First Description of Factors Influencing the Outcome of Developmental Dysplasia of the Hip in Children’s Medical Center

Mehrzad Mehdizadeh; Nasir  Babakhan Kondori; Afrooz Zandifar; Hooman Alizadeh

doi:10.5812/iranjradiol.95805

First Description of Factors Influencing the Outcome of Developmental Dysplasia of the Hip in Children’s Medical Center

authors:

avatar Mehrzad Mehdizadeh ¹ , Nasir Babakhan Kondori ^{2
, *} , Afrooz Zandifar ¹ , Hooman Alizadeh ¹

1 Department of Radiology, Children’s Medical Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran

2 Department of Radiology, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran

how to cite: Mehdizadeh M, Babakhan Kondori N , Zandifar A, Alizadeh H. First Description of Factors Influencing the Outcome of Developmental Dysplasia of the Hip in Children’s Medical Center. I J Radiol. 2020;17(3):e95805. https://doi.org/10.5812/iranjradiol.95805.

Abstract

Background:

There are several factors may have an impact on the prognosis of developmental dysplasia of the hip (DDH). They may change the outcome and treatment if they are present in a patient.

Objectives:

The objective of this study is to determine the association of those factors with the outcome.

Patients and Methods:

The study was performed on 74 infants with DDH in Children’s Medical Centre. After obtaining informed consent and ethical approval, patients with DDH confirmed by ultrasound were included, and possible risk factors including severity of DDH based on the Graf criteria, follow-up length, age, gender, laterality, type of delivery, amniotic fluid index, fetal anomalies, birth order of children, and methods of treatment were collected and compared against treatment response.

Results:

There were 58 female and 19 male patients with a mean age of 6.54 weeks. Bilateral DDH was found in 31 females and nine males. The average alpha and beta angles were 53.19 ± 5.7 and 66.53 ± 6.6 degree, respectively. The severity of DDH had a significant association with treatment response (P = 0.003). Recovery was better in females than in males (P = 0.031). In addition, the first‐born infants had a better response (P = 0.001). A meaningful connection (P = 0.01) was noted between the amniotic fluid index as well as renal/limb anomalies and treatment response. Type of delivery (cesarean versus vaginal) or fetal presentation had no significant association with treatment response (P > 0.05).

Conclusion:

Factors with a negative impact on DDH outcomes include the severity of DDH, male gender, higher birth order, oligohydramnios, renal and limb anomalies.

Keywords

Newborn Perinatal Risk Factors Screening Ultrasound Developmental Dysplasia of the Hip

1. Background

The frequency of developmental dysplasia of the hip (DDH) is 0.8 - 1 per 1000 births (1). If it is not detected and not corrected in early infancy, it can interfere with normal development and leads to anatomical and functional disorders in adulthood (2). Although there is no definite etiology for DDH, a group of genetic and environmental factors including ligament laxity, breech presentation, postnatal hip joint positions like swaddling, female gender, first delivery, and family history may play a role (3, 4).

Physical examinations (Ortolani, Barlow, Galeazzi or Allis) only have 28.1% sensitivity for DDH (5). Therefore, ultrasound for earlier diagnosis and X-ray for older children should be performed. The treatment aim is to maintain good contact between the femoral head and acetabulum. For this purpose, flexion and abduction in a physiological position are recommended. For older children, however, closed/open reductions may be considered based on their age and conditions (6-8). The severity of DDH and treatment are determined based on the Graf criteria (Table 1). Type 1 does not need treatment. Type 2a should be observed. The Pavlik harness is the treatment of choice for types 2b, 2c, D, 3 and 4. However, open reduction sometimes is required for older babies.

Table 1.

Types of DDH Based on Graf Classification

Type	Maturity	Bony roof	α Angle (Bony angle), °	Bony rim	Cartilage root	β Angle, °	Age
Type I	Mature	Good	≥ 60	Sharp	Good coverage femoral head	Ia = β ≤ 55; Ib = β > 55	All
Type II a+	Immature but appropriate for age	Adequate	50 - 59	Blunt	Coverage femoral head		< 3 mo
Type II a-	Immature and inappropriate for age	Deficient	50 - 59	Rounded	Coverage femoral head		< 3 mo
Type II b	Delay in development	Deficient	50 - 59	Rounded	Coverage femoral head		> 3 mo
Type II c	Stable or unstable	Severely deficient	43 - 49	Rounded /flat	Still coverage femoral head	β < 77	All
Type D	Decentering hip	Severely deficient	43 - 49	Rounded /flat	Displaced	β > 77	All
Type III	Eccentric hip	Poor	< 43	Flat	Labrum pressed upwards		All
Type IV	Eccentric hip	Poor	< 43	Flat	Labrum pressed downwards		All

Abbreviation: DDH, developmental dysplasia of the hip.

