ORIGINAL  
Niger J Paed 2013; 40 (2): 150 –153  
Yilgwan CS  
John C  
Abok I I  
Pattern of acute respiratory  
infections in hospitalized children  
under five years of age in Jos  
Nigeria  
Okolo SN  
DOI:http://dx.doi.org/10.4314/njp.v40i2,8  
Accepted: 19th September 2012  
Abstract Background: Acute res-  
piratory infections are the com-  
monest cause of acute morbidity in  
children especially those under five  
in the developing countries. Clini-  
cal diagnosis is of utmost impor-  
tance considering the unavailability  
of radiological and microbiological  
services in most primary care set-  
tings in most developing countries.  
Methodology: Thirty nine children  
with symptoms of acute respiratory  
infection attending our emergency  
room over a one year period were  
recruited. Each had a CXR and  
blood culture ordered by the at-  
tending physician on admission.  
=25.6+19.1, Males = 13.8+14.2,  
t=2.2, p=0.03). Bronchiolitis was  
the commonest ARI seen in infants,  
tonsillitis in children beyond in-  
fancy while pneumonia was seen in  
all age groups. The cardinal feature  
of each disease entity was Fever,  
cough, breathlessness, tachycardia  
and hypoxemia in those with Pneu-  
monia; Catarrh, nasal congestion  
and tachypnoea in those with bron-  
chiolitis, while fever and vomiting  
were seen in those with pharyngo-  
tonsilitis.  
Conclusion: This review highlights  
the common ARI in our setting.  
Efforts need to be intensified on the  
identification of children with ARI  
in the children emergency room  
with the aim of prompt and appro-  
priate management in order to meet  
the MDG targets.  
Yilgwan CS  
(
)
John C, Abok I I, Okolo SN  
Department of Paediatrics  
University of Jos  
Nigeria.  
Email: yilgwan@hotmail.com,  
yilgwanc@unijos.edu.ng  
Tel: +2348180310979  
Results: Thirty nine subjects were  
admitted with ARI with a hospital  
prevalence of 43.5/1000 person per  
year (39/897). Mean age was  
1
8.75+17.23 mo, (Females  
Introduction  
While the use of pulse oximetry has been deployed in  
several centres, its application and interpretation remains  
a challenge.  
We sort therefore to examine the pattern of ARI in our  
environment, vis-a-vis age, sex, anthropometric find-  
ings, clinical symptoms and signs and pulse oximetry  
reading in ARI as seen in our hospital.  
Acute respiratory infections are the commonest cause of  
acute morbidity in children ,e2specially those under five  
1
in the developing countries. Viral and bacterial organ-  
isms have been i,m4 plicated as causative agents for most  
3
ARI in children. Most diagnosis of ARI is made in the  
presence of clinical features and where available also  
radiolog,5ical appearances especially in the case of Pneu-  
4
monia. However, radiological services in most cases  
are only available in tertiary care facilities with few radi-  
ologists available for specialist interpretation of films.  
Patients and methods  
6
,7  
This then makes clinical diagnosis imperative and of  
utmost importance considering the high burden and the  
case fatal8it,9y rate for children with ARI in developing  
countries. There are features that are highly suggestive  
Thirty nine children with symptoms of acute respiratory  
infection attending the emergency room of the Jos uni-  
versity teaching hospital over a one year period were  
recruited. Each had a CXR ordered by the attending  
physician on admission. All children with symptoms of  
ARI necessitating admission were recruited. However  
subjects with cardiovascular, pulmonary, or neurological  
congenital defects, or if 6weeks and below as well as  
those with chronic respiratory tract disorders or diseases  
(R)  
of ARI and have been defined by WHO in the ARI  
1
0
case management for primary health care providers.  
While this is very useful, few applications exist to dis-  
tinguish the various forms of ARI-pneumonia. Bron-  
chiolitis and others like pharyngotonsilitis.  
1
51  
while 3(27.3%) had pharyngotonsillitis. In the age group  
6 month and above, all 9(100%) were seen with pneu-  
were excluded.  
