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Parasitology Proficiency Testing Program

GENERAL CRITIQUE FOR 03 October 2005

The purpose of the New York State Proficiency Testing Program in the category of Parasitology General is to monitor the performance of applicant laboratories in detecting and identifying parasites in fecal emulsions, fecal smears, and blood films.

SAMPLE PREPARATION AND QUALITY CONTROL

All emulsions and slides used in this test were prepared by a commercial source. The emulsions were dispensed into the vials from pools which were continuously mixed during the loading process. Numerous samples of each test specimen were selected at random by the Parasitology Unit of the David Axelrod Institute for Public Health, and were checked to confirm their contents. Extensive quality control tests were also conducted by the supplying vendor and a detailed quality control report was submitted to the New York State Parasitology Laboratory for inspection and verification. Samples were authenticated by 80% of participating laboratories and/or referee laboratories.

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GENERAL ANSWER KEY FOR 03 October 2005

SAMPLECORRECT ANSWERS POINTS
06-FHymenolepis nana20
06-GNecator americanus/Ancylostoma duodenale20
06-HNO PARASITES SEEN20
06-IEntamoeba coli20
06-JPlasmodium falciparum20

TOTAL POSSIBLE POINTS 100

SAMPLE 06-F Report Helminths Only

RESULTS OF PARTICIPATING LABS

ORGANISM NUMBER REPORTED PERCENT REPORTEDREFEREE RESULTS STATUS
Hymenolepis nana149/1549710/10Correct
Trichuris trichiura08050Incorrect
Hymenolepis diminuta010.60Incorrect
Entamoeba histolytica010.60Incorrect
No Parasites Seen010.60Incorrect

QUALITY CONTROL

Participating and referee laboratories agreed that Hymenolepis nana was the correct response (97 and 100%). Quality control examination of 4% of this sample revealed an average of 8 ova per coverslip. Rare Entamoeba histolytica cysts are also present but should not have been reported because "Helminths Only" was requested. Other tests performed include Direct Immunofluorescent Assay and ELISA for Giardia lamblia and Cryptosporidium sp. which were negative for both organisms. A modified acid-fast stained smear was also negative.

DIAGNOSTIC CHARACTERISTICS

Click here for larger image of Hymenolepis nana Hymenolepis nana also known as the dwarf tapeworm is an intestinal cestode acquired by ingesting eggs from the environment or rarely by ingesting infected beetles. Internal autoinfection is also possible. H. nana is the only human tapeworm that doesn't have an intermediate host and transmission occurs from person to person. It has a worldwide distribution and is more commonly seen in children. The diagnostic stage is the egg recovered in stool. These eggs are spherical, thin shelled, and measure 30 to 47 microns in diameter. They have a six hooked oncosphere with two polar thickenings from which filaments arise. These filaments are visible in the space between the embryo and the outer shell. Eggs of H. nana can be confused with the eggs of Hymenolepis diminuta and careful measurement with a calibrated ocular micrometer is essential. The eggs of H. diminuta are much larger measuring 70-85 microns.
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SAMPLE 06-G Report All Parasites

RESULTS OF PARTICIPATING LABS

ORGANISM NUMBER REPORTED PERCENT REPORTEDREFEREE RESULTS STATUS
Necator americanus/Ancylostoma duodenale153/1549910/10Correct
Blastocystis hominis352303No Penalty
Entamoeba coli322103No Penalty
Endolimax nana02010Incorrect
Entamoeba hartmanni02010Incorrect
Ascaris lumbricoides02010Incorrect
Hymenolepis nana010.60Incorrect

QUALITY CONTROL

Participating and referee laboratories agreed that Hookworm was the correct response (99 and 100%). Quality control examination of 4% of this sample revealed an average of 6 ova per coverslip. Also present in rare numbers are Blastocystis hominis and Entamoeba coli Other tests performed include Direct Immunofluorescent Assay and ELISA for Giardia lamblia and Cryptosporidium sp. which were negative for both organisms. A modified acid-fast stained smear was also negative.

