<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">ACT</journal-id><journal-title-group><journal-title>Advances in Computed Tomography</journal-title></journal-title-group><issn pub-type="epub">2169-2475</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/act.2014.32004</article-id><article-id pub-id-type="publisher-id">ACT-46623</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>COMPUTER SCIENCE &amp; COMMUNICATIONS</subject><subject>MEDICINE &amp; HEALTHCARE</subject></subj-group></article-categories><title-group><article-title>The Impact of Enteric Contrast on Radiologist Confidence in Intravenously Enhanced MDCT of the Abdomen and Pelvis: A Randomized Controlled Trial</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Christopher</surname><given-names>M. Garcia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Steven</surname><given-names>Boe</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bret</surname><given-names>Coughlin</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>David</surname><given-names>M. O’Sullivan</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Douglas</surname><given-names>Moote</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Michael</surname><given-names>T. O’Loughlin</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Devika</surname><given-names>Jajoo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Steve</surname><given-names>Lee</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Research, Hartford Hospital, Hartford, USA</addr-line></aff><aff id="aff1"><addr-line>Department of Radiology, Hartford Hospital, Hartford, USA</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>Christopher.michael.garcia@gmail.com(CMG)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>09</day><month>06</month><year>2014</year></pub-date><volume>03</volume><issue>02</issue><fpage>18</fpage><lpage>23</lpage><history><date date-type="received"><day>29</day>	<month>March</month>	<year>2014</year></date><date date-type="rev-recd"><day>29</day>	<month>April</month>	<year>2014</year>	</date><date date-type="accepted"><day>4</day>	<month>May</month>	<year>2014</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
	After
Institutional Review Board approval, 109 patients ≥ 18 years old undergoing
intravenously enhanced Computed Tomography (CT) of the abdomen and pelvis were
prospectively enrolled and randomized into two arms. Patients with a history of
inflammatory bowel disease, Crohn disease and ulcerative colitis were excluded.
The control arm received routine enteric contrast and intravenous contrast. The
experimental arm did not receive oral contrast, but received the standard dose
of intravenous (IV) contrast. One of four experienced body radiologists
reviewed the studies and rated his/her confidence on a scale of 1 (no
confidence) to 10 (all confident findings have been made). Confidence levels
were compared between groups. The 109 subjects were distributed 54 (49.5%) in
the control arm and 55 (50.5%) in the experimental arm. The average confidence
level in the control arm was 8.7 ± 0.9 versus 8.4 ± 1.1 in the experimental arm, which is not statistically significant (p
value = 0.09). Among radiologists, the average confidence levels ranged from 6
- 10 in the control arm and 7 - 10 in the experimental arm. No examinations
were repeated for technical considerations in either group. No studies were
repeated in the experimental group in order to administer oral contrast. When
each radiologist was compared to the others, there were no differences in
confidence level between pairs in the control arm; however, there were
statistically significant differences in confidence level among three pairs of
radiologists for the experimental arm. There was no statistically significant
difference in radiologist confidence level between intravenously enhanced
abdomen and pelvis CTs with enteric contrast and without enteric contrast.
