What s hot where its hot: Update in travel and tropical medicine Jay S. Keystone Medisys Travel Health Edward C. Keystone RDU Mt.
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1 What s hot where its hot: Update in travel and tropical medicine Jay S. Keystone Medisys Travel Health Edward C. Keystone RDU Mt. Sinai Hospital
2 Outline of this very talk malaria cysticercosis leishmaniasis travellers diarrhea 2
3 Interval between arrival and symptom onset USA 2010 N=1484 MMWR 2011;60:1-15 Interval mo. % P.falciparum N=489 %P.vivax N=98 < >
4 Interval between arrival and symptom onset USA 2010 N=1484 MMWR 2011;60:1-15 Interval mo. % P.falciparum N=489 %P.vivax N=98 < % >
5 Interval between arrival and symptom onset USA 2010 N=1484 MMWR 2011;60:1-15 Interval mo. % P.falciparum N=489 %P.vivax N=98 < % 74 % >
6 Pf Malaria onset according to preexisting immunity EID (2) February 53% Non-immunes n=197 36% Semi-immunes n=63 55% 11% 25% 6% 2% 3% 3% 2%
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9 I want to run a few tests on you, just to cover my ass.
10 Thick film Thin film
11 Thick film Thin film diagnosis speciation
12 Thick film Thin film If the first film is negative repeat it x 2 q12-24 hrs. diagnosis speciation
13 Binax ICT NOW test : Histidine rich protein II+ malaria aldolase Kain,Am J Trop Med 60;2003: Low + Pf High + Pf
14 9
15 Parasite Sensitivity Specificity P.falciparum 99% 94% P.vivax 94% 100% 9
16 Why admit with low Pf parasitemia?
17 Why admit with low Pf parasitemia? Once upon a time (2011) there was 35 year old woman who returned from West Africa with 3 day history of fever.
18 Why admit with low Pf parasitemia? Once upon a time (2011) there was 35 year old woman who returned from West Africa with 3 day history of fever. -looks unwell
19 Why admit with low Pf parasitemia? Once upon a time (2011) there was 35 year old woman who returned from West Africa with 3 day history of fever. -looks unwell -thrombocytopenia & mild anemia
20 Why admit with low Pf parasitemia? Once upon a time (2011) there was 35 year old woman who returned from West Africa with 3 day history of fever. -looks unwell -thrombocytopenia & mild anemia -P.faciparum parasitemia 1.1%
21 Why admit with low Pf parasitemia? Once upon a time (2011) there was 35 year old woman who returned from West Africa with 3 day history of fever. -looks unwell -thrombocytopenia & mild anemia -P.faciparum parasitemia 1.1% 9 hours later : parasitemia 30%
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23 Malarone Coartem
24 Good Twin Evil Twin
25 Good Twin Better twin
26 Artemether lumefantrine vs. Atovaquone proguanil Parameter Atovaquone proguanil (Malarone) Artemether lumefantrine(coartem) Efficacy fatty meal few treatment failures PCT 4 days FCT 2 days few treatment failures PCT 2 days FCT 1 day Safety well tolerated more GI upset and headache Convenience once daily doses over 3 days 6 doses over 3 days Cost (USD)
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30 Why does Keystone recommend atovaquone/ proguanil for only 3 days after exposure...is he nuts or has he got a good lawyer? 16
31 NEJM 2008:359:
32 18
33 18
34 Clinical Infectious Diseases 2012;54(2):
35 Clinical Infectious Diseases 2012;54(2):232 9 effective dose intervals supportive of weekly dosing post-exposure prophylaxis 4 days after challenge was 100% effective 19
36 Oct 31,
37 Malaria summary VFRs at increasing risk of severe malaria VFRs present with malaria later than nonimmunes Rapid diagnostics are ideal when expertise in diagnosis is sub-optimal Admit all with P.falciparum malaria Atov/proguanil may be D/C d early post -exposure Mefloquine is safe for prevention in all trimestersof pregnancy. 21
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45 Fluconazole treatment of L.major in Iran; RT n=120 J Acad Derm 2011;64:606-8 Cure at 6 weeks: (60/group) 48% w 200 mg 81% w 400 mg Adverse events: bothersome 200 mg -none 400mg - 1 incr. LFTs and 1 incr. creatinine - 75% cheilitis;15% nausea 29
46 Fluconazole treatment of CL in Brazil due to L.(V)braziliensis CID 2011;53:693-5 method:n=28 Tx x 4 weeks ;no response..d/c; response..con t to cure; well tolerated dose mg/kg number cure % duration (range) (4-12) (4-10) (4-5) 30
47 Summary: Fluconazole in Tx of leishmaniasis Saudia Arabia: 200 mg > placebo in L.major Iran: 400mg > 200 mg in L.major Brazil: 8mg/kg > 6.5 mg/kg > 5 mg/kg in L.braziliensis Bottom-line: considering A/Es to SAGluconate. & liposomal ampho.b, fluconazole reasonable 1st choice when systemic therapy is required. 31
48 Journal of Antimicrobial Chemotherapy
49 Cryotherapy +/- SAG infiltration weekly x 1-3 Journal of Antimicrobial Chemotherapy
50 in Iran International Journal of Dermatology 2004;43:
51 in Iran International Journal of Dermatology 2004;43: IL+cryo Cryo IL 33
52 Special Mention: Notable Scott P. Leishmania - a parasitized parasite. N Engl J Med May 5;364(18): Science&2011;&331:775/8.& Some Leishmania parsites contain an RNA virus which promotes the production of pro-inflmammatory molecules such as TNF α, IL-6, CXCL10, and CCL5. The response to the virus is mediated by the TLR 3 gene product (TLR3), an RNA receptor that is expressed within the same endosomal compartment as the parasites. Viral RNA released by dead parasites soon after infection binds to TLR3 and results in the production of cytokines and chemokines that enhance inflammatory responses and 34 thus exacerbate disease.
