Candidates who wish to repeat one or more items with<strong>in</strong> a procedure may do so at their discretion, if they havenot begun the next procedure. However, Candidates who have begun the next procedure and wish to return to aprior procedure to repeat one or more items, or perform one or more omitted items, are expected to redo theentire procedure (this is unlike CSE where Candidates who have left a skill must redo the entire skill). TheseCandidates must announce this <strong>in</strong>tent to the SP and return to the first item <strong>in</strong> the procedure (except for anygeneral station procedures such as greet<strong>in</strong>g the Patient). In repeat<strong>in</strong>g the procedure, all <strong>of</strong> the prior marksrecorded by the Exam<strong>in</strong>er are erased, and the Candidate proceeds and is evaluated as if perform<strong>in</strong>g the entireprocedure for the first time. Candidates are strongly discouraged from repeat<strong>in</strong>g Procedure 1: Preparation <strong>of</strong>Both Medications due to time constra<strong>in</strong>ts.Candidates are responsible for facilitat<strong>in</strong>g Video Record<strong>in</strong>gs. Occasionally, the SP may ask a Candidate torepeat one or more items if the SP is not able to observe it.Some items require the Candidate to give <strong>in</strong>structions to the Patient, who will be portrayed by the SP. Thus,some items are <strong>in</strong>teractive between the Candidate and the SP.Some items require the Candidate to state cl<strong>in</strong>ical f<strong>in</strong>d<strong>in</strong>gs to the SP. Candidates are rem<strong>in</strong>ded that specificperformance items <strong>in</strong> each station, as <strong>in</strong>dicated on the evaluation form, require that the obta<strong>in</strong>ed f<strong>in</strong>d<strong>in</strong>gs bestated to the SP verbally <strong>in</strong> the same manner as they should be entered <strong>in</strong>to a patient record. Speak<strong>in</strong>g clearlyand audibly is important for these performance items, s<strong>in</strong>ce these items also test communication skills.Candidates should <strong>in</strong>dicate to the SP when they have completed the station by stat<strong>in</strong>g “I am f<strong>in</strong>ished.”Any procedural questions that Candidates have should be addressed directly to the NCCTO staff. No othercommunication should occur between Candidates and SPs or among Candidates dur<strong>in</strong>g the CSE,<strong>in</strong>clud<strong>in</strong>g rotation time before the station. “Communication” <strong>in</strong>cludes conversation, text messag<strong>in</strong>g, andpass<strong>in</strong>g notes, as examples. In addition, no communication is to occur among Candidates before leav<strong>in</strong>gthe test center.Candidates must not leave the test center until dismissed nor re-enter the test center after dismissal. Candidatesmust return their badges, and Candidates must not remove any test<strong>in</strong>g materials from the test center.Candidate Orientation Information: SpecificWhen obta<strong>in</strong><strong>in</strong>g the Patient’s allergy history, the Candidate must <strong>in</strong>quire about all 4 allergies <strong>in</strong> order to receivecredit for this item (Item 3).This station <strong>in</strong>tegrates IV <strong>in</strong>jection, as would be done for fluoresce<strong>in</strong> angiography, with the <strong>in</strong>tramuscular<strong>in</strong>jection <strong>of</strong> ep<strong>in</strong>ephr<strong>in</strong>e. This is cl<strong>in</strong>ically realistic s<strong>in</strong>ce a needle/syr<strong>in</strong>ge filled with 1:1000 ep<strong>in</strong>ephr<strong>in</strong>e couldbe prepared prior to perform<strong>in</strong>g fluoresce<strong>in</strong> angiography <strong>in</strong> the event the patient experiences an anaphylacticreaction due to the <strong>in</strong>jection <strong>of</strong> fluoresce<strong>in</strong> sodium dye. Prepar<strong>in</strong>g the