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ETHIOPIAN JOURNAL OF
PEDIATRICS AND CHILD
HEALTH
July 2009, Volume V, Number 5
Original articles
The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in Tikur
Anbessa Hospital
Mikyas Demissie ,M.D. , Sileshi Lulsesed, M.D.
Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital
Kalid Asrat, MD, Amha Mekasha, MD, MSc
Gullian Barre Syndrome in Children At Tikur Anbessa Specialized Hospital
Tigist Bacha, MD
Assessment of quality of care of sick under-five children in referral hospitals in Ethiopia.
Sirak Hailu, MD, Solomon Emyu, MD/MPH, Fisseha Mamo, MPH, Tolawaq Kejela MD
Management of severe acute malnutrition in children using community based therapeutic care approach: a
review of three years data from southern Ethiopia.
Efrem Teferi, MD Shiferaw Teklemariam, MD, MPH , Lopiso Erosie, BSC, MPH , Abel Hailu, MD,
Tefera Belachew, MD, MSc, DLSHTM, Mohammed A Yassin, MD, MSc, PhD
Review article
Child Survival: Progress Towards meeting MDG4
Assaye Kassie, MD
Case report
A Case Report : Optic glioma in a child with NF1
Kalid Asrat, MD
The Ethiopian Journal of Pediatrics and Child Health aims to contribute towards the improvement
of child health in developing countries, particularly in Ethiopia. The journal publishes original
articles, reviews, case reports pertaining to health problems of children.
Editorial board
Amha Mekasha, MD, Msc
Assaye Kassie, MD
Sirak Hialu, MD
Tedbab Degife, MD
Editor-in-chief
Table of contents
Original articles
The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in Tikur
Anbessa Hospital
Mikyas Demissie ,M.D. , Sileshi Lulsesed, M.D.
Clinical Predictors of Pneumonia Among Under-five Children At Tikur Anbesa Specilaized Hospital
Kalid Asrat, MD, Amha Mekasha, MD, MSc
Gullian Barre Syndrome in Children At Tikur Anbessa Specialized Hospital
Tigist Bacha, MD
Assessment of quality of care of sick under-five children in referral hospitals in Ethiopia.
Sirak Hailu, MD, Solomon Emyu, MD/MPH, Fisseha Mamo, MPH, Tolawaq Kejela MD
Management of severe acute malnutrition in children using community based therapeutic care approach: a
review of three years data from southern Ethiopia.
Efrem Teferi, MD Shiferaw Teklemariam, MD, MPH , Lopiso Erosie, BSC, MPH , Abel Hailu, MD,
Tefera Belachew, MD, MSc, DLSHTM, Mohammed A Yassin, MD, MSc, PhD
Review article
Child Survival: Progress Towards meeting MDG4
Assaye Kassie, MD
Case report
A Case Report : Optic glioma in a child with NF1
Kalid Asrat, MD
4
The Prevalence of Nosocomial Infections and Associated Risk Factors in Pediatric Patients in
Tikur Anbessa Hospital
Mikyas Demissie, MD, Sileshi Lulseged, MD, Msc
Abstract
Little is known about nosocomial infections and associated risk factors among children in Ethiopia.
The aim of the study is to generate data on nosocomial infection in children that will serve as a base for
further studies and to develop prevention interventions. A case control study was done on 111 cases and
222 controls from pediatrics wards of Tikur Anbessa Hospital, Aug 2002-Dec 2003. Nosocomial infection
rate was 5 per 100 discharges. A total of 143 nosocomial infections were detected in 111 cases. The
commonest infection was pneumonia 39.8%. Specimen for culture and sensitivity was taken from
63/143(44.1%) infections and organisms were isolated in 43 infections. And 14 different type of bacteria
were found. E coli, klebsiella pneumoniae and pseudomonas species were the most frequently isolated
organisms. The resistance to ampicillin was 91.9% , gentamycin 67.2%, , ceftriaxone 50%, norfloxacin
18.3%, and ciprofloxacin 15.4%. Age less than one year, malnutrition, admission to orthopedics unit,
peripheral intravenous line and prolonged hospitalization were significantly associated with nosocomial
infection. In conclusion surveillance for high risk patients, education of health personnel, proper isolation
technique, hand washing or use of glove and gowns, avoid prolonged hospitalization when possible and
reestablishment of infection control committee are needed for prevention of nosocomial infection. And
antimicrobial therapy should be guided based on drug susceptibility pattern of bacteria isolated from patients
with nosocomial infection in the hospital.
Introduction
Nosocomial infections result in considerable
morbidity
of
care
and
hospitalization
mortality,
and
prolongation
increases
patient
outbreak
klebsiella
the
immunodeficiency
of
gentamycin-resistant
most
common
cause
(14-16).
of
secondary
The
cumulative
aspiration
into
lower
airway
leading
to
6
allowing antimicrobial resistant microorganisms
source
of
highly
resistant
organisms.
have
infection(11,12,18,20,21).
nosocomial
were excluded.
neonates and those who were discharged from
controls
ward.
from
registration
book
excluding
7
Data was collected from charts of cases and
sex,
general
primary
diagnosis,
weight,
length,
anaesthesia
while
Long
duration
nasotracheal
chemotherapy,
of
Operational Definitions:
use
of
steroid,
level
or
orotracheal
intubation
is
identify
been
nosocomial
infections
have
8
and p-value and odds ratio calculation. P-value
factors.
Results
December
2003,
excluding
neonatal
and
nosocomial infection
surgery.
from
cases.
63/143(44.1%)
nosocomial
infections.
9
from pus and the remaining 7(11.1%) were from
positive
nosocomial
Waterlow classification,
isolated
in
43/63(68.3%)
organism
pneumoniae,
followed
pseudomonas
of
by
klebsiella
species,
ward, infection at
and
Table 3.
(Table 5)
Among
222
controls,
175(78.8%)
were
10
21(18.9%) died. Children with nosocomial
death
when
compared
to
those
without
Discussion
infection
by
was
gastroenteritis,
pneumonia
and
followed
whether
the
isolated
coagulase
negative
11
Disruption of the physical barrier occurs in burn
study
since
canula
related
12
Table 1. Distribution of nosocomial infection by site , Tikur Anbessa hospital, August 2002-December 2003.
.Site of nosocomial infection
Pneumonia
Gastroenteritis
Primary blood stream infection
Urinary tract infection
Skin and soft tissue infection
Upper respirator tract infection
Surgical wound infection
Central Nervous System infections
Others
Systemic infection
Total
frequency
57
17
15
13
13
9
8
2
7
2
143
%
39.9
11.9
10.9
9.1
9.1
6.3
5.6
1.4
4.9
1.4
100
8
(18.2)
2
(10.5)
0
Skin &
soft
tissue
(%)
27
1
(61.4)
(2.3)
General
5
0
7
1
surgery
(26.3)
(36.8)
(5.3)
Neuro
0
1
3
2
surgery
(10)
(30)
(20)
Plastic
1
0
0
1
0
surgery
(50)
(50)
Burn unit
1
1
0
3
4
(7.1)
(7.1)
(21.4)
(28.6)
Tumor
0
1
1
11
1
therapy
(3.2)
(3.2)
(35.5)
(3.2)
ENT
0
0
1
3
0
(16.7)
(50)
Orthopedics
1
1
6
2
4
(5.9)
(5.9)
(35.3)
(11.8)
(23.5)
Total
8
13
9
57
13
SWI=surgical wound infection UTI=urinary tract infection
URTI= upper respiratory tract infection CNS= central nervous system
primary
blood
stream
infection(
%)
5
(11.4)
0
0
0
2
(14.3)
8
(25.8)
0
0
15
Systemic
infectio(%)
(%)infection
infectiom
Total
Pneumo
nia
(%)
Other(%)
Pediatrics
CNS(%)
Service
Gastro
Enteritis (%)
Table 2. Site of nosocomial infections by the service in Tikur Anbessa hospital, August 2002-December 2003.
4
(9)
2
(10.5)
1
(10)
0
44
1
(5.3)
1
(10)
0
1
(5.3)
1
(10)
0
19
10
1
(7.1)
6
(19.3)
1
(16.7)
2
(11.8)
17
14
3
(9.7)
1(16.
7)
0
1
(7.1)
0
17
1
(5.5)
2
31
143
Table 3 Types of organism isolated from children with nosocomial infection in Tikur Anbessa hospital, August 2002December 2003.
Organism isolated
Frequency
%
Escherichia coli
11
17.7
Klebsiella pneumoniae
9
14.5
Pseudomonas species
9
14.5
Coagulase negative staphylococci 6
9.7
Acinetobacter species
5
8.1
Klebsiella oxytoca
4
6.5
Salmonella species
4
6.5
Staphylococcus aureus
3
4.8
Proteus vulgaris
3
4.8
Citrobacter species
3
4.8
Shigella species
2
3.2
Group A streptococci
1
1.6
Morganella morgagne
1
1.6
Enterobacter cloaca
1
1.6
Total
62
100
14
Table 4 Drug susceptibility pattern of bacteria isolated from children with nosocomial infections in Tikur Anbessa Hospital,
August 2002- December 2003.