3
Informed consent was sought from care givers of all  
eligible children and only those who consented to par-  
ticipate in this study were recruited into the study. All  
children were evaluated by the attending physicians (1  
of 4 of the investigators)  
monia while none were seen with either bronchiolitis or  
tonsillitis.  
Frequency of common symptom encountered  
Data was collected using a standardised questionnaire  
which included information such as cough, fast breath-  
ing/rapid breathing, fever or hypothermia, nasal conges-  
tion, catarrh or vomiting. Axillary temperature and the  
status of the child (quiet or fussy/crying) were recorded.  
Hypoxaemia detected using pulse oximetric readings  
Fever was found in all the children with pneumonia and  
tonsillitis but only present in 25% of those children seen  
with bronchiolitis.  
Cough was a prominent symptom seen in 80% of chil-  
dren with pneumonia, while only 20% of those with  
bronchiolitis and none of those with tonsillitis presented  
with cough.  
Breathlessness was seen in 75% of the children with  
pneumonia, while 25% of children with bronchiolitis  
and none of those with tonsillitis had breathlessness.  
Catarrh was seen in 100% of those children with bron-  
chiolitis while none of the children with pneumonia or  
pharyngotonsilitis had catarrh.  
Vomiting was seen in only those children with pneumo-  
nia (25%) and those with tonsillitis (50%). This is as  
shown in table1  
(
SaO2) measured three times using a Nellcor N10 oxime-  
ter with an adhesive sensor attached to the child's index  
finger was noted.  
A complete chest examination was done. The presence  
of nasal flaring, retractions, wheezing or grunting was  
established with the child's chest naked, and the respira-  
tory rate was determined by counting the respiratory  
movements for one minute. Auscultation for breath  
sound character and quality was done while the presence  
of abnormal respiratory sounds (crepitations, rhonchi,  
reduced breath sounds) were also recorded. All cases of  
ARI had chest radiograph against which we compared  
the clinical features being studied. Children with a his-  
tory of rapid breathing, a history of difficulty drinking,  
tachypnoea ( respiratory rate greater than 40 breaths/  
minute for children older than 12 months, and greater 50  
breaths/minute for children aged 3-12  
months),wheezing, nasal flaring, or chest in drawing in  
the presence of a pulmonary parenchymal density com-  
patible with pneumonia on chest radiograph as inter-  
preted by the paediatric radiologist were defined as hav-  
ing pneumonia. While those with painful swallowing,  
vomiting and pharyngeal hyperaemia and exudates in  
the tonsilar crypts were classified as tonsillitis.  
Table 1: Frequency of symptoms encountered by morbidity  
type  
%
of children  
Symptom  
Fever  
Pneumonia  
Tonsillitis Bronchiolitis  
100  
80  
100  
25  
25  
0
Cough  
Breathlessness  
Catarrh  
75  
0
25  
0
20  
100  
80  
Nasal congestion  
0
0
Vomiting  
25  
50  
0
Cardiorespiratory parameters  
Data so generated was analysed using the Stata IC 10  
statistical software.  
The mean respiratory rate by age was 47±13.5  
(
(
range=30-80) for those aged 0-11 months, 33.6±6.9  
range=22-48), for those age 12-35 months and  
3
5.8±10.5 (range=24-52) for those age 36-60 months.  
Results  
When stratified by diagnosis, the mean respiratory rate  
was 54.6±8.77 in children with bronchiolitis, 51.0±14.1  
in those with pneumonia and 34.0±8.99 in those with  
acute tonsillitis.  
During the study period, a total of 113 children were  
admitted into the unit, out of which 78 (69.0%) were  
children 5years and below. From this, 39(50%) were  
diagnosed with acute respiratory tract infection. Males  
were 22(59.0%) and Females 16(41.0%).  
Mean age was18.75mo+17.23, (Females =25.6+19.1,  
Males = 13.8+14.2, t=2.2, p=0.03). The 0-11months old  
accounted for 48.7% (19) of the patients seen. This was  
followed by the 12-36 month group with 28.2% (11)  
while the 36-60 month old group were 23.1 % (9).  
