]. In this study, the sensitivity and specificity of detection of the affected labrum were 90.3% and 83.3%, respectively, which were consistent with previous reports [24-26].

As another secondary adaptive change, thickened or elongated ligamentum teres often requires surgical excision, especially in grade III DDH. The stress is concentrated on a small area of the acetabular roof and may lead to high rates of avascular necrosis of the femoral head. Therefore, the hypertrophied ligament trees should be removed in the surgery to achieve optimal results. Devitt et al [27] reported that MRI can be used to rule out partial tears of the ligamentum teres with sufficient sensitivity (91%) and PPV(67%) and accuracy (64%) but relative low specificity (9%) and NPV (31%). In our study, 25 hips with thickened ligamentum teres were identified in the surgery, 23 of them were detectable by MRI. And the sensitivity (92%) and specificity (83.3%), PPV (88.5%), NPV (88.2%) and accuracy (88.4%) for detecting thickened ligamentum teres were much higher in our reports, which may be partly attributed to higher resolution 3.0T MRI used in this study. AVN is one of the most common serious complication of DDH [28]. In the study, bilateral AVN were shown on 2 of 4 patients with elongated ligamentum teres during 3.5 years follow up, which led to the surgery. One of the possible reasons is that ligamentum teres exerts abnormally high pressure on ossific nucleus for a long time before surgery, indicating the early diagnosis by MRI and surgical removal of elongated ligamentum teres will be the key to decrease the occurrence of AVN.

The iliopsoas tendon passes between the acetabulum and the displaced femoral head and may obstruct concentric reduction [29]. The iliopsoas muscle atrophy often occurs on the affected hip as a result of biomechanical changes after DDH. Therefore, complete tenotomy of the iliopsoas muscle is recommended due to its advantages such as lower risk of avascular necrosis of the femoral head and decreased pressure on the hip joint. Keeney et al [24] reported that the three-dimensional (3D) MRI was quite useful in diagnosing the iliopsoas muscle atrophy and was helpful in predicting the reduction difficulty. In our study, preoperative MRI has a high diagnostic efficiency, and its sensitivity, specificity, positive predictive value, negative predictive value and accuracy are highly consistent with postoperative pathology. The preoperative MRI would be helpful to identify the iliopsoas muscle atrophy.

In our research, there was good consistency between the two senior radiologists of MRI in thickening of the ligamentum teres, inversion of the labrum, atrophy of the iliopsoas muscle, fibrofatty pulvinar tissue and joint effusion (ICC > 0.72), indicating that MRI has good repeatability in the diagnosis of DDH and is suitable for preoperative diagnosis and postoperative evaluation and follow-up.

There were significant differences in the number of boys and girls in the study, with European scholars reporting a male-to-female ratio of about 1:7 and a unilateral incidence of about 90%, with left side more likely to be affected than right side (3:1) [30]. In our group, there were 9 boys and 30 girls, with the incidence of DDH in girls much higher than that in boys. This may have something to do with genetics [30]. In addition, during childbirth, the mother will secrete a large amount of relaxation hormone, in order to achieve the purpose of relaxing ligaments and expanding the birth canal. Girls are more sensitive to this relaxation hormone than boys, and have more loose soft tissue around the hip. If there is resistance during delivery, hip dislocation is more likely to occur, which is also the reason why DDH rates are higher in girls than boys.

DDH is more common in the left hip [30]. In this group of DDH cases, there were 25 left hip lesions and 18 right hip lesions. Due to the insufficient sample size, the difference of prediction accuracy of left and right hip joints was not further studied.

This study has some limitations. It was a retrospective study, and the sample size of this study was small. Given these limitations, prospective and global sample studies may be necessary to confirm the diagnostic capability of MRI.

In conclusion, MR could adequately detect thickened fibrofatty pulvinar tissue, joint effusion, inversion of the labrum, and iliopsoas muscle atrophy, thickened round ligament. These irreducible factors can be observed by MRI before surgery and help orthopedist select a suitable operation such as closed or open reduction. MRI technology can provide abundant morphological information for acetabular development and has important clinical value for DDH diagnosis and surgical treatment.

DDH:the developmental dysplasia of the hip; MRI:magnetic resonance imaging; ACR:American College of Radiology; US:ultrasonography; DR: digital radiography; AVN:avascular necrosis; T1-W :T1-weighted; SE:spin-echo; TR :repetition time; TE :echo time; STIR :short inversion time inversion recovery; PACS :the Picture Archiving and Communication Systems; PPV:positive predictive values; NPV:negative predictive values; ICC:intra-class correlation coefficient; CI:confidence interval.

Acknowledgements

This work was supported by Science and Technology for Peoples Livelihood of Suzhou [SS201746], General Social Development Project of Jiangsu [BE2017670] and National Natural Science Foundation of China [81773439].

