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African Journal of Biomedical Research
Ibadan Biomedical Communications Group
ISSN: 1119-5096
Vol. 5, Num. 3, 2002, pp. 97-102
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African Journal of Biomedical Research, Vol. 5, No. 3, Sept,
2002, pp. 97-102
A STUDY OF WOUND
INFECTIONS IN TWO
HEALTH INSTITUTIONS IN ILE-IFE, NIGERIA.
SHITTU A.O*., KOLAWOLE
D.O. AND
OYEDEPO E.A.R.
1Department
of Biochemistry and Microbiology, University of Zululand,
KwaDlangezwa 3886, Republic of South Africa;
2Department
of Microbiology, Obafemi Awolowo University, Ile-Ife, Nigeria.
*Address for correspondence: bayo_shittu@yahoo.com Telephone: +27-035-902-6095;
Fax: + 27-035-902-6189
Received: June
2002
Accepted: September, 2002
Code Number: md02021
The microbiological
analysis of wound infection in 102 patients was undertaken in the outpatient
departments of the University
Teaching Hospital and the Health Centre in Ile-Ife, Nigeria.
The location and type of wound was considered and identification of bacterial
isolates was determined by standard microbiological techniques. Forty per cent
of wound types was attributed to trauma and in most cases, were located at the
extremities. A total of one hundred and sixty two bacterial isolates were obtained
from wound cultures. In 39 cases, cultures were monomicrobial, 55 cultures were
polymicrobial but no bacterial isolate was obtained in eight cases. Staphylococcus
aureus was the predominant microorganism (25%) followed by Escherichia coli (12%),
Pseudomonas aeruginosa (9%) and Staphylococcus epidermidis (9%). The diversity
of microorganisms and the high incidence of polymicrobic flora in this study
give credence to the value of identifying one or more bacterial pathogens from
wound cultures. Continuous dialogue between the microbiology department and wound
care practitioners and education of patients on personal hygiene is strongly
advised.
INTRODUCTION
A wound is a breach in the skin
and the exposure of subcutaneous tissue following loss of skin integrity provides
a moist, warm, and nutritive environment that is conducive to microbial colonization
and
proliferation. (Bowler et al, 2001). Infection in a wound delays healing
and may cause wound breakdown, herniation of the wound and complete wound dehiscence.
(Alexander, 1994). In spite of technological advances that have been made in
surgery and wound management, wound infection has been regarded as the most common
nosocomial infection especially in patients
undergoing surgery (Dionigi et al, 2001). It is an important cause of
illness resulting in a prolongation of hospital stay, increased trauma care,
treatment costs, and general wound management practices become more resource
demanding (Bowler et al, 2001).
The severity of the complications
depends largely on
the infecting pathogen and on the site of infection (Terry, 1985; Garner et
al, 1988) and in general, a wound can be considered infected if purulent
material is observed without the confirmation of a positive culture. The control
of wound infections has become more challenging due to widespread bacterial resistance
to antibiotics and to a greater incidence of infections
caused by methicillin-resistant Staphylococcus aureus, polymicrobic flora
and by fungi. The knowledge of the causative agents of wound infection has therefore
proved to be helpful in the selection of empiric antimicrobial therapy and on
infection control measures in health institutions.
This study investigated
the bacteriology of patient's
infected wounds in two health institutions in Ile-Ife, Nigeria.
MATERIAL AND METHODS
Sample population: One
hundred and two patients participated in the study. They were made up of 70males
and 32 females between the ages of 2 and 72 years. The patients presented for
wound dressing in the outpatient departments of the Obafemi Awolowo University
Teaching Hospitals Complex (O.A.U.T.H.C) and the Health Centre, Ile-Ife. The
wound types include boils, whitlow, abscesses, permicitis, trauma wounds, burns,
systemic ulcers, insect bites and swelling of no specific etiology. Wound sites
were categorised as head and neck; back and abdomen; breast; armpit; arm; hand;
thigh and groin;
leg and foot regions.
