Efecto experimental de las radiaciones ionizantes en el pulmón:
Mini-Review Article Epidemiology of typhoid and paratyphoid fever in India
Suman Kanungo1, Shanta Dutta2, and Dipika Sur1 1Division of Epidemiology, National Institute of Cholera and Enteric Diseases, Kolkata, India 2Division of Microbiology, National Institute of Cholera and Enteric Diseases, Kolkata, India
Abstract Enteric fever (typhoid and paratyphoid fever) is a major human bacterial infection. Although the disease is not common in industrialised countries, it remains an important and persistent health problem in developing nations. Hospital-based studies and outbreak reports from India indicate that enteric fever is a major public health problem in this country, with Salmonella enterica serovarTyphi (S. Typhi)the most common aetiologic agent but with an apparently increasing number of cases due to S. Paratyphi A (SPA). Because risk factors such as poor sanitation, lack of a safe drinking water supply and low socio economic conditions in resource-poor countries are amplified by the evolution of multidrug resistant salmonellae with reduced susceptibility to fluoroquinolone, treatment failure cases have been reported in India, which is associated with increased mortality and morbidity. Vaccination, which requires strict planning and proper targeting of the vulnerable age groups, is considered to be an effective tool in controlling this disease in endemic areas, given there is development of a conjugate vaccine against both serovars (S. Typhi and S. Para A). Key Words: Typhoid, multidrug resistance, Salmonella Typhi and Paratyphi, antimicrobials, vaccination J Infect Developing Countries 2008; 2(6):454-460. Received 14 June 2008 - Accepted 19 September 2008 Copyright 2008 Kanungo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Introduction
persistent health problem in developing nations [2].
Clinical syndromes caused by Salmonella infection
Hospital-based studies and outbreak reports from India
in humans are broadly divided into two groups. The
indicate that enteric fever is a major public health
first, enteric fever, is transmitted by contaminated water
problem in this country, with Salmonella Typhi (S.
or food, and is caused mainly by Salmonella enterica
Typhi)the most common aetiologic agent but with an
serovarTyphi (typhoid fever) or Salmonella enterica
apparently increasing number of cases due to S.
serovar Paratyphi A, B or C (paratyphoid fever). The
Paratyphi A. S. Paratyphi B and S. Paratyphi C are
secondly, a range of clinical syndromes including
relatively uncommon in India. There have been two
diarrhoeal disease, is caused by a large number of non-
large-scale studies in India on the incidence of blood
typhoidal Salmonella serovars (NTS) [1]. Salmonellae
culture confirmed typhoid fever, one among individuals
under 40 years old [3] and another among children 6 to
facultative anaerobic bacilli that ferment glucose,
17 years old [4], but as yet, none on paratyphoid fever.
reduce nitrate to nitrite, and synthesise peritrichous
Thus, the actual burden of paratyphoid fever in India
flagella when motile. Salmonella is a genus in the
and its incidence and characteristics relative to typhoid
family Enterobacteriaceae that has more than 2,300
fever are poorly understood. In a study conducted in
serotypes, based on the presence of three main antigens:
Punjab that examined 340 enteric fever cases, 334 S.
somatic O antigen (lipopolysaccharide cell wall
Typhi and 6 Paratyphi A isolates were identified [5].
component), surface Virulent (Vi) antigen (S. Typhi and
This scenario, however, has changed as recent studies
S. Paratyphi C only), and flagellar H antigen. Here we
have highlighted the increasing occurrence of
will restrict our description to the epidemiology of
Typhoid fever incidence varies substantially in
Asia. Very high typhoid fever incidence has been found
Burden of enteric fever in India
in India and Pakistan [11]. In comparison, typhoid fever
frequency was moderate in Vietnam and China and
industrialised countries, it remains an important and
intermediate in Indonesia. [12]. Worldwide, the
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
emergence of multidrug resistant S. Typhiand S.
Researchers from New Delhi, India, reported that S.