Antibiotics
No. of isolates
sensitive
Intermediate
Resistant
tested
sensitive
Ampicillin
62
4(6.5%)
1(1.6%)
57(91.9%)
Gentamycin
61
20(32.8%)
0
41(67.2%)
Norfloxacin
60
47(78.3%)
2(3.3%)
11(18.3%)
Trimethoprim58
10(17.2%)
2(3.5%)
46(79.3%)
Sulfamethoxazole
Tetracycline
58
13(22.4%)
2(3.5%)
43(74.1%)
Chloramphenicol
55
8(14.5%)
0
47(85.5%)
Ceftriaxone
36
13(36.1%)
5(13.9%)
18(50%)
Augmentin
31
8(25.8%)
5(16.1%)
18(58.1%)
Doxycycline
25
5(20%)
1(4%)
19(76%)
Amoxicillin
24
2(8.3%)
1(4.2%)
21(87.5%)
Naldixic Acid
22
12(54.5%)
0
10(45.5%)
Nirofurantoin
19
6(31.6%)
1(5.3%)
12(63.1%)
Amikacin
14
11(78.6%)
1(7.1%)
2(14.3%)
Ciprofloxacin
13
9(69.2%)
2(15.4%)
2(15.4%)
Penicillin G
13
0
2(15.4%)
11(84.6%)
Erythromycin
13
4(30.8%)
3(10%)
6(46.2%)
Methicillin
11
2(18.2%)
3(27.3%)
6(54.5%)
Carbencillin
8
2(25%)
3(37.5%)
3(37.5%)
Kanamycin
4
0
2(50%)
2(50%)
Cephalotin
4
0
2(50%)
2(50%)
Cloxacillin
3
0
2(66.7%)
1(33.3%)
Lincomycin
3
1(33.3%)
2(66.7%)
0
14
15
Table 5 Risk factors associated with nosocomial infection in pediatric patients, Tikur Anbessa Hospital, August 2002December 2003.
Variables
Age in month
Weight for
height
Peripheral
intravenous line
Use of
antineoplastic
chemotherapy
Duration of stay
before
discharge
Service
1-11
12-59
60-119
120-180
>=90%
80-89%
70-79%
<70%
No
Yes
No
Yes
Control
Number
35
85
52
50
143
44
22
7
23
199
215
7
%
15.8
38.3
23.4
22.5
66.2
20.4
10.2
3.2
10.4
89.6
96.8
3.2
Case
Number
31
33
27
20
58
21
19
8
3
108
89
22
%
27.9
29.7
24.3
18
54.7
19.8
17.9
7.6
2.7
97.3
80.2
19.8
<7 days
8-14 days
15-21days
>21 days
74
62
40
46
33.3
27.9
18
7.2
2
19
16
74
1.8
17.1
14.4
66.7
General surgery
Pediatrics
Plastic surgery
ENT
Neurosurgery
Orthopedics
Burn unit
Tumor therapy
unit
72
90
10
14
6
21
4
5
32.4
40.5
4.5
6.3
2.7
9.5
1.8
2.3
16
38
2
4
5
15
7
24
14.4
34.2
1.8
3.6
4.5
13.5
6.3
21.6
OR
P value
2.21(1.03-4.79)
0.97(0.48-1.97)
1.30(0.61-2.76)
1
1
1.18(0.62-2.24)
2.13(1.02-4.46)
2.82(0.88-9.13)
1
4.16(1.15-17.82)
1
7.59(2.94-20.35)
0.042
0.937
0.577
6.373(2.16-18.83)
0.741(0.296-1.856)
1.155(0.421-3.169)
0.709
0.0447
0.09
0.94(0.41-2.18)
3.68(1.46-9.30)
2.28(0.52-10.04)
0.025
7.566(1.009-56.708)
0.000001
0.006(0.00-12)
0.00032
0.00005
0.00000
13.43(2.65-68.08)
9.29(1.74-48.64)
70.15(13.96-352.46
0.079
0.785
0.945
0.096
0.012
0.003
0.000
1.68(0.42-6.71)
1.21(0.19-7.56)
1.83(0.36-9.21)
2.89(0.53-15.59)
4.86(1.31-18.01)
4.89(0.93-25.83)
1778.85(0.00-34)
1
11.34(2.4-73.44)
14.8(3.02-98.38)
59.52(13.41368.48)
1
1.9(0.94-3.89)
0.90(0.0-5.09)
1.29(o.31-5.001)
3.75(o.85-16.41)
3.21(1.26-8.27)
7.88(1.77-37.27)
21.6(6.47-77.05)
15
16
References
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
20.
21.
Jarvis W.R : Epidemiology of nosocomial infections in pediatric patients. Pediatr. Infect. Dis. J. 1987; 6: 344-51
Moss W. An outbreak of getamycin-resistant klebsiella bacteremia at a children's hospital. Ethiop Med J. 1992;
30: 197-205
Worku B. Klebsiella oxytoca outbreak at Ethio-Swedish childrens hospital (ESCH). Ethiop Med J. 1997; 35:17783
Cooper R.G., Sumner C. Hospital infection data from a childrens hospital Med J. Aust. 1970; 2:1110-13
Gardner P, Carles D.G Infection acquired in a pediatric hospital. J. Pediatr. 1972; 81: 1205-1210
Wenzel R.P, Osterman C.A., Hunting K.J. Hospital acquired infection 11. Infection rates by site, service and
common procedures in a university hospital. Am. J. Epidemiol. 1976; 104: 645-51
Welliver R.C., Mc Laughlin S. Unique epidemiology of nosocomial infection in a childrens hospital. Am. J. Dis.
Child. 1984; 138: 131-5
Gaynes R.P., Edward J.R., Jarvis W.R., Culver D. H, Tolson J. S., Martone W. J. Nosocomial infection among
neonates in high- risk nurseries in the United States. Pediatrics. 1996; 98: 357-61
Sohn A. H., Garret D. O., Sinkovitz- Cochran R.L., Grohskopf L. A., Levine G. L., Stover B.H., Seigel J.D.,Jarvis
W.R. Prevalence of nosocomial infections in neonatal intensive care unit patients: Results from the first national
point prevalence survey.J.Pediatr .2001;133:821-827.
Behrman R, Kleigman R, Jenson H. T lymphocyte, B lymphocyte and Natural Killer cells.-In: Buckley R., ed ;
Infection control and prophylaxis.-In: Fisher, ed. Nelson, Text Book of pediatrics, 17th ed. New Delhi, Elsevier,
2004:683, 866, 1184.
Feigin, Cherry. Nosocomial infections.-In: Huskin W.C., Goldman D.A., eds., Textbook of pediatric infectious
disease, 4th ed. Philadelphia, Elsevier, 1998; 2545-85.
Fleming C.A., Balaguera H.U., Craven D.E., Risk factors for nosocomial preumonia.Med chinics of north
America 2001;85:1545-1563.
Knittle M.A., Eitzman D.V., Baer H, Role of hand contamination of personnel in the epidemiology of gram
negative nosocomial infections: J.pediatr 1975; 86:433-437.
Chandra R.K: Nutrition, immunity, and infection: Present knowledge and future direction.Lancet.1983; 1:688-91.
Puri S, Chandra P.K: Nutritional regulation of host resistance and predictive value of immunlogic test in
assessement of outcome. Pediatric Clinics of North America.1985; 32:499-516.
Bhattacharyya N, Kosloske A.M., Macarlhia C.Nosocomial infection in pediatric surgical patients: a study of 608
infants and children: J.pediatr.Surg.1993; 28:338-343.
Bhattacharyya N, Koslosk A.M., postoperative wound infectious in pediatric surgical patients: A study of 676
infants and children. J.pediatr surg.1990; 25:125-129.
Haley R.W., Houton T.M., Culver D.H., Stanley R.C., Emori T.G., Hardisan C.D., Quade D, Schauchtman
R.H.Schaberg D.R., shah B.V., Schat, G.D., Nosocomial infections in U.S. Hospitals, 1975-1976 estimated
frequency by selected characteristics of patients AM J Med 1981; 70: 947-959.
Calis R, Torres A, Gatell J.M., Almale M, Rodringuez-Roisin R.,Aqustin vidal A. Noscomial preumonia. A
multivariate analysis of risk and prognosis. Chest 1988; 93:318-24.
Price D.J., Sleigh J.D., Control of infection due to klebsiella aerogenes in a neurosurgical unit by withdrawal of all
antibiotics. Lancet 1970; 2:1213-1215.
Young L.S. Nosocomial infection in the immuocompromised adult. Am. J .Med 1981; 70:398-403.
16
17
22.
23.
24.
25.
26.
27.
28.
Garlsand I.S.,Nelson D.B., Cheah T.E., Hennes H.H., Johnson T.M. infectious complications during peripheral
intravenous therapy with Teflon catheters: a prospective study.pediatr infect dis. J. 1987; 6: 918-921.
Tully J.L., Friedland F.H., Baldini L.M., Goldmann D.A., Complications of intravenous therapy with steel needles
and Teflon catheters. Am. J Med 1981; 70:702-6.
Ducel.G, Fabry.J, Nicolle.L; Prevention of hospital acquired infections A Practical Guide 2nd
edition.WHO/CDS/EPH/2002.12
Garner J.S., Jarvis W.R., Emori T. G., Horan T.C. , Hughes J .M.. CDC definition for nosocomial infections. Am J
Infect Control 1988;16:128-140.
Waterlow. J.C. Note on the assessement and classification of protein energy malnutrition in children. Lancet
1973; 2:87-98.
Classification of infantile malnutrition. Lancet 1970; 2: 302-303.
Grady R., Safety profile of quinolone antibiotics in the pediatric population. Pediatr Infect Dis J 2003; 22: 112832.
Acknowledgements
I thank Dr Fithun Lulseged and staff at the statistics office who helped me collect data. I also extend my gratitude to Dr
Adamu Adissie and Dr Firew Mekonnen who helped me in the analysis of the data.