</p></abstract><kwd-group><kwd>Enteric Contrast</kwd><kwd> Outpatient CT</kwd><kwd> Confidence</kwd><kwd> Oral Contrast</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Although protocols vary by institution, equipment, setting and clinical question, the default protocol in our practice for outpatient contrast-enhanced abdominal CT scans includes both enteric and IV contrast administration. Recently, the justification for enteric contrast in the emergency department has been questioned in multiple reports. Studies demonstrate the non-superiority of enteric contrast studies in diagnosing appendicitis [<xref ref-type="bibr" rid="scirp.46623-ref1">1</xref>] -[<xref ref-type="bibr" rid="scirp.46623-ref4">4</xref>] and traumatic bowel injury [<xref ref-type="bibr" rid="scirp.46623-ref5">5</xref>] . The majority of those studies focus on appendicitis, probably due to its clear surgical endpoint and relatively high prevalence. Other studies continue to demonstrate that regardless of the presence of enteric, intravenous, or even rectal contrast, multidetector computed tomography (MDCT) is highly sensitive and specific in diagnosing acute appendicitis [<xref ref-type="bibr" rid="scirp.46623-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.46623-ref7">7</xref>] and other acute processes [<xref ref-type="bibr" rid="scirp.46623-ref8">8</xref>] .</p><p>The routine use of enteric contrast in the outpatient setting has multiple direct and indirect effects, including increased cost, decreased practice efficiency, patient inconvenience and sometimes discomfort. Enteric contrast in oncology patients has been associated with lower patient satisfaction scores [<xref ref-type="bibr" rid="scirp.46623-ref9">9</xref>] . Although the vast majority of research in this area is performed in the emergency setting, the advantages of withholding enteric contrast in the emergency department may translate to routine intravenously enhanced MDCT of the abdomen and pelvis in the outpatient setting. Our purpose in this randomized controlled trial is to evaluate the impact of enteric contrast in intravenously enhanced MDCT of the abdomen and pelvis on radiologist confidence in the outpatient setting.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Study Design</title><p>The trial was conducted following IRB approval and registration with a national database  (www.clinicaltrials.gov, NCT01655550). Following informed consent, 109 patients ≥ 18 years old undergoing intravenously contrast-enhanced CT of the abdomen and pelvis were prospectively enrolled and randomized into two arms in a one-to-one fashion between April 2012 and May 2013, inclusive. The control arm received routine enteric and IV contrast. The experimental arm did not receive enteric contrast, but received the standard dose of IV contrast. All patients ingested 6 ounces of water immediately prior to the scan. One of four experienced body radiologists with 13, 16, 16 and 24 years of practice beyond training was assigned, based on availability, to re- view each case and rate his/her confidence on a scale of 1 (no confidence) to 10 (confident all findings have been made). Interpreting radiologists underwent a one-hour training session in selecting the appropriate confi- dence level, where pilot cases were reviewed and scored. Axial images as well as coronal and sagittal recon- structions were provided for interpretation in both groups. See <xref ref-type="fig" rid="fig1">Figure 1</xref> for the ten point scale of confidence le- vels. Briefly, a confidence level of 10 corresponded to “Excellent study. Confident all findings have been made” and a level of 1 corresponded to “Non diagnostic study. Study needs to be repeated”. A level of 5 corresponded to “Somewhat limited study. May have missed a finding”. Confidence levels were compared between groups.</p><p>Patients with a history of inflammatory bowel disease, Crohn disease and ulcerative colitis were excluded. Other exclusion criteria were allergy to IV contrast, pregnancy, and unwilling or unable to give informed consent. Patients with specific requisitions for CT enterography were excluded. Patient age, height, weight and body mass index were obtained prospectively.</p></sec><sec id="s2_2"><title>2.2. CT Technique</title><p>Computed tomography scans were performed in two outpatient radiology offices. CT scans were performed on a GE VCT Light Speed 64 slice MDCT scanner with a 70-second scan delay after intravenous administration of 100 mL of Omnipaque 300<sup>TM</sup> (GE Healthcare, Waukesha, WI) at a rate of 3 ml per second. Auto milliampere dose modulation was used, with eye, thyroid and breast bismuth shields. 40% Adaptive Statistical Iterative Re- construction was used. Subjects in the control arm ingested 450 mL of Readicat II<sup>&#174;</sup> Barium Sulfate suspension 2.1% w/v, 2.0% w/w (E-Z-Em, Lake Success, NY) one hour before their scheduled appointment time.