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FoodNet Hemolytic Uremic Syndrome (HUS) Surveillance
ICR 201805-0920-010 · OMB 0920-0978 · Object 83476201.
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Case ID_____________p1 A A CDC’s FoodNet Hemolytic Uremic Syndrome (HUS) Surveillance Case Report Form 1A. Case ID [caseid] YYYYYearXXFipscode001Record ___________________________________________ 2A. State ID [stateid] ___________________________________________ 3A. FoodNet Person ID (if applicable) [personid] ___________________________________________ 4A. Site [site] ___________________________________________ 5A. Date entered [denter] ____/____/____ Demographic Information Instructions: Complete the following demographic information as it pertains to the patient diagnosed with HUS. 6A. Date of Birth [dob] ____/____/____ 7A. State of Residence [state] _______________________________________________ 8A. County of residence [county] _______________________________________________ 9A. Sex [sex] Male (1) Female (2) Unknown (9) 10A. Ethnicity [ethnicity] Hispanic (1) 11A. Race [race] Black (1) Non-Hispanic (2) White (2) Unknown (9) Asian (3) American Indian / Alaska Native (4) Pacific Islander / Native Hawaiian (5) Multi-Racial (6) Other (12) Unknown (9) Clinical Information Instructions: Complete the following by interviewing the attending physician and/or reviewing patient's medical record. 12A. Is the date of HUS diagnosis known? [dhusunk] yes(1) no(0) 13A. Date of HUS diagnosis? [dhus] ____/____/____ 14A. Did the patient have diarrhea in the 3 weeks before HUS diagnosis? [diarrhea] yes (1) no (0) unknown (9) if yes 17A. 15A. Date of diarrhea onset [donset] ____/____/____ 16A. Did stools contain visible blood at the time? [stoolblood] yes (1) no (0) unknown (9) Was diarrhea treated with antimicrobial medications? [abxdiar] if yes 18A. Types of antimicrobials used to treat diarrhea: (check all that apply) (0,1) yes (1) no (0) unknown (9) Azithromycin (Zithromax, Z-Pak) [abxd_azithromycin] Ceftriaxone (Rocephin)[abxd_ceftriaxone] Ciprofloxin (Cipro) [abxd_cirpofloxin] Levofloxacin (Levaquin) [abxd_levofloxacin] Metronidazole (Flagyl) [abxd_metronidazole] Piperacillin [abxd_piperacillin] Tazobactam [abxd_tazobactam] Trimethoprim Sulfamethoxazole (Bactrim, Septra) [abxd_trimethoprimsul] Vancomycin (Vancocin) [abxd_vancomycin] Other (specify in comments) [abxd_other] __________________________________[abxdoth] Unknown [abxd_unknown] Last updated 6/13/2016 Case ID_____________p2 A A Clinical Information Continued 19A. Did the patient have contact with another person with diarrhea or HUS during the 3 weeks before HUS diagnosis (include daycare, household, etc)? [contact] yes (1) no (0) unknown (9) 20A. Was the patient treated with an antimicrobial medication (ANY antibiotic) for any other reason than diarrhea during the 3 weeks before HUS diagnosis? [abxnotdiar] yes (1) no (0) unknown (9) if yes 21A. Reason treated with antimicrobial [abxndreason] 22A. Types of antimicrobials used to treat conditions other than diarrhea: (check all that apply) (0,1) _______________________________ Azithromycin (Zithromax, Z-Pak) [abxnd_azithromycin] Ceftriaxone (Rocephin)[abxnd_ceftriaxone] Ciprofloxin (Cipro) [abxnd_cirpofloxin] Levofloxacin (Levaquin) [abxnd_levofloxacin] Metronidazole (Flagyl) [abxnd_metronidazole] Piperacillin [abxnd_piperacillin] Tazobactam [abxnd_tazobactam] Trimethoprim Sulfamethoxazole (Bactrim, Septra) [abxnd_trimethoprimsul] Vancomycin (Vancocin) [abxnd_vancomycin] Other (specify in comments) [abxnd_other] ___________________________[abxndoth] Unknown [abxnd_unknown] Other medical conditions present during 3 weeks before HUS diagnosis: 23A. Other gastrointestinal illness [gastro] yes (1) no (0) unknown (9) 24A. Urinary tract infection [uti] yes (1) no (0) unknown (9) 25A. Respiratory tract infection [rti] yes (1) no (0) unknown (9) 26A. Other acute illness[acute] yes (1) no (0) unknown (9) if yes ______________________________ Describe [acutedesc] 27A. Pregnancy [preg] yes (1) no (0) unknown (9) 28A. Kidney disease [kidn] yes (1) no (0) unknown (9) 29A. Immune compromising condition or medication [immcomp] yes (1) no (0) unknown (9) if yes 30A. Malignancy [malig] yes (1) no (0) unknown (9) 31A. Transplanted organ or bone marrow [transpl] yes (1) no (0) unknown (9) 32A. HIV infection [hiv] yes (1) no (0) unknown (9) 33A. Steroid Use (parenteral or oral) [ster] yes (1) no (0) unknown (9) Other, describe [immother] yes (1) no (0) unknown (9) ______________________[immotherdesc] Laboratory values within 7 days before and 3 days after HUS diagnosis Instructions: Record the correct unites or convert to the correct units before entering into the HUS database, especially for platelet count (e.g., enter a platelet count of 33,700/mm3 as 33.7) 34A. Highest serum creatinine [cre] ______ mg/dL (suggested range: 0.10-30.00) 35A. Highest serum BUN [bun] ______ mg/dL (suggested range: 4.0-100.0) 36A. Highest WBC [wbc] ______K/mm3 (suggested range: 0.50-125.00) 37A. Lowest hemoglobin [hgb] ______ g/dL (suggested range: 2.0-30.0) Last updated 6/13/2016 Case ID_____________p3 A A Laboratory Values Continued 38A. Lowest hematocrit [hct] ______ % (suggested range: 0.0-100.0) 3 (suggested range: 3.0-600.0) 39A. Lowest platelet count [plt] ______ K/mm 40A. Microangiopathic changes [rcfrag] yes (1) no (0) unknown (9) not tested (7) Other laboratory findings within 7 days before and 3 days after HUS diagnosis: 41A. Blood (or heme) in urine [burine] yes (1) no (0) unknown (9) not tested (7) 42A. Protein in urine [purine] yes (1) no (0) unknown (9) not tested (7) 43A. RBC in urine by microscopy [rburine] yes (1) no (0) unknown (9) not tested (7) Epi Information Instructions for Hospital Discharge Data: All records meeting the ICD9-or ICD10-CM codes specified in the surveillance protocol should be reviewed even if the case had already been identified through Active Surveillance in order to obtain potentially missing information. If a case is captured through HDD and was previously identified through the network of practitioners, sites should check that the abstracted information from active surveillance is current and complete. In the event that additional information is available, this should be included in the FoodNet HUS surveillance system. If a discrepancy is identified, the most current information should be used. 44A. How was patient’s illness first identified by public health (state or local health department or EIP)? [firstident] Report of HUS case by a physician or service participating in the FoodNet HUS active surveillance network (1) Report of HUS case by a non-participating physician or service (2) Routine STEC infection active surveillance (3) Retrospective review of hospital discharge data (4) Other (specify in comments) (7) _____________________________[fidentothdesc] Unknown (9) 45A. Date reported to public health or identified by hospital discharge data review [dphreport] ____/____/____ 46A. Was hospital discharge data review completed for this case (to verify or supplement information)? [hddrev] yes (1) no (0) unknown (9) 47A. Date of HDD (hospital discharge data) review [dhdd] ____/____/____ 48A. Is this case epidemiologically linked to a confirmed or probable Shiga toxin-producing E.coli (STEC) case?[epilink] yes (1) no (0) unknown (9) 49A. Is this case outbreak related? [outbreak] yes (1) no (0) unknown (9) Form A Comments, Composite Variables, and Status 50A. Completed by (initials): [aby] _______________________________ 51A. Comments [commentsa] _______________________________ 52A. Age at HUS Diagnosis [age] Number in years (round-up) 53A. Is the patient a resident of the FoodNet catchment area [fncatch] 1(in catchment), 0 (not in catchment), blank (incomplete) 54A. Is this a FoodNet pediatric post diarrheal case [postdiarrheal] 1(Yes), 0 (No), blank (incomplete) 55A. Year reported? [reportedyear] ____________ (e.g. 2016) 56A. Complete? [a_case_report_form_complete] incomplete (0) unverified (1) complete (2) Last updated 6/13/2016 Case ID_____________p4 B B CDC’s Foodnet Hemolytic Uremic Syndrome Surveillance Microbiology Report Form Instructions: Enter the most relevant microbiology tests associated with this HUS case by specimen source. If multiple positive stool specimens were tested, prioritize specimens tested by the SPHL or CDC. Include positive stool with any evidence of STEC, and, if applicable, serum sent to CDC for testing of abxbodies against STEC and/or one other positive specimen if additional results are available. In addition, you will be prompted to enter negative results (if applicable) only for evidence of STEC. Stool Specimen 1B. Was stool collected? yes (1) no (0) unknown (9) [stoolspec] 2B. Date stool specimen collected [dstoolspec] ____/____/____ 3B. State Lab ID: [stoolslabsid] _____________________________ Instructions: Answer below questions as they pertain to the stool specimen collected at each lab. You will be asked about other specimens in the other pathogens section. 4B. Questions Was this specimen forwarded to the lab? Was testing performed at lab? Was a Shiga toxin test performed? (e.g. PCR, EIA) Shiga toxin test result Shiga toxin type Was a CIDT for E. coli O157 performed? (e.g. Immunocard Stat) CIDT result? Did the test include H7? Was a culture for E.coli O157 performed? Was E.coli O157 isolated? Was a culture for E.coli nonO157 performed? Was E.coli non-O157 isolated? O Antigen Clinical Lab yes (1) no (0) unk (9) [sspecsent] yes (1) no (0) unk (9) [ctest] yes (1) no (0) unk (9) [cstxtest] positive (1) negative (2) [cstxresult] stx1 (1) stx2 (2) stx1 & stx2 (3) undifferentiated(9) [cstxgene] yes (1) no (0) unk (9) [co157cidt] positive (1) negative (2) [co157cidtresult] yes (1) no (0) unk (9) [cidth7] yes (1) no (0) unk (9) [co157cult] yes (1) no (0) unk (9) [co157isol] N/A N/A N/A State or Local PHL yes (1) no (0) unk (9) [fspecsent] yes (1) no (0) unk (9) [stest] yes (1) no (0) unk (9) [sstxtest] positive (1) negative (2) [sstxresult] stx1 (1) stx2 (2) stx1 & stx2 (3) undifferentiated(9) [sstxgene] yes (1) no (0) unk (9) [so157cidt] positive (1) negative (2) [so157cidtresult] N/A yes (1) no (0) unk (9) [so157cult] yes (1) no (0) unk (9) [so157isol] yes (1) no (0) unk (9) [snono157cult] yes (1) no (0) unk (9) [snono157isol] O26(1) O111(2) O103(3) O121 (4) O45(5) O145(6) rough(-2) und (-3) not found(-1) CDC Lab (Federal) N/A yes (1) no (0) unk (9) [ftest] N/A positive (1) negative (2) [fstxresult] stx1 (1) stx2 (2) stx1 & stx2 (3) undifferentiated(9) [fstxgene] N/A N/A N/A N/A yes (1) no (0) unk (9) [fo157isol] yes (1) no (0) unk (9) [fnono157cult] yes (1) no (0) unk (9) [fnono157isol] [foant] [foantoth] [soant] H Antigen H7 pos (1) H7 neg (2) non-motile(3) not tested(4) [chant] 5B. Was immunomagnetic separation (IMS) used to identify common STEC serogroups? [ims] [shant] [shantoth] [fhant] [fhantoth] yes (1) no (0) unknown (9) O157 [imssero_O157] O26 [imssero_O26] O45 [imssero_O45] O103 [imssero_O103] O111 [imssero_O111] O121 [imssero_O121] O145 [imssero_O145] 7B. Was whole genome sequencing (WGS) performed on this isolate? (at state or CDC) [wgs] yes (1) no (0) unknown (9) 8B. Sequencing ID: [wgsid] _____________________________ 6B. What serogroup(s) did the IMS procedure target? (check all that apply) (0,1) Last updated 6/13/2016 Case ID_____________p5 B B CDC Serology Tests yes (1) no (0) unknown (9) 9B. Has patient serum or plasma been sent to CDC for testing for antibodies to O157 or other STEC? [antio157] 10B. Date serology specimen collected? [dserum] ____/____/____ 11B. State laboratory ID for serum [serumslabsid] _____________________________ 12B. Was there more than one serology result for this case? [multiserol] yes (1) no (0) unknown (9) 13B. Questions LPS type Titer IgG O157(1) O111(2) [igg1] Interpretation of IgG Positive Negative [igginterp1] (1) (2) [igm1] Interpretation of IgM Positive Negative [igminterp1] (1) (2) [lpstype1] [lsptype2] [igg2] [igginterp2] (1) (2) [igm2] [igminterp2] (1) (2) [lpstype3] [igg3] [igginterp3] (1) (2) [igm3] [igminterp3] (1) (2) Titer IgM Other Pathogens (co-infections) and Other Specimens 14B. Questions Were any other pathogens identified? Specimen source Test type Pathogen Clinical Lab State or Local PHL CDC Lab (federal) yes(1) no(0) unk(9) yes(1) no(0) unk(9) [cothpath] [sothpath] Same stool used for STEC Same stool used for STEC testing testing culture(1) CIDT(2) culture(1) CIDT(2) [cothpathttyp] [sothpathttyp] [cpath] [spath] Other Specimens (second specimen) yes(1) no(0) unk(9) [fothpath] Same stool used for STEC testing culture(1) CIDT(2) [fothpathttyp1] [fpath] yes(1) no(0) unk(9) Was any other specimen collected? Date other specimen collection Specimen source [othspec] ____/____/____ [dothspec] [specsrc] culture(1) non-culture (CIDT)(2) [othspecttyp1] [othspecpath1] culture(1) non-culture (CIDT)(2) [othspecttyp2] [othspecpath2] Test type 1 Pathogen 1 Test type 2 Pathogen 2 Where positive? (check all that apply) (0,1) Other specimen State lab id clinic [osp_clinic] State or local [osp_phl] CDC [osp_cdc] [osslabsid] Form B Comments, Composite Variables, and Status 15B. Completed by (initials): [bby] _______________________________ 16B. Comments [commentsb] _______________________________ 17B. Is there an STEC isolate? [stecisolate] 1(Yes), 0 (No), blank (incomplete) 18B. Is there evidence of STEC by serology [stecbyserology] 1(Yes), 0 (No), blank (incomplete) 19B. Is there any evidence of Shiga toxin? [anystx] 1(Yes), 0 (No), blank (incomplete) 20B. Complete? [b_microbiology_form_complete] incomplete (0) unverified (1) complete (2) Last updated 6/13/2016 Case ID_____________p6 C C CDC’s Foodnet Hemolytic Uremic Syndrome Surveillance Chart Review Form Instructions: Complete after patient has been discharged; use hospital discharge summary, consultation notes and DRG coding sheet. Complete one composite form for all institution where hospitalized. Hospitals 1C. Was patient hospitalized? [hospital] yes(1) no(0) unknown(9) 2C. Date of first admission: [dadmis] ___/____/___ 3C. Date of last discharge: [ddisch] ___/____/___ Complications Did any of the following complications occur during this admission: 4C. 6C. 8C. 10C. 12C. Pneumonia [pne] Seizure [szr] Paralysis or hemiparesis [par] Blindness [bln] Other major neurologic sequelae [ner] if yes, Describe: [nerdesc] yes (1) no (0) yes (1) no (0) yes (1) no (0) yes (1) no (0) yes (1) no (0) unknown (9) unknown (9) unknown (9) unknown (9) unknown (9) Date of onset if yes 5C. [dpne] If yes 7C. [dszr] If yes 9C. [dpar] if yes 11C. [dbln] if yes 13C. [dner] _____________________________ Were any of the following procedures performed during this admission: 14C. 15C. 19C. 20C. Peritoneal dialysis [pdial] Hemodialysis [hdial] yes (1) no (0) unknown (9) yes (1) no (0) unknown (9) Transfusion with: 16C. packed RBC or whole blood [prbc] 17C. platelets [pltt] 18C. fresh frozen plasma [ffpl] yes (1) no (0) unknown (9) yes (1) no (0) unknown (9) yes (1) no (0) unknown (9) Plasmapheresis [phres] Laparotomy or other abdominal surgery* [surg] (*other than insertion of dialysis catheter) if yes Describe: [surgdesc] yes (1) no (0) unknown (9) yes (1) no (0) unknown (9) _____________________________ Discharge 21C. Condition at discharge [conddc] dead (1) alive (0) if dead 22C. Date deceased [ddead] ____/____/____ if alive 23C. Requiring dialysis [reqdial] yes (1) no (0) unknown (9) 24C. With neurologic deficits [neurodef] yes (1) no (0) unknown (9) Form C Comments, Composite Variables, and Status 25C. Completed by (initials): [cby] _______________________________ 26C. Comments [commentsc] _______________________________ 27C. Length of Stay? (Days) [los] Number in Days 28C. Complete? [c_chart_review_form_complete] incomplete (0) unverified (1) complete (2) Last updated 6/13/2016
| File Type | application/pdf |
| File Title | FoodNet Hemolytic Uremic Syndrome (HUS) Surveillance |
| Author | CDC User |
| File Modified | 2016-12-20 |
| File Created | 2016-12-20 |