Sacroiliac Distraction Test: Difference between revisions

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== Description and Purpose<br>  ==


The SIJ (Sacroiliac Joint) Distraction (Colloquially know as Gapping) test is used to add evidence, positive or negative, to the hypotheses of an SIJ sprain or dysfunction when used in the”Laslett SIJ Cluster testing”. This test stresses the anterior sacroiliac ligaments (Cook and Hegedus 2013, Cook et al 2007, Laslett 2008, Laslett et al 2005, Laslett et al 2003). This test has also been described as the Transverse Anterior Stress Test or the Sacroiliac Joint Stress Test[1][2].
== Description and Purpose  ==


== Technique<br> ==
The SIJ ([[Sacroiliac Joint]]) Distraction (Colloquially know as Gapping) test is used to add evidence, positive or negative, to the hypotheses of an SIJ sprain or dysfunction when used in the Laslett [[Sacroiliac Joint Special Test Cluster|SIJ Cluster testing]]. This test stresses the anterior sacroiliac ligaments.<ref name=":0">Cook, C, Hegedus, E. (2013). Orthopedic Physical Examination Test: An Evidence Based Approach. New Jersey: Prentice Hall.</ref><ref name=":1">Cook, C., Cleland, J., Huijbregts, P. (2007). Creation and Critique of Studies of Diagnostic Accuracy: Use of theS methodological Quality Assessment Tool. J Manipulative Physiol Ther, 15(2), 93-102.</ref><ref name=":2">Laslett M, (2008). Evidence-Based Diagnosis and Treatment of the Painful Sacroiliac Joint. J Man Manip Ther. 2008; 16(3): 142–152.</ref><ref name=":3">Laslett M, Aprill C, McDonald B, Young S (2005). Diagnosis of sacroiliac joint pain: validity of individual provocation tests and composites of test. Man Ther. 2005;10:207-218.</ref><ref name=":4">Laslett M, Young SB, Aprill CN, McDonald B, (2003). Diagnosing painful sacroiliac joints: A validity study of a McKenzie evaluation and sacroiliac joint provocation tests. Aust J Physiother 2003;49:89–97.</ref> This test has also been described as the Transverse Anterior Stress Test or the Sacroiliac Joint Stress Test.


1. The patient lies supine and the examiner applies a vertically orientated, posteriorly directed force to both the anterior superior ilac spines (ASIS) (Cook and Hegedus 2013 , Laslett 2008, Laslett et al 2005, Laslett et al 2003).
== Technique  ==


<br>Note: Cook and Hegedus (2013) suggest applying a sustained force for 30 seconds before applying a repeated vigorous force in an attempt to reproduced the patient’s symptoms. However, Laslett (2008) does not suggest any timings or changes in force.  
[[Image:Laslett 2008 SIJ Distraction test.png|thumb|right|200px|SI Distraction Test - Vertically oriented pressure is applied to the anterior superior iliac spinous processes directed posteriorly, distracting the sacroiliac joint.]]


Because of the lack of standardisation in the technique it is quite feasible different therapists will practise this test different ways, giving rise to variability in response and lowering the inter-tester reliability (Laslett et al 2005, Levin et al 2005). No evidence to suggest either method is preferable (Levin et al 2005), therefore, more evidence needed.
1. The patient lies supine and the examiner applies a vertically orientated, posteriorly directed force to both the anterior superior iliac spines (ASIS)<ref name=":0" /> <ref name=":2" /><ref name=":3" /><ref name=":4" />


<br>2. The presumed effect is a DISTRACTION of the anterior aspect of the sacroiliac joint. (Laslett et al 2005, Laslett et al 2003)
<br>Note: Cook and Hegedus (2013) suggest applying a sustained force for 30 seconds before applying a repeated vigorous force in an attempt to reproduced the patient’s symptoms. However, Laslett (2008) does not suggest any timings or changes in force.  
 
<br>3. A test is positive if it reproduces the patient's symptoms. This indicates SIJ dysfunction or a sprain of the anterior sacroiliac ligaments (Cook and Hegedus 2013, Cook et al 2007, Laslett 2008, Laslett et al 2005, Laslett et al 2003)  
 
<br>'''However, this test should be used in concordance within a SIJ testing cluster to ensure maximum reliability and validity when confirming hypotheses''' (Albert et al 2000, Kokmeyer et al 2002, Laslett 2008, Laslett et al 2005,Laslett et al 2003, Ozgocmen et al 2008, Robinson et al 2007). See Laslett SIJ testing cluster for further information<br><br>
 
(Picture Goes here)


<br>  
Because of the lack of standardisation in the technique it is quite feasible different therapists will practise this test different ways, giving rise to variability in response and lowering the inter-tester reliability.<ref name=":3" /><ref name=":5">Levin U, Nilsson-Wikmar L, Stenström CH (2005). Variability within and between evaluations of sacroiliac pain with the use of distraction testing. J Manipulative Physiol Ther. 2005 Nov-Dec;28(9):688-95.</ref> No evidence to suggest either method is preferable<ref name=":5" />, therefore, more evidence needed.


