Imtiaz All Khan ( Department of Paediatrics, Dow Medical College and Civil Hospital, Karachi. )
Dure Samin Akram ( Department of Paediatrics, Dow Medical College and Civil Hospital, Karachi. )
The microbiological pattern of proven early neonatal sepsis is reported between the period of 1st January, 1984 to 31st December, 1985.
Of 198 blood cultures, 30(43.5%) and 53 (41.0%) were positive in 1984 and 1985, respectively. There was considerable variability in the spectrum of organisms in these two years. The type of organisms found and their sensitivity to antibiotics was marked different from that reported in Western literature. Most organisms were found to be resistant to commonly used antibiotics. Cefotaxime and Tobramycin were most effective, while Fosfomycin was found to be effective against enterococci (JPMA 37: 327: 1987).
Neonatal Sepsis is a clinical syndrome characterised by symptomatic and systemic illness and bacteria in the blood1. Its incidence in the West is approximately 1/1000 in full term and 4/1000 in premature babies.2 The figures have remained fairly constant over the past 30 years3-5 although the type of organisms causing disease have changed over a number of years2.
The pattern of etiological agents usually differs from country to country. For example in Latin America Salmonella and in Spain Listeria Monocytogenes is frequently involved in causing sepsis2,4-6
Scant published data is available from Pakistan on the common organisms involved in sepsis and their pattern of sensitivity to commonly used antibiotics. This study was undertaken to identify organisms causing neonatal sepsis together with their sensitivity pattern to antibiotics. An attempt was also made to establish any change in the sensitivity pattern over the course of two years.
PATIENTS AND METhODS
The data included is on patients admitted between 1st January, 1984 uptil 31st December, 1985. Only early sepsis (less than 1 week of age) wau studied as babies beyond one week of age are not admitted to our nursery. Hospital and. home deliveries were included to determine if the causative organisms and/or their sensitivity pattern varied with environment.
Criteria used to include babies in the study consisted of symptoms and signs commonly associated with sUspected sepsis (Table-I).
After a detailed history and physical examination, blood was drawn for culture and complete blood count. Other cultures e.g. CSF, Urine and Umbllcal Swab were obtained as and when indicated.
Blood cultures were inoculated on Dextrose broth (oxoid) and Thioglycollate broth, and incubated aerobically and anaerobically. Subcultures and gram stains were done 48 hours later. Blood agar and Mac Conkey agar were used for sub.cultures which were again incubated aerobically and anaerobically
Groeth obtained form different media was co-rtlaued by microscopic and gram – stain examination. Catalase and Staph slide test (Biomerieux) were performed for identification of streptococci and staphylococci respectively. Streptex (Weilcome) was used for grouping streptococci (Lancefield grouping). Oxidase test was used to identify gram negative bacilli. Oxidase positive bacilli were put through the oxiferm tube (Roche) and oxidase negative through the Entero tube II (Roche).
Cultures other than blood were inoculated intO a bottle of Stuart’s transport medium (modi. fled oxoid) and later plated onto two blood agar plates (for aerobic and anaerobic incubation) and Mac Conkey agar. A gram stain was also done at the time of moculation and after incubation. Further identification procedures were as for blood cultures.
Every baby suspected of having sepsis was given Ampicillin and Tobramycin initially. Later Cephradine and Tobramycin were used routinely as initial reports revealed high resistance of most organisms to Ampicillin. Antibiotics were changed, as needed, after the results of the culture were obtained, or if the baby’s clinical condition did not improve within 48 hours. The antibiotics were continued for ten days, but the duration was increased in those with meningitis or delayed recovery. A baby was kept on antibiotics on clinical grounds even if the blood culture was negative.
Neonatal Sepsis was more predominant in males in both the years, though mortality did not seem to vary uniformly between the two sexes. Mortality, evaluated according to gestational age and environment at birth (home or hospital), also did not show a statistically significant difference (p0.05 by chi square). The etiolo. gical pattern of neonatal sepsis was found to be very different in this study as compared to reported literature. Although E. Coli was found to be the most common etiological agent causing sepsis in 1984, there was a high frequency of infection due to Kiebsiella and, Salmonella in 1985. The change could partly be attributed to environmental factors in the nursery between 1984 and 1985 since between April 1984 and July 1985, newborns were admitted in a make shift nursery due.to building renovation.
Hemolytic Streptococcus group ‘B’ is the most frequently incriminated organism causing neonatal sepsis in Western literature. It was not grown in any of the blood cultures in this study although special methods were used to isolate it.
Commonly used antibiotics e.g. Ampicillin had a very low sensitivity pattern to most organisms as reported in Table IV and V. Cefotaxime and Tobramycin, in combination, were found to be the most effective broad spctrum antibiotics in this study, although a few resistant strains did appear.
Fosfomycin had a limited spectrum with a high rate of sensitivity towards Enterococci and Staphylococci.
Due to financial constraints and consequent lack of medical facilities in most of our hospitals routine blood cultures cannot be obtained in every case of suspected sepsis. It is however recommended to monitor blood cultures periodically on a random basis, to assess changes that might occur over a period of time.
1. Behrman, R.E. and Vaughan, V.C. Nelson’s textbook of pediatrics. 12th ed. Philadelphia, Saunders, l983,p.403.
2. McIntosh, K. Bacterial infections of the newborn, in Schaffer’s diseases of the newborn. 5th ed. Philadelphia, Saunders, 1984, p. 729.
3. Wilson, H.D. and Eichenwald, H.F. Sepsis neona torum. Pediatr. Clin. North Am., 1974;21:571.
4. Freedman, R.M., Ingram, D.L., Gross, I., Ehren Kranz, R.A., Warshaw, LB. and Baltimore, R.S. A half century of neonatal sepsis at Yale. Am. J.Dis. Child., 1981;135: 140.
5. Hargiss, C. and Larson, F. The epidemiology of staphylococcus aureus in a newborn nursery from 1970 through 1976. Pediatrics, 1978; 61:348.
6. Siegel, J.D. and McCracken, G.H Sepsis neona torum.N.Engl.J. Med., 198l;304:642.
7. Placzek, M.M. and Whitelaw, A. Early and late neonatal septicaemia. Arch. Dis. Child., 1983; 58: 728.