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Revista de la Facultad de Medicina Humana

versión impresa ISSN 1814-5469versión On-line ISSN 2308-0531

Rev. Fac. Med. Hum. vol.22 no.2 Lima abr./jun 2022  Epub 16-Mar-2022

http://dx.doi.org/10.25176/rfmh.v22i2.4275 

Original article

Microbiological profile of microorganisms isolated from patients in critical care units of a Hospital in Lambayeque, Peru, 2019-2020

Marco Antonio Chilon-Chavez1 

Jery Giankarlo Muñoz-Inga1 

Heber Silva-Díaz2 

1Facultad de Medicina Humana, Universidad de San Martín de Porres. Chiclayo, Perú

2Dirección de Investigación, Hospital Regional Lambayeque. Chiclayo, Perú

ABSTRACT

Objective:

To describe the microbiological profile of microorganisms isolated from patients in critical care units of a hospital in the Lambayeque region in 2019-2020.

Methods:

Descriptive, retrospective, cross-sectional study with a quantitative approach. A census study was carried out on 332 patients from critical care units (CCUS) with a positive microbiological culture registered in the file of the microbiology laboratory of the Lambayeque Regional Hospital in 2019-2020. The statistical software Info stat v8 was used for statistical analysis.

Results:

The median age was 50 years, predominantly male (55.1%). The most frequent culture sample was bronchial secretion (35.8%). The most frequently isolated microorganisms were A. baumannii complex (27.7%) resistant to meropenem and imipenem with 90.7% and 89.3% respectively, P. aeruginosa (13.9%) resistant to cefepime with 55.8% and 61.1% for Piperacillin / tazobactam, E. coli (11.1%) resistant to ampicillin with 94.7%; and K. pneumoniae (9.9%) resistant to ampicillin / sulbactam by 79.2%.

Conclusion:

The most frequent microorganisms isolated from the study population were the A. baumannii complex, P. aeruginosa, E. coli and K. pneumoniae; isolated mainly from respiratory secretions, of which the first two showed high resistance to carbapenems and aminoglycosides, and in the next two, half were ESBL.

Keywords: Intensive Care Units; Drug Resistance; Anti-Infective agents; Microbiology; Hospitals.(fuente: MeSH NLM).

INTRODUCTION

Antimicrobial resistance, a process between microorganisms and antimicrobials where the drug loses efficacy, becoming a complex challenge for public health, this natural phenomenon is currently accelerated by the misuse of antimicrobials1,2.

Currently, it is common to identify microbiological isolates in the hospital environment and outside of it, with resistance levels ranging from multidrug-resistant (MDR), extremely resistant (XDR), and even pan-resistant, in which no type of antimicrobial has an effect. With respect to the latest estimates for the Prevention and Control of Diseases of the United States (CDC), these microorganisms have a high economic impact of 35 million additional dollars in medical expenses; in turn, they are the cause of more than 2 million infections and 23,000 deaths annually in the US3.

In the CCUs, there is a diversity of microorganisms that are exposed to different antiseptic agents, which causes them to generate a specific resistance for each antimicrobial group. In these units, patients are found in a vulnerable state due to their homeostatic and immunological instability, which makes them more easily infected by these microorganisms4.

Antimicrobial resistance is understood as the mechanisms that can produce various types of microorganisms in response to the use of drugs that are used for the treatment and prophylaxis of diseases caused by these. This is increased with its indiscriminate use by the population5.

There are two types of resistance, intrinsic, specific properties of bacteria, whose same species are invariability resitant to some groups of antibiotics. On the other hand, the acquired type is revealed in therapeutic failures in patients infected with these bacterial strains that, through certain mechanisms,become resitant to the drug that was usually sensitive6.

Worldwide, as in India, it was shown that the most frequent species isolated in critical care units were Staphylococcus aureus and Klebsiella pneumoniae, both resistant to cephalosporins. In addition, more than half of the S. aureus found were S. aureus resistant to methicillin (MRSA), and none of them were resistant to linezolid and vancomyc7.