Paratyphi Astrains has been shown to be
Typhi (75.7%) was the predominant serovar isolated
geographically heterogeneous [12-13], underscoring the
during the study period followed by S. Paratyphi A
importance of continuing microbiological surveillance
(23.8%) [17]. The maximum number of enteric fever
cases occurred during April to June (dry season)
antimicrobial resistance profile at the country level.
followed by July to September (monsoon season) [19].
Studies completed in Kolkata urban slums show a
Transmission, seasonality and risk factors of
seasonal variation of the incidence of both typhoid and
enteric fever
paratyphoid fever, with monsoon months being the
Humans are the only reservoir for these organisms.
The main source of infection is the stool of infected
persons; other sources are contaminated water, food,
Figure 1. Month-wise variation of typhoid and paratyphoid
and possibly flies. Lack of sanitation and clean running
water cause contamination for long periods of time in
resource-poor countries. Contaminated surface water
further contaminates the water supply. In addition, it is
seldom possible for the population in poor countries
either to boil their drinking water, or to sterilise the
Enteric disease is caused by both waterborne and
food-borne infectious agents which gain access via the
gastrointestinal tract. The onset depends mainly on the
virulence of the organism and the infective dose.
Humans can be both cases and carriers. They usually
secrete the organism for an average of 6 to 8 weeks and
3 3 3 3 3 3 3 3 4 4 4 4 4 4 4 4 4 4 4 4 5 5 5 5 5 5 5 5 5 5 5 5 6 6 6 6 6 6 6 6
carrier status usually diminishes after 6 to 8 months [1].
In India, enteric disease is most prevalent in urban
areas, with incidence approaching one percent of the
Exposure of the individual to contaminated food or
population annually in some endemic areas [15]. water correlates closely with the risk for enteric fever.
Usually children 15 years of age and younger are more
Since public health interventions, such as water
susceptible, most probably because adults develop
improvement or vaccination campaigns, are usually
immunity from recurrent infection and sub-clinical
implemented for groups of individuals, a large enteric
cases. A large-scale community study performed in an
fever surveillance study was conducted and factors were
Indian urban slum showed incidence as high as 2 per
analysed which correlate with enteric fever on an
1,000 population per year for children under five, and
individual level alongside factors associated with high-
5.1 per 1,000 population per year for children under ten
and low-risk areas with enteric fever incidence [18].
[16]. Another study in Northern India showed that the
Thus the individual level data were linked to a
majority of cases occurred in children aged 5 to 12
population-based geographic information system. In the
years and 24.8% of cases were in children up to 5 years
study, individual and household level variables were
of age [17]. Salmonella serovars showed an age-related
fitted in Generalized Estimating Equations (GEE) with
bias, with paratyphoid fever more common in adults.
the logit link function to take into account the likelihood
One study from Kolkata showed the incidence of
that household factors correlated within household
paratyphoid fever was lower (0.8/1000/year), and the
members. Over a 12-month period, 80 typhoid fever
mean age of paratyphoid patients was older (17.1 years)
cases and 47 paratyphoid fever cases were detected
compared to typhoid fever (incidence 1.4/1000/year,
among 56,946 residents in two bustees (slums) of
Kolkata, India. Residents in areas with a high risk for
Typhoid fever is usually observed throughout the
typhoid and paratyphoid fever had lower literacy rates
year. Some studies show a peak of the disease from July
and economic status, a bigger household size, and
to September, as it coincides with the rainy season
resided closer to water bodies and study treatment
when the chance of water contamination is high,
centres than residents in low-risk areas. Predictors for
both typhoid and paratyphoid fever were found to be
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
similar [18]. In contrast, a study conducted in Jakarta,
pattern) a range of nonspecific symptoms may be
