Travel Medicine Flashcards

1
Q

Big three issues for travel medicine

A

1) Vaccine use in travel
2) Management of traveler’s diarrhea
3) Prevention of malaria

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2
Q

When to schedule pretravel clinic visit

A

Pretravel advice should be sought 4–6 weeks before departure to best prepare the traveler and ensure that appropriate vaccinations can be provided

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3
Q

Key counseling points for travel medicine visit

A

All travelers should be advised on vaccine-preventable illnesses/required immunizations, avoidance of insects, malaria chemoprophylaxis if visiting an area of risk, prevention and self-treatment of TD, and responsible behaviors (e.g., wearing seatbelts, helmets on motorcycles).

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4
Q

Altitude sickness prevention and management

A

Altitude sickness should also be discussed if high-altitude destinations are planned or patients have a history of altitude sickness. a. Prophylaxis with acetazolamide is usually effective and can hasten recovery if symptoms develop. b. Dexamethasone may also be used, but is more commonly considered as an adjunct in descent.

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5
Q

Percentage of malaria and typhoid in the US from visiting friends and relatives

A

About 50% of malaria imported into the United States in 1999–2003 occurred in VFR travelers. c. Around 75% of imported typhoid cases also occurred in this population.

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6
Q

Most serious infection in returning travelers

A

Malaria, specifically Plasmodium falciparum malaria, is the most serious infection in returning travelers and remains the most common cause of death.

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7
Q

Early fever in returning travelers

A

If fever develops beyond 21 days, dengue, rickettsial infections, Zika virus, and viral hemorrhagic fevers are less likely.

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8
Q

Malaria incubation period

A

Incubation period is often 1–4 weeks but can be longer, depending on the patient’s immune status, dos- ing of chemoprophylaxis, and infecting Plasmodium strain. Febrile patients presenting before 7 days are unlikely to be infected unless exposed to infected mosquitoes before travel.

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9
Q

Rabies incubation period

A

20-60 days (can be months to years)

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10
Q

Incubation period: anthrax

A

Cutaneous: 1 day; Pulmonary: 1-7 days

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11
Q

Incubation period: plague

A

Bubonic plague: 2-6 days

Pneumonic plague: 1-3 days

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12
Q

DEET cutoffs by age

A

For travelers with children and/or infants (older than 2 months) DEET is considered safe, but the concentration should not exceed 30%. c. DEET should not be used in infants younger than 2 months. 4. An alternative to DEET is picaridin,

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13
Q

Purposes of thick and thin smears for malaria

A

Thick smears screen large amounts of blood for the presence of parasites.

health department. 5. Thin smears are used to determine the infecting Plasmodium spp. with significant implications for pharmacotherapy.

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14
Q

Most important diagnosis for returning traveler

A

Any traveler presenting with fever and a history of travel to a malaria-endemic area in the past 3 months should be considered to have malaria until ruled out.

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15
Q

Malaria chemoprophylaxis regimens starting 1-3 weeks before travel

A

Chloroquine & mefloquine; continue 4 weeks after return

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16
Q

Malaria ppx regimes, start 1-2 days before travel

A

Atovaquone/proguanil - continue 1 week after
Primaquine - continue 1 week after
Doxycycline - continue 4 week after

17
Q

Treatment of uncomplicated malaria

A
Artemether/lumefantrine x3 days
Atovaquone/proguanil x 3 days
Hydroxychloroquine x48 hours
Chloroquine x48 hours
mefloquine x2 doses
Quinine + (doxycycline or tetracycline or clindamycin) x7 days
18
Q

Incubation periods for travelers diarrhea

A

Incubation period is typically up to 3 days, but can be within hours for bacterial and viral pathogens versus some protozoal pathogens, which may take 1–2 weeks and is less likely to present early in travel.

19
Q

Average duration of untreated travelers diarrhea

A

Average duration of untreated diarrhea is 4–5 days, but is pathogen-dependent. Comparatively, proto- zoal pathogens may cause diarrhea for weeks to months if left untreated.

