Concurrent Validity of Calipers and Ultrasound Imaging
to Measure Interrecti Distance. Cynthia M. Chiarello, J. and Adrienne McAuley. J Orthop Sports Phys Ther 2013;43(7):495-503.
Laura
Scheufele PT, DPT, WCS
August 7,
2013
Primary Aim: To determine the concurrent validity of digital nylon
calipers in comparison to ultrasound imaging (USI) for the measurement of
interrecti distance (IRD). Secondary purpose was to describe the IRD seen in
typical adult males and females.
Subjects: A
sample of convenience of 56 individuals (11 men, 45 women: 22 nulliparous and
23 parous)
Exclusion criteria: If pregnant; had
scarring from previous abdominal surgery such that, on observation of the
abdomen, the linea alba or umbilicus was obscured or deformed; had
rheumatological or connective tissue disease; or had any medical condition that
would prohibit active abdominal contraction.
Study Design: Clinical
measurement, concurrent validity criterion standard.
Methods: Each
subject positioned in hook-lying and two measurement sitesmarked with water-soluble
pen: 4.5 cm above the umbilical midpoint and 4.5 cm below the umbilical
midpoint. No umbilical measurement taken secondary to technical difficulties
with USI (also previously reported in other studies as well). Measurements
taken in two positions: 1) the abdominal muscles at rest (arms at side) and 2)
with active contraction of the abdominals (arms crossed over chest and head
raised only until spine of the scapulae off the table surface.)
Caliber measurements taken first (to avoid marks being distorted by the
ultrasound gel) by a single examiner (examiner #1).This examiner palpated for
the medial borders of the right and left rectus abdominis muscle bellies at the
marked locations. The inside measurement jaws of the caliper were positioned at
the locations of the palpating fingers, perpendicular to the direction of the
muscles, and adjusted to the perceived IRD width. Examiner #1 would leave the
room and examiner #2 would enter to complete the USI measurements. Each
examiner was blinded from the other’s findings.
The USI assessmentperformed with the patient still positioned hooklying. A
5-MHz curvilinear transducer perpendicular to the abdominal surface at each
marked location. The onscreen image of the IRD was captured and then the measuring
feature was used to measure the IRD. The examiner determining the location of
the medial borders, using the onscreen cursor to mark the distance between the
muscle bellies.
A
separate study performed to establish each tester’s own reliability. 8 subjects
measured with calipers and 6 with USI. Three measurements for each location
both at rest and with abdominal muscle contracted performed on the same day. Intrarater
reliability found to be very high for each tool, with intraclass correlation
coefficients (ICCs) ranging between 0.90 to 0.99.
Results:
The nulliparous women had the
smallest IRD in both locations and with both tools except the rest position
below the umbilicus, which was the smallest in the men subgroup.
Validity of the measurements taken
with the caliper as compared to the USI was different above versus below the
umbilicus.
Above umbilicus: No statistical
difference (P> .05) in IRD values
between the 2 measurement tools in both rest and contracted positions.
Below umbilicus: The IRD
measurements using calipers were significantly larger (P< .0001) than when using USI for both rest and contracted
positions. Low agreement between the 2 measurement tools below the umbilicus.
Table 3 summarizes the mean averages
of each subset
Discussion: Ultrasound
is considered the best available clinical tool to assess IRD, but it not
readily available for most clinicians. A digital nylon caliper is a cost
effective clinical tool but previously its use was not validated. The caliper
measurements above the umbilicus were comparable to the USI both when at rest
and with abdominals contracted (considered good to excellent validity), but not
with the measurements below the umbilicus. In this location the measurements
were overestimated compared to the USI. Speculation about the cause of this difference
may have been due to 1) inaccurate identification of the medial borders using
manual palpation with the caliper measurement (possibly related to greater
adipose tissue in the area 2) the measurements could have been taken at different
depths or 3) the caliper jaws could have produced an outward pressure against
the muscle belly, thus increasing the distance.
Significant variances in IRD noted
between gender and parity, as well as location above or below the umbilicus. There
is no current standard for defining DRA, and thus clinicians need to be careful
when interpreting measurements.
Strengths: Examiners blinded from each other’s assessment. Inclusion of
males and females.
Weaknesses: Relatively small sample size. Unable to compare measurements
at the level of umbilicus. In order to prevent the marking from being wiped
off, not able to randomize order of measurement.
Conclusion:Calipers
are a valid tool for measuring IRD above the umbilicus in males and females
when using USI as the criterion standard, but not for the location below the
umbilicus.
Impact on practice: This
is an important first step towards establishing an inexpensive evaluation tool
for DRA that is validated. Ultimately
this may pave the way for additional studies to establish which treatments for
DRA is evidence based as well.
Thought questions:
1)
Where do we go from here regarding
research? 2) How are clinicians currently assessing DRA? What parameters do you use as “normal”/abnormal? Does this study change how you are going to assess?
3) How are clinicians treating DRA?
Other notable research:
Mota et al (JOSPT 2012) reported on
test-retest reliability of ultrasound measurement of IRD. This study evaluated 24
healthy females at positions 2 cm above and below the umbilicus and assessed
during rest, an “abdominal crunch” and with a drawing-in maneuver. Ultrasound
found to be a reliable measurement for measuring IRD at rest and during abdominal
crunch and drawing in maneuver. The lowest ICC value (0.50) found below the
umbilicus during contraction. The test-retest measurements across days showed
good reliability during rest and drawing-in maneuver (ICC 0.78 and 0.74) and
very good above with rest, abdominal crunch, and drawing in ( ICC 0.87, 0.83,
and 0.90).
Mota et al (Manual Therapy 2012)
reported on the reliability of IRD measurement by palpation and compared to
ultrasound in 20 healthy females. Palpation found to be sufficiently reliable
to be used in clinical practice, but ultrasound found to be more accurate and
valid.
Beer et al (Clinical Anatomy 2009)
investigated the normal width of the linea alba in 150 nulliparous women
between the ages of 20 to 45 yo with ultrasound. Chose 3 reference points:
level of xiphoid, 3 cm above umbilicus, and 2 cm below the umbilicus. Broad
ranges of widths were observed, with the widest reference point 3 cm above the
umbilicus. Mean widths as follows: Level of xiphoid 7 +/- 5 mm, 3 cm above
umbilicus: 13 +/- 7 mm, and 2 cm below umbilicus 8 +/- 6 mm. Defined the normal
width ( 10th and 90th percentiles taken) as up to 15 mm
level of xiphoid, up to 22 mm 3 cm above umbilicus, and up to 16 mm 2 cm below
the umbilicus in nulliparous women.
Spitznagle (Int Urogynecol J 2007)
reported on the prevalence of DRA in an urogynecolgical population, differences
in characteristics of patients with and without DRA, and the relationship of
DRA to support-related PFD diagnoses. A relationship was noted between the
presence of DRA and SUI, FI and POP.
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