Indonesia, showed that the risk factors are more
associated with typhoid fever. These include chills,
prevalent outside the household in paratyphoid rather
constipation, diarrhoea, weakness, dizziness, nausea and
Chronic carriers of typhoid play a crucial role in
cough. Diarrhoea may be a presenting feature especially
spreading the disease throughout the community. The
in immunocompromised cases and infants. Classical
first essential factor in carrier prevention of infection
clinical features of the disease were comparable among
includes educating the general public as well as
patients under and above 5 years of age but other
identifying all possible carriers and sources of
manifestations, such as hepatomegaly, anaemia and
complications, are generally more frequent in children
Invasive salmonellosis due to NTS in India
Rare symptoms, including ―Rose spots‖, relative
Typhoid is a highly adapted invasive disease that is
bradycardia and—in severe cases—neuropsychiatric
restricted to humans and shows little association with
symptoms such as muttering and delirium have also
the immunocompromised. In contrast, non-typhoidal
been reported [15]. Late diagnosis or failure to respond
salmonelloses have a broad vertebrate host range, an
to treatment may lead to serious complications,
epidemiology that often involves foods and animals,
including gastrointestinal hemorrhage, perforation of
and a dramatically more severe and invasive
the gut, and shock. There is evidence of pancreatitis
[23]; splenic infarction [24] in some cases due to
particular in those with HIV. The prevalence of non-
typhoid. There is also evidence of vertical transmission
typhoidal Salmonella (NTS) bacteraemia has risen in
of the pathogen with high mortality and morbidity in
many countries and is probably related to the increase in
HIV infection [21]. Although invasive disease caused
by NTS has been recently reported from many African
Treatment
and Asian countries, the infection is relatively unknown
Antibiotic therapy is the only effective treatment for
in India. One study from Thailand [22] reported a total
enteric fever. In the past, the drug of choice was
of 135 patients with NTS bacteraemia. Salmonella
chloramphenicol. It was the standard treatment until
group C was predominant. The most common
plasmid-mediated resistance to this drug emerged.
underlying disease was HIV infection. Up to 30% of
Because of severe adverse effects, a high relapse rate
NTS isolates were identified as multidrug resistant. In
and widespread bacterial resistance to chloramphenicol,
one disease burden study from Kolkata, only one isolate
ampicillin (1g given orally every 6 hours) and
of S. Typhimurium and one isolate of S. Dublin were
trimethoprim-sulfamethoxazole (TMP-SMX; double
identified (not published) from 1,500 blood culture
strength tablet given twice a day) became the mainstay
With the emergence of multidrug resistant S. Typhi
Clinical Features
in the late 1980s, typhoid disease was found to be
Typhoid fever is a severe, contagious and life-
resistant to treatment with most of the commonly used
threatening systemic disease caused by Salmonella
antibiotics such as chloramphenicol, ampicillin, TMP-
Typhi which may result in persistent fever with or
SMX, streptomycin and tetracycline. A study in the
without severe complications. Typhoid often presents
mid-1990s in Bangalore showed resistance to
with misleading symptoms, thus making it extremely
difficult to diagnose. Paratyphoid fever relates to a
nalidixic acid to be as high as 95% with 90% sensitivity
group of enteric illnesses caused by strains of
to norfloxacin and ciprofloxacin [26]. Multidrug
Salmonella Paratyphi A, B and C. Paratyphoid fever
resistant outbreaks have been reported in 1995 from
bears similarities with typhoid fever, but its course is
Bangalore with 76% resistance to ampicillin, 64% to
more benign with fewer complications [1].
chloramphenicol, and 75% to tetracycline [27]. Another
Hallmarks of enteric fever include abdominal pain
study in Karnataka completed in 1999 showed very
and high fever, with fever being the main presenting
high resistance to chloramphenicol and cotrimoxazole
feature (as high as 75% of the cases) in the initial
[28]. Recently multidrug resistance was seen in S.