17
18
Abstract
This is a six years retrospective descriptive study conducted in the pediatric and child health department of Tikur Anbessa
Hospital from September, 2001 September, 2006 G.C to assess the pattern of acute flaccid paralysis (AFP) and the
clinical and epidemiologic features of Guillain Barre syndrome (GBS).
Data was collected from medical records of all patients admitted with diagnosis of AFP, and analyzed using standard
statistical tests with SPSS version 14 software. Out of 70 admitted cases of AFP, forty six (65.7%) were males and 24
(34.3%) were females. Sixty seven cases (95.7%) were diagnosed to have GBS and the rest three were compatible with
poliomyelitis, transverse myelitis and post injection neuritis. Out of the 70 cases 66 (94.3%) have received at least one
dose of polio vaccination and the rest 4 (5.7%) were never vaccinated.
Out of the cases diagnosed to have GBS, 44 (65.7%) met NNCDS diagnostic criteria. History of antecedent event was
obtained in 31/67 (46.3%) patients. Majority of the patients 45 (67.17%) presented with ascending reflexes quadriparesis,
2 (2.98%) patients with descending areflexic quadriparesis, 19(28.35%) only with lower limb involvement and 1 (1.5%)
with typical miller-fisher type. Sensation was affected in 4 patients.
Cytoalbuminological dissociation was found in 27(40.3%). There were 11 deaths (16.4%) of whom five were admitted to
ICU the rest six didnt. This study showed that the commonest cause of AFP is GBS which is associated with high
mortality. This high mortality rate 11/67 (16.42%) is attributed to absence of pediatrics ICU, late arrival to Hospital after
onset of illness, and poor supportive care.
18
19
INTRODUCTION
Acute flaccid paralysis (AFP) is the clinical condition
GBS.
transverse
myelitis
and
metabolic
(2,5,6,7)
19
Results
due to neuropathy,
2. Areflexia or hyporeflexia
trunk,
data.
50
NO of AFP Cases
40
30
20
10
0
Amhara
Oromiya
SNNPR
Region
Addis Ababa
21
25.0%
20.0%
15.0%
10.0%
5.0%
0.0%
1993
Fig 2. AFP cases distribution
per year
1994
1995
1996
1997
1998
Admition Year
Frequency
3
1
5
1
1
11
Percentage
27.2
9.1
45.4
9.1
9.1
100
21
22
Table 2: CSF analysis Result
Frequency
Percent
4.5
10.4
27
40.3
21
31.3
9
67
13.4
100.0
from 1 day to 14.0 days the mean being 3.44 days. The
mixed
axonal
and
demyelinating.
22
Discussion
This is the first study done on pattern of AFP and clinical and
can see the mortality rate from GBS is high some of which
For five cases stool sample for polio was not taken out of
encouraged.
24
References
1. Acute Flacc
2. id paral
3. ysis surveillance: Ministry of Health and WHO Ethiopia June 2006: 5
4. Koul R, Chacko A, Javed H et al Acute flaccid paralysis in Australian children. . J Paediatr Child Health.
2003; 39 (1):22-6.
5. Hahn AF. Guillain-Barre syndrome. Lancet 1998; 352: 635-41.
6. Lovecchio F, Jacobson S. Approach to generalized weakness and peripheral neuromuscular disease.
Emerg Med clin N am 1997; 15(3):605-23
7. Rehman A, Idris M, Elahi M, Arif A. Guillain-Barre syndrome. The leading cause of Acute Flaccid Paralysis
in Hazara Division. J ayub Med Coll Abbottabad 2007;19:26-28.
8. Rasul CH, Das PL, Alam S, Ahmed S, Ahmed M. Clinical profile of acute flaccid paralysis. Med J Malaysia.
2002 ; 57 (1):61-5.
9. Molinero MR, Varon D, Holden KR, Sladky JT, Molina IB, Cleaves F. Epidemiology of childhood GuillainBarre syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999.
J Child Neurol. 2003; 18(11):741-7..
10. Kuwabara S. Guillain-Barre syndrome: epidemiology, pathophysiology and management. Drugs.
2004;64(6):597-610. .
11. Berhane Beyene, Ayele Gebremariam, Tilahun Teka et al. Laboratory and Epidemiology communications,
Regional Distribution of Acute Flaccid Paralysis Cases in Ethiopia in 2000 2002. Jpn.J.Infect. Dis., 2004;
52:. 72.
12. Harvey B.Sarnat. Neuromuscular Disorders. In: Richard E. Behrman, Robert M. Kliegman and Hal B.
Jenson, Editors. Nelson Text Book of Pediatrics, 17th Edition .Philadelphia Pennsylvania, 2004:2080-81.
13. Asbury Ak. Assessment of current diagnostic criteria for Guillian-Barre syndrome. Ann Neurol
1990:27(suppl):s21-4
14. Zenebe Melaku, Guta Zenebe, Abera Bekele .Guillaian barre syndrome in Ethiopian patients. Ethiop Med J
2005; 43( 1) :21
15. Bahemuka M. Guillain-Barre syndrome in Kenya: a clinical review of 54 patients.
J Neurol. 1988; 235(7):418-21.
16. Howlett WP, Vedeler CA, Nyland H, Aarli JA. Gullian-Barrre syndrome in Northern Tanzania: a comparison
of epidemiological and clinical findings with western Norway. Acta Neurol Scand 1987:75:95-100.
17. Osuntookun BO, Agebebi K. Prognosis of GuillainBarre syndrome. Medicine in the African Region: The
Nigerian experience. Neurol Neurosurg Psychatry 1973:36:478-83.
24
25
Acknowledgments:
I extend my thanks to Dr. Ahmed Bedru for his invaluable advice in the conduct of the research. Ato Tilahun
Zimita for his assistance in data entry and analysis.
25
26
ABSTRACT
Background: About 10-20% of sick children presenting to a primary care facility require referral to hospital for
inpatient care. Improvement of the quality of pediatric referral care has a major contribution to the child survival
efforts by ensuring the continuum of care and averting mortality.
Objective: To assess the quality of care for children in selected referral hospitals based on the minimum standards
derived from the WHO Pocket book of Hospital Care for Children, 2005 and thereby to initiate pediatric referral care
quality improvement process in the country.
Methods: A qualitative assessment of pediatric referral care was conducted in 8 hospitals selected by convenient
sampling, January July 2008. A team composed of experienced pediatricians and health officer used an adapted
WHO hospital assessment tool to assess the quality of triage, emergency care and case management practices &
hospital infrastructure and support services.
Results: None of these hospitals were practicing the standard triaging process by assessing children immediately on
arrival for emergency and priority signs. All of them were not appropriately organized and fully equipped to handle
pediatric emergencies effectively. Overall, the case management of common neonatal and childhood illnesses was
not optimal. Generally, there was shortage of some essential drugs and lack of materials such as nasal prongs, infant
and child size bag & masks, nebulizers, heaters and oxygen concentrators. Hygienic facilities were below the
expected standard. Staff were not trained in ETAT (Emergency Triage Assessment and Treatment) and there were
no protocols for pediatric referral care. There was no clearly designated high dependency area where very sick
children receive highest attention and no special rooms for providing appropriate neonatal care in majority of the
hospitals. The overall case fatality rate was 11% (10-16%) but first 24 hours mortality could not be determined due to
problems with the recording system.
Conclusions: The quality of pediatric referral care needs serious attention and coordinated efforts utilizing the
opportunity of the national hospital management initiative and the BPR (Business Process Re-engineering) to
institutionalize ETAT and standards of hospital care for children. This has to be complemented with availing of
appropriate job aids, essential supplies and equipments, and improvement of health worker skills through training,
clinical mentoring and regular supportive supervision.
1
26
27
practices, and care at the first-level hospital. On the
basis of current guidelines, it has been estimated that
10% to 20% of sick children who present for primary
care (i.e., the most severely ill) require referral to a
first referral or district hospital. The quality of care
provided in these hospitals is likely therefore to have
a major impact on the health and lives of millions of
children each year.
INTRODUCTION
The Ethiopian health service delivery system is
organized as a four-tier system, characterized by a
Primary Health Care Unit (PHCU) 1st tier, then the
district hospital 2nd tier, zonal hospital 3rd tier and
specialized hospital- 4th tier. Services given at each
level of these tiers have a crucial role in averting the
morbidity and mortality burden of children and
contributing a lot to the achievement of healthy
society. In relation to this, Ethiopia has developed a
comprehensive national child survival strategy, which
is part of the national HSDP-3, and is implementing
the IMNCI approach at a wide scale at health facility
and community levels. Currently the national IMNCI
coverage of the country at Health Center levels is
about 60%. These interventions at a community and
frontline health facilities (PHCU) levels are very
important to address the majority of the health
problems of children and also to make the services
close and easily available to the society.
27
28
RESULTS
General hospital information
All surveyed hospitals had isolated pediatrics OPD
and ward except Bishoftu hospital whose pediatric
inpatient room was part of the adult medical ward.
Separate pediatric waiting area and archive rooms
were found in only 3 and 2 hospitals respectively. Six
of the 8 hospitals had separate room for admitting
paediatric infectious cases while only 3 had separate
28
29
The pediatric service in these hospitals caters for
children up to the age of 14 years. Based on available
data for the period July 2006 to June 2007, there
were on average 29 (range 12-66) children seen in
the Paediatric OPD with about 5 admissions per day
(range 1-9). The two commonest causes of OPD
attendance and admission were severe pneumonia
and diarrhoea with severe dehydration or dysentery.