DIAGNOSTIC CHARACTERISTICS

Click here for larger image of Necator americanus Necator americanus(Hookworm) infection occurs in warm moist areas through skin penetration of filariform larvae from the soil. The larvae migrate through the heart and lungs, are swallowed, and take up residence in the small intestine where the adults mature. The diagnostic stage is the egg passed in stool. They are oval and measure approximately 60 X 40 microns. They have a thin shell with a space between the shell and the developing embryo. Development is usually at the 8 to 32 cell stage. These eggs are indistinguishable from those of Ancylostoma duodenale.

SAMPLE 06-H Report All Parasites

RESULTS OF PARTICIPATING LABS

ORGANISM NUMBER REPORTED PERCENT REPORTEDREFEREE RESULTS STATUS
NO PARASITES SEEN152/1549910/10Correct
Cryptosporidium sp.010.60Incorrect
Necator americanus/Ancylostoma duodenale010.60Incorrect
Blastocystis hominis010.60Incorrect

QUALITY CONTROL

Participating and referee laboratories agreed that NO PARASITES SEEN was the correct response (99 and 100%). Quality control examination of 4% of this sample revealed no parasites. Other tests performed include Direct Immunofluorescent Assay and ELISA for Giardia lamblia and Cryptosporidium sp. which were negative for both organisms. A modified acid-fast stained smear was also negative.

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SAMPLE 06-I Report Protozoa Only

RESULTS OF PARTICIPATING LABS

ORGANISM NUMBER REPORTED PERCENT REPORTEDREFEREE RESULTS STATUS
Entamoeba coli149/1549710/10Correct
No Parasites Seen03020Incorrect
Entamoeba histolytica02010Incorrect
Giardia lamblia010.60Incorrect
Plasmodium falciparum010.60Incorrect

QUALITY CONTROL

Participating and referee laboratories agreed that Entamoeba coli was the correct response (97 and 100%). Quality control examination of 4% of this sample showed organisms in every 8-10 100X oil emersion fields. The cysts measure between 10-20 microns and contain 5-8 nuclei.

DIAGNOSTIC CHARACTERISTICS

Click here for larger image of Entamoeba coli cyst Entamoeba coli is distributed worldwide and is nonpathogenic. The trophozoites vary in size from 15-50 microns with an average range of 20-25 micrometers. They have a single nucleus that generally has a large diffuse karyosome and irregular peripheral chromatin. The cytoplasm is generally granular and vacuolated. The cysts measure between 10-35 microns with an average range of 15-25 microns. Most of the cysts noted in this sample were in the 10-20 micron size range. The mature cysts have 8 nuclei that have uneven peripheral chromatin and large diffuse karyosomes. Chromatin bars are less common than in Entamoeba histolytica and have pointed ends. Infection occurs by ingesting contaminated food or water.

SAMPLE 06-J Report All Parasites

RESULTS OF PARTICIPATING LABS

ORGANISM NUMBER REPORTED PERCENT REPORTEDREFEREE RESULTS STATUS
Plasmodium falciparum138/1519110/10Correct
Babesiasp.07050Incorrect
No Parasites Seen03020Incorrect
Plasmodium vivax02010Incorrect
Entamoeba coli010.60Incorrect

QUALITY CONTROL

Participating and referee laboratories agreed that Plasmodium falciparum was the correct response (91 and 100%). Quality control examination of 4% of this sample revealed parasites in every 6-8 oil emersion fields. Infected red blood cells are not enlarged and do not contain Schüffner's stippling. The only stage observed is the ring stage trophozoite.

DIAGNOSTIC CHARACTERISTICS

Click here for larger image of Plasmodium falciparum Plasmodium falciparum is one of the four species of Plasmodium known to infect humans. It causes the most dangerous and severe form of malaria and is always considered to be a medical emergency. Death may occur rapidly if proper treatment is not started immediately. Its distribution is limited to the tropics, primarily Africa and Asia. P. falciparum invades all ages of RBC's and so the parasitemia can exceed 50%. The usual stages seen in the peripheral blood are rings and gametocytes. Schizogony occurs in the internal organs so it is rare to seen other stages although they may be present in cases of severe malaria. The infected RBC's are not enlarged nor do they contain Schüffner's dots. The rings are generally small, and may have one or two chromatin dots. Applique´ forms are also characteristic. Gametocytes are rounded to banana-shaped and contain a single well defined chromatin and coarse rice-grain like pigment