stages. Usually the incubation period is 1 to 14 days. In
Typhi but less in S. Paratyphi A isolates. However,
addition to fever up to 39°C, (with a typical step-ladder
resistance to nalidixic acid was comparable in both
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
Ciprofloxacin for adults, excluding pregnant
women, is presently the treatment of choice. There is a
Diagnosis and Treatment of Chronic Carriers of
dramatic increase in nalidixic acid-resistant isolates
with reduced susceptibility to fluoroquinolones (FQs),
In developed countries where adequate medical
although all isolates are susceptible to third-generation
facilities exist, it is important to screen all patients,
cephalosporins. Patients infected with such strains may
suspects and contacts. Three negative stool cultures and
not be responsive to treatment with ciprofloxacin,
one negative Vi antigen blood test should be the
which could lead to reports of treatment failure
minimum requirements before a proven case of typhoid
cases[15]. One study from Kolkata reported the
fever is determined non-infectious. However, the Vi test
isolation of one S. Typhi strain which demonstrated
is of little use in tropical and subtropical countries
high-levels of ciprofloxacin and norfloxacin resistance
with 16 ug/mL of MIC [29]. Indian studies showing
evidence of emergence of fluoroquinolone resistance
The treatment of the chronic carrier is a difficult
[30] are similar in pattern to results from other Asian
problem. Trials with ampicillin have shown some
success but even prolonged ampicillin administration in
Pregnant women and children most often receive
the convalescent stage may not prevent the carrier state
ceftriaxone injections. However, all these drugs can
cause adverse effects and long-term use can lead to the
development of antibiotic resistance. Together, these
aureomycin in patients who were excreting the typhoid
constitute about 80% of the world’s typhoid burden,
bacillus showed that about 25% continued to excrete the
where various rates of multi drug resistance (16 to 37%)
bacillus after completion of the treatment. Presently, it
and nalidixic acid resistance (5 to 51%) were found
still appears that prophylaxis remains the best method
during 2002-2004 [30]. However, there is now evidence
for preventing the spread of typhoid fever by chronic
that strains previously resistant to chloramphenicol have
carriers who have not responded to both conservative
become sensitive to treatment with chloramphenicol
and operative treatment. To date, ciprofloxacin and
[31]. Another study showed a change in resistance
norfloxacin are found to be more effective drugs than
patterns to conventional anti-typhoid microbials such as
prolonged courses of ampicillin or co-trimoxazole [14].
ampicillin and chloramphenicol from 84% to 14% [32].
A study conducted in Kolkata observed that recent
Prevention and Control S. Paratyphi A isolates from Kolkata, India, were
As the main route of typhoid transmission (enteric
fever as a whole) is faeco-oral by contaminated food
chloramphenicol, to which this organism was sensitive
and water, the disease remains a serious problem in the
in earlier years [33]. There was also evidence of an
developing world where it is confounded by low socio-
upsurge of S. Paratyphi A in Kolkata [34]. In the global
economic conditions and overcrowding. Cost-of-illness
context, there is evidence of increased incidence of
studies have shown that the burden of disease increases
enteric infections due to S. Typhi Vi-phage- type E1
in most countries upon the emergence of multi-drug
and S. Paratyphi A phage type PT1 in the western world
resistant forms of enteric fever (unpublished data).
among those who had traveled to India and Pakistan in
Hence, a need for prevention and control has gained
enormous importance in recent years. As humans are
The latest studies showed evidence of significant
the only reservoir of this faeco-orally transmitted
resistance to ciprofloxacin and early evidence of
disease, preventive measures include improvement of
resistance to ceftriaxone [36]. These observations
correspond with the global picture. In Vietnam,
However, instituting these measures requires a huge
uncomplicated typhoid fever cases due to MDR S.
investment, making it an almost unachievable task,
Typhi with reduced susceptibility to fluoroquinolones
especially in resource-poor countries where they are
have been shown to be successfully treated with a 7-day
needed most. For comprehensive control measures,
course of azithromycin [37]. There have been reports
cases need to be diagnosed early followed by provision
of isolation and emergence of S. Paratyphi A since 1996
of prompt and appropriate treatment. Carriers need to be
from across India, especially from central India and
identified efficiently and early treatment instituted.