The mean bed capacity of the assessed hospitals
was 39 (range 11-68) and the average bed
occupancy rate was 58% (range 31% in Zewditu &
90% in Ambo). Children under 5 account for 64% of
admissions to the pediatric wards. Based on available
data from 5 hospitals, the average daily emergency
patient load was 7 and the average all cause mortality
in under fives was 11% (10-16%).
Drugs
Glucose 40% i.v.
Glucose 5% i.v.
Normal saline i.v.
Ringers lactate i.v.
Epinephrine (Adrenaline) s.c.
Corticosteroids i.v. or p.o.
Furosemide i.v.
Diazepam i.m., i.v.
Phenobarbital i.m., i.v.
Paracetamol
Ampicillin inj.
Benzyl penicillin
Cloxacillin
3rd generation Cephalosporins
Chloramphenicol
Gentamicin
*All anti-malaria drugs
Digoxin
F75 milk
F100 milk
Ready to Use Therapeutic Food
Vitamin K i.m. injection
ORS
Emergency area
Ward
Pharmacy/store
5 (63%)
6 (75%)
6 (75%)
8 (100%)
8 (100%)
6 (75%)
5 (63%)
5 (63%)
0 (0%)
6 (75%)
6 (75%)
5 (63%)
5 (63%)
3 (38%)
3 (38%)
5 (63%)
4 (50%)
3 (50%)
2 (25%)
3 (50%)
2 (25%)
0 (0%)
6 (75%)
6 (75%)
7 (88%)
6 (75%)
7 (88%)
7 (88%)
5 (63%)
5 (63%)
5 (63%)
0 (0%)
6 (75%)
4 (50%)
5 (63%)
5 (63%)
4 (50%)
3 (38%)
5 (63%)
4 (50%)
4 (50%)
6 (75%)
7 (88%)
5 (63%)
0 (0%)
7 (88%)
7 (88%)
8 (100%)
7 (88%)
8 (100%)
7 (88%)
7 (88%)
5 (63%)
5 (63%)
0 (0%)
8 (100%)
7 (88%)
7 (88%)
6 (75%)
5 (63%)
4 (50%)
6 (75%)
8 (100%)
6 (75%)
6 (75%)
7 (88%)
6 (75%)
3 (38%)
8 (100%)
29
30
Table 2: Availability of essential Equipments & supplies
No
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
Equipments
Resuscitation table/area
Torch
Otoscope
Scales for children
Stethoscopes
Thermometers
Heat source
Lumbar puncture set
Oxygen source:
oxygen cylinder
oxygen concentrator
central supply
Flow-meters for oxygen?
Equipment for the administration of oxygen?
nasal prongs
catheters
Masks
Self inflating bags for resuscitation
Masks
infant size
child size
adult size
Butterflies and/or cannulas of paediatric size
NG-tubes, paediatric size
Suction equipment
Nebulisers for administration of Salbutamol
Emergency area
Ward
Pharmacy/ store
5 (63%)
4 (50%)
5 (63%)
7 (88%)
7 (88%)
8 (100%)
1 (13%)
5 (63%)
7 (88%)
7 (88%)
1 (13%)
0 (0%)
7 (88%)
7 (88%)
0 (0%)
7 (88%)
0 (0%)
3 (38%)
2 (25%)
4 (50%)
6 (75%)
8 (100%)
7 (88%)
8 (100%)
2 (25%)
6 (75%)
7 (88%)
7 (88%)
1 (13%)
0 (0%)
7 (88%)
7 (88%)
0 (0%)
7 (88%)
1 (13%)
3 (38%)
3 (38%)
4 (50%)
6 (75%)
7 (88%)
8 (100%)
7 (88%)
0 (0%)
3 (38%)
4 (50%)
4 (50%)
0 (0%)
0 (0%)
5 (63%)
6 (75%)
0 (0%)
6 (75%)
0 (0%)
2 (25%)
0 (0%)
3 (38%)
1 (13%)
7 (88%)
4 (50%)
5 (63%)
0 (0%)
0 (0%)
4 (50%)
1 (13%)
7 (88%)
7 (88%)
7 (88%)
0 (0%)
0 (0%)
2 (25%)
0 (0%)
7 (88%)
7 (88%)
6 (75%)
0 (0%)
Emergency care
Most of the surveyed hospitals (5/8) were not
appropriately organized, fully staffed and equipped to
handle pediatric emergencies effectively. Most of
these hospitals were not practicing the standard
triage process by assessing children immediately on
arrival for emergency or priority signs before
administrative procedures. However, three hospitals,
two of them implementing the new hospital
improvement initiative, had assigned qualified nurses
30
31
Table 3: Summary of grading of the emergency setup in the hospitals
Standards and criteria
No
1
2
3
4
5
6
7
8
9
10
Children are assessed for severity/ priority signs (triaged) immediately on arrival as per
the ETAT standard
Patients do not have to wait for their turn, registration, payment etc. before a first
assessment is done and action taken.
A wall chart or job aid for identifying children by severity of condition is located in the
emergency admissions area.
Drugs, equipment and supplies
Essential drugs for emergency conditions (anticonvulsants, glucose, iv fluids) are
always available and free of charge to the family
Essential lab tests (glucose, Hb or PCV) are available and results are obtained timely
Essential equipment (needles and syringes, naso-gastric tubes, oxygen equipment,
self-inflating resuscitation bags with masks of different sizes, nebulisers or spacers) is
available
Staffing
A qualified staff member is designated to carry out triage.
A health professional is available without delay to manage children determined to have
an emergency condition.
Case management
Staff doing triage is trained in the ETAT guidelines and can implement them
appropriately when the emergency room gets busy during peak hours
Staff is skilled in the management of common emergency conditions and starts
treatment without delay: Management of convulsions, lethargy, severe respiratory
distress, shock and severe dehydration.
Good
To be
improved
0 (0%)
8 (100%)
0 (0%)
8 (100%)
0 (0%)
8 (100%)
0 (0%)
8 (100%)
4 (50%)
4 (50%)
0 (0%)
8 (100%)
3 (38%)
5 (63%)
3 (38%)
5 (63%)
0 (0%)
8 (100%)
0 (0%)
8 (100%)
Pediatrics ward
Table 4 summarizes the status of the 8 hospitals against the WHO standards and criteria for pediatric wards.
31
32
32
33
Table 4: Standard's for children ward
No
Good
Children are seen in OPD only by the designated health professional in the designated
room/area.
Closest attention for the most seriously ill
The most seriously ill children are cared for in a section where they receive closest
2
attention.
Separate ward for children.
4
Children are kept in a separate ward or separate area of a ward.
Severely ill children are kept apart from adults in wards such as for infectious diseases
5
or intensive care.
Children with surgical conditions are at least kept in a separate room, with staff aware of
6
the special needs for children such as feeding and warmth.
7
Arrangements are made to meet these needs.
8
In cold climates, the ward has an efficient and safe heat source.
Separate room for sick neonates with mothers
9
Sick new-borns are kept separate from healthy babies.
10
Mothers of sick new-borns are rooming in with their babies, and have adequate facilities.
Hygiene and accident prevention
Staff has access to hand washing facilities The ward is kept clean and dangerous items
11
are inaccessible for children
12
Sharps are disposed of in a special container preventing accidents
Hygienic and sufficient services facilitate the stay of mother and child
13
There are sufficient and adequate toilets which are easily accessible
Mothers have access to running water and to an appropriate space, near the ward, to
14
wash themselves and their child.
1
To be
improved
6/7 (86%)
1/7 (14%)
0 (0%)
8 (100%)
7 (88%)
1 (13%)
4 (50%)
4 (50%)
3 (38%)
5 (63%)
1 (13%)
0 (0%)
7 (88%)
8 (100%)
3 (38%)
0 (0%)
5 (63%)
8 (100%)
3 (38%)
5 (63%)
8 (100%)
0 (0%)
0 (0%)
8 (100%)
0 (0%)
8 (100%)
15
Mothers have access to a washing facility, in order to wash her and her childs clothes.
0 (0%)
8 (100%)
16
17
4 (50%)
6 (75%)
4 (50%)
2 (25%)
33
34
In the majority of cases, differential diagnosis of fever
was not considered exhaustively and investigations
were incomplete. In some instances planned LP tests
were not done and patients were treated empirically.
Inappropriate choice and administration of antibiotics
was observed and documentation of patient progress
and treatment given was not up to the standard in
almost all hospitals. Overall, patient records and
monitoring charts were poorly recorded.
Monitoring of patients
All admitted children were assessed by a doctor at
admission and majority of them were re-evaluated
about once a day during working days and upon
consultation during weekends. A qualified nurse was
available 24 hours per day in the children's wards in
all hospitals and a medical doctor in 6 of them.
Nutritional status was assessed at admission using
weight for age in most hospitals. All patients had
individual charts, vital sign and medication sheets, but
the case histories, progress notes and the other
34
35
Neonatal care
Early and exclusive breastfeeding, skin to skin
contact and proper thermal protection was not
practiced adequately in almost all hospitals. Eye and
Vitamin K prophylaxis and immunizations were given
routinely in only 2 hospitals. Neonatal resuscitation
flow chart was available in only one hospital.
Good
2/6 (33%)
1/6 (17%)
To be improved
4/6 (67%)
4/6 (67%)
1/6 (17%)
5/6 (83%)
1/6 (17%)
5/6 (83%)
Summary
The following table and figures 1 & 2 show the
summarized score by major sections of the
assessment and by facility. Table 6 is a summary
sheet showing the details of the summary scores of
the 8 hospitals in the different service areas.