syr<strong>in</strong>ges for both procedures at thebeg<strong>in</strong>n<strong>in</strong>g <strong>of</strong> the station also results <strong>in</strong> appropriate streaml<strong>in</strong><strong>in</strong>g <strong>of</strong> items perta<strong>in</strong><strong>in</strong>g to handwash<strong>in</strong>g and thedonn<strong>in</strong>g <strong>of</strong> protective gloves. The gloves that are donned <strong>in</strong> perform<strong>in</strong>g an <strong>in</strong>travenous <strong>in</strong>jection for fluoresce<strong>in</strong>angiography may be left on through perform<strong>in</strong>g an <strong>in</strong>tramuscular <strong>in</strong>jection <strong>of</strong> ep<strong>in</strong>ephr<strong>in</strong>e. If desired, Candidatesmay wash their hands while wear<strong>in</strong>g the protective gloves.A standard multi-use medication vial will be provided labeled “25% fluoresce<strong>in</strong> sodium” with an expirationdate; however, the solution <strong>in</strong> the vial will be clear. The <strong>National</strong> <strong>Board</strong> recognizes that <strong>in</strong>jectable fluoresce<strong>in</strong>sodium is also commonly available <strong>in</strong> s<strong>in</strong>gle-use glass ampules.While the medication vials are labeled appropriately (“25% fluoresce<strong>in</strong> sodium” for IV <strong>in</strong>jection and “1:1000ep<strong>in</strong>ephr<strong>in</strong>e” for IM <strong>in</strong>jection), the solutions <strong>in</strong> both vials are clear. Thus, after withdraw<strong>in</strong>g the medications3
<strong>in</strong>to two separate syr<strong>in</strong>ges (us<strong>in</strong>g the 5mL syr<strong>in</strong>ge for fluoresce<strong>in</strong> sodium and the 1mL syr<strong>in</strong>ge for ep<strong>in</strong>ephr<strong>in</strong>e),the only dist<strong>in</strong>guish<strong>in</strong>g factors between the medications will be the volume conta<strong>in</strong>ed <strong>in</strong> the syr<strong>in</strong>ges (3.0 mL <strong>of</strong>fluoresce<strong>in</strong> sodium for IV <strong>in</strong>jection and 0.4 mL <strong>of</strong> 1:1000 ep<strong>in</strong>ephr<strong>in</strong>e for IM <strong>in</strong>jection) as well as the size <strong>of</strong> thesyr<strong>in</strong>ges. Thus, it will be important for the Candidate to ensure that the correct medication is be<strong>in</strong>g <strong>in</strong>jected.The syr<strong>in</strong>ges may be marked with either cc or mL scales; .1 cc is equal to .1 mL.For the preparation for <strong>in</strong>tramuscular <strong>in</strong>jection <strong>of</strong> ep<strong>in</strong>ephr<strong>in</strong>e, a standard multi-use medication vial will beprovided labeled “1:1000 ep<strong>in</strong>ephr<strong>in</strong>e” with an expiration date. The <strong>National</strong> <strong>Board</strong> recognizes that that<strong>in</strong>jectable ep<strong>in</strong>ephr<strong>in</strong>e solution is also available <strong>in</strong> commercially available auto-<strong>in</strong>jectors (e.g., EpiPen ® ).For safety purposes, Candidates should not hold the vial with their other (“free”) hand when <strong>in</strong>sert<strong>in</strong>g the needle<strong>in</strong>to the vial (Items 10 and 18).IM <strong>in</strong>jection <strong>of</strong> 1:1000 ep<strong>in</strong>ephr<strong>in</strong>e solution is to be performed <strong>in</strong> the deltoid muscle pad on the simulated arm.The <strong>National</strong> <strong>Board</strong> recognizes that <strong>in</strong>jection <strong>of</strong> ep<strong>in</strong>ephr<strong>in</strong>e to treat an anaphylactic reaction is usuallyadm<strong>in</strong>istered <strong>in</strong>tramuscularly <strong>in</strong> the outer thigh <strong>of</strong> a patient. However, the <strong>Board</strong> views the skills needed toperform IM <strong>in</strong>jection <strong>in</strong> the deltoid muscle pad <strong>of</strong> the simulated arm to be similar to the adm<strong>in</strong>istration <strong>of</strong>ep<strong>in</strong>ephr<strong>in</strong>e by <strong>in</strong>jection at another anatomical site as performed cl<strong>in</strong>ically.Candidate must verbalize “bevel up” when <strong>in</strong>sert<strong>in</strong>g the needle <strong>in</strong>to the arm for the IV <strong>in</strong>jection.Candidates may assume that the Patient’s deltoid does not show any signs <strong>of</strong> any tenderness dur<strong>in</strong>g palpation(Item 47).Candidate Orientation Information: Scor<strong>in</strong>g, Adm<strong>in</strong>istrative Irregularities, and AppealsThe <strong>National</strong> <strong>Board</strong> uses quantitative and qualitative data analysis to evaluate exam<strong>in</strong>ation uniformity andfairness <strong>in</strong> order to identify potentially poor measurement. Quantitative data are derived from a statisticalcomposite Exam<strong>in</strong>er analysis to assess <strong>in</strong>terrater (i.e., <strong>in</strong>ter-Exam<strong>in</strong>er) reliability to detect possible harshness <strong>in</strong>grad<strong>in</strong>g. Qualitative data are based on Test Incident Reports completed by Candidates and <strong>Exam<strong>in</strong>ers</strong> thatdocument any adm<strong>in</strong>istrative irregularities (e.g., malfunction<strong>in</strong>g equipment). Candidates who feel that theirperformance may have been adversely affected by an adm<strong>in</strong>istrative irregularity dur<strong>in</strong>g CSE are responsible forcomplet<strong>in</strong>g, and strongly encouraged to complete, a Test Incident Report. The process for complet<strong>in</strong>g a TestIncident Report will be described dur<strong>in</strong>g the Candidate Orientation at the beg<strong>in</strong>n<strong>in</strong>g <strong>of</strong> the CSE session.NCCTO Staff review all Test Incident Reports completed by Candidates at the conclusion <strong>of</strong> the CSEsession. <strong>Exam<strong>in</strong>ers</strong> may also <strong>in</strong>itiate a Test Incident Report if they feel it is warranted. Each completed TestIncident Report is reviewed by the NCCTO Staff for confirmation <strong>of</strong> its occurrence and assessment <strong>of</strong> itspotential impact on Candidate performance. NBEO ® retest policy dictates that repeat tests are provided only dueto adm<strong>in</strong>istrative irregularities (e.g., equipment failure, loss <strong>of</strong> electrical power, or an unacceptable patient) oncethe irregularity is corrected. NCCTO Staff are permitted to approve provisional retests on exam day because <strong>of</strong>the time-sensitive nature <strong>of</strong> the CSE process. However, only NBEO review <strong>of</strong> a retest and its accompany<strong>in</strong>gdocumentation can determ<strong>in</strong>e if the retest was warranted or if the orig<strong>in</strong>al test results should be accepted. Thisdeterm<strong>in</strong>ation will be made by NBEO staff prior to scor<strong>in</strong>g <strong>of</strong> the retest, to avoid any bias. Thus, if the needarises, Candidates are strongly encouraged to complete a Test Incident Report immediately after the f<strong>in</strong>al examcycle and before leav<strong>in</strong>g the test center. Test Incident Reports will not be accepted from Candidates once theyhave left the test center.If the <strong>National</strong> <strong>Board</strong> concludes that potentially poor measurement may have contributed to a fail<strong>in</strong>gperformance on CSE or ISE, the <strong>National</strong> <strong>Board</strong> will <strong>of</strong>fer to re-exam<strong>in</strong>e that Candidate, free-<strong>of</strong>-charge. Theoccurrence <strong>of</strong> potentially poor measurement is not an <strong>in</strong>dication <strong>of</strong> grad<strong>in</strong>g with prejudice, but rather a randomor unexpected no-fault outcome. The <strong>National</strong> <strong>Board</strong> will contact Candidates if such a re-exam<strong>in</strong>ation isappropriate.4