The mean oxygen saturation by age was 96.3±2.08  
(
(
(
range=92-99) for those age 0-11 months, 95.8±4.8  
range=82-98), for those age 12-35 months and 96.6±1.9  
range=93-99) for those age 36-60 months. When strati-  
fied by diagnosis, the mean oxygen saturation was  
9
7.8±0.71% in those with bronchiolitis, 95.5±3.40% in  
those with pneumonia and 97.5±0.55% in those with  
acute tonsillitis.  
Patient distribution by diagnosis of ARI  
The mean pulse rate by age was 131.5±22.5 (range=98-  
Of the 19 infants seen, aged 0-11 months, 8(42.1%) each  
had bronchiolitis and pneumonia, while 3(15.8%) had  
pharyngotonsillitis. Similarly, among the 12-36mo olds  
seen, none had bronchiolitis, 8(72.7%) had pneumonia  
1
1
62) for those age 0-11 months, 121.0±17.4 (range=100-  
53), for those age 12-35 months and 136.0±28.6  
(
range=160-168) for those age 36-60 months. When  
stratified by diagnosis, the mean pulse rate was  
1
52  
1
bronchiolitis, pneumonia and tonsillitis respectively.  
This is shown in table 2  
22.0±24.7, 134.4±23.2 and 117.3±14.3 in those with  
cough been predominant features in pneumonia while  
cough and catarrh were more frequent in bronchiolitis.  
Pharyngotonsilitis had more of fever and vomiting and  
less cough. Reports have shown bronchiolitis to be com-  
monly associate20d with nasal congestion, catarrh and  
breathlessness. The course of bronchiolitis is usually  
variable and dynamic ranging from transient events such  
as nasal blockade to progressive respiratory distress  
from lower respiratory tract inflamma2t0i,2o1n and obstruc-  
Table 2: Cardio-respiratory parameters by morbidity of  
Subjects  
Diagnosis  
RR  
SO2  
PR  
Bronchiolitis 44.6±8.77 97.8±0.71 122.0±24.7  
Pneumonia  
Tonsillitis  
41.0±14.1 95.5±3.40 134.4±23.2  
34.0±8.99 97.5±0.55 117.3±14.3  
tion. As reported by other researchers  
fever was not  
a common feature of bronchiolitis in our study. How-  
ever, we did not find cou0gh as a prominent symptom  
Commonest features of ARI  
2
unlike what Fattouh et al reported in Egypt. Since all  
our patients with bronchiolitis were younger than 6  
months where cough is not so prominent with respira-  
tory infections, it is not surprising that fewer than 25  
percent of our children reported cough as a symptom.  
The cardinal feature of each disease entity was Fever  
(
100%), cough (80%), breathlessness (75%), tachycardia  
and hypoxemia in those with Pneumonia. Catarrh  
100%), nasal congestion (80%) and tachypnea(80%) in  
those with bronchiolitis. Fever (100%) and vomiting  
100%) in those with pharyngotonsilitis. (Table 1 and 2)  
(
On the other hand, that we found pharyngotonsilitis as-  
sociated2commonly with fever and vomiting is not sur-  
(
2
prising. Though pharyngotonsilitis is an acute respira-  
tory infection, its onset is sudden and usually character-  
ized by symptoms of fever and sore throat, naus2ea, vom-  
Discussions  
2
iting, headache, and rarely, abdominal pain. Cough  
and breathlessness are not prominent features especially  
since it is an upper tract infection without the usual lung  
parenchyma inflammation and the lower tract obstruc-  
tion seen in pneumonia and other lower tract infections.  
Clinical features and aetiologies of ARI differ from age  
to age and so also the pat1te1rns of the different ARI  
within the same age group. Typical features of ARI  
include but are not limited to cough, breathlessness, ca-  
tarrh, fever etc. Differences in features are seen in de-  
gree of respiratory distresses, hypoxaemia and age of  
In general, pneumonia was more associated with hypox-  
aemia than bronchio3litis and pharyngotonsilitis similar  
1
2
typical presentation. This was amply demonstrated in  
our study.  