35
36
Table 6: Details of summary score of the 8 hospitals in the different service areas
No
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
Good
5
4
6
1
3
1
2
2
5
1
1
1
2
30
To be improved
3
2
1
5
3
2
6
2
8
5
6
5
1
7
6
4
6
1
4
4
5
84
222
2.98
2
4
1
6
7
1
4
3
68
NB: - ** = Five of 8 hospitals had a summary score of 3 out of 5, while 3 hospitals has a summary score of 2 out of 5 for
emergency drugs, supplies and equipment section.
36
37
Figure 1: Average summary score of the different pediatric care services out of a maximum score of 5
2.3
2.4
2.5
Hospital administration
2.5
Monitoring
Access to hospital
2.6
2.6
2.8
Supportive care
2.8
2.9
3.0
3.0
3.1
3.3
Diarrhoea mgt
3.3
3.6
Cough mgt
3.8
Laboratory support
4.4
HIV/AIDS mgt
0.0
1.0
2.0
3.0
4.0
37
5.0
38
Figure 2: Total summary score of the 8 hospitals, out of a total score of 5
5.0
4.0
3.4
3.1
2.9
3.0
3.0
2.9
3.1
3.0
Yirgalem
Zewditu
score
2.6
2.0
1.0
0.0
Adama
Ambo
Bishoftu
Debre Birhan
Dessie
Yekatit 12
Hospitals
Despite the potential limitations, this study provides
some basic information about the status of pediatric
hospital care that could guide the national efforts in
improving the quality of referral care for children.
38
39
essential for the proper implementation of ETAT.
Even though the current quality improvement process
through the hospital BPR initiative is a very good
opportunity for the overall improvement of hospital
care for children, the centralized triaging mechanism
that keeps patients of all age groups together in one
waiting area is not conducive for the effective
implementation of the ETAT standards.
Generally, there was lack of some essential drugs
and materials such as nasal prongs, infant and child
size bag & masks, nebulizers, heaters and oxygen
concentrators. The total absence of long acting
parenteral
anti-convulsants
poses
serious
shortcoming in the management of pediatric
neurologic emergencies.
In almost all hospitals, there was no clearly
designated and properly arranged/equipped high
dependency area where very sick children receive
highest attention. Majority of the hospitals (5/8) do not
have any special arrangement and facilities for
providing appropriate neonatal care.
Hygienic facilities were below the expected standard
in majority of the hospitals and none of the hospitals
provide appropriate routine pediatric diet for children.
Overall, the case management of common neonatal
and childhood illnesses was not optimal. None of the
hospital staff had been trained in ETAT and there
were no job aids or protocols for pediatric referral
care which could partly contribute to the problems
observed in the case management.
In summary, the quality of pediatric referral care
needs serious attention and coordinated systematic
improvement effort using the opportunity of the
national hospital management initiative and the BPR
process to institutionalize ETAT and standards of
hospital care for children. This has to be
complemented with availing of appropriate job aids,
essential supplies and equipment, and improvement
of health worker skills through training, clinical
mentoring and regular supportive supervision.
39
40
RECOMMENDATIONS
1. The ETAT standards should be incorporated into the Ethiopian Hospital Management Initiative blue print and the
BPR documents by the FMOH to ensure its systematic implementation.
2. National plan of action should be developed for systematic and phased implementation of ETAT in referral
hospitals.
3. Staff should be trained in ETAT through in-service courses & ETAT should also be introduced into the pre-service
teaching to ensure its sustainability.
4. National pediatric referral care protocol & job aids should be availed in all hospitals
5. Coordinated efforts and more resources needed for availing essential drugs, supplies and equipments in all
hospitals.
6. All hospitals should have arrangements/rooms for the care of sick neonates, high-dependency areas for critically
sick children and isolation rooms for infectious cases.
7. Efforts should be made to improve the hygienic facilities & the quality of routine hospital diet for children.
8. The recording and reporting system in the hospitals need to be improved and pediatric data should be
disaggregated by appropriate age categories.
9. Mechanisms for regular supportive supervision and mentoring needed to achieve sustained improvement in the
quality of pediatric referral care.
10. The Ethiopian Pediatric Society, the Medical teaching institutions, WHO, UNICEF and other partners should
support the quality improvement process.
40
41
ACKNOWLEDGEMENTS
We would like to thank the FMOH especially the former Family Health and Health Services Departments, the
Directors and staff of the surveyed hospitals for facilitating the whole process. We are very grateful to the World
Health Organization for the financial and technical support provided for the assessment. Sincere gratitude is
expressed to Dr Neghist Tesfaye (FMOH), Dr Teshome Desta (WHO/ICST-ESA), Dr Wilson Were (WHO/HQ)
and Prof. Elizabeth Molyneux (Queen Elizabeth Central Hospital, College of Medicine, Blantyre/Malawi) for their
valuable technical support.
41
42
Management of severe acute malnutrition in children using community based therapeutic care approach:
a review of three years data from southern Ethiopia.
Efrem Teferi, MD1, Shiferaw Teklemariam, MD, MPH1 , Lopiso Erosie, BSC, MPH1 , Abel Hailu, MD1
Tefera Belachew, MD, MSc, DLSHTM2, Mohammed A Yassin, MD, MSc, PhD1,3
Abstract
The objective of the study is to assess the outcome of community-based therapeutic care (CTC) for children with severe
malnutrition in Southern Ethiopia. Diagnosis of severe malnutrition was made based on anthropometric measurement and
all children received therapeutic food according to the protocol and were discharged from the feeding program when they
their weight for height was more than 80% of the reference for 2 consecutive weeks. Data on the number of admissions,
discharges, weight gain and length of stay in the program were recorded using standard formants and reports were sent to
the Regional Health Bureau monthly. The data was entered using EPI-Info proportions and means were compared using
chi-square test. This is a retrospective review of reports retained in the Bureau. A total of 12,316 patients with severe acute
malnutrition, 56.2% marasmic and 43.8% kwashiorkor cases were treated in CTC program from 2003 to 2005. The average
cure and death rates were 91% (9871) and 2.5% (217) and the average weight gain was 5.3 and 5.8 grams /kg/day and the
average length of stay was 49 and 42 days for cases of Marasmus and Kwashiorkor, respectively. Except for weight gain
and length of stay, our findings exceeded the minimum sphere standards for treatment outcome measures. In conclusion
the CTC approach has a comparable outcome to Therapeutic feeding centers and could be expanded quickly during
emergency situation. As majority of patients are treated at home, the workload for the health worker would be reduced, so it
is an alternative approach for management of severe malnutrition where human resource and space in health facilities are
limited.
42
43
Introduction
Ethiopia has a long history of food insecurity and
nutritional problems affecting a large proportion of the
population. (1) Even during a relatively non-drought
years, malnutrition in children in Ethiopia is extremely
high exposing the survival of this group of the population
at a great threat. An estimated 47% of Ethiopias underfive children are moderately or severely stunted
contributing to an under five-mortality rate of 123/1000
live births. (2) Ethiopia stands 6th among countries with
the highest number of under-five deaths in the world, with
more than 472,000 under-five dying each year, (3)
Malnutrition, even in its milder form, accounts directly or
indirectly for 53% of all under-five deaths in Ethiopia (4).
43
44
CTC was introduced in SNNPR in 2003 and expanded in
2004 and 2005. It integrates supplementary and
therapeutic feeding with an emphasis on outreach and
community based support. In out patient therapeutic
program (OTP), the therapeutic product used is ready to
use (plumpy nut and BP 100 biscuit) with outpatient drug
treatment protocol. There were few referrals for inpatient
treatment, which includes those with complication and
who were admitted in stabilization centers (SC) and
Results
A total of 12,316 patients with severe acute malnutrition,
56.2% marasmic and 43.8% kwashiorkor cases were
treated in CTC program from 2003 to 2005. Of these,
1540 (12.5%) were treated in 2003, 1955 (16%) in 2004
and 8791(71%) in 2005. The majority (90%) of the cases
were age between 6 months to 5 years old. The average
cure and death rates for the region were 91% (9871) and
2.5% (217) respectively. The highest (99%) cure rate
44
45
2. The outcome of patients treated in CTC was
comparable to those treated in TFC in the region during
However, there was statistically significant difference in
the mean length of stay which were 21 and 25 vs. 42 and
49 days for marasmus and kwashiorkor patients
respectively and the average weight gain of 13.4 and14
the same period with cure rate of 91% vs. 87% (p>0.05)
and death rates of 2.5% vs. 3.6% (p>0.05), respectively.
vs. 5.3 and 5.8 g/kg/day for patients treated in TFC than
in CTC (p<0.01 for both) (Table 3). A similar trend was
observed when the outcome from the CTC program was
compared to the sphere standard as shown in Table 4.
Discussion
Given the spatial arrangement of health service
units and their limited capacity to handle a large
number
of
cases
of severe acute malnutrition during emergency and
crisis in Ethiopia, seeking an alternative solution for
management of such cases cannot be overlooked.
Community base therapeutic care provides a
promising alternative option to the TFCs and facilitybased stabilization centers (9-12). Though CTC
cannot totally replace an inpatient therapeutic care
as some cases with complications, such as
infections, may still need an inpatient care, it is
complementary to therapeutic and supplementary
feeding programs (9).
45
46
was no information on the follow up of individual
cases and suffers incompleteness and missing data.