Authors' contributions

Huihui Jia and Liang Wang collected data and wrote the draft. Mao Sheng contributed to the elaboration of the ideas developed in the manuscript and made critical amendments. Yan Chang and Yongrui Song contributed to the data collection and interpretation. Xiaodong Yang provided the statistical analysis. All authors read and approved the final manuscript.

Funding

National Natural Science Foundation of China [81773439]; Science and Technology for Peoples Livelihood of Suzhou [SS201746]; General Social Development Project of Jiangsu [BE2017670].

Availability of data and material

All data generated or analyzed during this study are included in this published article and its supplementary information files.

Ethics approval and consent to participate

Institutional review board/ethics committee approval was obtained from the Institutional Review Board of Children’s Hospital of Soochow University (Suzhou, China), and was performed in accordance with the ethical guidelines of the Declaration of Helsinki. Animals were not used in this study. The patients gave consent to the submission of this study.

Consent for publication

Written informed consent was obtained from the patient/parents/legal guardians for publication of this study and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Competing interests

The authors declare that they have no competing interests.

Author details

¹Department of Radiology, Children′s Hospital of Soochow University, Suzhou, 215000, P.R.China.

²Department of Orthopaedics, The Affiliated Suzhou Science& Technology Town Hospital of Nanjing Medical University, Suzhou, 215000, P.R.China.

³Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163, P.R.China.

⁴Department of Orthopaedics, Children′s Hospital of Soochow University, Suzhou, 215000, P.R.China.

Clinical practice guideline: early detection of developmental dysplasia of the hip. Committee on Quality Improvement, Subcommittee on Developmental Dysplasia of the Hip. American Academy of Pediatrics. Pediatrics, 2000. 105(4): p. 896-905.
Nemeth, B.A. and V. Narotam, Developmental dysplasia of the hip. Pediatr Rev, 2012. 33(12): p. 553-61.
Ali Ahmed Raba, Qais Gasibat. Developmental Dysplasia of the Hip: Management of Graf IIa.Dysplastic Hip. 2020, 10(02):p.247-254.
Moraleda, L., et al., [Dysplasia in the development of the hip]. Rev Esp Cir Ortop Traumatol, 2013. 57(1): p. 67-77.
Albinana, J., et al., Acetabular dysplasia after treatment for developmental dysplasia of the hip. Implications for secondary procedures. J Bone Joint Surg Br, 2004. 86(6): p. 876-86.
Jones, D., An assessment of the value of examination of the hip in the newborn. J Bone Joint Surg Br, 1977. 59(3): p. 318-22.
Christian A. Barrera, Sara A. Cohen, Wudbhav N. Sankar, et al. Imaging of developmental dysplasia of the hip: ultrasound, radiography and magnetic resonance imaging.Pediatric Radiology.2019, 49(12):p.1652-1668.
Atweh, L.A. and J.H. Kan, Multimodality imaging of developmental dysplasia of the hip. Pediatr Radiol, 2013. 43 Suppl 1: p. S166-71.
George J S , Kulkarni V , Bellemore M , et al. Importance of early diagnosis for developmental dysplasia of the hip: A 5﹜ear radiological outcome study comparing the effect of early and late diagnosis. Journal of Paediatrics and Child Health, 2020.10.
Akgul, T., et al., Radiological results of modified Dega osteotomy in Tonnis grade 3 and 4 developmental dysplasia of the hip. J Pediatr Orthop B, 2014. 23(4): p. 333-8.
Dibello D, Odoni L, Pederiva F, et al, MRI in Postreduction Evaluation of Developmental Dysplasia of the Hip:Our Experience.J Pediatr Orthop. 2019, 39(9):449-452.
Duffy, C.M., et al., Magnetic resonance imaging evaluation of surgical management in developmental dysplasia of the hip in childhood. J Pediatr Orthop, 2002. 22(1): p. 92-100.
Nguyen Jie C, Back Susan J, Barrera Christian A, et al. Developmental dysplasia of the hip: can contrast-enhanced MRI predict the development of avascular necrosis following surgery?. Skeletal Radiology,2020,10.
Yong BiCheng, Li YiQiang, Li JingChun, et al. Post-operative radiograph assessment of children undergoing closed reduction and spica cast immobilization for developmental dysplasia of the hip: does experience matter?.International Orthopaedics,2018,.42(11):2725-2731.
Starr, V. and B.Y. Ha, Imaging update on developmental dysplasia of the hip with the role of MRI. AJR Am J Roentgenol, 2014. 203(6): p. 1324-35.
Rosenbaum DG, Servaes S, Bogner EA, et al. MR imaging in postreduction assessment of developmental dysplasia of the hip: goals and obstacles.Radiographics,2016.36(3):p.840-854.
Douira-Khomsi, W., et al., Magnetic resonance evaluation of acetabular residual dysplasia in developmental dysplasia of the hip: a preliminary study of 27 patients. J Pediatr Orthop, 2010. 30(1): p. 37-43.
Krasny, R., et al., MR-anatomy of infants hip: comparison to anatomical preparations. Pediatr Radiol, 1991. 21(3): p. 211-5.
Li, L.Y., et al., Development of the osseous and cartilaginous acetabular index in normal children and those with developmental dysplasia of the hip: a cross-sectional study using MRI. J Bone Joint Surg Br, 2012. 94(12): p. 1625-31.
Jaremko, J.L., C.C. Wang, and S. Dulai, Reliability of indices measured on infant hip MRI at time of spica cast application for dysplasia. Hip Int, 2014. 24(4): p. 405-16.
Chin, M.S., B.W. Betz, and M.A. Halanski, Comparison of hip reduction using magnetic resonance imaging or computed tomography in hip dysplasia. J Pediatr Orthop, 2011. 31(5): p. 525-9.
Studer K, Williams N, Studer P, et al. Obstacles to reduction in infantile developmental dysplasia of the hip. Journal of Children's Orthopaedics. 2017, 11(5):p.358-366.
Benjamin, H. and W. John, Developmental dysplasia of the hip Orthopaedics and Trauma, 2009. 23: p. 162-168.
Keeney, J.A., et al., Magnetic resonance arthrography versus arthroscopy in the evaluation of articular hip pathology. Clin Orthop Relat Res, 2004(429): p. 163-9.
Chan, Y.S., et al., Evaluating hip labral tears using magnetic resonance arthrography: a prospective study comparing hip arthroscopy and magnetic resonance arthrography diagnosis. Arthroscopy, 2005. 21(10): p. 1250.
Schmid, M.R., et al., Cartilage lesions in the hip: diagnostic effectiveness of MR arthrography. Radiology, 2003. 226(2): p. 382-6.
Devitt, B.M., et al., Preoperative diagnosis of pathologic conditions of the ligamentum teres: is MRI a valuable imaging modality? Arthroscopy, 2014. 30(5): p. 568-74.
Tiderius, C., et al., Post-closed reduction perfusion magnetic resonance imaging as a predictor of avascular necrosis in developmental hip dysplasia: a preliminary report. J Pediatr Orthop, 2009. 29(1): p. 14-20.
Fukiage, K., N. Yamasaki, and S. Suzuki, Visualization of developmental dysplasia of the hip in infants by using three-dimensional magnetic resonance imaging. J Pediatr Orthop B, 2014. 23(2): p. 107-11.
Jon CC, Michael KD. Developmental dysplasia of the hip. Surgery, 2007, 25(4): 176-180.