2
to what Shann et al, in Papua New Guinea reported in  
their clinical assessment of ARI in children an0d the  
1
WHO clinical criteria for the diagnosis of ARI. Like  
I13n,14this study we found, as has been reported severally  
bronchiolitis in infancy, pharyngotonsilitis in older  
children and pneumonia cutting across all age groups as  
well a,1s5 being the commonest ARI in our environ-  
2
3
the Shann study , the present study made use of the  
added clinical finding of crepitations in the diagnosis of  
pneumonia. Crepitations had been demonstrated to give  
an added strength in the diagnosis of pneumonia.  
1
ment. Younger children especially infants are predis-  
posed to viral bronchiolitis because placentally transmit-  
ted anti-RSV maternal antibody, even if present in high  
conce6ntration, provides partial but incomplete protec-  
1
Conclusion  
tion. On the other hand, pneumonia is caused by a  
5,7  
wide range of organism with most been virulent. Be-  
sides, the absence of vaccine against the common under  
five causes of pneumonia in our national immunization  
schedule is a significant contributor to the high preva-  
lence17of pneumonia found in children under five years  
old.  
This study showed that the commonest acute respiratory  
infections encountered in our emergency room were  
pneumonia, bronchiolitis and pharyngotonsilitis. Bron-  
chiolitis is a frequent infection in infants while pharyn-  
gotonsilitis occur commonly in children beyond infancy.  
On the other hand, pneumonia cuts across all age group.  
Furthermore, the common features seen in the emer-  
gency room associated with pneumonia were cough,  
breathlessness, tachycardia and hypoxemia while bron-  
chiolitis was more commonly associated with infancy,  
breathlessness, catarrh, and nasal congestion. Pharyngo-  
tonsilitis was seen in association with fever and  
We also found a higher proportion of infants compared  
with other age groups presenting with ARI similar to  
previous reports where infants have been shown to be  
generally more predisposed to infections as a result of  
their relatively immature adaptive im8mune system com-  
1
pared to older children and adults. Also, degradation  
vomiting.  
of maternal antibodies, cessation of breastfeeding, and  
been at child-care centres increases the r9isk of infections  
1
Limitation  
especially respiratory tract infections. It is thus not  
surprising that even in this study the proportion of chil-  
dren with ARI decreased with age.  
The small sample size here will preclude drawing hasty  
inferences however our findings still give some insight  
on the current problem as seen in our facility. Secondly,  
Typical features seen in each entity showed fever and  
1
53  
our studied population consisted of only children admit-  
ted in the EPU rather than the whole paediatric cases  
seen in the facility with a diagnosis of ARI. Since most  
ARI will be mild and may not necessarily be admitted,  
that group seen in the outpatient clinic will be invariably  
missed.  
Acknowledgement  
We sincerely appreciate the Nursing staff in the unit and  
our residents who helped in patient management  
Conflict of interest: None  
Funding: None  
Reference  
1
.
Oyejide CO, Osinusi K. Acute  
respiratory tract infection in chil-  
dren in Idikan Community, Ibadan,  
Nigeria:severity, risk factors, and  
frequency of occurrence. Reviews  
of Infectious Diseases 1990; 12:  
S1042–1046.  
Rudan I, Tomaskovic L, Boschi-  
Pinto C, Campbell H: Global esti-  
mate of the incidence of clinical  
pneumonia among children under  
five years of age. Bull WHO 2004;  
9. Williams BG, Gouws E, Boschi-  
17. Effect of a conjugate pneumococ-  
cal vaccine on the occurrence of  
respiratory infections and antibi-  
otic use in day-care center atten-  
dees. Pediatr Infect Dis J,  
Pinto C, Bryce J, Dye C: Estimates  
of worldwide distribution of child  
deaths from acute respiratory in-  
fections. Lancet Infect Dis 2002, 2  
(1):25-32.  
10. World Health Organization. Tech-  
nical basis for the WHO recom-  
mendations on the management of  
pneumonia in children at first level  
health facilities. Geneva: World  
Health Organization, 1991. (WHO/  
ARI/91.20).  
11. Ohiaeri CN, Akinsulie OA and  
Renner JK. Pattern of presentation  
and risk factors of acute respira-  
tory infection in under five old in  
Mushin local government area of  
Lagos State. Nig Ot J Hosp med  
2003;13:24-26.  