Laslett 2008 -&nbsp;"The distraction test” (testing right and left SIJ simultaneously).<br>Note: Vertically oriented pressure is applied to the anterior superior iliac spinous processes directed posteriorly, distracting the sacroiliac joint.<br>  
<br>2. The presumed effect is a DISTRACTION of the anterior aspect of the sacroiliac joint.<ref name=":3" /><ref name=":4" />  


Videos showing demonstration of technique (No copyright intended)
<br>3. A test is positive if it reproduces the patient's symptoms. This indicates SIJ dysfunction or a sprain of the anterior sacroiliac ligaments<ref name=":0" /><ref name=":1" /><ref name=":2" /><ref name=":3" /><ref name=":4" />


http://www.youtube.com/watch?v=jRYEuPWzGDE&amp;NR=1<br>http://www.youtube.com/watch?v=Q2tRicO91ng <br>
<br>'''However, this test should be used in concordance within a SIJ testing cluster to ensure maximum reliability and validity when confirming hypotheses'''<ref name=":10">Albert H, Godskesen M, Westergaard J (2000). Evaluation of clinical test used in classification procedures in pregnancy-related pelvic joint pain. Eur Spine J. 2000; 9(2):161-166</ref><ref name=":11">Kokmeyer DJ, Van der Wurdd P, Aufdemkampe G, Fikenscher TC (2002). The reliability of multitest regimens with sacroiliac pain provocation tests. J Manipulative Physiol Therapy. 2002;25(1):42-48</ref><ref name=":2" /><ref name=":4" /><ref name=":6">Ozgocmen S, Bozgeyik Z, Kalcik M, Yildrim A (2008). The value of sacroiliac pain provocation tests in early active sacroilitis. Clin Rheumatol. 2008;27:1275-1282</ref><ref name=":8">Robinson HS. Brox JI. Robinson R. Bjelland E. Solem S. Telje T (2007). The reliability of selected motion- and pain provocation tests for the sacroiliacjoint. Manual Therapy. 12(1):72-9, 2007 Feb.</ref> See Laslett SIJ testing cluster for further information


== Evidence<br> ==
<clinicallyrelevant id="83474654" title="Sacroiliac Distraction Test" />
== Evidence  ==


The Diagnostic Accuracy of the Distraction test for SIJ dysfunction is described below (Original data from Cook and Hegedus (2013).  
The Diagnostic Accuracy of the Distraction test for SIJ dysfunction is described below (Original data from Cook and Hegedus (2013).  


 
{| cellspacing="1" cellpadding="1" border="1" width="800"
 
{| width="800" border="1" cellpadding="1" cellspacing="1"
|-
|-
| Author
| Author  
| Reliability
| Reliability  
| Sensitivity
| Sensitivity  
| Specificity
| Specificity  
| LR+
| LR+  
| LR-
| LR-  
| QUADAS Score (0-14) Cook and Hegedus 2013
| QUADAS Score (0-14) Cook and Hegedus 2013  
| QUADAS Score (0-14) Gunning 2013
| QUADAS Score (0-14) Gunning 2013  
| CEBM (0-5) With qualitative J
| CEBM (0-5) With qualitative J  
| Study Conclusion
| Study Conclusion
|-
|-
| Albert et al 2000
| Albert et al 2000  
| 84%
| 84%  
| 4-14 (Average = 9)
| 4-14 (Average = 9)  
| 100
| 100  
| NA
| NA  
| NA
| NA  
| 7
| 7  
| 7
| 7  
| '''Score = 4<br>Patient Spectrum<br>'''535 women fulfilling broad inclusion criteria with daily pain at gestation week 33.'''<br>Reference Standard<br>'''Reference standard performed on all participants'''<br>Independent blind comparisons with Gold standard<br>'''No gold standard used but 2 examinations performed by individual and blinded assessors'''<br>Test characteristics<br>'''Presented as expected but without likelihood ratios'''<br>Reproducibility<br>'''Method and all analyses detailed clearly. All reproducible
| '''Score = 4<br>Patient Spectrum<br>'''535 women fulfilling broad inclusion criteria with daily pain at gestation week 33.'''<br>Reference Standard<br>'''Reference standard performed on all participants'''<br>Independent blind comparisons with Gold standard<br>'''No gold standard used but 2 examinations performed by individual and blinded assessors'''<br>Test characteristics<br>'''Presented as expected but without likelihood ratios'''<br>Reproducibility<br>'''Method and all analyses detailed clearly. All reproducible  
| Test has reasonable specificity and inter-rater reliability and should be used as an assessment tool in pregnant women
| Test has reasonable specificity and inter-rater reliability and should be used as an assessment tool in pregnant women
|-
|-
| Blower and Griffin 1984
| Blower and Griffin 1984  
| 63%
| 63%  
| Not tested
| Not tested  
| 89
| 89  
| NA
| NA  
| NA
| NA  
| 5
| 5  
|  
|  
6 - Reference standard used but minimal description. 2 studies reported in 1. Very messy study.
6 - Reference standard used but minimal description. 2 studies reported in 1. Very messy study.  
 


<br>


|  
|  
Score = 2
Score = 2  


'''Patient Spectrum'''
'''Patient Spectrum''' Consecutive admissions of AS patients with varying stages of progression.  
Consecutive admissions of AS patients with varying stages of progression.


