The Case of the Missing Appendix

The correct initial diagnostic imaging test to evaluate pediatric abdominal pain for appendicitis is an ultrasound.  It carries none of the risks associated with CT imaging – except for the increased risk of a non-diagnostic evaluation.  It is also highly operator dependent and suffers in centers without sufficient volume of abdominal ultrasonography.

This study evaluates the subset of ultrasonography reports with the dreaded result “Appendix not visualized.”  Overall, 37.7% of 662 consecutive ultrasonographic studies at the authors’ institution failed to visualize the appendix.  Of interest to these authors were the “secondary signs” of appendicitis – free fluid, pericecal inflammatory changes, prominent lymph nodes, and phlegmon.

Their results are quite complicated – and, woefully, not terribly helpful.  Free fluid in females – useless.  Free fluid in males – more helpful if there’s a lot, but still only 2 cases of appendicitis out of the 5 males with a moderate/large amount of free fluid.  Lymph nodes – useless.  Pericecal fat changes – 1 out of 4.  Phlegmon – 2 out of 2.

So, there’s some information here.  Secondary signs with “Appendix not visualized” are typically not diagnostic alone – but, depending on the summation of other clinical findings, may yet be enough to obviate supplemental CT.

“Appendix Not Seen: The Predictive Value of Secondary Inflammatory Sonographic Signs” 
www.ncbi.nlm.nih.gov/pubmed/23528502

Chloride-Restriction & More JAMA Inadequacy

“The implementation of a chloride-restrictive strategy in a tertiary ICU was associated with a significant decrease in the incidence of AKI and use of RRT.”

Pretty clear, eh?  This article is one of several in a line of folks working to divorce us from normal saline.  The argument is that this hypernatremic, hyperchloremic solution, when given for large-volume resuscitation in the critically ill, leads to metabolic acidosis and decreased urine output.  This study, sponsored by Baxter, the makers of Plasma-Lyte, is an open-label, before-and-after design.  One year, they gave whatever fluid they wanted – mostly saline.  The next year, saline-containing fluids were restricted, and they used 20% albumin, lactated ringers (Hartmann’s solution), or Plasma-Lyte.

Firstly, the primary outcome doesn’t match their clinicaltrials.gov registration.  They’ve changed it from mean base excess during hospital stay to two primary outcomes that weren’t even both previously defined as secondary outcomes – increase in creatinine from baseline and incidence of acute kidney injury according to the RIFLE classification.

Then, they offer two positive results from their study – a decrease in the incidence of AKI and the use of renal replacement therapy.  The authors use RIFLE as their indicator of AKI – but they don’t pre-define which categories of RIFLE they use, and lump “Injury” and “Failure” together to a composite endpoint to gain statistical significance.  Otherwise, it’s a 7.4% control and 5.4% intervention difference in “Failure” that doesn’t reach statistical significance – and considering the mean baseline creatinine was lower in the intervention period, it ought to be expected to reach the failure definition less frequently.

The difference in rise of creatinine reaches statistical significance – but they’ve hidden the details in their online supplement  The mean serum creatinine in the baseline period rises from 10.4 mmol/L to 11.0 mmol/L, and in the intervention period from 10.3 mmol/L to 10.7 mmol/L.  This might be statistically significant, but hardly clinically significant.  Luckily, the authors use a skewed y-axis to distort and magnify the difference in their graph of these results.

Lastly, the RRT difference reported in their six-month study period is befuddling.  The overall rate of RRT in the entire year of their baseline period is 7.9%, while the rate of RRT in the entire year of their intervention period is 7.4%.  Yet, in the six months reported for this study, they report RRT use of 10% in the baseline period and 6.3% for the intervention period.  This implies the authors retrospectively selected their study period in order to magnify the effect of the RRT difference.  This difference in RRT also doesn’t match the 2% absolute difference in RIFLE classification for “failure” during the study period.  This implies the open-label nature of the study influenced the frequency of RRT use, as the authors may have exerted control over an outcome measure.

As far as patient-oriented outcomes go, after all this splitting of hairs, ICU length of stay was no different, the incidence of long-term dialysis was no different, and mortality was no different.  This is also a “bundle-of-care” study, with multiple different chloride-poor and chloride-rich fluids in use, which confounds the generalizability of the results.

Maybe chloride-sparing therapy is important.  But these authors are guilty of distorting and misleading with their presentation of results – and the JAMA editors, again, have failed us.

“Association Between a Chloride-Liberal vs Chloride-Restrictive Intravenous Fluid Administration Strategy and Kidney Injury in Critically Ill Adults”
www.ncbi.nlm.nih.gov/pubmed/23073953

Credit for much of the insight into this article goes to Greg Press, who prepared this article for last month’s Journal Club at UT-Houston – but he is in no way responsible for this unhinged rant.

Tongue Blade For Mandible Fractures

The “tongue blade test” is one of the fun, functional tests in Emergency Medicine.  If you’ve got facial trauma and you’re concerned about a mandible fracture, simply align a wooden tongue blade over the molars in a patient’s mouth and have them bite down firmly.  Then, twist the blade medially.  If the patient is not limited by pain, they’ll be able to hold the blade until it breaks.  If they’re limited by pain, such as in the presence of a mandible fracture, the patient won’t be able to hold the blade until it breaks.

This is an observational study enrolling 190 eligible patients for the tongue blade test in the presence of suspected mandible fracture.  66 patients had negative (normal) tongue blade tests, while 124 had positive (abnormal) tests.  All patients received a CT for definitive diagnosis.  There were 5 false negatives and 29 false positives.  Therefore, the sensitivity of the test is 95% and specificity 68%.  These results are consistent with some prior reviews of this test’s characteristics.

Not a “zero miss” test, but, depending on the pre-test likelihood based on other clinical factors, a very useful screening test.

“Re-evaluating the diagnostic accuracy of the tongue blade test: still useful as a screening tool for mandibular fractures?”
www.ncbi.nlm.nih.gov/pubmed/23490109