There are still some controversies regarding risk factors and whether they ever have any impact on the outcome.

2. Objectives

The current study aimed at determining possible risk factors and their effects on treatment response. Good knowledge about these factors could predict DDH outcome and may change the threshold in which a surgeon may shift toward a more aggressive treatment in earlier stages.

3. Patients and Methods

The current descriptive- analytical study was conducted in Tehran, Iran from November 2014 to June 2017. Parents were informed of the details of the study, and informed consent was obtained. Ethical approval was obtained by the ethical committee of this center. The sample size was calculated by the Pukak equation, considering a 95% confidence level, 80% strength, 5% error, and 3 per 1000 frequency. Eighty-four patients out of 399 patients who were referred for hip ultrasound either had DDH or type 2a Graf ultrasound. All of them were younger than 18 weeks. Those who did not attend follow-up ultrasound or those with teratologic dislocation, i.e., myelomeningocele, arthrogryposis, chromosomal abnormalities, lumbosacral disorders, or neuromuscular dislocations, were excluded. In the end, 74 patients were included (Figure 1).

Figure 1.

Study population in our survey

Data were collected using hip ultrasound and questionnaires. The questionnaire contained information about family members, birth order, age, gender, type of delivery, presentation, family history of DDH, and associated anomalies including club foot, torticollis, and meningocele. An ultrasound exam was performed after two weeks from the onset of treatment. In some cases, further follow-up ultrasound exams were done every four weeks, and treatment response was assessed based on ultrasound morphology, alpha and beta angles. We used a 5-MHz linear probe of an ultrasound machine (50-G Siemens, Erlangen, Germany) to obtain coronal views in lateral decubitus. The alpha and beta angles were measured.

Statistical analysis was performed using SPSS version 18 (SPSS Inc. Released 2009. PASW Statistics for Windows, Version 18.0. Chicago: SPSS Inc.). The results were expressed as mean ± standard deviation (SD) for quantitative, and as frequency and percentage for qualitative data. Patients were divided into two groups: the responsive group who had normal ultrasound report of Graf type 1 at the end of treatment and the non-responsive group who did not show complete recovery to type 1 Graf. The relationship between the treatment response and study variables including gender, age, family history, presentation, type of delivery, and associated anomalies were measured using the chi-square test for qualitative variables and t-test for quantitative ones. To assess the predictor factors on treatment response, simple and multiple logistic regression were used. To evaluate the relationship between predictor variables (including gender, gestational age at birth, type of delivery, fetal presentation, amniotic fluid volume, order of children, family history of DDH, limb anomalies and renal anomalies) and treatment response, crude and adjusted odds ratio (OR) and 95% confidence Interval (CI) were used. In all items, results were considered statistically significant if P value was less than 0.05.

4. Results

The current study included 58 female and 19 male infants with a mean age of 6.54 weeks. Bilateral DDH was observed in 31 female and nine male patients. All infants were monitored for 3 - 38 weeks (average 6.4). Two infants had just one follow-up ultrasound, 52 patients had two ultrasounds, and the rest underwent 3 - 7 ultrasound exams (Figures 2-5). From all 114 hip joints, 63 (55.3%) hips were left-sided, and 51 (44.7%) were right-sided. Mean alpha and beta angles were 53.18 ± 5.7 (range: 39 - 59) and 66.53 ± 6.6 (range: 53 - 83) degrees, respectively. Graf type of involvement was 2a+ in 47 hips, 2a- in 19 hips, 2b in eight hips, 2c in seven hips, type D in 12 hips, type 3 in 13 hips, and the remaining eight hip joints had type 4.

Figure 2.

Five-week infant with type II a+ developmental dysplasia of the hip (DDH). Ultrasound measures: alpha 55 and beta 65 degree.

Figure 3.

Nine-week infant. The same patients in Figures 1 after 4 weeks shows complete recovery to type 1 (alpha = 63 and beta = 54).

Figure 4.

Three-week infant with type D developmental dysplasia of the hip (DDH). Ultrasound measures: alpha 47 and beta 82 degree.

Figure 5.

Eleven-week infant. The same patients in Figures 3 after 8 weeks of Pavlik cast shows complete recovery to type I (alpha = 62 and beta = 59).

