2
15
occurred in 159,%14 of our cases as similarly noted in the
same studies.
severe anemia in 12.8% of the child. The indiscriminate
antibiotic use, delayed presentation and choice of less
effective antibiotic at admission could have contributed
to a higher rate of bowel perforation in up to 10.3% of
our cases compared to a rate of 0.5–1% ob6 served to re-
sult from inappropriate or delayed therapy.
Isolation of salmonella in cultured specime1n,1s0,,1t2he most
important diagnostic tool and gold standard,
was
not a predominant finding in our study, with only 10.3%
positive culture for Salmonella typhi. Although blood
culture was done in 82.1% of patients due to logistic
challenges, the yield was still much lower than what was
reported in similar but older reports that h7-a9,d14findings in
The limitations of this study include amongst others,
being a retrospective review that reported on a limited
number of children. Because ABUTH is a tertiary refer-
ral facility in Zaria, some other children ill with typhoid
fever could have been treated in other lower level and
private health facilities or at home. A community-based
investigation of disease outbreak in the residential settle-
ments of the children could have best revealed the epide-
miological pattern of the problem, including the detec-
tion of,5milder cases and chronic carriers of Salmonella
the range of 60-85% positive cultures.
The poor
yield from cultures could have been partly due to pre-
admission antibiotic use, often with multiple drugs,
common to all the children studied. In the same manner,
Widal test was positive in only 46.2%7-o9,f14our cases, a
frequency less than that in other reports.
Use of anti-
biotics before hospital presentation is known to depress
typhoid antibody production resulting in low titres de-
tectable by Widal test just as it also leads10t,1o1,i1n2,h20ibition of
growth of salmonellae on culture media.
1
typhi. Nevertheless, our findings suggest that typhoid
fever had assumed public health importance in the
settlements from where these children resided in the
reporting period, a significant proportion of whom were
aged under-5. The findings support a need for provision
of adequate uninterrupted potable water supply, environ-
mental sanitation, inclusion of vaccination against
Salmonellae for infants in the National Immunization
Schedule1,4a,5n,1d3,2p1ublic health education on water and food
hygiene.
The switch to ceftriaxone or ciprofloxacin in 61.1% of
children initially started on chloramphenicol at time of
admission suggests a significant reduction in clinical
efficacy of the latter drug. The negative preliminary
culture results in majority of cases could be partly attrib-
uted to the observed indiscriminate use of antibiotics.
These findings concur with observations that resistance
to chloramphenicol constitutes a significant problem that
has rendered it less effective with high ra1-t3e,1s1,o12f treatment
failure, relapse and chronic carrier rates.
Author contributions
Umar LW: Literature search and review, data analysis
and initial draft and final manuscript writing.
Adelaiye H, Adebiyi M, Adeoye GO, Ahmad HR,
Giwa F: Coordination of data collection
Conflict of interest: None
There was no mortality even though potentially life-
threatening complications of bowel perforation and
progression to progression to bowel perforation
Funding: None
(
in 10.3%) and septic shock (in 10.3%) occurred with
References
1
.
WHO Background document.
Communicable Disease Surveil-
lance and Response Vaccines and
Biologicals: The diagnosis, treat-
ment and prevention of typhoid
fever 2003. WHO/V&B/03.07.
Crump JA, Mintz ED. Global
Trends in Typhoid and Paraty-
phoid Fever. Clin Infectious Dis
6. Stephens I., Levine MM. Manage-
12. Akinyemi K, Smith S, Oyefolu A,
Coker A. Multidrug resistance in
Salmonella enterica serovar typhi
isolated from patients with typhoid
fever complications in Lagos, Nige-
ria. Public Health 2005; 119: 321–327.
13. Clasen T, Schmidt W-P, Rabie T,
Roberts I, Cairncross S. Interven-
tions to improve water quality for
preventing diarrhoea: systematic
review and meta-analysis. Brit
ment of typhoid fever in children.
Pediatr Infectious Dis J 2002; 21
(2): 157-159.
7. Johnson AOK, Aderele WI. En-
teric fever in childhood. J Trop
Med Hyg 1981; 84: 29-35.
8. Abraham G, Teklu B. Typhoid
fever: Clinical analysis of 50
Ethiopian patients. Ethiop Med J.
1981; 19:41-6.
9. Scrag J, Rubidge C, Wallace HL.
Typhoid fever in African and In-
dian children in Durban. Arch Dis
Child 1969; 44: 18-28.
10. Baker S, Favorov M, Dougan G.
Searching for the elusive typhoid
diagnostic. BMC Infectious Dis-
eases 2010; 10: 45. Accessed at:
http://ww.biomedcentral.com/1471
-2334/10/45.
11. Parry CM, Threlfall EJ. Antim-
icrobial resistance in typhoidal and
non-typhoidal salmonellae. Curr
Opin Infect Dis 2008; 21: 531-8.
2
3
.
.
2
012. 50: (2); 241-246.
Crump JA, Luby SP, Mintz ED.
The global burden of typhoid fe-
ver. Bull World Health Organ
Med J 2007; 334: 782.
14. Duggan MB, Beyer L. Enteric fever
in young Yoruba children Arch Dis
Child 1975; 50: 67-71.
15. Timothy MED, Ashley EM, Dalli-
more EA, Keng EC. Relative bra-
dycardia is not a feature of enteric
fever in children. Clinic Infectious
Dis 1999; 28 (3): 582-586.
2
004; 82: 346-53.
4
.
Mweu E, English M. Typhoid
fever in children in Africa. Trop
Med Int Health 2008; 13: 1-9.
Ochiai RL, Acosta CJ, Danovaro-
Holliday MC, et al. A study of
typhoid fever in five Asian coun-
tries: disease burden and implica-
tions for control. Bull World
5
.
16. Bhutta ZA. Enteric fever. In Klieg-
man RM, Behrman RE, Jenson
HB, Stanton BMD (Eds), Nelson
Health Organ 2008; 86: 260-8.
th
Textbook Pediatrics 18 edition,
Philadelphia, WB Saunders
(Publishers). 2007; 1186-90.