Collection of samples: All
the wounds were judged as infected by the presence of purulent material. Before
wound cleansing and dressing conducted by a nurse, the exudate from each wound
site was carefully taken using sterile cotton-tipped applicators (Sterilin,
U.K) and transferred to the research laboratory. It was immediately applied
to freshly prepared blood agar plates (Oxoid, U.K), streaked and incubated
aerobically at 37oC for 24 hours. Bacterial colonies on blood agar plates were
later Gram stained. Characterization of bacterial isolates was based on standard
microbiological methods.6 They include Gram stain, morphological and cultural
characteristics on nutrient agar, spore stain, motility and carbohydrate fermentation
tests, nitrate reduction, catalase, hydrogen sulphide production and indole
production. Other tests include citrate utilization, gelatin liquefaction,
Methyl Red-Voges Proskaeur test, coagulase, haemolysis on blood agar, morphological
and cultural characteristics on mannitol salt and eosin-methylene
blue agar.
RESULTS
Isolation of bacterial
species: One hundred and sixty two bacterial isolates were
recovered from various infected wounds averaging 1.6 bacteria per specimen.
Positive growth was observed in 95% of wound cultures. One microorganism
was present in 39 wound cultures, several microorganisms in 55 cultures,
and in eight cultures, no bacterial isolate was obtained from the cultured
material. Eleven bacterial genera and seventeen species were identified
(Table I).
Staphylococcus aureus was
the most frequently isolated microorganism (25%) followed by Escherichia coli,
(12%) Pseudomonas aeruginosa (9%) and Staphylococcus epidermidis (9%). The
staphylococci were the predominant Gram positive organism (41%) and the family
Enterobacteriaceae constituted 37% of the total number of isolates. Bacterial
isolates identified as Klebsiella pneumoniae, Enterobacter cloacae, Proteus
spp and Pseudomonas spp accounted for less than seven percent of the total
number of isolates. A total of forty per cent of wounds was attributed to
trauma and forty-two percent of isolates were recovered from this wound type
(Table II).
Table I Bacterial Isolates Recovered
From Patients Wounds
ORGANISM
|
N
(%)
|
%
|
Staphylococcus aureus
|
41(25.3)
|
41.4
|
Staphylococcus epidermidis
|
15(9.3)
|
Staphylococcus sp
|
11(6.8)
|
Bacillus sp
|
13(8.0)
|
8.0
|
Streptococcus sp
|
2(1.2)
|
1.2
|
Diplococcus sp
|
1(0.6)
|
1.2
|
Aerococcus sp
|
1(0.6)
|
Escherichia coli
|
20(12.3)
|
37.7
|
Enterobacter cloacae
|
2(1.2)
|
Enterobacter aerogenes
|
7(4.3)
|
Klebsiella pneumoniae
|
3(1.9)
|
Proteus vulgaris
|
11(6.8)
|
Proteus mirabilis
|
10(6.2)
|
Proteus sp
|
3(1.9)
|
Serratia marcensens |
5(3.1)
|
Pseudomonas aeruginosa
|
15(9.3)
|
10.5
|
Pseudomonas sp
|
2(1.2)
|
TOTAL |
162(100)
|
|
Fifteen bacterial species were
identified from trauma wounds
followed by boils (10) and abscess (9) respectively.