A study, conducted at the Latin American level, reported that the most frequently isolated bacteria in critical care units were Escherichia coli and K. pneumoniae resistant to ampicillin, cefazolin, and piperacillin/tazobactam8.

In 2014, in a social security hospital in Chiclayo, it was shown that the most frequently isolated bacteria in the Intensive Care Unit (ICU) were K. pneumoniae, 27.3%; Pseudomonas aeruginosa, 13.6% and E. coli, 11.5% resistant to cephalosporins and sensitive to carbapenems and aminoglycosides9.

The objective of this study was to describe the microbiological profile of the microorganisms isolated from patients in the critical care units of a hospital in the Lambayeque region in 2019-2020. This research allowed us to have quality control for treating infections that occur, unlike other hospitals in the region.

METHODS

Design and study area

A descriptive, retrospective, cross-sectional study with a quantitative approach was carried out in the CCUs of the Lambayeque Regional Hospital (HRL).

Population and sample

The study population was patients from the HRL CCUs with positive microbiological culture, treated from April 2019 to March 2020. The study was census.

The unit of analysis was the microbiological cultures registered in the HRL microbiology laboratory during the study period. Patients from critical care units with positive microbiological culture recorded in the HRL microbiology laboratory file were excluded.

Variables and instruments

The microbiological profile is a document that includes frequency and resistance data corresponding to microorganisms isolated from patients cared for in a certain place, space, and time, to which statistical interpretation is added10.

The samples were processed by the VITEK® system in the study, automated bacterial identification, and antimicrobial susceptibility study system. The identification of bacteria is based on the inoculation of a suspension of microorganisms on cards with certain panel of biochemical reactions. Antimicrobial susceptibility is carried out similarly through cards containing standardized dilutions of different antibiotics corresponding to the susceptibility cutoff points established as of 201811.

Epidemiological variables were also studied: age and gender; laboratory variables: service of origin and type of sample; microbiological variables: isolated microorganism and antimicrobial susceptibility (sensitive, intermediate, and resistant).

Procedures

The record of results of positive microbiological isolates of patients admitted to critical care units between April 2019 and March 2020 was reviewed.

Statistical analysis

In a database created in the Microsoft Excel 2019 program, it was The information obtained from the laboratory record was processed and subsequently sent to the statistical software Info stat v8, for its corresponding analysis. Descriptive statistics were performed, calculating absolute and relative frequencies for the categorical variables; and measures of central tendency and dispersion for the quantitative variables, taking into account their normal distribution according to the Kolmogorov-Smirnov goodness-of-fit test

Ethical aspects

The study in question was reviewed by the San Martin de Porres University (Official Letter No. 23 - 2021 - CIEI-FMH-USMP) and HRL (Inv_Code: 0211-086-19 CEI) for its approval. The confidentiality of the results obtained from the patients under study was always maintained, assigning codes to their names and surnames for their identification. ikewise, the custody of said information will be in charge exclusively of the researchers; the corresponding permits were requested from the hospital to carry out the research. the risks of participating in the study were minimal.

RESULTS

The study included 332 microbiological records of patients treated in critical care units of the HRL, during 2019 and 2020. The study population was characterized by a median age of 50 years, with an interquartile range (IQR) of 28 to 66. Likewise, the median age in the Pediatric Special Care Unit (PCU) and ICU was one year (IQR= 1 - 8) and 51 years (IQR= 36 - 70), respectively.

Table 1, shows the demographic characteristics of the study population, where there is a predominance of the male sex (55.1%) and the age group of 18 to 59 years (57.2%).