20
Q

Etiology of travelers diarrhea

A

Disease etiology is predominantly secondary to bacterial enteropathogens (up to 85%); however, viruses and protozoa/parasites should also be considered causative pathogen

21
Q

Role of prophylaxis in travelers diarrhea

A

Antimicrobial prophylaxis is not currently endorsed by the IDSA guidelines and should only be used in travelers for whom development of diarrhea would be more likely to lead to complications.

considered for antimicrobial prophylaxis: a. Patients who should avoid dehydration b. History of stroke/transient ischemic attack c. Insulin-dependent diabetes mellitus d. Chronic renal failure e. Patients with possibility of complex diarrheal episodes i. Inflammatory bowel disease ii. AIDS iii. Patients with ileostomies/colostomies

22
Q

Travelers diarrhea prophylaxis medications and duration

A

Ppx regimens:
Bismuth 2 tabs q6h
Cipro qd-bid
Rifaximin qd-bid ac

If indicated, prophylactic antimicrobials should be taken for the duration of the trip, but limited to no longer than 3 weeks.

23
Q

Activity of antimicrobials vs TD pathogens

A

Fluoroquinolones are effective against most bacterial pathogens except for C. jejuni.

Rifaximin is not considered active against mucosally invasive pathogens such as Shigella, Salmonella, or Campylobacter.

Azithromycin is a useful alternative where Campylobacter spp. are more common

24
Q

Zika virus sexual transmission

A

Sexual transmission from infected travelers to non-traveler partners has occurred within 20 days of first sexual contact in all transmissions studied to date.

In males, the CDC recommends the use of condoms and/or abstaining from sexual activity for at least 6 months after exposure or travel to an area of risk because of documented viral persistence in semen.

In females, the CDC recommends 8 weeks of consistent condom use or abstinence after exposure or travel to an area of risk.

25
Q

Zika virus natural history

A

Clinical presentation a. Clinical illness usually mild b. Around 20% of infections are symptomatic c. Incubation period is about 6 day

26
Q

Ebola virus natural history

A

Clinical presentation a. Incubation period is 2–21 days, with a mean of about 7 days

Most patients infected do not have hemorrhagic manifestations of disease

27
Q

Chikungunya natural history

A

Clinical presentation a. Most infected people are symptomatic. Less than 15% experience asymptomatic seroconversion. b. Incubation period 3–7 days (range 1–12 days) c. Primary clinical symptoms include fever and polyarthralgia (usually bilateral).

Chikungunya Virus 1. Overview a. Single-stranded RNA virus b. Transmitted by A. aegypti and A. albopictus, which also transmit Zika and dengue viruse

28
Q

Symptoms: chikungunya vs dengue

A

C: more arthralgias
D: more lab abnormalities (neutropenia, thrombocytopenia)

29
Q

Dengue natural history

A

Typical incubation period is 3–14 days (mean 7 days) with symptoms following three phases: i. Initial febrile phase – Characterized by high temperature with headache, myalgias, vomiting, and joint pain

Critical phase (a) Typically occurs around the time of defervescence (b) Some patients experience a systemic vascular leak syndrome that manifests as hemocon- centration, hypoproteinemia, pleural effusions, and ascites. (c) Clinicians should be aware of this phase because patients can rapidly deteriorate to den- gue shock syndrome.

30
Q

West Nile Virus natural history

A

Clinical presentation a. Incubation is 2–14 days; may be longer in immunocompromised patients b. Most infected travelers are asymptomatic. c. Around 25% of infected patients develop abrupt febrile illness called West Nile fever.

Less than 1% of patients will develop meningitis or encephalitis after infection, which represents severe disease. h. Symptoms are consistent with a typical meningitis clinical picture, including: i. Abrupt fever and headache ii. Signs of meningeal irritation iii. Photophobia

mortality associated with severe disease (neuroinvasive disease) is about 10% and approaches 20% in those older than 70