'''Reference Standard'''
'''Reference Standard'''  


Performed on all participants
Performed on all participants  


'''Independant Blind comparisons with Gold Standard'''
'''Independent Blind comparisons with Gold Standard'''  


No gold standard used/ Blind testing of index test but not reference standard
No gold standard used/ Blind testing of index test but not reference standard  


'''Test Characteristics'''
'''Test Characteristics''' Specificity produced but not sensitivty  
Specificity produced but not sensitivty


'''Reproducibility'''
'''Reproducibility'''  


<br>


| Test has reasonable reliability and sensitivity and can be used to aid assessment of AS with LBP
| Test has reasonable reliability and sensitivity and can be used to aid assessment of AS with LBP
|-
|-
| Kokmeyer et al 2002
| Kokmeyer et al 2002  
| 46%
| 46%  
| Not tested
| Not tested  
| Not tested
| Not tested  
| NA
| NA  
| NA
| NA  
| NA
| NA  
| Abstract only
| Abstract only  
|  
|  
'''Score = 2 (Abstract only)<br>Patient Spectrum<br>'''78 subjects with varying degress of LBP'''<br>Reference Standard<br>'''Unclear from abstract'''<br>Independent blind comparisons with Gold standard<br>'''Unclear from abstract'''<br>Test characteristics<br>'''Unclear from abstract'''<br>Reproducibility<br>'''Well described and detailed method'''<br>'''
'''Score = 2 (Abstract only)<br>Patient Spectrum<br>'''78 subjects with varying degress of LBP'''<br>Reference Standard<br>'''Unclear from abstract'''<br>Independent blind comparisons with Gold standard<br>'''Unclear from abstract'''<br>Test characteristics<br>'''Unclear from abstract'''<br>Reproducibility<br>'''Well described and detailed method'''<br>'''  


| Test is best when used within a multitest cluster of 5 SIJ tests.
| Test is best when used within a multitest cluster of 5 SIJ tests.
|-
|-
| Laslett et al 2005
| Laslett et al 2005  
| Not tested
| Not tested  
| 60
| 60  
| 81
| 81  
| 3.2
| 3.2  
| 0.5
| 0.5  
| 12
| 12  
| 12 - Full usage of normally available clinical data not allowed. Unclear if intermediate results reported.
| 12 - Full usage of normally available clinical data not allowed. Unclear if intermediate results reported.  
| Score = 5<br>'''Patient Spectrum'''<br>48 subjects with broad spectrum. Accepting range of buttock pain with/without Lumbar or lower limb symptoms. Excluded if midline pain above L5<br>'''Reference Standard'''<br>Every subject received reference standard diagnosis via Fluroscopy contrast guidance of a diagnostic spinal injection.<br>'''Independent blind comparisons with Gold standard<br>'''Therapist and Radiologist blinded to opposite assessment. Gold standard diagnostic spinal injection used.<br>'''Test characteristics'''<br>Presented as expected<br>'''Reproducibility'''<br>Concisely and clearly detailed method and results analysis<br>
| Score = 5<br>'''Patient Spectrum'''<br>48 subjects with broad spectrum. Accepting range of buttock pain with/without Lumbar or lower limb symptoms. Excluded if midline pain above L5<br>'''Reference Standard'''<br>Every subject received reference standard diagnosis via Fluroscopy contrast guidance of a diagnostic spinal injection.<br>'''Independent blind comparisons with Gold standard<br>'''Therapist and Radiologist blinded to opposite assessment. Gold standard diagnostic spinal injection used.<br>'''Test characteristics'''<br>Presented as expected<br>'''Reproducibility'''<br>Concisely and clearly detailed method and results analysis<br>  
| Test best used when used within a multitest cluster (Laslett et al 2005)
| Test best used when used within a multitest cluster (Laslett et al 2005)
|-
|-
|  
|  
Laslett and Williams 1994
Laslett and Williams 1994  


(Cited Cook and Hegedus 2008)
(Cited Cook and Hegedus 2008)  