Orissa. The isolates were sensitive to chloramphenicol
Additionally, a strong surveillance system should be in
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
place for early detection of both cases and carriers.
the efficacy of the Vi vaccine bound to nontoxic
Most policy makers in developing countries resort to a
recombinant Pseudomonas aeruginosa exotoxin A
comprehensive approach to prevent typhoid through
(rEPA) among children 2 to 5 years of age showed that
immunisation, thus combining a short-term measure
it is safe and immunogenic and has more than 90%
with long-term solutions. An effective vaccine against
efficacy in this age group [42]. A large-scale,
S. Para A is not available to date.
community-based demonstration trial of the Vi vaccine
has recently been concluded in Kolkata, India, among a
Vaccines
population of 60,000 with a coverage of 69%. The
Vaccination of high-risk populations is considered
results are awaited. If proven effective, this vaccine can
the most promising strategy for the control of typhoid
be incorporated in India’s public health program.
fever. The concept of vaccination against typhoid began
Despite the availability of these vaccines and the
in the 1960s when field trials showed the effectiveness
WHO’s recommendation for the use of vaccines among
of a killed vaccine, reporting a protection rate of
school children in endemic areas, the use is quite
approximately 70% after two doses [39]. It was a heat-
limited because of cost, lack of proper data, and the
inactivated, phenol preserved, whole cell typhoid and
vaccine’s ineffectiveness in children under 2 years of
paratyphoid vaccine constituting S. Typhi, S Paratyphi
age. In view of the increasing number of infections with
A and S. Paratyphi B. The vaccine had a reasonable
S. Paratyphi A, development of a suitable vaccine
protection level but severe reactogenicity due to the
against S. Paratyphi A is urgently needed.
presence of extra protein components from S. Paratyphi
A and B. The World Health Organization (WHO)
Conclusion
recommended discontinuation of this vaccine as it
The existence of multidrug-resistant bacteria is a
evoked unacceptable adverse effects; it was thereafter
serious and growing problem in the treatment of
typhoid, especially in the developing world. This
In the 1980s, two licensed, newer generation, well-
situation has been further complicated by the emergence
tolerated typhoid vaccines were available, which
of quinolone resistant strains with reduced susceptibility
promised protection without significant adverse effects:
to FQs, which is a major concern of clinicians who treat
the live, attenuated oral vaccine, Ty21a, and the
enteric fever. When bacteria prove to be resistant to
injectable subunit Vi polysaccharide vaccine. Studies
standard antibiotics, morbidity and mortality rates
conducted in Chile showed that 3 doses of Ty21a
increase. Failure to treat an infection properly leads to
conferred a protection of around 62% over a 7-year
prolonged illness, thus increasing the chance of
period and almost 80% protection against typhoid fever
developing a carrier state in which persons are
over a surveillance span of 5 years. [40]. The same trial
contagious and able to spread the resistant strain to
showed that the vaccine conferred significant protection
others. As plasmid-mediated mutagenesis among
against paratyphoid B fever using pool data from two
circulating strains occurs much more quickly than the
different sites [41]. Both the Ty21a and Vi
development of new drugs, there is always a fear that
polysaccharide (PS) vaccine provide significant
highly lethal strains of resistant bacteria will evolve,
protection against typhoid by distinctly different
leaving physicians with no effective way to combat
immune mechanisms. Vi stimulates the IgG antibody
them. Therefore, vaccination has been proven to be an
while Ty21a induces humoral and cell-mediated
effective way of controlling typhoid in resource-poor
immune responses but not the Vi antibody [42].
countries, especially in vulnerable age groups, mainly
The Vi vaccine has been targeted for accelerated
introduction into public health programs, due to several
However, the proportion of prevalence of typhoid
advantages it has over Ty21a, including consistent
and paratyphoid around the globe is changing due to
efficacy results (64-77%) even in areas of high typhoid
altered urbanisation and food habits. As the risk factors
incidence [ 43]; a single-dose regimen; the lack of
for both diseases may not coincide, the typhoid vaccine
is not found to be protective against paratyphoid. Some
requirements. A review article showed that both the
other strategy, such as the development of a suitable
Ty21a and Vi vaccines are less toxic and equally
conjugate vaccine against both serovars, is required to
effective than the conventional vaccine [40]. In South
control the endemicity of the disease in developing
Africa, Vi provided a protection coverage of 55% over
a 3-year period [44]. A study done in Vietnam to elicit
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
predictors for typhoid and paratyphoid fever in Kolkata, India.