IMMUNOASSAY RESULTS

CRYPTOSPORIDIUM IMMUNOASSAY RESULTS

METHOD 06-F 06-G 06-H 
 NEGATIVEPOSITIVENEGATIVEPOSITIVENEGATIVEPOSITIVE
BD ColorPAC110120120
MCC Para-Tect Crypto/Giardia DFA010010010
Meridian ImmunoCard STAT Crypto/Giardia080090090
Meridian Merifluor Crypto/Giardia200140200
Meridian Premier Crypto01001000
Remel ProSpecT Crypto EIA240250260
TechLab/Wampole Test EIA040040040
Other01001000

GIARDIA IMMUNOASSAY RESULTS

METHOD 06-F 06-G 06-H 
 NEGATIVEPOSITIVENEGATIVEPOSITIVENEGATIVEPOSITIVE
BD ColorPAC130140140
MCC Para-Tect Crypto/Giardia DFA010010010
Meridian ImmunoCard STAT Crypto/Giardia090090090
Meridian Merifluor Crypto/Giardia140140140
Meridian Premier Giardia01001000
Remel ProSpecT Giardia EIA310330330
Remel ProSpecT Giardia EZ03003000
Remel Xpect Giardia/Crypto030030030
TechLab/Wampole Test EIA0400500401
Other010010010

October 2005 DISTRIBUTION OF SCORES

SCORE NO. OF LABS PERCENT
100 125 78
90-99 11 07
80-89 20 12
70-79 01 0.6
60-69 01 0.6
40-49 02 01
20-39 01 0.6
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GRADING

The answer key was derived from the response of all participating laboratories as per CLIA Regulations,Part 493, Subpart I, Section 493.917. These regulations can be viewed at www.phppo.cdc.gov These regulations state that 80% or more of participating laboratories or referee laboratories must identify the parasite for it to be correct. Similarly, less than 20% of the participating laboratories or referees finding parasites or ova is an incorrect response. Organisms reported by 20-80% of the participating laboratories or referees are "Unauthenticated", and are not considered for grading.

Each sample has a maximum value of 20 points. Credit is given according to the formula:

Number of correct responses by lab

# Correct Parasites Present + # Lab's Incorrect Answers
X 100

IMPORTANT REMINDERS

The next Parasitology Proficiency Test is scheduled for February 06, 2006. You are responsible for notifying us before February 13, 2006 if you do not receive your test. Proficiency test results must be postmarked by February 21, 2006 or you will receive a zero. These requirements are clearly stated in your NYS Proficiency Testing Handbook provided by the NYS Clinical Laboratory Evaluation Program or can be accessed via the internet at www.wadsworth.org/labcert/clep/ProgramGuide/WebGuide.pdf.

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NEWS AND NOTES

Policy changes made by the Clinical Laboratory Evaluation Program now allow for the CQ holder for a particular category to sign the attestation statement instead of the Laboratory Director. Starting with the February 05, 2001 test event we will now accept Director's and/or CQ holder's signatures on the attestation statement.

The Clinical Parasitology Lab of the NYSDOH offers two mailing kits for the submission of specimens. One kit contains vials of PVA and Formalin and the other does not. These kits can be ordered by calling 518-474-4175 and requesting kit DOH-2117. Please be sure to specify whether you need preservatives or not. Remember that the NYS Parasitology Lab only accepts specimens preserved in appropriate fixatives for the test requested.

Two one day Malaria Workshops are scheduled for April 11 and 12, 2006. These workshops will be presented in conjunction with the NLTN and will be held at Long Island University C.W. Post Campus in Brookville, NY. Registration forms will be sent to all permitted laboratories. For further information call 800-536-NLTN or visit NLTN web site.

Web site questions or comments or to request a different file format (pdf.,doc.,wpd.) contact:
E-mail: Parasit@wadsworth.org.

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