| 69%
| 69%  
| Not tested
| Not tested  
| Not tested
| Not tested  
| NA
| NA  
| NA
| NA  
| NA
| NA  
| Unable to obtain paper
| Unable to obtain paper  
| Unable to obtain paper
| Unable to obtain paper  
| NA
| NA
|-
|-
| McCombe et al 1989
| McCombe et al 1989  
| 36%
| 36%  
| Not tested
| Not tested  
| Not tested
| Not tested  
| NA
| NA  
| NA
| NA  
| NA
| NA  
| Abstract only
| Abstract only  
| Score = 0 (Abstract only)<br>'''Patient Spectrum'''<br>83 subjects but unclear in abstract how met or inclusion criteria. Unclear as to extent and type of LBP<br>'''Reference Standard'''<br>Unclear from abstract. Study tests inter-rater reliability of multiple tests but still unclear<br>'''Independent blind comparisons with Gold standard'''<br>Unclear from abstract<br>'''Test characteristics'''<br>Unclear from abstract<br>'''Reproducibility'''<br>Some description of methods and analysis in abstract but not reproducible.<br>
| Score = 0 (Abstract only)<br>'''Patient Spectrum'''<br>83 subjects but unclear in abstract how met or inclusion criteria. Unclear as to extent and type of LBP<br>'''Reference Standard'''<br>Unclear from abstract. Study tests inter-rater reliability of multiple tests but still unclear<br>'''Independent blind comparisons with Gold standard'''<br>Unclear from abstract<br>'''Test characteristics'''<br>Unclear from abstract<br>'''Reproducibility'''<br>Some description of methods and analysis in abstract but not reproducible.<br>  
| NA
| NA
|-
|-
| Ozgocmen et al 2008
| Ozgocmen et al 2008  
| Not tested
| Not tested  
| 23
| 23  
| 81
| 81  
| 1.24
| 1.24  
| 0.94
| 0.94  
| 10
| 10  
| 10 – unclear if MRI interpreted with physio findings. Withdrawls not explained. No intermediate results.
| 10 – unclear if MRI interpreted with physio findings. Withdrawls not explained. No intermediate results.  
| Score = 4<br>'''Patient Spectrum'''<br>Unclear as to how subjects were recruited from clinic and unclear as to extent of dysfunction, except present for 3 months +<br>'''Reference Standard'''<br>MRI used on all tests subjects<br>'''Independent blind comparisons with Gold standard'''<br>Physiotherapists were blinded of MRI results while assessing subject.<br>'''Test characteristics'''<br>Presented as expected<br>'''Reproducibility'''<br>Very detailed method and analysis<br>
| Score = 4<br>'''Patient Spectrum'''<br>Unclear as to how subjects were recruited from clinic and unclear as to extent of dysfunction, except present for 3 months +<br>'''Reference Standard'''<br>MRI used on all tests subjects<br>'''Independent blind comparisons with Gold standard'''<br>Physiotherapists were blinded of MRI results while assessing subject.<br>'''Test characteristics'''<br>Presented as expected<br>'''Reproducibility'''<br>Very detailed method and analysis<br>  
| Test has acceptable reliability when used in early stage sacroilitis. However, reliability, sensitivity and specificity improved when in a multi-test cluster.
| Test has acceptable reliability when used in early stage sacroilitis. However, reliability, sensitivity and specificity improved when in a multi-test cluster.
|-
|-
| Potter and Rothstein 1985
| Potter and Rothstein 1985  
| 94%
| 94%  
| Not tested
| Not tested  
| Not tested
| Not tested  
| NA
| NA  
| NA
| NA  
| NA
| NA  
| 5 – No reference measure used. Study investigate inter-rate reliability.
| 5 – No reference measure used. Study investigate inter-rate reliability.  
| Score = 3<br>'''Patient Spectrum'''<br>17 subjects with wide range of symptoms. Unilateral buttock pain, 1 year + with/without lumbar or lower limb pain or paraesthesia. Accepted pts who would normally be tested for SIJ dysfunction.<br>'''Reference Standard'''<br>Reference standard identical to index test but carried out on every subject by independent and blind assessor<br>'''Independent blind comparisons with Gold standard'''<br>No gold standard used but assessors independent and blind of each other.<br>'''Test characteristics'''<br>Only reliability and assessor agreement assessed<br>'''Reproducibility'''<br>Very detailed and specific description of method and analyses<br>
| Score = 3<br>'''Patient Spectrum'''<br>17 subjects with wide range of symptoms. Unilateral buttock pain, 1 year + with/without lumbar or lower limb pain or paraesthesia. Accepted pts who would normally be tested for SIJ dysfunction.<br>'''Reference Standard'''<br>Reference standard identical to index test but carried out on every subject by independent and blind assessor<br>'''Independent blind comparisons with Gold standard'''<br>No gold standard used but assessors independent and blind of each other.<br>'''Test characteristics'''<br>Only reliability and assessor agreement assessed<br>'''Reproducibility'''<br>Very detailed and specific description of method and analyses<br>  
| Reliability of test is poor
| Reliability of test is poor
|-
|-
| Robinson et al 2007
| Robinson et al 2007  
| 82%
| 82%  
| Not tested
| Not tested  
| Not tested
| Not tested  
| NA
| NA  
| NA
| NA  
| NA
| NA  
| 10 – Reference standard not independent of index test + clinicians deprived of pain localisation on examination
| 10 – Reference standard not independent of index test + clinicians deprived of pain localisation on examination  
| Score = 3<br>'''Patient Spectrum'''<br>61 subjects with either AS, post partum pelvic pain or no pain.<br>'''Reference Standard'''<br>Tests performed on every subject twice but 2 random, separate, independent and blind assessors in a random order.<br>'''Independent blind comparions with Gold standard'''<br>Reference standard same as index test and not gold standard. Assessors were independent and blinded.<br>'''Test characteristics'''<br>Only reliability and assessor agreement reported.<br>'''Reproducibility'''<br>Well detailed methodology and analyses<br>
| Score = 3<br>'''Patient Spectrum'''<br>61 subjects with either AS, post partum pelvic pain or no pain.<br>'''Reference Standard'''<br>Tests performed on every subject twice but 2 random, separate, independent and blind assessors in a random order.<br>'''Independent blind comparions with Gold standard'''<br>Reference standard same as index test and not gold standard. Assessors were independent and blinded.<br>'''Test characteristics'''<br>Only reliability and assessor agreement reported.<br>'''Reproducibility'''<br>Well detailed methodology and analyses<br>  
| Reliability of the test is moderate to good. However, test is better when performed in a multi-test cluster.<br>
| Reliability of the test is moderate to good. However, test is better when performed in a multi-test cluster.<br>
|-
|-
| Russell et al 1981
| Russell et al 1981  
| Not tested
| Not tested  
| 11
| 11  
| 90
| 90  
| 1.1
| 1.1  
| 0.98
| 0.98  
| 5
| 5  
| PUBmed indexed but no abstract available therefore, not obtained
| PUBmed indexed but no abstract available therefore, not obtained  
| Unable to obtain
| Unable to obtain  
| Test not valid (van der Wruff cited Russell et al 1981)
| Test not valid (van der Wruff cited Russell et al 1981)
|-
|-
| Average (Mean)
| Average (Mean)  
| 65.4%
| 65.4%  
| 25.75
| 25.75  
| 88.2
| 88.2  
| 1.85
| 1.85  
| 0.81
| 0.81  
| 7.8
| 7.8  
| 7.8
| 7.8  
| 2.57
| 2.57  
| Test is acceptable used on its own, but it is best used within a cluster
| Test is acceptable used on its own, but it is best used within a cluster
|}
|}