46
47
-11Table 1: Outcome of cases of severe acute malnutrition treated in the CTC program from 20032005, South Ethiopia
Woredas
Total Discharged
Dalocha
Lanfuro
Malgano
Boricha
Arbegona
Bensa
Bedessa
Shebedino
Awssa Zu.
Boloso Sore
Offa
Damot Gale
Humbo
Sodo Zurria
Modulla
Karat
Total
762
907
1159
1255
248
213
399
575
748
2593
801
578
159
278
313
1328
12316
680
901
1011
1152
230
68
237
518
535
2586
741
521
149
207
163
1132
10831
Zone
Silte
Sidama
Wolaita
Kembata T.
Konso
631
795
815
1140
215
61
206
495
479
2408
641
514
142
185
141
1003
9871
92.79
88.24
80.61
98.96
93.48
89.71
86.92
95.56
89.53
93.12
86.50
98.66
95.30
89.37
86.50
88.60
90.9
19
21
14
16
1
2
20
7
11
43
20
4
5
9
6
19
217
2.8
2.3
1.4
1.4
0.4
2.9
8.4
1.4
2.1
1.7
2.7
0.8
3.4
4.3
3.7
1.7
2.5
47
48
-12Table 2: Mean length of stay and average weight gain for cases of severe acute malnutrition
admitted to the Community based Therapeutic care program from 2003 to 2005, South Ethiopia.
Centers
days
Marsmus
Kwashiorkor
Marasmus
Kwashiorkor
Dalocha
63
47
5.2
4.0
Lanfuro
61
40
5.6
5.1
Malgano
37
32
7.8
10.0
Shebedino
40
32
4.6
5.0
Awassa Zu.
59
47
3.0
2.8
Arbegona
58
50
5.2
4.4
Boricha
45
32
6.0
5.5
Bedessa
70
66
3.0
18.0
Offa
62
52
3.9
3.1
Sodo Zur.
40
42
7.5
4.8
Boloso So.
58
52
5.0
4.2
Damot Ga.
36
33
5.4
4.4
Humbo
41
30
5.5
3.8
Modulla
32
30
5.3
6.3
Karat
39
37
6.0
5.6
Regional average
49.4
41.5
5.3
5.8
48
49
-13-
Cure
rate
Death
rate
weight
gain
Marasmus
Kwashiorkor
Marasmus
Kwashiorkor
TFC
87.2
3.6
25
21
14
13.4
CTC
91
2.5
49
42
5.3
5.8
Table 4: Outcome of children treated by the Community based Therapeutic care e program from
2003- 2005 compared to the minimum sphere standard, South Ethiopia.
Indicator
Cure rate
Death rate
Mean weight gain
Mean duration of stay
90.9%
<10%
2.5%
>8grams/kg/day
30-40 days
42-49 days
49
50
*Guideline for management of severe acute malnutrition,FMOH,2007, Referrence.22
References
1. Birhane G. Running a national early warning system: the Ethiopian experience, Addis Ababa Relief
and Rehabilitation commission, 1991.
2. CSA & ORC Macro (Central Statistical Authority (Ethiopia) and OCR Macro), 2006, Ethiopia
Demographic and Health Survey 2005. Addis Ababa, Ethiopia and Calverton, Maryland, U.S.A:
Central Statistical Authority and OCR Macro.
3. Robert E Black, Saul S Morris, Jennifer Bryce. Where and why are 10 million children dying every
year? The Lancet 2003;28: 361,
4. BASICS II. Basic support for institutionalizing child survival. The Second Child Survival Revolution,
Summary of the Lancet Child Survival Series: BASICS II, 2003.
5.
Pelletier, D., & E. Frongillo. 2002. Changes in Child Survival are Strongly Associated with
Changes in Malnutrition in Developing Countries. FANTA, Academy for Educational Development:
Washington DC, USA.
6. Federal Ministry of Health, Family Health Department. National strategy for child survival in
Ethiopia, Addis Ababa, July 2005.
7. WHO. Reducing severe and moderate malnutrition in Children. Bull WHO 1995, 73(4): 443-48.
8. Teferi E et al. Treatment Outcome of children admitted to Therapeutic Feeding centers in Southern
Region. (in press).
9. De Waal, A. Taffesse, L. Carruth . Child survival during the 20022003 droughts in Ethiopia,
Special Issue:
50
51
11. Collins, S. Changing the Way we Address Severe Malnutrition during Famine. The Lancet 2001,
358:498-501.
12. Collins, S. and Sadler, K. The Outpatient care for severely malnourished children in emergency
relief programs: a retrospective cohort study. The Lancet 2002, 360:1824-30.
13. Community based therapeutic care (CTC) in Ethiopia. Proceeding of workshop in Addis Ababa,
Ethiopia, 22- 23 June 2004.
14. Federal MoH/UNICEF/MOST. Guideline for enhanced outreach strategy (EOS) for child survival
interventions, revised version, Addis Ababa. July 2005.
15. EL HadjiIssakhaDiop, Nicolle Idohou, Marieb am Adeline Ndour, Andre Brined and Salimata Wade.
Comparison of
the efficacy of ready to use food and liquid milk Based diet for rehabilitation of severely
malnourished children. Am Clin Nutr 2003; 78: ; 302-7.
16. Steve Collins, Kate Sadler, Outpatient care for severely malnourished children in emergency relief
programmes; a retrospective Cohort study. The Lancet 2002;360;1824-30.
17. Community based approach to managing severe malnutrition, Proceedings of an interagency
workshop, Dublin October 2003.
18. Federal Ministry of Health . National guideline for the management of severe acute malnutrition for
Ethiopia. MoH, Addis Ababa, May 2004.
51
52
Acknowledgments
We would like to thank members of Laboratory and Research Department for their valuable comments on
the draft. We also thank save the children USA, International Medical Corpus, Action Contra La Faim for
helping to implement the program and health workers in zones and woreda for working hard to save the
lives of patients. I t would have been difficult to implement the program with out the help of UNICEF (United
Nations Childrens Fund), who provided therapeutic products drugs, and conducted trainings in cooperation
with Regional Health Bureau.
52
53
CHILD SURVIVAL: PROGRES TOWARDS MEETING MDG4
Assaye Kassie1
Abstract
Few causes are responsible for the majority of under-five deaths in Ethiopia: pneumonia (28%), neonatal causes
(25%), malaria (20%), diarrhea (20%), measles (4%) and AIDS (1%). To prevent these deaths, and to achieve
Millennium Development Goal 4 (MDG4) (to reduce by two thirds, between 1990 and 2015, the under 5 mortality
rate), it is necessary to ensure the implementation of cost-effective interventions that are listed in the National Child
Survival Strategy.
There are examples of remarkable achievements in coverage increase within short time periods, including training of
30,000 Health Extension Workers (HEWS) in the last 4 years, rapid increase, from 1% in 2005 to 42% in 2007, in
percentage of children under the age of five years who slept under a Long Lasting Insecticide-treated Nets (LLINs),
and increase in coverage of Vitamin A supplementation from 45 % in 2005 to 91% in 2007. These successes can
serve as benchmarks to scaling up of other interventions.
Among the major killers, the ones that are poorly addressed are childhood pneumonia and perinatal problems which
are the leading causes of under-five mortality in Ethiopia. Realizing the continuum of care approach at delivery level
and sustaining it over time, and searching for an alternative way of improving access to treatment of childhood
pneumonia and essential newborn care, are crucial challenges for child survival in Ethiopia.
Furthermore, there is growing consensus that a primary bottleneck to achieving MDGs in low-income countries is
health systems that are too fragile and fragmented to deliver the volume and quality of services to those in need. Major
shortfalls are identified in the health workforce, lack of donor coordination, and week information systems. It is for this
reason that the Health Sector Development Programme (HSDP) in Ethiopia is focusing on cost-effective health
interventions and on health systems strengthening in order to achieve the dual goals of improving population health
and reducing health inequalities.
53
54
54
55
Other, 2%
Measles, 4%
AIDS, 1%
Neonatal, 25%
Diarrhea, 20%
Malnutrition
57%
HIV/AI
DS
Malaria, 20%
Pneumonia,
28%
Congenital
4%
Causes of
neonatal
deaths
followed
by
perinatal
asphyxia
prematurity/low birth weight (Figure 2).
Other
7%
Diarrhoea
3%
Tetanus
7%
and
Asphyxia
25%
Preterm birth
17%
Infection
37%
55
56
survival series estimated that, with 99% coverage
sufficient evidence for effect in prevention or
treatment, it would be possible to prevent 65% of
deaths
due to pneumonia, 55% of deaths due to
neonatal complications, 91% of deaths due to
malaria, 88% of deaths from diarrhea, 100% of
deaths from measles, and 48% of those due to
AIDS (12).
160
165
153
140
123
120
109
89
80
HSDP I
95
54
II
40
0
1990
1995
Current Trend
2000
2005
Years
2010
2015
MDG Trend
Figure 3. Trend in under 5 Mortality Rate in the period 1990-2005 and projections until
2015 in Ethiopia.
56
57
4) Opportunities to achieve MDG4:
implementation of child survival interventions
An integrated approach is in place in order to
achieve MDG 4, with:
Focus on the community: Ethiopia is investing
a lot in the Health Extension Program (HEP) to
reach the poorest of the poor with basic and
essential life saving care by focusing mainly on
the mothers, newborns and children of the rural
population.