References
19. Mohanty S, Renuka K, Sood S, Das BK, Kapil A (2006)
Miller SI, Pegues DA (2000) Salmonella Species, Including
Antibiogram pattern and seasonality of Salmonella serotypes in
Salmonella typhi In: Madell GL., Bennett JE, Dolin R.
North Indiaan tertiary care hospital. Epidemiol Infect 134: 961-
Principles and Practice of Infectious Disease. 5th edition. New
20. Vollaard AM, Ali S, van Asten HA, Widjaja S, Visser LG,
Crump JA, Luby SP, Mintz ED (2004) The global burden of
Surjadi C, van Dissel JT (2004) Risk factors for typhoid and
typhoid fever. Bull World Health Org 82: 346–53.
paratyphoid fever in Jakarta, Indonesia, JAMA, J American
Sinha A, Sazawal S, Kumar R, Sood S, Reddaiah VP, Singh B,
Rao M, Naficy A, Clemens JD, Bhan MK (1999) Typhoid
fever in children aged less than 5 years. Lancet; 354:734-37.
immunocompromised adults. J of Infections 56:413-422.
Chuttani CS, Prakash K, Gupta P, Grover V, Kumar A (1977)
22. Kiratisin P (2008) Bacteraemia due to non-typhoidal
Controlled field trial of a high-dose oral killed typhoid vaccine
Salmonella in Thailand: clinical and microbiological analysis.
in India. Bull of the World Health Org 55: 643-44.
Trans R Soc Trop Med Hyg 102(4):384-8. Epub 2008 Mar 5.
Pathania NS and Sachar RS (1965) Typhoid and paratyphoid
23. Kadappu KK, Rao PV, Srinivas N, Shastry BA (2002)
fever in Punjab (India): a study of 340 cases. Am J Trop Med
Pancreatitis in enteric fever. Ind J Gastroenterol 21(1): 32-33.
24. Mehta LK, Arya SC, Mathai G (2007) Infarction of spleen in
Rodrigues C, Shenai S, Mehta A (2003) Enteric fever in
typhoid fever. Saudi Med J. Feb;28(2):271-72.
Mumbai, India: the good news and the bad news. (letter)
25. Raveendran R, Wattal C, Sharma A, Kler N, Garg P, Gujral K,
Khera N (2007) Vertical transmission of Salmonella paratyphi
Padmapriya V, Kenneth J, Amarnath SK (2003) Re-emergence
of Salmonella paratyphi A: a shift in immunity? (letter).
26. Navaneeth BV, Suganthi N, Belwadi MR (2001) Antibiotic
National Medical Journal of India; 16: 47-48.
resistance among common bacterial enteric pathogens isolated
Sood S, Kapil A, Dash N, Das BK, Goel V, Seth P. (1999)
from stool. Ind J Paediatr 68(7): 687-8.
Paratyphoid fever in India: An emerging problem. (letter)
27. Rathish KC, Chandrashekar MR, Nagesha CN (1995) An
outbreak of multidrug resistant typhoid fever in Bangalore. Ind
Kapil A, Sood S, Reddaiah VP, Das B, Seth P. (1997)
Paratyphoid fever due to Salmonella enterica serotype
28. Ciraj AM, Seetha KS, Gopalakrishna BK, Shivananda PG
Paratyphi A. (letter) Emerging Infectious Diseases; 3: 407
(1999) Drug resistance pattern and Phage types of Salmonella
10. Singh B, Saxena SN (1964) Blood culture positive cases of
typhi isolates in Manipal, South Karnataka. Ind J Med Sci
enteric group of fevers in Delhi. Ind J Med Res; 52:539-44.