 
<br>


Sensitivity – The possibility of a positive test resulting in someone with the pathology<br>Specificity – The probability of a negative test resulting in someone without the pathology<br>Positive Likelihood Ratio (LR+) –The ratio of a positive test result in people with the pathology to a positive test result in people without the pathology.<br>Negative Likelihood Ratio (LR-) – The ratio of a negative test result in people with the pathology to a negative test result in people without the pathology.<br>Reliability – Likelihood of results from test to be reproduced again (Expressed as percentage or as decimal)  
Sensitivity – The possibility of a positive test resulting in someone with the pathology<br>Specificity – The probability of a negative test resulting in someone without the pathology<br>Positive Likelihood Ratio (LR+) –The ratio of a positive test result in people with the pathology to a positive test result in people without the pathology.<br>Negative Likelihood Ratio (LR-) – The ratio of a negative test result in people with the pathology to a negative test result in people without the pathology.<br>Reliability – Likelihood of results from test to be reproduced again (Expressed as percentage or as decimal)  


<br>
#A systematic review by van der Wurff et al (2000b)<ref>van der Wurff P, Meyne W, Hagmeijer RHM (2000b). Clinical tests of the sacroiliac joint: A systematic methodological review. Part 2: Validity. Manual Therapy Volume 5, Issue 2, May 2000, Pages 89–96</ref> found that ¾ of studies included which looked at distraction found that it was not a valid test and 2/3 in van der Wurff et al (2000a)<ref>van der Wurff P, Meyne W, Hagmeijer RHM (2000a). Clinical tests of the sacroiliac joint: A systematic methodological review. Part 1: Reliability. Manual Therapy Volume 5, Issue 2, May 2000, Pages 89–96</ref> found it unreliable.
#Stuber 2007<ref name=":9">Stuber KJ (2007). Specificity, sensitivity, and predictive values of clinical tests of the sacroiliac joint: a systematic review of the literature. J Can Chiropr Assoc. 2007 March; 51(1): 30–41.</ref> found only one study in a systematic review investigating Distraction Test.<ref>Laslett M, Aprill C, McDonald B, Young S (2005). Diagnosis of sacroiliac joint pain: validity of individual provocation tests and composites of test. Man Ther. 2005;10:207-218.</ref> Stuber 2007 reported 60% sensitivity. The search excluded any papers which didn’t compare to a gold standard. This explains why only one study in Stuber 2007 was included as most of the studies from Cook and Hegedus (2013) did not utilize a gold standard comparative.
#New evidence has come out since then suggesting the test is&nbsp;sufficiently and reasonably reliable and valid when used independently but is best when used in a cluster<ref name=":2" /><ref name=":3" /><ref name=":4" /><ref name=":6" /><ref name=":8" /><ref name=":9" />
#Gold standard/Reference standard for SIJ dysfunction is a sacroiliac joint injection confirmed under fluoroscopy or CT-guidance using a local anesthetic solution. The injection is performed twice on 2 separate visits with the diagnosis being confirmed when the patient reports a significant change in relief from pain. Maigne et al 1998, Maigne et al (1996)<ref>Maigne JY, Aivaliklis A, Pfefer F (1996). Results of sacroiliac joint double block and value of sacroiliac pain provocation tests in 54 patients with low back pain. Spine 1996;21:1889-1892</ref> and Schwarzer et al (1995)<ref>Schwarzer AC, April CN, Bogduk N (1995). The sacroiliac joint in chronic low back pain. Spine 1995;20:31-37</ref> have used at least a 75 percent change in relief of pain before a response to injection is considered positive and the SIJ deemed the source of pain. However, there is some debate that injection into ligament posterior to joint rather than an intra-articular injection is actually more effective<ref>Borowsky CD, Fagen G.(2008) Sources of sacroiliac region pain: insights gained from a study comparing standard intra-articular injection with a technique combining intra- and peri-articular injection. Arch Phys Med Rehabil. Nov;89(11):2048-56</ref><ref>Murakami E, Tanaka Y, Aizwa T (2007). Effect of peri-articular and intra-articular lidocaine injections for sacroiliac joint pain: prospective comparative study. J Ortoped Science. 2007;12:274-280.</ref>


== Conclusion  ==


'''Notes:'''
Although this test does have moderate to good reliability<ref name=":8" /> and is reasonably accurate in diagnosing SIJ dysfunction/sprain<ref name=":3" />,the evidence shows that it is [[Sacroiliac Joint Special Test Cluster|best used when used within a cluster]] <ref name=":10" /><ref name=":11" /><ref name=":2" /><ref name=":3" /><ref name=":4" /><ref name=":6" /><ref name=":8" />
 
*Ham et al 1996 used the Distraction test as a measure for pelvic fracture so it was not included from Cook and Hegedus (2013).
*Ozgocmen et al 2008 assessed patients with acute sacroilitis
*QUADAS score replicated from Cook and Hegedus (2013). Originally produced by Whitling et al (2003). Cook and Hegedus (2013) citied Whitling et al (2005). It is a quality tool to assess Diagnostic Accuracy Studies (Whitling et al 2003).
 