</p><fig id="fig1"><label>Figure 1</label><caption><p> Confidence level worksheet used by radiologist</p></caption><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\2-2590050x\cd9ac61a-60d2-4673-aea3-94309a7e3641.png"/></fig></sec><sec id="s2_3"><title>2.3. Data Analysis</title><p>The data analyst was blinded with respect to patient allocation. The nature of enteric contrast does not allow for blinding of the interpreting radiologists. Continuous data were assessed for normality and found to be normally distributed. Inferential statistics comprised chi-square tests for categorical data and Student’s t-tests for two- group comparisons. One-way analysis of variance with post hoc Scheff&#233;’s multiple range tests were used for comparisons involving more than two groups. Statistical analyses were conducted with IBM SPSS v. 21 (IBM, Armonk, NY 2013), using an a priori alpha level of 0.05 such that all results yielding p &lt; 0.05 were deemed statistically significant.</p></sec></sec><sec id="s3"><title>3. Results</title><p>The 109 subjects were distributed 54 (49.5%) in the control arm and 55 (50.5%) in the experimental arm. At baseline, there were no differences between groups with respect to age or BMI (<xref ref-type="table" rid="table1">Table 1</xref>). The most common indication for contrast enhanced CT scans in both groups was cancer staging, 36/56 (64%) in the control group and 38/55 (69%) in the experimental group. Abdominal pain was the next most likely indication 8/56 (15%) in the control group and 10/55 (18%) in the experimental group (<xref ref-type="table" rid="table2">Table 2</xref>).</p><p>Among radiologists, the average confidence levels ranged from 6 - 10 in the control arm and 7 - 10 in the experimental arm. The average confidence level (+/− standard deviation) in the control arm was 8.7 &#177; 0.9 versus 8.4 &#177; 1.1 in the experimental arm, with a p value of 0.09. One reader had a statistically significant difference in confidence level; average confidence level of 8.6 in the enteric contrast group versus 7.7 in the no enteric contrast group, with a p value of 0.005. Other readers did not have a statistically significant difference (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>There was no overall difference in confidence level by reader in the control group (ANOVA, p = 0.923), with all inter-reader differences (i.e., 1 vs. 2, 1 vs. 3, etc.) p &gt; 0.93. However, there was a significant difference in confidence level by reader in the experimental group (ANOVA, p &lt; 0.001), with individual differences seen between readers 1 and 3 (Scheff&#233;’s, p = 0.011), readers 1 and 4 (Scheff&#233;’s, p &lt; 0.001), and readers 2 and 4 (Scheff&#233;’s, p = 0.001).</p><p>A post hoc power analysis of our data revealed that group sample sizes of 54 and 55 achieved 40% power to detect a difference of 0.3 between the null hypothesis that both group means were 8.7 and the alternative hypothesis that the mean of group 2 was 8.4, with known group standard deviations of 0.9 and 1.1, using a two-sided t-test with a significance level (alpha) of 0.05.</p><p>No examinations were repeated for technical consideration in either group. In 69% of studies in the experimental group, the radiologist felt that the addition of enteric contrast would not have impacted the confidence level. There were 9 studies in each group where follow-up examinations were recommended. No follow up recommendations were made due to inadequate bowel evaluation or to follow up abnormalities in the small or large bowel.</p><table-wrap id="table1"  position="float"><object-id pub-id-type="pii">Table 1</object-id><label>Table 1</label><caption><p>. Subject data in the control group and the experimental group</p></caption><table><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Enteric contrast</th><th align="center" valign="middle" >No enteric contrast</th><th align="center" valign="middle" >p value (Student t-test)</th></tr></thead><tbody><tr><td align="center" valign="middle" >Subject n (%)</td><td align="center" valign="middle" >54 (49.5%)</td><td align="center" valign="middle" >55 (50.5%)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Age, years (mean &#177; SD)</td><td align="center" valign="middle" >60.4 &#177; 13.2</td><td align="center" valign="middle" >61.2 &#177; 11.2</td><td align="center" valign="middle" >0.743</td></tr><tr><td align="center" valign="middle" >Male/Female</td><td align="center" valign="middle" >18/36</td><td align="center" valign="middle" >26/29</td><td align="center" valign="middle" >0.138</td></tr><tr><td align="center" valign="middle" >BMI, kg/m<sup>2</sup> (mean &#177; SD)</td><td align="center" valign="middle" >28.9 &#177; 5.9</td><td align="center" valign="middle" >28.5 &#177; 6.1</td><td align="center" valign="middle" >0.764</td></tr></tbody></table></table-wrap><table-wrap id="table2"  position="float"><object-id pub-id-type="pii">Table 2</object-id><label>Table 2</label><caption><p>. Total number of examinations by indication in each arm</p></caption><table><thead><tr><th align="center" valign="middle" >Indication</th><th align="center" valign="middle" >Enteric Contrast (n = 56)</th><th align="center" valign="middle" >No Enteric Contrast (n = 55)</th></tr></thead><tbody><tr><td align="center" valign="middle" >Cancer Staging</td><td align="center" valign="middle" >36 (64%)</td><td align="center" valign="middle" >38 (69%)</td></tr><tr><td align="center" valign="middle" >Abdominal Pain</td><td align="center" valign="middle" >8 (14%)</td><td align="center" valign="middle" >10 (18%)</td></tr><tr><td align="center" valign="middle" >Other</td><td align="center" valign="middle" >12 (21%)</td><td align="center" valign="middle" >7 (13%)</td></tr></tbody></table></table-wrap><table-wrap id="table3"  position="float"><object-id pub-id-type="pii">Table 3</object-id><label>Table 3</label><caption><p>. Average confidence levels, standard deviation and p values for both arms with subgroup analysis</p></caption><table><thead><tr><th align="center" valign="middle"  rowspan="2"  >Radiologist</th><th align="center" valign="middle"  colspan="3"  >Confidence level</th><th align="center" valign="middle" ></th></tr></thead><tbody><tr><td align="center" valign="middle" >Group</td><td align="center" valign="middle" >N</td><td align="center" valign="middle" >Mean &#177; SD</td><td align="center" valign="middle" >p value (Student t-test)</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >Enteric Contrast</td><td align="center" valign="middle" >54</td><td align="center" valign="middle" >8.7 &#177; 0.9</td><td align="center" valign="middle" >0.090</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >No Enteric Contrast</td><td align="center" valign="middle" >55</td><td align="center" valign="middle" >8.4 &#177; 1.1</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Radiologist 1</td><td align="center" valign="middle" >Enteric Contrast</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >8.6 &#177; 0.7</td><td align="center" valign="middle" >0.005</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >No Enteric Contrast</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >7.7 &#177; 0.6</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Radiologist 2</td><td align="center" valign="middle" >Enteric Contrast</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >8.7 &#177; 0.8</td><td align="center" valign="middle" >0.14</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >No Enteric Contrast</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >7.8 &#177; 1.0</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Radiologist 3</td><td align="center" valign="middle" >Enteric Contrast</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >8.9 &#177; 1.0</td><td align="center" valign="middle" >0.88</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >No Enteric Contrast</td><td align="center" valign="middle" >14</td><td align="center" valign="middle" >8.8 &#177; 1.2</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Radiologist 4</td><td align="center" valign="middle" >Enteric Contrast</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >8.8 &#177; 1.2</td><td align="center" valign="middle" >0.13</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >No Enteric Contrast</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >9.4 &#177; 0.7</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>Barium and water soluble enteric contrast agents have been in use for approximately a century, first in fluoroscopic examinations and now in CT [<xref ref-type="bibr" rid="scirp.46623-ref10">10</xref>] . Historically, enteric contrast was unquestionably necessary due to slow acquisition, bowel motion and relatively decreased contrast enhancement. Newer techniques and faster acquisitions have markedly improved temporal and spatial resolution of CT scans of the abdomen and pelvis, and therefore the need for enteric contrast should be reassessed. The use of enteric contrast in abdomen and pelvis CT has been both defended and called into question in recent years in multiple applications. Results from our study suggest that the addition of enteric contrast does not significantly add to the diagnostic confidence of the interpreting radiologist with intravenously enhanced studies. However, when readers were stratified individually, one reader did have a statistically significant difference in confidence level. Another reader had a higher confidence level in the group without enteric contrast, though the results are not statistically significant (p = 0.125). This suggests that personal preference and comfort level with/without routine enteric contrast may impact the confidence level of some radiologists. Examples of scored examinations at both extremes can be found in <xref ref-type="fig" rid="fig2">Figure 2</xref> and <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p><p>Although the aim of this study was to assess the role enteric contrast plays in the experience of the interpreting radiologist, one must also consider its impact on the patient. Patients need to pick up the bottle of contrast</p><fig-group id="fig2"> <caption><title>Figure 2</title><p> Coronal images without enteric contrast. (a) One of the lowest confidence levels, 7. Lack of intra-abdominal fat limits differentiation of bowel loops and potential pathology; (b) One of the highest levels, 10. Presence of intra-abdominal fat provides contrast between bowel loops, despite the lack of enteric contrast</p></caption><fig id ="fig2_1"><label>(a)</label><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\2-2590050x\8bcc2f54-3e49-499a-8d74-4c524dfead87.png"/></fig><fig id ="fig2_2"><label>(b)</label><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\2-2590050x\a18cf599-ae7d-421d-9f2e-b4699fd2d44b.png"/></fig></fig-group><fig-group id="fig3"> <caption><title>Figure 3</title><p> Coronal images with enteric contrast. (a) One of the lowest confidence levels, 6. Distribution of enteric contrast is limited to the distal small bowel and proximal large bowel; (b) One of the highest levels, 10. There is fairly uniform distribution of enteric contrast along with adequate intra-abdominal fat</p></caption><fig id ="fig3_1"><label>(a)</label><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\2-2590050x\9d8a99af-6244-448a-8a8c-1e21d22425ae.png"/></fig><fig id ="fig3_2"><label>(b)</label><graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://file.scirp.org/Html/htmlimages\2-2590050x\e1254978-7182-4bd7-b3df-05ce378ec317.png"/></fig></fig-group><p>from the office or arrive early to their appointment. This additional step may adversely affect workflow in a busy outpatient office and can be a significant inconvenience for patients with limited mobility and access. A study in cancer patients reported that patients found that enteric contrast was the least pleasant experience, outranking intravenous cannulation and intravenous contrast injection [<xref ref-type="bibr" rid="scirp.46623-ref9">9</xref>] . Concern for perforated viscus is a concern specific to barium enteric contrast agents, but less of an issue in the ambulatory population. Another concern studied in the emergency setting includes prolonged gastric emptying, which can impact general anesthesia if an urgent surgical finding is identified.</p><p>The impact on the imaging center is increased cost. The list price of the enteric contrast agent used in this study (Readicat II<sup>&#174;</sup> Barium Sulfate suspension 2.1% w/v, 2.0% w/w) is $131.77 for 24 bottles of the flavored variety and $135.12 for 24 bottles of the unflavored variety. Less direct, but nonetheless important factors include additional staff necessary to appropriately screen and protocol cases for enteric contrast as well as distribute the contrast to the patient.</p><p>Positive enteric contrast may add to increased radiation exposure in the setting of automatic exposure control. A study comparing water with positive enteric contrast revealed an 11% increase in CTDIvol in patients who received positive enteric contrast (11.8 mGy versus 13.1 mGy, respectively) [<xref ref-type="bibr" rid="scirp.46623-ref11">11</xref>] . This benefit would need to be balanced with the potential risk of needing a repeat CT scan attributable to withholding enteric contrast. In our trial, no scan was repeated for this reason.</p><p>Limitations in our trial include a small sample size and the subjective analysis of confidence level by each interpreting radiologist. Recruitment was slower than expected. Of the 490 patients who scheduled CT examinations at eligible offices, 355 of them declined even initial contact with investigators. It is possible that this could have introduced selection bias into the study. Anecdotally, patients with a history of cancer were particularly concerned with whether an accurate comparison could be made with their prior study. Diagnostic accuracy would be an objective endpoint, but difficult when assessing multiple disease processes that are not necessarily pathologically proven. Radiologist bias may be a concern, since there is no way to blind radiologists to study technique. The comfort of radiologists in interpreting CT without enteric contrast is likely multifactorial including the study indication, practice setting and style and training.</p></sec><sec id="s5"><title>5. Conclusion</title><p>Our findings indicate that the decision to routinely use enteric contrast may not be justified, given the lack of additional confidence it imparts. Further research is needed to evaluate the effect of enteric contrast on diagnostic accuracy in the outpatient setting.</p></sec><sec id="s6"><title>Acknowledgements</title><p>We thank the CT and Call Center staff of Jefferson Radiology particularly Rebecca Rudnick as well as Luce Buhl and Crystal Kollmorgan.</p></sec></body><back><ref-list><title>References</title><ref id="scirp.46623-ref1"><label>1</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>LAITURI</surname><given-names> C.A.</given-names></name>,<name name-style="western"><surname> FRASER</surname><given-names> J.D.</given-names></name>,<name name-style="western"><surname> AGUAYO</surname><given-names> P.</given-names></name>,<name name-style="western"><surname> FIKE</surname><given-names> F.B.</given-names></name>,<name name-style="western"><surname> GAREY</surname><given-names> C.L.</given-names></name>,<name name-style="western"><surname> SHARP</surname><given-names> S.W.</given-names></name>,<name name-style="western"><surname> OSTLIE</surname><given-names> D.J. </given-names></name>,<name name-style="western"><surname> ST PETER</surname><given-names> S.D. </given-names></name>,<etal>et al</etal>. 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