53 Leishmania summary Fluconazoleis may be a reasonable option for systemic therapy; larger studies are needed. Old world leish and non-brasiliensis species may be managed with Pentostam infiltration plus cryotherapy. Toll-like receptors may be an NB factor in leish pathogenesis 35
54 EID 2012:18:
55 Myanmar N= ~500/group 23% Laos 18% Burundi 26% Bhutan 23% 37
56 38
57 Stages of parenchymal neurocysticercosis vescicular viable
58 Stages of parenchymal neurocysticercosis vescicular viable degenerating dying
59 Stages of parenchymal neurocysticercosis vescicular viable degenerating dying colloidal life support
60 Stages of parenchymal neurocysticercosis vescicular viable degenerating dying colloidal life support calcified dead
61 Meta-analysis drug therapy for neurocysticercosis Del Brutto,Ann Int Med 2006;145:43-51
62 Meta-analysis drug therapy for neurocysticercosis Del Brutto,Ann Int Med 2006;145:43-51
63 Cochrane database review Viable lesions in adults, albendaole = placebo for recurrence of seizures (116 participants, one trial); albendazole > placebo for lesion resolution (RR 0.56,); 192 participants, two trials). Non-viable lesions in children, seizure recurrence; albendazole > no treatment (RR 0.49), 329 participants, four trials). No difference in the persistence of lesions at follow up (570 participants, six trials). 42
64 Author s conclusions Viable lesions: albendazole may reduce the number of lesions. Non-viable (dying) lesions: seizure recurrence was substantially lower with albendazole, 43
65 Pediatr Infect Dis J 2009;28: ) 44
66 December1996
67 January 1997
68 Clinical Infectious Diseases 2001; 33:
69 Neurocysticercosis summary Albendazole treatment of viable parasites reduces number of lesions Albendazole treatment of dying parasites reduces seizure recurrence Calcified cystercerci provoke oedema and seizures Albendazole plus praziquntel may be better than albendazole alone 48
70 Do travellers adhere to food and water precautions? Kozicki, Int. J. Eidem ;169-72
71 Do travellers adhere to food and water precautions? NOT a Chance! Kozicki, Int. J. Eidem ;169-72
72 Do travellers adhere to food and water precautions? NOT a Chance! 97% of travellers make a food and water faux pas within 72 hours of arrival Kozicki, Int. J. Eidem ;169-72
73 Etiology of Travellers Diarrhea Agent Percent EAEC + ETEC* Salmonella, shigella, campy Protozoa (giardia,crypto.eh) 0-5 Viruses (rotavirus,norovirus**) 0-20 Unknown * SE Asia : ETEC 7% Campylobacter 32% Am.J.TMH 2009;8:609 ** norovirus: 20% BMC Infect Dis. 2010;10:131.
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75 Text 52
76 India Mexico Guatemala Antibiot. EAEC (3) ETEC (98) EAEC ETEC (270) NAL CIP AZM RIF Text MIC90 CLSI breakpoints 52
77 India Mexico Guatemala Antibiot. EAEC (3) ETEC (98) EAEC ETEC (270) NAL CIP AZM RIF Text MIC90 CLSI breakpoints 52
78 Epidemiology of Travelers Diarrhea J Travel Med 2005; 12:
79 Epidemiology of Travelers Diarrhea J Travel Med 2005; 12:
80
81 JTM 2009;16:186 55
82 3 Scenarios presented to 60 physicians in Phuket,Mombasa,Goa (~20/site) Scenario: fever, diarrhea, abd pain, fever Results: rehydration:73% symptomatic Tx: 100% IM/IV: 59% antibiotics : 73% (FLQ,CFT, TMS,AMX) JTM 2009;16:186 55
83 3 Scenarios presented to 60 physicians in Phuket,Mombasa,Goa (~20/site) Scenario: fever, diarrhea, abd pain, fever Results: rehydration:73% symptomatic Tx: 100% IM/IV: 59% antibiotics : 73% (FLQ,CFT, TMS,AMX) JTM 2009;16:186 55
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85 Travellers diarrhea ETEC and EAEC most frequent cause of TD; norovirus and campylobacter increasingly NB. Drug resistance of enteric pathogens on the rise FLQ for Africa and W. hemisphere; azithromycin for Indian SC and SE Asia Self-treatment of TD avoids risk of unsterile injections by local physicians. 57
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