#Score of 7-14 “yesses” has typically been seen to indicate a high quality diagnostic accuracy study while a score below 7 indicates a poor quality diagnostic accuracy study (de Graaf et al 2006, Sehgal et al 2005, Shah et al 2005).
#However, Cook and Hegedus (2013) suggest a score of 10 “yesses” should be associated with a high quality study and a score below 10 should be associated with poor designed studies (Cook and Hegedus 2010, Hardaker et al 1990, Hegedus et al 2007).<br>
 
*A&nbsp;systematic review by van der Wurff et al (2000b) found that ¾ of studies included which looked at distraction found that it was not a valid test and 2/3 in van der Wurff et al (2000a) found it unreliable.
*Stuber (2007) found only one study in a systematic review investigating Distraction Test (Laslett et al 2005). Stuber (2007) reported 60% sensitivity. The search excluded any papers which didn’t compare to a gold standard. This explains why only one study in Stuber (2007) was included as most of the studies from Cook and Hegedus (2013) did not utilise a gold standard comparative.
*New evidence has come out since then suggesting the test is&nbsp;sufficiently and reasonably reliable and valid when used independantly but is best when used in a cluster (Laslett et al 2008, Laslett et al 2005, Laslett et al 2003, Robinson et al 2007, Ozgocmen et al 2008, Stuber 2007)
*Gold standard/Reference standard for SIJ dysfunction is a sacroiliac joint injection confirmed under fluoroscopy or CT-guidance using a local anesthetic solution.
 
#The injection is performed twice on 2 separate visits with the diagnosis being confirmed when the patient reports a significant change in relief from pain.
#Schwarzer et al (1995), Maigne et al 1998 and Maigne et al1996 have used at least a 75 percent change in relief of pain before a response to injection is considered positive and the SIJ deemed the source of pain.
#However, there is some debate that injection into ligament posterior to joint rather than an intra-articular injection is actually more effective (Murakami et al 2008, Borowski et al 2007)


*A brief search on PUBmed and Medline with the search term (sacroiliac joint AND (distraction test OR gapping test OR Transverse Anterior Stress Test OR Sacroiliac Joint Stress Test)) returned 27 results on PUBmed showing no other studies other than the ones published in Cook and Hegedus (2013)<br>
== See Also ==
 
<div>
= Conclusion =
* http://www.physio-pedia.com/Posterior_pelvic_pain_provocation_test_(aka_Thigh_Thrust_aka_Posterior_Shear)
 
* http://www.physio-pedia.com/Sacral_Thrust_Test
Although this test does have moderate to good reliability (Robinson et al 2007) and is reasonably accurate in diagnosing SIJ dysfunction/sprain (Laslett et al 2005) the evidence shows that it is best used when used within a cluster (Albert et al 2000, Kokmeyer et al 2002, Laslett 2008, Laslett et al 2005,Laslett et al 2003, Ozgocmen et al 2008, Robinson et al 2007).
* http://www.physio-pedia.com/Gaenslen_Test
 
</div>
See Laslett Cluster Testing for further information
 
Link to Laslett Testing<br>
 
 
 
 
 
 
 
 
 
 
 
 
 
= Resources =
 
<br>
 
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Latest revision as of 22:31, 31 January 2021

Description and Purpose[edit | edit source]

The SIJ (Sacroiliac Joint) Distraction (Colloquially know as Gapping) test is used to add evidence, positive or negative, to the hypotheses of an SIJ sprain or dysfunction when used in the Laslett SIJ Cluster testing. This test stresses the anterior sacroiliac ligaments.[1][2][3][4][5] This test has also been described as the Transverse Anterior Stress Test or the Sacroiliac Joint Stress Test.

Technique[edit | edit source]

SI Distraction Test - Vertically oriented pressure is applied to the anterior superior iliac spinous processes directed posteriorly, distracting the sacroiliac joint.

1. The patient lies supine and the examiner applies a vertically orientated, posteriorly directed force to both the anterior superior iliac spines (ASIS)[1] [3][4][5]


Note: Cook and Hegedus (2013) suggest applying a sustained force for 30 seconds before applying a repeated vigorous force in an attempt to reproduced the patient’s symptoms. However, Laslett (2008) does not suggest any timings or changes in force.

Because of the lack of standardisation in the technique it is quite feasible different therapists will practise this test different ways, giving rise to variability in response and lowering the inter-tester reliability.[4][6] No evidence to suggest either method is preferable[6], therefore, more evidence needed.


2. The presumed effect is a DISTRACTION of the anterior aspect of the sacroiliac joint.[4][5]


3. A test is positive if it reproduces the patient's symptoms. This indicates SIJ dysfunction or a sprain of the anterior sacroiliac ligaments[1][2][3][4][5]


However, this test should be used in concordance within a SIJ testing cluster to ensure maximum reliability and validity when confirming hypotheses[7][8][3][5][9][10] See Laslett SIJ testing cluster for further information

Sacroiliac Distraction Test video provided by Clinically Relevant

Evidence[edit | edit source]

The Diagnostic Accuracy of the Distraction test for SIJ dysfunction is described below (Original data from Cook and Hegedus (2013).

Author Reliability Sensitivity Specificity LR+ LR- QUADAS Score (0-14) Cook and Hegedus 2013 QUADAS Score (0-14) Gunning 2013 CEBM (0-5) With qualitative J Study Conclusion
Albert et al 2000 84% 4-14 (Average = 9) 100 NA NA 7 7 Score = 4
Patient Spectrum
535 women fulfilling broad inclusion criteria with daily pain at gestation week 33.
Reference Standard
Reference standard performed on all participants
Independent blind comparisons with Gold standard
No gold standard used but 2 examinations performed by individual and blinded assessors
Test characteristics
Presented as expected but without likelihood ratios
Reproducibility
Method and all analyses detailed clearly. All reproducible
Test has reasonable specificity and inter-rater reliability and should be used as an assessment tool in pregnant women
Blower and Griffin 1984 63% Not tested 89 NA NA 5

6 - Reference standard used but minimal description. 2 studies reported in 1. Very messy study.


