Microbial Spectrum and Antiobiotic Sensitivity Patterns in Neonatal Blood Cultures: A NICU Based Study from Quetta, Pakistan
DOI:
https://doi.org/10.51253/pafmj.v76iSUPPL-1.11430Keywords:
Acinetobacter baumannii, Blood culture, Klebsiella pneumoniae, Neonate, Sepsis, Serratia marcescensAbstract
Objective: To document the microbial spectrum and antibiotic sensitivity patterns in blood cultures of suspected neonatal sepsis.
Study Design: Cross-sectional study.
Place and duration: Neonatal Intensive Care Unit (NICU) of Combined Military Hospital, Quetta, Pakistan from May 2023 to Oct 2023.
Methodology: The study analzyed neonates diagnosed with sepsis based on specific risk factors and clinical signs of bacterial infections. A thorough clinical assessment was conducted to confirm the presence of suspected sepsis. Specimens of neonates were processed using standard microbiological techniques for culture and sensitivity analysis.
Results: In a total of 119 neonates, 68(57.1%) were boys. The median age was 2.00 days (1.00-4.00). Culture proven sepsis was found in 33(27.7%) specimens. Among 33 neonates with culture proven sepsis, Serratia marcescens, Acinetobacter baumannii, and Klebsiella pneumoniae were found to be the most frequent isolates, noted in 16(48.5%), 4(12.1%) and 4(12.1%) cases, respectively. Serratia marcescens were found to be highly resistant (100.0%) to ampicillin, cefipime, cefotaxime, and doxycyclin whereas these were 100.0% senstivie to Tazocin. Acinebobacter baumanni were found resistant 3rd generation cephalosporins but found 100.0% sensitive to Polymyxin B. Klebsiella pneumoniae were 100% sensitive to Polymyxin B. Enrerococcus species were 100.0% sensitive to Linezolid.
Conclusion: Gender, birth weight, gestational age, and mode of delivery had significant association with culture-proven neonatal sepsis. The identification of Serratia marcescens, Acinetobacter baumannii, and Klebsiella pneumoniae as most commonly found isolates and high resistance patterns to most commonly antibiotics highlight the imperative for precise antibiotic selection guided by local resistance profiles.
Downloads
References
1. Ministry of Health, Annual Health Bulletin, KMT Press, Thimphu, 2015. Available at:
https://www.moh.gov.bt/wp-content/uploads/ftps/annual-health-bulletins/Annual%20Health%20Bulletin-2015 (Accessed on October 120, 2025)
2. Odabasi IO, Bulbul A. Neonatal Sepsis. Sisli Etfal Hastan Tip Bull 2020; 54(2): 142-158.
https://doi.org/10.14744/SEMB.2020.00236
3. Vergnano S, Sharland M, Kazembe P, Mwansambo C, Heath PT. Neonatal sepsis: an international perspective. Arch Dis Child Fetal Neonatal Ed 2005, 90: 220-224.
https://doi.org/10.1136/adc.2002.022863
4. Shaikh M, Hanif M, Gul R, Hussain W, Hemandas H, Memon A. Spectrum and antimicrobial susceptibility pattern of micro-organisms associated with neonatal sepsis in a Hospital in Karachi, Pakistan. Cureus 2020; 12(10): e10924.
https://doi.org/10.7759/cureus.10924
5. Milton R, Gillespie D, Dyer C, Taiyari K, Carvalho M, Thomson K, et al. Neonatal sepsis and mortality in low-income and middle-income countries from a facility-based birth cohort: an international multisite prospective observational study. Lancet Glob Health 2022; 10(5): e661-e672.
https://doi.org/10.1016/S2214-109X(22)00043-2
6. Ershad M, Mostafa A, Dela Cruz M, Vearrier D. Neonatal sepsis. Curr Emerg Hosp Med Rep 2019; 7(3): 83-90.
https://doi.org/10.1007/s40138-019-00188-z
7. Yadav P, Yadav SK. Progress in diagnosis and treatment of neonatal sepsis: A review article. J Nepal Med Assoc 2022; 60(247): 318-324. https://doi.org/10.31729/jnma.7324
8. Eichberger J, Resch E, Resch B. Diagnosis of neonatal sepsis: The role of inflammatory markers. Front Pediatr 2022; 10: 840288. https://doi.org/10.3389/fped.2022.840288
9. Pek JH, Yap BJ, Gan MY, Seethor STT, Greenberg R, Hornik CPV, et al. Neurocognitive impairment after neonatal sepsis: protocol for a systematic review and meta-analysis. BMJ Open 2020; 10(6): e038816.
https://doi.org/10.1136/bmjopen-2020-038816
10. Tann CJ, Kohli-Lynch M, Nalugya R, Sadoo S, Martin K, Lassman R, et al. Surviving and thriving: Early intervention for neonatal survivors with developmental disability in Uganda. Infants Young Child 2021; 34(1): 17-32.
https://doi.org/10.1097/IYC.0000000000000182
11. Niyoyita JC, Ndayisenga J, Omolo J, Niyompano H, Bimenyimana PC, Dzinamarira T, Nsekuye O, Chavez I, Hakizayezu F. Factors associated with neonatal sepsis among neonates admitted in Kibungo Referral Hospital, Rwanda. Sci Rep 2024; 14(1): 15961.
https://doi.org/10.1038/s41598-024-66818-z
12. Shehab El-Din EM, El-Sokkary MM, Bassiouny MR, Hassan R. Epidemiology of neonatal sepsis and implicated pathogens: A study from Egypt. Biomed Res Int 2015; 2015: 509484.
https://doi.org/10.1155/2015/509484
13. Srinivasa S, Arunkumar D. Bacterial isolates and their antibiotic susceptibility patterns in neonatal sepsis. Curr Pediatr Res 2014; 18(2): 83-86.
14. Chaurasia S, Sivanandan S, Agarwal R, Ellis S, Sharland M, Sankar MJ. Neonatal sepsis in South Asia: huge burden and spiralling antimicrobial resistance. BMJ 2019; 364: k5314.
https://doi.org/10.1136/bmj.k5314
15. Vergnano S, Menson E, Kennea N, Embleton N, Russell AB, Watts T, et al. Neonatal infections in England: the NeonIN surveillance network. Arch Dis Child Fetal Neonatal Ed 2011; 96(1): F9-F14. https://doi.org/10.1136/adc.2009.178798
16. Stoll BJ, Hansen NI, Sánchez PJ, Faix RG, Poindexter BB, van Meurs KP, et al. Early onset neonatal sepsis: the burden of group B Streptococcal and E. coli disease continues Pediatrics 2011; 127(5): 817-826. https://doi.org/10.1542/peds.2010-2217
17. Irshad M, Hayat M, Parvez H, Ihsan Ullah, Zia ur Rehman. Neonatal sepsis; Diagnostic accuracy of C-reactive protein (CRP) in the diagnosis of neonatal sepsis. Professional Med J 2019; 26(4): 608-614.
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Syed Moeed Ahmed, Muhammad Shoaib, Waqas Ahmed, Samrina Yasmeen, Hina Muhammad Ali, Najeebullah

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.