Table 1.  Demographic characteristics of patients treated in the critical care units of the Lambayeque Regional Hospital, 2019-2020 (N= 332) 

Demographic characteristics N %
Sex    
Female 149 44,9
Male 183 55,1
Age (years)    
0 a 17 34 10,2
18 a 59 190 57,2
60 to more 108 32,5

While inTable 2, the laboratory characteristics of the study population, the most frequently obtained samples with positive culture were from the respiratory tract (TR= Bronchial secretion, Tracheal aspirate, Bronchoalveolar lavage) 57.8%; for urine culture, it was 22.9%, and the service of origin was ICU 91.3%

Table 2.  Laboratory characteristics of patients with culture positive microbiological from the critical care units of the Lambayeque Regional Hospital, year 2019-2020(N=332) 

Laboratory characteristics N %
Type of sample    
Bronchial secretion 119 35,8
Urine culture 76 22,9
Tracheal 50 15,1
Blood culture 26 7,1
Catheter tip 25 7,5
Bronchoalveolar lavage 23 6,9
Wound secretion 4 1,2
Cerebrospinal fluid 2 0,6
Tissue 3 0,9
Others 4 1,2
Department of origin    
PCU 29 8,7
ICU 303 91,3

AndTable 3shows the microbiological characteristics of the study population; approximately 50.0% of the E. coli and K. pneumoniae regardless of the sample's origin, were extended-spectrum beta-lactamases (ESBL). Gram-negative bacteria represented 70.7% of the microbial isolates.

Tabla 3.  Microbiological characteristics of microbial isolates from patients from the critical care units of the Lambayeque Regional Hospital , year 2019-2020 

Microbiological characteristics N %
Microbial type (N=332)    
Bacteria 287 86,4
Fungus 45 13.6
ESBL producers (N=36)    
E. coli 18 50,0
K. pneumoniae 18 50,0
Isolated microorganism (N=332)    
A. baumannii complex 92 27,7
P. aeruginosa 46 13,9
E. coli 37 11,1
K. pneumoniae 33 9,9
Candida albicans 26 7,8
S. haemolyticus 19 5,7
S. epidermidis 15 4,5
C. tropicalis 13 3,9
S. aureus 11 3,3
Stenotrophomonas maltophila 8 2,4
Proteus mirabilis 7 2,1
P. mallei 5 1,5
C. glabrata 4 1,2
Enterococcus faecalis 3 0,9
C. krusei 2 0,6
Enterobacter cloacae 2 0,6
Serratia marcescens 2 0,6
S. hominis 2 0,6
Enterobacter aerogenes 1 0,3
Moraxella spp 1 0,3
Morganella morganii 1 0,3
S. mitis 1 0,3
S. saprophyticus 1 0,3

Finally,Table 4shows the E. coli with a high sensitivity profile to carbapenems such as meropenem, followed by ertapenem; and finally amikacin.

Sensitivity for the cephalosporin group was low; for urine samples, ceftriaxone obtained 5% while nitrofurantoin retains its high antimicrobial response. Amikacin and meropenem maintain their response to K. pneumoniae;For the TR samples, cefepime had a low response together with ciprofloxacin.

Resistance was maintained for trimethoprim/sulfamethoxazole in E. coli and for the first(Cefazolin) and third (ceftriaxone and ceftazidime) generation cephalosporins; the highest percentages of k. pneumoniae were for ampicillin/sulbactam and ceftazidime.

Table 4.  Sensitivity profile of E. coli and K. pneumoniae of the microbial isolates of patients rom the critical care units of the Lambayeque Regional Hospital, year 2019-2020,according to sample type 