12. Lozano JM.Epidemiology of hy-  
poxaemia in children with acute  
lower respiratory infection Int J  
Tuberc Lung Dis 5(6):496–504  
13. Koch A, Mølbak K, Homøe  
P,Sørensen P, Hjuler T, Ehmer M  
Risk Factors for Acute Respiratory  
Tract Infections in Young  
2001;20:951-958  
18. Dahl MS, Tessin I, Trollfors B.  
Invasive group B streptococcal  
infections in Sweden: Incidence,  
predisposing factors and progno-  
sis. Int J Infect Dis 2003;7:113-9.  
19. Nafstad P, Brunekreef B, Skrondal  
A, and Nystad W.Early respiratory  
infections, asthma and allergy: 10  
year follow up of the Oslo birth  
cohort. Pediatrics 2005;116;e255  
20. Fattouh AM, Mansi YA, El-anany  
MG, El-kholy AA and El-karaksy  
HA. Acute lower respiratory tract  
infection due to respiratory  
2
3
.
.
8
2:895-903.  
Robertson SE, Roca A, Pedro P et  
al. Respiratory syncytial virus  
infection: denominator-based stud-  
ies in Indonesia, Mozambique,  
Nigeria and South Africa. Bull-  
WHO 2004; 82: 914–922.  
Klig JE, Chen L. Lower respiratory  
infections in children. Current  
Opinion in Pediatrics 2003; 15:  
4
5
.
.
syncytial virus in a group of Egyp-  
tian children under 5 years of age  
Italian Journal of Pediatrics 2011;  
37:14-20  
1
21–126.  
Tagbo, BN, AC Ude. Use of clini-  
cal parameters other than respira-  
tory rate in predicting pneumonia  
in under five children in Enugu,  
Nigeria. J Coll Med 2001; 6: 116-  
21. Nokes DJ, et al. Respiratory  
syncytial virus epidemiology in a  
birth cohort from Kilifi district,  
Kenya: infection during the first  
year of life. Journal of Infectious  
Diseases 2004; 190: 1828–32.  
22. Brooks I. Diagnosis and manage-  
ment of pharyngotonsilitis. Israeli  
Journal of Emergency Medicine  
2008;8:26-34  
23. Shann F, Hart K, Thomas D. Acute  
lower respiratory tract infections in  
children: possible criteria for se-  
lection of patients for antibiotic  
therapy and hospital admission.  
1984. Bull WHO. 2003; 81(4): 301  
–305.  
1
19  
Greenlandic Children. Am J Epide-  
miol 2003;158:374–384  
6
.
Redd SC, Patrick E, Vreuls R,  
Metsing M, Moteetee M. Compari-  
son of the clinical and radiographic  
diagnosis of paediatric pneumonia.  
Trans R Soc Trop Med Hyg. 1994  
May-Jun;88(3):307-10  
14. Selwyn BJ. The epidemiology of  
acute respiratory tract infection in  
young children: comparison of  
findings from several developing  
countries. Coordinated Data Group  
of BOSTID Researchers. Rev In-  
fect Dis 1990;12(suppl 8):870–88  
7
8
.
.
Rudan I, Boschi-Pinto C, Biloglav  
Z, Mulholland K, Campbell H:  
Epidemiology and etiology of  
childhood pneumonia. Bull WHO  
1
5. Monto AS. Studies of the commu-  
nity and family: acute respiratory  
illness and infection. Epidemiol  
Rev 1994;16:351–73.  
2
008, 86:408-416B.  
1
6. Odisho SM , Al-Bana AS, Yaas-  
sen NY. Detection of Respiratory  
syncytial virus infection in a sam-  
ple of infants in Iraq. Iraqi J Med  
Sci, 2009; VOL.7 (4):11-19  
Simoes AF, Cherian T, Chow J,  
Shahid-Salles S, Laxminarayan R,  
John TJ: Acute Respiratory Infec-  
tions in Children. Disease Control  
Priorities in Developing Countries  
Washington: Oxford University  
Press, second 2006.