Table 2: The distribution of bacterial isolates in relation to location and
types of wound infection
Body Regions
|
Wound type
|
1
|
2
|
3
|
4
|
5
|
6
|
7
|
8
|
9
|
10
|
11
|
12
|
13
|
14
|
15
|
16
|
17
|
18
|
Head&Neck; n=4
|
Boil (1)
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
Trauma (2)
|
1
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
Postoperative (1)
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Back&Abdomen; n=3
|
Boil (2)
|
2
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
Postoperative (1)
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
Breast; n=3
|
Boil (2)
|
1
|
|
|
|
|
|
|
|
|
|
|
1
|
1
|
|
|
1
|
|
|
Abscess (1)
|
1
|
|
|
|
|
|
|
1
|
1
|
|
|
|
|
|
|
|
|
|
Armpit; n=2
|
Boil (2)
|
1
|
|
1
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
Arm; n=2
|
Postoperative (1)
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
Trauma (1)
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
Hand; n=27
|
Boil (1)
|
|
|
|
1
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
Trauma (7)
|
3
|
|
|
1
|
1
|
|
|
|
|
1
|
|
|
1
|
1
|
|
|
|
1
|
Postoperative (3)
|
1
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
1
|
Insect bite (1)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
Whitlow (12)
|
6
|
7
|
|
|
|
|
|
2
|
|
|
|
|
|
|
|
1
|
|
1
|
Abscess (2)
|
1
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
Inflammation (1)
|
1
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Thigh & Groin; n=15
|
Boil (2)
|
1
|
|
|
1
|
|
|
|
|
|
|
|
|
1
|
|
1
|
|
|
|
Trauma (1)
|
|
|
|
1
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
Postoperative (1)
|
1
|
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
Abscess (6)
|
4
|
|
|
|
|
|
|
2
|
|
1
|
|
|
1
|
1
|
|
|
1
|
|
Permicitis (2)
|
|
1
|
|
1
|
|
|
|
1
|
|
|
|
1
|
|
|
|
1
|
|
|
Burns (1)
|
|
|
1
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
Ulcers (1)
|
1
|
|
|
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
Inflammation (1)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
Leg; n=27
|
Boil (6)
|
2
|
|
|
1
|
|
|
|
1
|
|
|
|
|
1
|
|
|
|
1
|
2
|
Trauma (16)
|
4
|
3
|
3
|
|
|
1
|
|
3
|
|
1
|
|
4
|
1
|
|
2
|
6
|
|
|
Postoperative (1)
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
Insect bite (2)
|
1
|
|
2
|
|
|
|
1
|
|
|
|
|
|
|
|
|
|
|
|
Ulcers (2)
|
1
|
1
|
|
|
|
|
|
2
|
|
|
1
|
|
1
|
|
|
1
|
|
|
Foot; n=19
|
Boils (2)
|
|
|
|
|
|
|
|
1
|
|
|
|
|
|
|
|
1
|
|
|
Trauma (14)
|
6
|
|
2
|
5
|
|
|
|
4
|
1
|
2
|
1
|
3
|
|
1
|
2
|
1
|
|
|
Postoperative (1)
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1
|
Insect bite (1)
|
|
|
1
|
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Inflammation (1)
|
1
|
1
|
1
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total
|
41
|
15
|
11
|
13
|
2
|
1
|
1
|
20
|
2
|
7
|
3
|
11
|
10
|
3
|
5
|
15
|
2
|
8
|
1 Staphylococcus aureus; 2 Staphylococcus epidermidis;
3 Staphylococcus spp; 4 Bacillus spp; 5 Streptococcus spp; 6
Diplococcus spp; 7 - Aerococcus spp; 8 Escherichia coli; 9 Enterobacter
cloacae; 10 Enterobacter aerogenes; 11 Klebsiella pneumoniae; 12 Proteus
vulgaris; 13 Proteus mirabilis; 14 Proteus spp; 15 Serratia marcensens;
16 Pseudomonas aeruginosa; 17 Pseudomonas spp; 18 No growth
A total of sixty-three isolates
(39%) were obtained from
wound types that required incision and drainage (I & D) to remove the exudate
and clean the underlying tissue (incised boils, whitlows, abscesses and
permicitis). S. aureus was the predominant microorganism constituting
31% of the total number of isolates recovered from these wound types.
The analysis of polymicrobial
infections showed that 31 (56.3%) out of the 55 polymicrobial cultures was
attributed to S. aureus with other microorganisms. They include ten
cases of S. aureus with Gram
positive organisms, nineteen cases of S. aureus with Gram negative organisms
and two cases involving S. aureus, Staphylococcus spp and a Gram negative organism.
Nine cases of polymicrobic infections involving Bacillus spp and Gram negative
organisms were recorded from a variety of wound types.
The location of wounds
in relation to wound types and organisms isolated from each wound site is shown
in Table II. Trauma wounds were mainly located at the leg and foot regions.