Micro organ Sample N (%) Antibiotics
Ampicilina-sulbactam (%) Amikacina (%) Cefepime (%) Ceftriaxona (%) Ceftazidima (%) Cefazolina (%) Ciprofloxacina (%) Ertapenem (%) Gentamicina (%) Imipenem (%) Meropenem (%) Nitrofurantoina (%) Piperacilina / tazobactam (%) Trimetoprim/sulfametoxazol (%)  
E. coli Orina 21 (56,8) 3/14 (21,4) 20/21 (95,2) 2/19 (10,5) 1/20 (5,0) 2/18 (11,1) 2/13 (15,4) 5/19 (26,3) 16/17 (94,1) 6/20 (30,0) 19/20 (95,0) 3/3 (100,0) 18/20 (90,0) 12/14 (85,7) 4/17 (23,5)  
TR 10 (27,0) 1/5 (20,0) 9/9 (100,0) 1/8 (12,5) 1/8 (12,5) 0/1 (0,0) 0/4 (0,0) 3/10 (30,0) 7/7 (100,0) 3/9 (33,3) 10/10 (100,0) 10/10 (100,0) 1/1 (100,0) SD 2/9 (22,2)  
Otros 6 (16,2) 2/4 (50,0) 3/3 (100,0) 2/4 (50,0) 2/5 (40,0) 0/1 (0,0) 0/1 (0,0) 2/4 (50,0) 3/3 (100,0) 5/5 (100,0) 5/5 (100,0) 5/5 (100,0) SD 1/1 (100,0) 0/3 (0,0)  
Todas 37 (100,0) 6/23 (26,1) 32/33 (97,0) 5/31 (16,1) 4/33 (12,1) 2/20 (10,0) 2/18 (11,1) 10/33 (30,3) 26/27 (96,3) 14/34 (41,2) 34/35 (97,1) 18/18 (100,0) 19/21 (90,5) 13/15 (86,7) 6/29 (20,7)  
K. pneumoniae Orina 10 (30,3) 1/8 (12,5) 8/10 (80,0) 1/10 (10,0) 1/8 (12,5) 1/9 (11,1) 0/3 (0,0) 1/10 (10,0) SD SD SD 1/2 (50,0) 0/8 (0,0) 5/8 (62,5) 1/8 (12,5)  
TR 18 (54,6) 2/13 (15,4) 17/18 (94,4) 4/17 (23,5) 3/15 (20,0) 1/2 (50,0) 0/4 (0,0) 6/16 (37,5) SD SD SD 17/18 (94,4) 0/1 (0,0) 1/2 (50,0) 4/12 (33,3)  
Sangre 5 (15,2) 0/3 (0,0) 3/5 (60,0) 1/4 (25,0) 0/2 (0,0) 1/3 (33,3) 0/3 (0,0) 1/4 (25,0) SD SD SD 3/5 (60,0) SD 1/3 (33,3) 1/3 (33,3)  
Todas 33 (100,0) 3/24 (12,5) 28/33 (84,9) 6/31 (19,4) 4/25 (16,0) 3/14 (21,4) 0/10 (0,0) 8/30 (26,7) SD SD SD 21/25 (84,0) 0/9 (0,0) 7/13 (53,9) 6/23 (26,1)  

Table 5.  Sensitivity profile of A. baumanni complex and P.aeruginosa of the microbial isolates of patients from the critical care units of the Lambayeque Regional Hospital, 2019-2020, according to sample type 

Micro organ Sample N (%) Antibiotics
Ampicilina-sulbactam(%) Amikacina(%) Cefepime (%) Ceftriaxona (%) Ciprofloxacina (%) Colistina (%) Gentamicina (%) Imipenem (%) Meropenem (%) Moxifloxacino(%) Piperacilina / tazobactam (%) Tobramicina (%) Trimetoprim/sulfametoxazol (%)
A. baumannii complex TR 77 (83,7) 8/63 (12,7) 17/72 (23,6) 9/74 (12,1) 2/45 (4,4) 9/74 (12,1) 30/30 (100,0) 9/73 (12,3) 9/71 (12,7) 8/73 (11,0) 1/10 (10,0) 3/25 (12,0) 6/37 (16,2) 7/71 (9,9)
Sangre 6 (6,5) 0/3 (0,0) 2/6 (33,3) 0/5 (0,0) 0/1 (0,0) 0/6 (0,0) 4/4 (100,0) 0/6 (0,0) 0/4 (0,0) 0/6 (0,0) 0/2 (0,0) 0/4 (0,0) 0/2 (0,0) 0/6 (0,0)
Otros 9 (9,8) 1/7 (14,3) 2/9 (22,2) 0/9 (0,0) 0/3 (0,0) 0/9 (0,0) 2/2 (100,0) 0/8 (0,0) 0/9 (0,0) 0/7 (0,0) 0/1 (0,0) 0/5 (0,0) 2/6 (33,3) 0/9 (0,0)
Todas 92 (100,0) 9/73 (12,3) 21/87 (24,1) 9/88 (10,2) 2/49 (4,1) 9/89 (10,1) 36/36 (100,0) 9/87(10,3) 9/84 (10,7) 8/86 (9,3) 1/13 (7,7) 3/34 (8,8) 8/45 (17,8) 7/86 (8,1)
P. aeruginosa TR 43 (93,5) 0/6 (0,0) 25/40 (62,5) 18/41 (43,9) SD 19/42 (45,2) 10/10 (100,0) 20/41 (48,8) 20/42 (47,6) 18/39 (46,1) 2/5 (40,0) 7/16 (43,7) 11/18 (61,1) SD
Otros 3 (6,5) 0/1 (0,0) 0/2 (0,0) 0/2 (0,0) SD 0/3 (0,0) 2/2 (100,0) 0/3 (0,0) 0/3 (0,0) 0/2 (0,0) SD 0/2 (0,0) 0/1 (0,0) SD
Todas 46 (100,0) 0/7 (0,0) 25/42 (59,5) 18/43 (41,9) SD 19/45 (42,2) 12/12 (100,0) 20/44 (45,5) 20/45 (44,4) 18/41 (43,9) 2/5 (40,0) 7/18 (38,9) 11/19 (57,9) SD