HEP
institutionalizes
and
standardizes the village health-care delivery
system to empower care-takers, families and
communities to take care of their own health. It
Child Survival Strategy: HSDP III is
incorporated as the de facto health component of
the Plan for Accelerated and Sustained
Development to End Poverty (PASDEP) (15).
Maternal and Child Health (MCH) are major
focuses of HSDP III, with Child Survival Strategy
being a major component of HSDP III.
Availability of Experienced Programs: there
are experienced programs relevant to child
health in Ethiopia, including EPI, Integrated
5) Benchmarks: scaling-up is possible
Through proper and rational utilization of
available opportunities in the country, it is
possible to scale up the implementation of high
impact child survival interventions. These are
some examples of successes and remarkable
achievements in coverage increase within short
time periods that can serve as benchmarks to
57
58
12,000,000
10,000,000
8,269,753
8,000,000
10,154,375
8,269,753
6,000,000
4,946,811
4,946,811
4,000,000
2,576,620
2,000,000
1,389,438
0
2004 - 1st
ROUND
2004 - 2nd
ROUND
2005 - 1st
ROUND
2005 - 2nd
ROUND
2006 - 1st
ROUND
2006 - 2nd
ROUND
2007 - 1st
ROUND
2007 - 2nd
ROUND
Figure 4. Coverage in Vitamin A supplementation among children aged 6-59 months in Ethiopia during
the period 2004-07.
58
59
59
60
References
1. Child health in Ethiopia. Background document for the National Child Survival Conference April
22-22, 2004, Addis Ababa, Ethiopia. World Health Organization, Addis Ababa.
2. [http://www.afro.who.int/cah/documents/situational_analysis/et_final_cs_situation_analysis.pdf.
Accessed June 2008].
3. CSA, 2006. Ethiopia Demographic and Health Survey 2005. Central Statistic Agency, Addis Ababa
and ORC Macro, Calverton.
4. Editorial, 2003. The worlds forgotten children. The Lancet, 361: 1.
5. FMOH, 2004. National review and planning meeting. Report of the Family Health Department of
the FMOH. Federal Ministry of Health, Addis Ababa.
6. FMOH, 2005a. National strategy for child survival. Family Health Department. Federal Ministry of
Health, Addis Ababa.
7. FMOH, 2005b. HSDP III. Health Sector Strategic Plan 2005/06-2009/10. Federal Ministry of
Health, Addis Ababa.
8. FMOH, 2007a. Health and health related indicators2006/07. Federal Ministry of Health, Addis
Ababa.
9. FMOH, 2007b. Annual performance report of HSDP III. EFY 1999 (2006/2007). Federal Ministry of
Health, Addis Ababa.
10. FMOH, 2008a. National Malaria Indicator Survey. Federal Ministry of Health, Addis Ababa.
11. FMOH, 2008b. IMNCI and C-IMNCI national review meeting. Report of the Family Health
Department of the FMOH. Federal Ministry of Health, Addis Ababa.
12. Gareth, J., Steketee, R., W., Black, R., E., Bhutta, Z. A., Morris S. S., and the Bellagio Child
Survival Study Group, 2003. How many children deaths can we prevent this year? The Lancet,
362: 65-71.
13. Gwatkin, D.R., 2000. Health inequalities and the health of the poor: What do we know? What can
we do? Bull. World Health Organ. 78, 3-17.
14. Lawn J., Kerber, K., 2006. Opportunities for Africas newborns. Practical data, policy and
programmatic support for newborn care in Africa. The partnership for maternal newborn and child
health, Cape Town.
15. MOFED, 2007. Ethiopia: Building on progress. A Plan for Accelerated and Sustained Development
to End Poverty (PASDEP). Annual Progress Report 2006/07. Ministry of Finance and Economic
Development, Addis Ababa.
16. Save The Children, 2006. New Report shows improvements in child survival in Africa , but more
than a million African babies die in the first month of life. Save The Children, US.
60
61
17. Schuftan C., 1990. The child survival revolution: a critique. Family practice, 7(4):329-332.
18. Travis, P., Bennet, S., Haynes, A., Pang, T., Bhutta, Z., Hyder, A.A., Pielemeier, N.R., Mills, A.,
Evans, T., 2004. Overcoming health-systems constraints to achieve Millennium Development
Goals. Lancet, 364: 900-906.
19. UNICEF, 1996. The state of the World Children 1996. The 1980s: Campaign for child survival.
page 1-5. United Nations Childrens Fund, New York.
20. UNICEF, 2006. Preliminary Report. Trends in Child Mortality in Eastern and Southern Africa 19902005. United Nations Childrens Fund, New York.
21. World Bank, 2003. The Millennium Development Goals for Health: Rising to the Challenges (draft).
World Bank, Washington, DC.
61
62
Abstract
A 10 year old female patient presented with progressive right eye proptosis ( Fig 1) and skin
rash of three years duration was seen at Tikur Anbessa Specialized Hospital, department of
pediatrics hematology /oncology unit. Physical examination showed mildly decreased visual acuity
and cafe au lait spot ( Fig 2) AND axillary freckling and Orbital CT ( Fig 3) showed right
intraorbital mass with an assessment of right optic nerve glioma she is to be started on weekly
vinblastine at a dose of 6mg/m2.
62
63
INTRODUCTION
Optic nerve glioma (also known as optic pathway
glioma) is the most common primary neoplasm of
the optic nerve. Along with reducing visual acuity
in the affected eye, the tumor sometimes
produces additional symptoms as it grows. A lowgrade form of this neoplasm, benign optic glioma,
occurs most often in pediatric patients. Another
form, aggressive glioma, is most common in
adults; it is frequently fatal, even with treatment.1
Optic-pathway glioma accounts for 1-5% of all
brain tumors in children [1]. About half of these
cases occur in children with neurofibromatosis
type 1 [2]. The diagnosis is usually rendered
before age 6 years, although there are some
reports of older ages [3,4]. The vast majority of
optic-pathway gliomas in children are pilocytic
astrocytomas [2,5]. The tumor may arise
anywhere along the optic pathway, from just
behind the globe to the lateral geniculate body
[5,6]. In patients with neurofibromatosis type 1,
the tumor is usually smaller than in sporadic
(non-neurofibromatosis type 1-associated) cases
[5,7].
The clinical presentation is variable. In patients
with neurofibromatosis type 1, 40-80% of opticpathway gliomas are asymptomatic at diagnosis,
whereas in sporadic cases, they are symptomatic
[3,5,8-10]. The most common signs are visionrelated: mainly visual loss, decreased visual
acuity, and strabismus. Other findings include
endocrine disturbances, signs of increased
intracranial pressure, and hydrocephalus
[2,5,8,9,10-13]. Ophthalmologic examination
may reveal decreased visual acuity, pathologic
visual fields, proptosis and more [9,10,13,14].
The generally young age of the children and high
prevalence of neurofibromatosis
type 1associated attention deficit hyperactivity disorder
render the ophthalmologic examination difficult,
and decrease its sensitivity and specificity [2,15].
Early diagnosis is important so that the tumor can
be carefully monitored and treatment can be
administered early, before visual deterioration.
The diagnosis can be made functionally by
visual-evoked potentials, but as is
Ababa University.
history
of
optic-pathway
gliomas
in
neurofibromatosis type 1 is considered
unpredictable [2,26]. Hence deciding
whether, or when, to initiate treatment becomes
difficult. The presence of an optic-pathway
glioma in a patient without neurofibromatosis
type 1 is considered an indication for treatment
[5]. Although neurofibromatosis type 1 is thought
to be relatively benign, given the risk of visual
impairment, blindness, neurologic deficits, or
death [27,28], patients affected by the tumor
should be monitored routinely for its size and
visual function, and an adverse change in either
should be considered an indication for treatment
[2]. If a glioma tends to remain stable, the
63
64
intervals between
magnetic resonance
examinations can be gradually increased [10].
Nevertheless, the subjective timing of imaging
scans and the lack of objective references to
identify deviations from normality place patients
at risk of either unnecessary or insufficient
neuroimaging. An optic-pathway glioma tends to
grow along the optic pathways by increasing its
width, rather than as one concentric mass that
grows in all directions [5]. As such, stereotypical
patterns of growth as seen on imaging scans of
children with optic-pathway glioma are often
highly comparable, because the tumor tends to
involve the same brain structure, and the
manner of growth is very similar.
CASE REPORT
Fig 1
64
65
Fig 2
65
66
Fig 3
Discussion
ophthalmologic
feasible.
and
Orbital
CT/MRI
if
66
67
References
1.
Alshail E, Rutka JE, Becker LE, Hoffman HJ. Optic chiasmatic-hypothalamic glioma. Brain Pathol
1997;7:799-806.
2.
Shuper A, Horev G, Kornreich L, et al. Visual pathway glioma: An erratic tumor with therapeutic
dilemmas. Arch Dis Child 1997;76: 259-63.
3.
4.
Listernick R, Ferner RE, Piersall L, Sharif S, Gutmann DH, Charrow J. Late-onset optic pathway
tumors in children with neurofibromatosis1. Neurology 2004;63:1944-6.
5.
Kornreich L, Blaser S, Schwarz M, et al. Optic pathway glioma: Correlation of imaging findings with
the presence of neurofibromatosis. AJNR 2001;22:1963-9.
6.
Liu GT, Brodsky MC, Phillips PC, et al. Optic radiation involvement in optic pathway gliomas in
neurofibromatosis. Am J Ophthalmol 2004;137:407-14.
7.
8.