All hip joints with type 2a involvement were just observed. Treatment by medical brace was done for 19 hips with type 2a. The Pavlik harness orthosis was applied for 15 hips including eight hips with type 2b and seven hips with type 2c. Closed reduction and the Pavlik harness orthosis were applied for 29 joints including 12 hips with type D, 11 hips with type 3, and six hips with type 4. Open reduction was performed for four joints including two type 3 hips and two type 4 hips. Recovery was observed in 98 involved hips (86%), however, 16 joints did not show improvement and required further treatment. Among the subjects, 55 infants were born by cesarean section and the other 19 by vaginal delivery. The cephalic presentation was observed in 68 subjects and breech presentation in the other six patients. Oligohydramnios was observed in four cases; while, 70 patients were reported normal during pregnancy. Forty-four patients were first child, nine patients had a positive family history, and nine patients had limb anomalies. Musculoskeletal anomalies include: clubfoot (8.8%), patella dislocation (0.9%), scoliosis (1.8%), radial dysgenesis (0.9%), and hydronephrosis (2.6%).

A better response was achieved in patients with type 2a and those with milder DDH based on Graf classification. For instance, 8.3% of type D, 53.8% of type 3, and all of the type 4 joints did not respond to treatment. Likewise, the mean alpha angle in the non-responsive group was 43.25 ± 3.2 degree in contrast with 54.02 ± 5 in the responsive group, which was significantly lower (P = 0.006). Similarly, the mean beta angle was 80 ± 7.1 degrees in the non-responsive group compared with 66.38 ± 5.6 in the responsive group, which was significantly higher (P = 0.034).

Of 114 affected hip joints, 89 hips (78%) were observed in female patients and the other 25 (22%) in male ones. Besides, 89.8% of affected hips in females and 72% in male patients showed complete recovery. Overall, 81.6% of treated cases were females and 18.4% were males. These results showed that response to treatment was better in females than males (P = 0.031). Being female increases the treatment response by a factor of 8.21.

Five (4.4%) patients had oligohydramnios history, only two of which (40%) had a good response during follow-up. The amniotic fluid had a significant correlation with response to treatment (P = 0.013). A normal amniotic fluid increases the treatment response by a factor of 16.92.

Among first-born children, 93.8% responded to treatment, the second-born children showed an 80.9% response rate, and the third- and next-born children showed only 42.85% recovery. Overall, 62.2% of the patients were first-born children, 34.7% second-born, and 3.1% next-born children. Treatment response was significantly better among first-born children (P = 0.001).

Treatment was also better (91%) in those without limb anomalies compared with those with anomalies (50%) (P = 0.001), and a significant connection between the presence of anomalies and failure to response (P = 0.002) was noted. Among limb anomalies, the ones associated with poor response were radial dysgenesis, scoliosis, and clubfoot in the order of frequency. Of the patients with renal anomalies, no one showed improvement, while in patients without renal problems, the response rate was 88.2%. Of all patients in the current study, 12.3% had limb anomalies. The average follow-up time in patients with anomalies was 9.6 weeks, and 8.6 weeks in patients without anomalies. Among the infants with limb anomalies, the ones with patellar dislocation had the longest follow-up, 22 weeks, while in scoliosis and clubfoot it was 3 weeks and 10.63 weeks, respectively. Fifty percent of patients with anomaly showed good response compared with a 91% response rate in the group without anomaly. Also, 43.8% of patients in the non-responsive group belonged to the anomaly group. Having no anomaly increases the treatment response by a factor of 5.02. Therefore, the presence of limb anomalies significantly decreased treatment response.

There was no significant correlation between the length of follow-up and response rate. (P = 0.30) Infants with good response attended more in the follow-up sessions. (P = 0.001) All patients that attended five sessions or more showed complete recovery. Twenty-five percent of cases that required further treatment due to their poor response, had only one and 50% of them had two follow-up sessions. Results also showed that gestational age at birth, birth weight, sidedness, laterality, type of delivery (cesarean versus vaginal), fetal presentation, and positive family history were not significantly connected with response to treatment. Natural delivery decreases the treatment response only by a factor of 0.12. Left hip involvement with 55.3% (63 joints) was more common than right side involvement. Of those with good response, 56.1% (64 joints) had left side involvement and 43.9% (50 joints) had right side involvement. However, the difference was not significant (Table 2).

Table 2.