11. Siddiqui FJ, Rabbani F, Hasan R, Nizami SQ, Bhutta ZA
29. Dutta S, Sur D, Manna B, Sen B, Bhattacharya M,
(2006) Typhoid fever in children: some epidemiological
Bhattacharya SK, Wain J, Nair S, Clemens JD, Ochiai RL.
considerations from Karachi, Pakistan. Int J Infect Dis 10
Salmonella enterica serovar Typhi in a community-based fever
12. Ochiai RL, Acosta CJ, Danovaro-Holliday MC, Baiqing D,
surveillance from Kolkata, India Int J Antimicrob Agents
Bhattacharya SK, Domi Typhoid Study Group (2008) A study
of typhoid fever in five Asian countries: disease burden and
30. Chau TT, Campbell JI, Galindo CM, Van Minh Hoang N, Diep
implications for controls. Bull World Health Org Apr
TS, Nga TT, Van Vinh Chau N, Tuan PQ, Page AL, Ochiai
RL, Schultsz C, Wain J, Bhutta ZA, Parry CM, Bhattacharya
13. Ochiai RL, Wang X, von Seidlein L, Yang J, Bhutta ZA,
SK, Dutta S et al. (2007) Antimicrobial drug resistance of
Bhattacharya SK, Agtini M, Deen JL, Wain J, Kim DR, Ali M,
Salmonella enterica serovar typhi in Asia and molecular
Acosta CJ, Jodar L, Clemens JD (2005) Salmonella paratyphi
mechanism of reduced susceptibility to the fluoroquinolones.
A rates, Asia. Emerg Infect Dis. 11 (11):1764-6.
Antimicrob Agents Chemother 51(12):4315-23. Epub 2007 Oct
14. Huckstep RL. Typhoid fever and other Salmonella Infections.
(1962) Chapter 27, online publication, published by E &S.
31. Dutta S, Sur D, Manna B, Bhattacharya SK, Deen JL, Clemens
Livingstone Ltd., Edinburgh and London. Available:
JD (2005) Rollback of Salmonella enterica serotype Typhi
resistance to chloramphenicol and other antimicrobials in
Kolkata, India. Antimicrob Agents Chemother 49(4):1662-3
15. Bhan MK, Bahl R, Bhatnagar S (2005) Typhoid and
32. Butt T, Ahmad RN, Salman M, Kazmi SY (2005) Changing
paratyphoid fever. Lancet. 2: 366(9487):749-62.
trends in drug resistance among typhoid Salmonallae in
16. Sur D, von Seidlein L, Manna B, Dutta S, Deb AK, Sarkar BL,
Rawalpindi, Pakistan. East Mediterr Health J 11(5-6):1038-44.
Kanungo S, Deen JL, et al. (2006) The malaria and typhoid
33. Mandal S, Mandal M, Pal NK (2006) Antibiotic resistance of
fever burden in the slums of Kolkata, India: data from a
Salmonella enterica serovar Paratyphi A in India. Emerging
prospective community based study, Trans R Soc Trop Med
and reemerging problem. J Post Grad Med 52: 163-166.
34. Palit A, Ghosh S, Dutta S, Sur D, Bhattacharya MK,
17. Walia M, R Gaind, P Paul, R Mehta, P Aggarwal, M Kalaivani
Bhattacharya SK (2006) Increasing prevalence of Salmonella et al. (2006) Age related clinical and microbiological
enterica serotype Paratyphi-A in patients with enteric fever in a
characteristics of enteric fever in India. Trans R Soc Trop Med
periurban slum setting of Kolkata, India. Int J Environ Health
18. Sur D, Ali M, von Seidlein L, Manna B, Deen JL, Acosta CJ,
Clemens JD, Bhattacharya SK (2007) Comparisons of
35. Lewis HC and Lawrence J (2006) Recent increase in S.
Paratyphi A phage type 1 and S. Typhi Vi-phage type E1 in
Kanungo et al. – Typhoid and paratyphoid fever in India
J Infect Developing Countries 2008; 2(6): 454-460.
