Form Approved
OMB Control No.: 0920-XXXX
Expiration date: XX/XX/XXXX
Form 1: Medical Tourism Case Intake Form
Instructions:
Health departments may use this form to notify the Centers for Disease Control and Prevention (CDC) of patients who have suffered an adverse health outcome(s) related to medical tourism. The form is divided into two parts.
Part A collects basic information about the patient, their travel history, the surgeries, treatments, or procedures received outside the United States, and the adverse health outcome(s) experienced related to the surgeries, treatments, or procedures received outside the United States. The interviewer should complete the form by speaking directly with the patient when possible. Alternatively, interviewing someone familiar with the circumstances surrounding the adverse health outcome (e.g., medical provider, relative, friend) or medical chart abstraction are acceptable. The medical chart review may be done in consultation with the patient interview. Verbal consent should be obtained from patients, and participation is voluntary.
Part B collects pertinent laboratory and radiology results obtained after the patient presents for medical care in the United States for the adverse health outcome(s). The interviewer should obtain this information from medical chart abstraction. When this is not possible, obtaining information from the treating medical provider or patient is acceptable. Additionally, you may include or refer to any previously completed health forms associated with the patient’s adverse health outcome(s) with this intake form. Please ensure any personally identifiable information (PII) is removed before submitting.
Key Definitions:
Medical Tourism:
Travel by a U.S. resident outside of the United States for the purpose of receiving healthcare or a U.S. resident presenting to a U.S. healthcare facility after receiving medical care outside the United States.
Adverse health outcome:
An unexpected problem, complication, or undesirable health outcome resulting from medical or dental surgeries, treatments, or other procedures. Examples include infections, blood clots, and other undesired post-treatment complications. Adverse health outcomes relevant to this data collection are those occurring after medical tourism.
PART A (interview to be completed by clinician or state/local health department)
Medical Tourism Case Intake Form
Case ID (CDC to complete):_________
Local Case ID (Local Health Jurisdiction to complete): _________
State Case ID (State/Territorial Health Jurisdiction to complete): _________
Patient Initials: ___________
Date form completed (MM/DD/YYYY): _______________________
If the interview was conducted in a language other than “English” please specify the name of the language here: ______________
Who did you interview to complete this form? (Select all that apply).
Patient
Friend or family member (specify relationship): ______________
Healthcare provider
Medical chart review
Other (please specify):_____________
Name of person completing the form: ______________________________
Title: ___________________________________
Organization: ___________________________________
Contact phone number: ___________________________________
Contact email: ___________________________________________
If you are transferring data from an earlier interview with the patient, list the interviewers' names, contact number, and interview date for these interviews:
Interview A: Name: __________________ Tel: _________________ Date: / /
Interview B: Name: __________________ Tel: _________________ Date: / /
Interview C: Name: __________________ Tel: _________________ Date: / /___
How did you find out about this medical tourist? Select all that apply.
Patient volunteered information about recent medical or dental surgery, treatment or procedure(s) received abroad when presenting for care in the United States
The clinician at the reporting US hospital/clinic identified the patient as a medical tourist when asking the patient about recent international travel history
US hospital/clinic’s laboratory
Laboratory surveillance system
Notification by domestic or international public health partner
Other (please specify):____________________
Patient interview/chart abstraction
1. How old were you (the patient) at time of surgery / treatment / procedure? Please report age in years. _________
2. Sex:
Male
Female
3. What is your (the patient’s) race/ethnicity? Select all that apply.
American Indian/Alaska Native
Asian
Black/African American
Hispanic/Latino
Middle Eastern or North African
Native Hawaiian/Pacific Islander
White
4. What is your (the patient’s) current state of residence? ______________________
5. What is your (the patient’s) county of residence? _____________________
Travel Information
6. When did you (the patient) depart from the United States? (MM/DD/YYYY): ___________________
7. What was your (the patient’s) primary method of travel from the United States to the country where the surgery/treatment/procedure(s) was received? Select best answer.
Air (e.g., plane, helicopter)
Land (e.g., train, automobile, or bus)
Sea (e.g., cruise travel, boat, or ferry)
8. When did you (the patient) return to the United States? (MM/DD/YYYY): ________________________
9. After the surgery/treatment/procedure, what was your (the patient’s) primary method of travel back to the United States? Select best answer.
Air (e.g., plane, helicopter)
Land (e.g., train, automobile, or bus)
Sea (e.g., cruise travel, boat, or ferry)
Surgery/treatment/procedure received outside the United States
10. What surgery/treatment/procedure(s) did you (the patient) have outside the United States. Select all that apply.
Bariatric or weight loss surgery
Cancer treatment
Cardiac surgery or procedure
Cosmetic surgery or procedure
Abdominoplasty (tummy tuck)
Breast augmentation
Buttock augmentation (e.g., “Brazilian butt lift”)
Liposuction
Rhinoplasty
Other (please specify): ________________
Dental surgery or procedure
Induced abortion (medical or surgical)
In vitro fertilization or other fertility procedure
Ophthalmologic surgery or procedure
Organ transplant
Orthopedic surgery
Stem cell therapy (distinct from stem cell transplant; e.g., stem cell injections)
Stem cell transplant
Other____________________________
11. What type of healthcare professional(s) performed the surgery/treatment/procedure? Check all that apply.
Medical Doctor Please specify type.