Table 1. The detection of labrum, ligamentum teres and the contracture of the iliopsoas muscle by MRI and pathology

	Pathology
MRI	Labrum			Ligamentum teres			Contracture of the iliopsoas muscle
MRI	(＋)	(—)	Total	(＋)	(—)	Total	(＋)	(—)	Total
(＋)	28	2	30	23	3	26	18	2	20
(—)	3	10	13	2	15	17	2	21	23
Total	31	12	43	25	18	43	20	23	43

* For labrum, Kappa = 0.718, 95% CI (0.488, 0.948)

* For ligamentum teres, Kappa = 0.759, 95% CI (0.561, 0.957)

* For contracture of the iliopsoas muscle, Kappa = 0.813, 95% CI (0.639, 0.988)

* The Kappa values indicate fairly good consistencies between MRI imaging and the pathology.

Table 2. Global interobserver consistency between the two senior radiologists of MRI

										Doctor 1
Doctor 2	Labrum						Ligamentum teres				Contracture of the iliopsoas muscle			Fibrofatty			Joint Effusion
	(＋)	(—)			Total		(＋)	(—)	Total		(＋)	(—)	Total	(＋)	(—)	Total	(＋)	(—)	Total
(＋)	23		0	23			24	0	24		18	0	18	31	0	31	26	0	26
(—)	5		15			20	10	9	19		3	22	25	0	12	12	0	17	17
Total	28		15			43	34	9	43		21	22	43	31	12	43	26	17	43

* For labrum, ICC = 0.88, 95% CI (0.777, 0.934)

* For ligamentum teres, ICC= 0.72, 95% CI (0.490, 0.850)

* For contracture of the iliopsoas muscle, ICC = 0.93, 95% CI (0.870, 0.962)

* For fibrofatty pulvinar tissue and joint effusion, ICC = 1.00

* The ICC values indicate fairly good consistencies between the two senior radiologists of MRI.

Assessment of irreducible aspects in developmental hip dysplasia by magnetic resonance imaging

Status:

Journal Publication

Version 2

Abstract

Figures

Background

Methods

Results

Discussion

Conclusions

Abbreviations

Declarations

References

Table

Status:

Journal Publication

Version 2