England and Wales, associated with travel to the Indian
Corresponding Authors:
subcontinent. EuroSurveill 11(10)( Euro Surveill. 2006 Mar
1. Dipika Sur, Div. of Epidemiology, National Institute of
Cholera and Enteric Diseases, Kolkata, India, P-33, CIT
36. Gupta A, Swarnakar NK, Choudhury SP (2001) Changing
Road, Scheme-XM, Beliaghata, Kolkata-700010, India
antibiotic sensitivity in enteric fever. J Trop Paediatr 47(6):
2. Shanta Dutta, Div. of Microbiology, National Institute of
37. Parry CM and Ho VA et al. (2007) Randomized controlled
Cholera and Enteric Diseases, Kolkata, India, P-33, CIT
comparison of ofloxacin, azithromycin, and an ofloxacin-
Road, Scheme-XM, Beliaghata, Kolkata-700010, India
azithromycin combination for treatment of multidrug resistant
and nalidixic acid-resistant typhoid fever. Antimocrobial
38. Bhattacharya SS, Dash Usha A (2007) Sudden rise in
Conflict of interest: No conflict of interest is declared.
occurrence of Salmonella paratyphi A infection in Rourkela, Orissa. Ind J of Med Microbiol 25: 78-79.
39. Levine MM, Ferreccio C, Abrego P, Martin OS, Ortiz E, Cryz
S (1999) Duration of efficacy of Ty21a, attenuated Salmonella typhi live oral vaccine. Vaccine 17 Suppl 2:S22-27.
40. Levine MM, Ferreccio C, Black RE, Lagos R, San Martin O,
Blackwelder WC (2007) Ty21a live oral typhoid vaccine and prevention of paratyphoid fever caused by Salmonella enterica Serovar Paratyphi B. Clin Infect Dis 45 Suppl 1:S24-8.
41. Lin FY, Ho VA, Khiem HB, Trach DD, Bay PV, Thanh TC,
Kossaczka Z, Bryla DA, Shiloach J, Robbins JB, Schneerson R (2001) The efficacy of a Salmonella Typhi Vi conjugate vaccine in two-to-five-year-old children. N Engl J Med 344 (17):1263-9
42. Levine M (2001) Centre for Vaccine Development, UMB, 9th
43. Acharya IL, Lowe CU, Thapa R et al. (1987) Prevention of
typhoid fever in Nepal with the Vi capsular polysaccharide of Salmonella typhi. A preliminary report. The New Eng J Med 317(18):1101-4.
44. Klugman KP, Koornhof HJ, Robbins JB, Le Cam NN (1996)
Immunogenicity, efficacy and serological correlate of protection of Salmonella typhi Vi capsular polysaccharide vaccine three years after immunization. Vaccine 14(5):435-8.
Dexamethasone (Decadron®) Information Sheet You are receiving this information sheet because your baby’s doctor has recommended dexamethasone (trade name Decadron®) for your baby. Dexamethasone is a powerful steroid medication that often helps a baby’s lungs to work more effectively, even when other medications and treatments have not helped. Dexamethasone can also produce side
ADI GUIDANCE PAPER ON DIAGNOSIS, STAGING AND MANAGEMENT OF ARONJ http://www.adi.org.uk/members/only/anti-resorptive-therapy/deliver.php/profsuzuki_cv.pdf PROFESSOR JON B. SUZUKI, DDS PHD MBA http://www.adi.org.uk/members/only/anti-resorptive-therapy/deliver.php/drlee_cv.pdf PROFESSOR CAMERON Y.S. LEE, DMD MD PHD The ADI Review Group: Rob Dyas David Offord Cemal Ucer Eddie Scher Tim Co