Guillamo JS, Creange A, Kalifa C, et al. Prognostic factors of CNS tumors in neurofibromatosis 1
(NF1): A retrospective study of 104 patients. Brain 2003;126:152-60.
9.
Czyzyk E, Jozwiak S, Roszkowski M, Schwartz RA. Optic pathway gliomas in children with and
without neurofibromatosis 1. J Child Neurol 2003;18:471-8.
10.
Listernick R, Charrow J, Greenwald M, Mets M. Natural history of optic pathway tumors in children
with neurofibromatosis type 1: A longitudinal study. J Pediatr 1994;125:63-6.
11.
Cnossen MH, Stam EN, Cooiman LC, et al. Endocrinologic disorders and optic pathway gliomas in
children with neurofibromatosis type1. Pediatrics 1997;100:667-70.
12.
Shuper A, Kornreich L, Michowitz S, Schwartz M, Yaniv I,Cohen IJ. Visual pathway tumors and
hydrocephalus. Pediatr Hematol Oncol 2000;17:463-8.
13.
Khafaga Y, Hassounah M, Kandil A, et al. Optic gliomas: A retrospective analysis of 50 cases. Int J
Radiat Oncol Biol Phys 2003;56:807-12.
14.
67
68
15.
Wolsey DH, Larson SA, Creel D, Hoffman R. Can screening for optic nerve gliomas in patients with
neurofibromatosis type I be performed with visual-evoked potential testing? J AAPOS 2006;10:30711.
16.
North K, Cochineas C, Tang E, Fagan E. Optic gliomas in neurofibromatosis type 1: Role of visual
evoked potentials. Pediatr Neurol 1994;10:117-23.
17.
Pepin SM, Lessell S. Anterior visual pathway gliomas: The last 30 years. Semin Ophthal.
2006;21:117-24.
18.
Van Es S, North KN, McHugh K, De Silva M. MRI findings in children with neurofibromatosis type
1: A prospective study. Pediatr Radiol 1996;26:478-87.
19.
Chateil JF, Soussotte C, Pedespan JM, Brun M, Le Manh C, Diard F. MRI and clinical differences
between optic pathway tumours in children with and without neurofibromatosis. Br J Radiol
2001;74:
24-31.
20.
Parsa CF, Hoyt CS, Lesser RL, et al. Spontaneous regression of optic gliomas: Thirteen cases
documented by serial neuroimaging. Arch Ophthalmol 2001;119:516-29.
21.
Chan MY, Foong AP, Heisey DM, Harkness W, Hayward R, Michalski A. Potential prognostic
factors of relapse-free survival in childhood optic pathway glioma: A multivariate analysis. Pediatr
Neurosurg
1998;29:23-8.
22.
Grill J, Laithier V, Rodriguez D, Raquin MA, Pierre-Kahn A, Kalifa C. When do children with optic
pathway tumors need treatment? An oncological perspective in 106 patients treated in a single
center. Eur
J Pediatr 2000;159:692-6.
23.
24.
Tow SL, Chandela S, Miller NR, Avellino AM. Long-term outcome in children with gliomas of the
anterior visual pathway. Pediatr Neurol 2003;28:262-70.
25.
Balcer LJ, Liu GT, Heller G, et al. Visual loss in children with neurofibromatosis type 1 and optic
pathway gliomas: Relation to tumor location by magnetic resonance imaging. Am J Ophthalmol
2001;131:442-5.
26.
Serova NK, Lazareva LA, Gorelychev SK, Ozerova VI, Pronin IN. A follow-up of patients with
anterior optic tract glioma concurrent with type 1 neurofibromatosis. Vestn Oftalmol 2006;122:3942.
68
69
27.
Luh GY, Bird CR. Imaging of brain tumors in the pediatric population. Neuroimag Clin North Am
1999;9:691-716.
28.
Acknowledgments
I would like to thank Dr David N Korones pediatric oncologist at Rocester medical center , New
York and Dr Ibrhaim Qaddumi , oncologist at St Jude Childrens Research hospital for their
constructive ideas and providing me with important references.
69
70
Abstract
The aim of the study is to identify simple clinical signs and symptoms in under five children which are
predictors of pneumonia at Tikur Anbesa Specialized Hospital (TASH), Department of Pediatrics and
Child Health, emergency and regular out-patient units. The design of the study is a prospective crosssectional study carried out during Aug 2004 Sep 2005. All children between the age of 2-59 months who
attended the regular and emergency pediatrics units at TASH during the study period who had either cough
or difficulty of breathing or chest x-ray evidence of pneumonia were included in the study. A calculated
sample of 164 was taken. Data analysis was done using SPSS and EPINFO version 1.1.2. Chi-square test
was used to calculate the differences in distribution of clinical signs and symptoms between groups with
and without chest x-ray (CXR) evidence of pneumonia.
A total of 179 patients were studied of whom 102 were males and 77 females (M:F 1:0.75). Clinical
symptoms and signs were related to CXR pneumonia. Tachypnea (94.5% with CXR pneumonia Vs 59.3%
without CXR pneumonia) and retraction (86.3% CXR Vs 40.6% without CXR pneumonia) were the best
clinical predictors of pneumonia. Tachypnea, flaring of alae nasi and retraction were also independently
associated with CXR pneumonia. Vomiting, refusal to feed, history of rapid breathing , grunting and chest
findings did not predict pneumonia.
In conclusion pneumonia is a significant cause of morbidity and mortality in developing countries like
Ethiopia . Using
simple clinical indicators pneumonia can be diagnosed by primary health workers and mortality can be
reduced
significantly.
70
71
INTRODUCTION
Around 10.6 million children die every year before reaching
their 5th birth day. Almost all of these deaths occur in low
income and middle income countries mainly in Africa and
south east Asia. Most deaths among under fives are still
attributable to just a handful of conditions, acute respiratory
infection(ARI) mostly pneumonia accounts for 19% of all
deaths(1,2,3,). Age Specific mortality
from lower
respiratory infection( LRI) in young Gambian children has
been estimated at 10 per 1000 each year(4 ) . In Ethiopia
infant mortality rate is 77 per 1000, under five mortality is
120 per 1000 (5), ARI being one of the major cause of
morbidity and mortality.
Taking these into consideration WHO in 1981 initiated a
programme for the control of ARI on a case management
of pneumonia. One of the strategies is to improve case
detection and patient management by primary health care
workers (7) and so reduce mortality. The aim of this study
is to evaluate the usefulness of simple clinical symptoms
and signs in the diagnosis of LRI, mainly pneumonia, which
can easily be used by primary health care workers. Despite
LRI (mainly pneumonia) being a condition commonly
encountered by clinicians, uncertainty remains over the
Ababa University.
71
72
A total of 179 children among whom 102 (57%) males and
77 (43%) females who fulfilled the inclusion criterias were
72
73
73
74
74
75
Discussion
In rural areas of developing countries the case fatality rate
from LRI in children is most likely to be reduced if primary
health care workers can identify the most serious forms of
LRI and deal with them appropriately, accurate guidelines
to detect LRI(pneumonia) who can be safely treated with
antibiotics as outpatients from those who require
immediate referral must be based on symptoms and signs
that can be readily assessed.
This study has attempted to look into clinical signs and
symptoms predictors of pneumonia in less than 5 year
children such as vomiting rapid breathing, tachypnea and
chest retraction, age and sex distribution ,frequency of
each clinical signs and symptoms at emergency and
regular pediatric out-patient department of TASH over one
year period. On a study done by Campbell, et al showed
that in infants a fever of >38.5c, refusal to feed (breast
feeding) or the presence of vomiting best correlated with
CXR pneumonia. In children aged 1-4 year, a fever of >
38.5c, RR >60/min are best correlated with CXR
pneumonia(11).Another study done by Cherian et al
showed that RR >50/min in infants and RR >40/min in
The Bangladesh study suggested that chest indrawing was
more specific as a sign
of
severe pneumonia
(17).Tachypnea has been exhaustively demonstrated to be
an excellent predictor of radiologically defined pneumonia
in a study done by Levantine J et al (10,14). In the present
study tachypnea and retraction are very specific signs of
CXR pneumonia, this is also consistent with other studies
done on the subject(10,14,17,18) and their usefulness is
further increased by their high sensitivity and are also
easier to teach to non medical staff like primary health care
workers. Vomiting, rapid breathing, fever, cough and
grunting were not satisfactory predictors of CXR
pneumonia.
Since our study is a hospital based study it should be
interpreted with caution when community health workers
(CHW) training and national guidelines are setup. Such
programmes must adopt policies that take into consideration
the health resource s available to implement them. In rural
areas of many developing countries including Ethiopia the
referral systems are poorly developed and much of the
primary care must be developed to CHWs, this should come
from community based studies.
In conclusion pneumonia is still the significant cause of
morbidity and mortality in developing countries like
Ethiopia . If pneumonia is diagnosed earlier using simple
clinical parameters which can also be used by non medical
staff like community health workers and other health
professional at each level mortality could be reduced
significantly. Tachypnea (94.5%) and retraction(86.3%) were
the best predictors of pneumonia as evidenced by
75
76
References
1.
2.
3.
4.
5.
6.
7.
8.
9.
10.
11.
12.
13.
14.
15.
16.
17.
18.
19.
2:125-8
76
77
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.Malnutrition and enteric parasitizes among under five children in Aynalem
Village, Tigray, Ethiop J HLth Dev 2000; 14:67-75
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books pub 2006: 110-120
77
78
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Acknowledgements
The printing of the Journal was made possible through the generous contribution of
UNICEF Ethiopia
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