Simple and Multiple Logistic Regression Analysis for Evaluation of Effects of Predictor Variables on Treatment Response of DDH^a

	Treatment response		Crude OR (95% CI)^b	Adjusted OR (95% CI)^c
	Positive	Negative	Crude OR (95% CI)^b	Adjusted OR (95% CI)^c
Sex			3.45 (1.13 - 10.51)	8.21
Female	80	9
Male^d	18	7
Gestational age at birth
Preterm^d	12	0	-	-
Term	86	16
Type of delivery				0.12
Cesarean^d	76	9	-
Vaginal	22	7
Fetal presentation
Breech^d	10	0	-	-
Cephalic	88	16
Amniotic fluid volume			11.07 (1.69 - 72.63)	16.92 (0.88 - 322.36)
Normal	96	13
Oligohydramnios^d	2	3
Order of children			0.23 (0.09 - 0.56)	0.29
First child	61	4
Second child	34	8
Third child or next children	3	4
Family history of DDH
Positive	14	2	-
Negative^d	84	13
Limb anomalies			7.69 (2.31 - 25.59)	5.02 (0.99 - 25.42)
Negative	91	9
Positive^d	7	7
Renal abnormality
Negative	98	13	-	-
Positive^d	0	3

Abbreviations: CI, confidence Interval; DDH, developmental dysplasia of the hip; OR, odds ratio.

^aValues are expressed as median (range).

^bSimple logistic regression.

^cMultiple logistic regression (there were all variables in the model).

^dReference category.

5. Discussion

In the current study, 74 infants (114 abnormal hip joints) were examined. Overall, there was a significant correlation between the severity of involvement according to the Graf criteria, male gender, higher birth order, oligohydramnios, and renal and limb anomalies and poor response. Most of the findings were compatible with those of the previous studies. However, in some results, differences were noticed which could be explained. For instance, the success rate was 45.5% in a study by Al-Essa et al. (9), which was lower than that of the current study in which 98 (86%) joints showed complete recovery. They treated 68.1% of infants younger than six months using the Pavlik harness orthosis, which is the first-line treatment in this age group, and the closed reduction was applied to 78% of older infants. Open reduction was only used for infants older than 18 months (9). This difference in the success rate can be attributed to the target population. In their study, all DDH cases had dislocation or dysplasia, while in the current study, most of the hip joints were type 2a, all of which showed good response.

Likewise, the current study revealed that DDH, by 56.2%, was more common in female patients. Studies showed that female cases are more prone to DDH due to estrogen effect (3). During follow-up, among the subjects that responded to treatment, 81.6% were female and 18.4% were male. The response rate was significantly higher in female patients in contrast with the results obtained by Omeroglu and Koparal (10), in which no association was found between gender and treatment response.

The average alpha angles on the first ultrasound in the responsive and non-responsive groups were 54.02 and 43.25 degrees and for beta angles, they were 66.38 and 80 degrees, respectively. Analysis of data showed that a decrease of alpha angle, which implies much severe DDH, significantly decreased treatment response. These findings were compatible with those of other studies, including White et al. (11), in which femoral head location in the inferior labrum was remarkably associated with better response, and a more superior or lateral location of the femoral head to the labrum was associated with treatment failure.

In the current study, the mean ages of the responsive and non-responsive groups were 6.32 and 7.88 weeks, respectively. Although the mean age of infants who were not treated successfully was higher, there was no significant correlation between age and treatment response. This difference can be attributed to the lower mean age in the current study, which was 6.54 ± 6.6 weeks. It can also be explained by the fact that patients older than 12 months were not included.

Follow-up length was 10 weeks in infants with positive family history, and 8.5 weeks in those without a family history. This finding may suggest that positive family history encourages families to attend more follow-up sessions. Overall, 87.5% of infants with family history and 86.5% of those without family history recovered. As a result, family history had no significant effect on the response rate. Omeroglu et al. examined the effect of variables including age, gender, side of involvement, family history, and other factors on response rate in infants with DDH. The results showed that side of involvement, family history, type of delivery, fetal presentation, and oligohydramnios had no significant correlation with response rate (10-12).

In conclusion, factors including the severity of hip involvement based on Graf criteria, male gender, higher birth order, oligohydramnios and renal and limb anomalies had a significant negative effect on treatment response. Although these risk factors seem to not change treatment choices, their presence could imply a more resistant DDH, which may encourage considering further treatment at an earlier stage. Overall, the success rate in the treatment of DDH is high which and for this reason, early detection and treatment of DDH is strongly suggested.

Footnotes

Authors' Contributions: Study concept and design: MM, HA, and AZ. Acquisition of data: MM, HA, and AZ. Analysis and interpretation of data: AZ and NB. Drafting of the manuscript: NB Critical revision of the manuscript for important intellectual content: NB and MM. Statistical analysis: AZ, HA, and MM. Administrative, technical, and material support: MM, AZ, HA, and NB. Study supervision: MM.
Clinical Trial Registration Code: The clinical trial registration code was IR.TUMS.MEDICINE.REC.1395.1928.a.
Conflict of Interests: There was no conflict of interest in our study.
Ethical Approval: The ethical approval was obtained from the Children’s Hospital Center Hospital.
Funding/Support: There was no funding or supporting source in our study.

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