Score = 2

Patient Spectrum Consecutive admissions of AS patients with varying stages of progression.

Reference Standard

Performed on all participants

Independent Blind comparisons with Gold Standard

No gold standard used/ Blind testing of index test but not reference standard

Test Characteristics Specificity produced but not sensitivty

Reproducibility


Test has reasonable reliability and sensitivity and can be used to aid assessment of AS with LBP
Kokmeyer et al 2002 46% Not tested Not tested NA NA NA Abstract only

Score = 2 (Abstract only)
Patient Spectrum
78 subjects with varying degress of LBP
Reference Standard
Unclear from abstract
Independent blind comparisons with Gold standard
Unclear from abstract
Test characteristics
Unclear from abstract
Reproducibility
Well described and detailed method

Test is best when used within a multitest cluster of 5 SIJ tests.
Laslett et al 2005 Not tested 60 81 3.2 0.5 12 12 - Full usage of normally available clinical data not allowed. Unclear if intermediate results reported. Score = 5
Patient Spectrum
48 subjects with broad spectrum. Accepting range of buttock pain with/without Lumbar or lower limb symptoms. Excluded if midline pain above L5
Reference Standard
Every subject received reference standard diagnosis via Fluroscopy contrast guidance of a diagnostic spinal injection.
Independent blind comparisons with Gold standard
Therapist and Radiologist blinded to opposite assessment. Gold standard diagnostic spinal injection used.
Test characteristics
Presented as expected
Reproducibility
Concisely and clearly detailed method and results analysis
Test best used when used within a multitest cluster (Laslett et al 2005)

Laslett and Williams 1994

(Cited Cook and Hegedus 2008)

69% Not tested Not tested NA NA NA Unable to obtain paper Unable to obtain paper NA
McCombe et al 1989 36% Not tested Not tested NA NA NA Abstract only Score = 0 (Abstract only)
Patient Spectrum
83 subjects but unclear in abstract how met or inclusion criteria. Unclear as to extent and type of LBP
Reference Standard
Unclear from abstract. Study tests inter-rater reliability of multiple tests but still unclear
Independent blind comparisons with Gold standard
Unclear from abstract
Test characteristics
Unclear from abstract
Reproducibility
Some description of methods and analysis in abstract but not reproducible.
NA
Ozgocmen et al 2008 Not tested 23 81 1.24 0.94 10 10 – unclear if MRI interpreted with physio findings. Withdrawls not explained. No intermediate results. Score = 4
Patient Spectrum
Unclear as to how subjects were recruited from clinic and unclear as to extent of dysfunction, except present for 3 months +
Reference Standard
MRI used on all tests subjects
Independent blind comparisons with Gold standard
Physiotherapists were blinded of MRI results while assessing subject.
Test characteristics
Presented as expected
Reproducibility
Very detailed method and analysis
Test has acceptable reliability when used in early stage sacroilitis. However, reliability, sensitivity and specificity improved when in a multi-test cluster.
Potter and Rothstein 1985 94% Not tested Not tested NA NA NA 5 – No reference measure used. Study investigate inter-rate reliability. Score = 3
Patient Spectrum
17 subjects with wide range of symptoms. Unilateral buttock pain, 1 year + with/without lumbar or lower limb pain or paraesthesia. Accepted pts who would normally be tested for SIJ dysfunction.
Reference Standard
Reference standard identical to index test but carried out on every subject by independent and blind assessor
Independent blind comparisons with Gold standard
No gold standard used but assessors independent and blind of each other.
Test characteristics
Only reliability and assessor agreement assessed
Reproducibility
Very detailed and specific description of method and analyses
Reliability of test is poor
Robinson et al 2007 82% Not tested Not tested NA NA NA 10 – Reference standard not independent of index test + clinicians deprived of pain localisation on examination Score = 3
Patient Spectrum
61 subjects with either AS, post partum pelvic pain or no pain.
Reference Standard
Tests performed on every subject twice but 2 random, separate, independent and blind assessors in a random order.
Independent blind comparions with Gold standard
Reference standard same as index test and not gold standard. Assessors were independent and blinded.
Test characteristics
Only reliability and assessor agreement reported.
Reproducibility
Well detailed methodology and analyses
Reliability of the test is moderate to good. However, test is better when performed in a multi-test cluster.
Russell et al 1981 Not tested 11 90 1.1 0.98 5 PUBmed indexed but no abstract available therefore, not obtained Unable to obtain Test not valid (van der Wruff cited Russell et al 1981)
Average (Mean) 65.4% 25.75 88.2 1.85 0.81 7.8 7.8 2.57 Test is acceptable used on its own, but it is best used within a cluster


Sensitivity – The possibility of a positive test resulting in someone with the pathology
Specificity – The probability of a negative test resulting in someone without the pathology
Positive Likelihood Ratio (LR+) –The ratio of a positive test result in people with the pathology to a positive test result in people without the pathology.
Negative Likelihood Ratio (LR-) – The ratio of a negative test result in people with the pathology to a negative test result in people without the pathology.
Reliability – Likelihood of results from test to be reproduced again (Expressed as percentage or as decimal)