Surgeon
Pain specialist
Primary care physician
Dermatologist
Anesthesiologist
Other (please specify): ________________
Nurse Practitioner
Nurse
Physician Assistant
Dentist
Other: _____________________________
Prefer not to answer
12a. When and where was the procedure(s) done? If any answer is unknown, please indicate this by writing “unknown”. If patient received procedures at multiple facilities outside the U.S., enter the narrative (details in question 12a, 12b, 12c) in the space at the end of Form 1 Part A.
Procedure(s) received:___________________________
Date(s) of procedure(s): ________________
Name of the person(s) who did the procedure(s): _____________________________
Facility name/address/city/country: ________________________________
Facility or Healthcare provider phone number: _________________________
Facility discharge date: _______________________
12b.Do you know of somebody else who experienced an adverse health outcome resulting from the surgery, treatment or procedures at this facility?
Yes
No
Declined to answer
12c. If yes, can you (the patient) provide the contact information for that person to the state/local health department? (NOTE: Personally Identifiable Information should not be transmitted to CDC)
Yes
No
Not Sure/Don’t Know
Declined to Answer
Adverse health outcome related to surgery/treatment/procedure received outside the United States
13. What adverse health outcome(s) did you (the patient) experience? Select all that apply. If an infection is present, please indicate the type of infection. Please include ICD-10 codes, if known. Additional space is provided if needed at the end of the section.
Infection type (Select all that apply).
Bloodstream
Skin/soft tissue (e.g., cellulitis, abscess, wound infection)
CNS (e.g., meningitis, brain abscess)
Bone (i.e., osteomyelitis)
Wound at site of procedure
Joint (i.e., septic arthritis)
Urinary tract
Sepsis
Other infection-related diagnosis, specify____________
Deep venous thrombosis
Pulmonary embolism
Death (cause of death): _____________ Date of death (MM/DD/YYYY):______
Other adverse health outcome: ___________________________
14. What date did you (the patient) start noticing symptoms related to the adverse health outcome? (MM/DD/YYYY): ________________________________________
15. What is your (the patient’s) current health status related to the adverse health outcome?
Recovered
Hospitalized/receiving inpatient care
Type of care (e.g., antibiotics, surgical revision, wound care): ________________
Resident of long-term care facility or subacute rehabilitation center receiving care
Type of care (e.g., antibiotics, wound care): ________________
At home of residence receiving outpatient care
Type of care: (e.g., antibiotics, wound care): ________________
Deceased
18. Additional Space for PART A Answer(s) (if needed) __________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
__________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
__________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
PART B (Medical Chart Abstraction)
19. Laboratory Results
Please note any results from labs completed as a result of the adverse health outcome. You may attach deidentified laboratory reports with this form. Alternatively, please describe the results below; extra space at the end of the form can be used if necessary. Please describe identified microorganisms, antimicrobial susceptibility results, and resistance mechanisms, if relevant. Options to enter additional results will be available in the electronic form.
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Result1 |
Result2 |
Result3 |
Date of test |
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Name of laboratory |
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Site of sample (Select one) |
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Type of result or test name |
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Organism identified |
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Resistance mechanisms |
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Antimicrobial Susceptibility Test results |
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20. If an isolate is available, has it been submitted for Whole Genome Sequencing?
Yes, (name of laboratory: __________________, date submitted (MM/DD/YYYY):______
No
Not sure/Don’t Know
N/A
21. Radiology Results. Please note any types of imaging procedures performed. If using paper form, attach deidentified imaging results here. Add additional details as necessary in the space provided at the end of the form. If using electronic form, may upload deidentified laboratory results here. Options to include multiple entries for each variable will be available in the electronic form.
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Result1 |
Result2 |
Result3 |
Date of test |
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Type of test (X-ray, CT, MRI, US, other: specify) |
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Body Site |
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Results
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22. Additional Space for PART B Answer(s) (if needed) __________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
__________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
__________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
Public reporting burden of this collection of information is estimated to average 10 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering, and maintaining the data needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden to CDC, Reports Clearance Officer, 1600 Clifton Rd., MS H21-8, Atlanta, GA 30333, ATTN: PRA (0920-XXXX).
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | Stoney, Rhett (CDC/NCEZID/DGMH/THB) |
File Modified | 0000-00-00 |
File Created | 2025-07-24 |