Wound infection at the extremities was observed in 27 cases at the hand and
leg regions respectively followed by 19 cases at the foot and 15 cases at the
thigh and groin regions of
the body. S. aureus was recovered from all the wound sites except the
arm and it was the most frequently isolated microorganism in wounds occurring
in all the regions of the body excluding the hand and leg.
DISCUSSION
Wound infection has been
a major concern among health care practitioners not only in terms of increased
trauma to the patient but also in view of it's burden on financial resources
and the increasing requirement for cost-effective management within the health
care system1. The
microbiological analysis reveals that S. aureus is the leading etiologic
agent of wound infection in these health institutions. This is similar to reports
in Nigeria, India, Thailand and Japan (Emele et al, 1999; Basak et
al, 1992) Tranet et al, 1998; Mashita et al, 2000). S.
aureus was the most frequently isolated microorganism from wounds caused
by incision to reach pus or fluid collection under the skin surface and from
wound
types observed in this study.
Microbiological investigations
have noted that this organism is the single causative bacterium in approximately
25 to 69% of
cutaneous abscess (Meislin et al, 1977; Brook et al, 1981; Mahdi et
al, 2000). The same microorganism has also been recognized as the most frequent
isolate in superficial infections seen in Hospital Accident and
Emergency Departments.
Nasal carriage of S.
aureus has been identified as an important risk factor for the acquisition
of S. aureus infection, although this may depend on an array of factors
that may either be
environmental or patient-related (Mahdi et al, 2000). The postulated sequence
of events which leads to infection is initiated with S. aureus nasal carriage
which is then disseminated via hand carriage to other body sites where infection
can occur with breaks in the dermal surfaces. The emergence of
methicillin-resistant S. aureus in wound infections has led to higher
treatment costs and prolongation of hospital stay with serious consequences in
infection control especially in developing countries. The number of trauma wound
infection observed in this study was high (40%).
The wounding agent range from
nail pricks on farm sites to door slams on fingers and motorcycle accidents.
Trauma is often associated with the development of local or systemic infection
and the situation in which injury or trauma occur as well as the location of
the injury may be predictive of the number and types of pathogens found in
the wound. Infecting microorganisms may be derived either from an exogenous
source (i.e. water-borne from water-related injury or microorganisms from soil
in a soil-contaminated injury) or the endogenous microflora of the patient
(File, 1995).
Fifteen bacterial species
were identified and forty two percent of the total number of isolates was recovered
from trauma wound infection. A high number of traumatic wound infections were
located on the leg and foot regions of the body i.e. the extremities. Traumatic
wound infection of the extremities is a common clinical problem and the high
frequency and variety of microorganisms confirms the view that microbiological
evaluation before
treatment should be strictly observed (Holzapfel et al, 1999).
Most of the wound infection
in these health institutions were polymicrobic in nature and in most cases,
associated with S.
aureus and other microorganisms. The variety of organisms observed in this
study support the need to obtain culture specimens from infected wounds for microbiological
evaluation and antibiotic susceptibility determination, so that adapted chemotherapy
can be prescribed. We believe that it will not only facilitate successful wound
management but also assist in the control of antibiotic usage and hence stem
the spread of antibiotic-resistant bacteria. The fact that anatomically incorrect
type of surgical incisions and wound debridement may delay wound healing brings
to focus that information regarding site, type of wound infection and clinical
symptoms should be considered along with the value of identifying one or more
bacterial pathogens. Continuous dialogue between the microbiology department
and wound care practitioners is
strongly advised.
We did not investigate
the impact of hygiene in the development of wound infection but we suggest
that education of patients on personal hygiene will be helpful in enhancing
wound healing and management of patients. This is with a view to saving cost,
time and providing prompt and
appropriate treatment for the patient.
Acknowledgements
The authors are grateful
to the nurses of the Out-patient Department of
the Obafemi Awolowo University Teaching
Hospitals Complex, for their assistance in the specimen collection. The project
was partly supported by grant 1425 LF,
awarded by the Obafemi Awolowo University Research
Committee. We thank Bongi Sigwebela (University of Zululand)
for assistance in the acquisition of research
articles.
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Communications Group
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