  1. A systematic review by van der Wurff et al (2000b)[11] found that ¾ of studies included which looked at distraction found that it was not a valid test and 2/3 in van der Wurff et al (2000a)[12] found it unreliable.
  2. Stuber 2007[13] found only one study in a systematic review investigating Distraction Test.[14] Stuber 2007 reported 60% sensitivity. The search excluded any papers which didn’t compare to a gold standard. This explains why only one study in Stuber 2007 was included as most of the studies from Cook and Hegedus (2013) did not utilize a gold standard comparative.
  3. New evidence has come out since then suggesting the test is sufficiently and reasonably reliable and valid when used independently but is best when used in a cluster[3][4][5][9][10][13]
  4. Gold standard/Reference standard for SIJ dysfunction is a sacroiliac joint injection confirmed under fluoroscopy or CT-guidance using a local anesthetic solution. The injection is performed twice on 2 separate visits with the diagnosis being confirmed when the patient reports a significant change in relief from pain. Maigne et al 1998, Maigne et al (1996)[15] and Schwarzer et al (1995)[16] have used at least a 75 percent change in relief of pain before a response to injection is considered positive and the SIJ deemed the source of pain. However, there is some debate that injection into ligament posterior to joint rather than an intra-articular injection is actually more effective[17][18]

Conclusion[edit | edit source]

Although this test does have moderate to good reliability[10] and is reasonably accurate in diagnosing SIJ dysfunction/sprain[4],the evidence shows that it is best used when used within a cluster [7][8][3][4][5][9][10]

See Also[edit | edit source]

References[edit | edit source]

  1. 1.0 1.1 1.2 Cook, C, Hegedus, E. (2013). Orthopedic Physical Examination Test: An Evidence Based Approach. New Jersey: Prentice Hall.
  2. 2.0 2.1 Cook, C., Cleland, J., Huijbregts, P. (2007). Creation and Critique of Studies of Diagnostic Accuracy: Use of theS methodological Quality Assessment Tool. J Manipulative Physiol Ther, 15(2), 93-102.
  3. 3.0 3.1 3.2 3.3 3.4 3.5 Laslett M, (2008). Evidence-Based Diagnosis and Treatment of the Painful Sacroiliac Joint. J Man Manip Ther. 2008; 16(3): 142–152.
  4. 4.0 4.1 4.2 4.3 4.4 4.5 4.6 4.7 Laslett M, Aprill C, McDonald B, Young S (2005). Diagnosis of sacroiliac joint pain: validity of individual provocation tests and composites of test. Man Ther. 2005;10:207-218.
  5. 5.0 5.1 5.2 5.3 5.4 5.5 5.6 Laslett M, Young SB, Aprill CN, McDonald B, (2003). Diagnosing painful sacroiliac joints: A validity study of a McKenzie evaluation and sacroiliac joint provocation tests. Aust J Physiother 2003;49:89–97.
  6. 6.0 6.1 Levin U, Nilsson-Wikmar L, Stenström CH (2005). Variability within and between evaluations of sacroiliac pain with the use of distraction testing. J Manipulative Physiol Ther. 2005 Nov-Dec;28(9):688-95.
  7. 7.0 7.1 Albert H, Godskesen M, Westergaard J (2000). Evaluation of clinical test used in classification procedures in pregnancy-related pelvic joint pain. Eur Spine J. 2000; 9(2):161-166
  8. 8.0 8.1 Kokmeyer DJ, Van der Wurdd P, Aufdemkampe G, Fikenscher TC (2002). The reliability of multitest regimens with sacroiliac pain provocation tests. J Manipulative Physiol Therapy. 2002;25(1):42-48
  9. 9.0 9.1 9.2 Ozgocmen S, Bozgeyik Z, Kalcik M, Yildrim A (2008). The value of sacroiliac pain provocation tests in early active sacroilitis. Clin Rheumatol. 2008;27:1275-1282
  10. 10.0 10.1 10.2 10.3 Robinson HS. Brox JI. Robinson R. Bjelland E. Solem S. Telje T (2007). The reliability of selected motion- and pain provocation tests for the sacroiliacjoint. Manual Therapy. 12(1):72-9, 2007 Feb.
  11. van der Wurff P, Meyne W, Hagmeijer RHM (2000b). Clinical tests of the sacroiliac joint: A systematic methodological review. Part 2: Validity. Manual Therapy Volume 5, Issue 2, May 2000, Pages 89–96
  12. van der Wurff P, Meyne W, Hagmeijer RHM (2000a). Clinical tests of the sacroiliac joint: A systematic methodological review. Part 1: Reliability. Manual Therapy Volume 5, Issue 2, May 2000, Pages 89–96
  13. 13.0 13.1 Stuber KJ (2007). Specificity, sensitivity, and predictive values of clinical tests of the sacroiliac joint: a systematic review of the literature. J Can Chiropr Assoc. 2007 March; 51(1): 30–41.
  14. Laslett M, Aprill C, McDonald B, Young S (2005). Diagnosis of sacroiliac joint pain: validity of individual provocation tests and composites of test. Man Ther. 2005;10:207-218.
  15. Maigne JY, Aivaliklis A, Pfefer F (1996). Results of sacroiliac joint double block and value of sacroiliac pain provocation tests in 54 patients with low back pain. Spine 1996;21:1889-1892
  16. Schwarzer AC, April CN, Bogduk N (1995). The sacroiliac joint in chronic low back pain. Spine 1995;20:31-37
  17. Borowsky CD, Fagen G.(2008) Sources of sacroiliac region pain: insights gained from a study comparing standard intra-articular injection with a technique combining intra- and peri-articular injection. Arch Phys Med Rehabil. Nov;89(11):2048-56
  18. Murakami E, Tanaka Y, Aizwa T (2007). Effect of peri-articular and intra-articular lidocaine injections for sacroiliac joint pain: prospective comparative study. J Ortoped Science. 2007;12:274-280.