Finally,Table 5shows that the isolates of P. aeruginosa were sensitive to amikacin and gentamicin. The two microorganisms were fully sensitive to colistin.

Isolates of Acinetobacter baumannii complex showed high resistance to carbapenems such as meropenem and imipenem. The resistance for P. aeruginosa was 42.1% for tobramycin; 48.8% for meropenem; 53.3% for ciprofloxacin;55.6% for imipenem;55,8% for cefepime and finally 61,1% for Piperacillin/tazobactam.

Regarding te susceptibility profile of the isolated fungi, a sensitivity of more than 90% was obtained for fluconazole and voriconazole.

DISCUSSION

This study describes the microbiological profile microorganisms isolated from patients in the critical care units of the HRL from 2019 to 2020. The male sex predominated with 51.1%, compared to the studies carried out in Colombia and India. Which reported the female sex with 51.6%8and 64.0%9, respectively.

The most frequently obtained culture-positive samples were bronchial secretion and urine culture, representing more than 50% of the total, with similar results to a study conducted in Arequipa12; In contrast, two studies in Colombia obtained a higher frequency in blood culture samples8and tracheal secretion13. It is observed that respiratory tract infections are more prevalent at the national level than systemic infections.

A. baumannii complex and P. aeruginosa were the most frequently isolated species, unlike a study conducted in India that reported S. aureus and K. pneumoniae7. On the other hand, two studies in Colombia reported E. coli as the most frequent species in the critical care unit8-13. Other studies carried out in Peru reported P. aeruginosa and E. coli as the most frequent species (Arequipa)12; while K. pneumoniae turned out to be the most frequent species in a hospital in Lambayeque9.

When analyzing the E. coli a sensitivity of 100% was obtained for meropenem and 96.3% for ertapenem, similar to a study carried out in Colombia8, and another in Lambayeque, where the sensitivity was more than 9 6%. for carbapenems. For the group of aminoglycosides (amikacin) the response was maintained as reported in a hospital in Lambayeque9.

strains E. coli presented a 94.7% resistance to ampicillin, 88,9% forcefazolin; 79,3% for trimethoprim/sulfamethoxazole with similar results in Colombia8.

Gram-negative bacilli, mainly enterobacteria, such as E. coli are producers of ESBL enzymes and these are capable of inactivating first and second-generation penicillins and cephalosporins, but als the plasmids that encode ESBLs carry resistance genes to other antimicrobials such as tetracyclines and co-trimoxazole, which is why the phenomenon of cross-ressitance is very frequent and the treatment of infections caused by these strains is more difficult14.

K. pneumoniae presented sensitivities greater than 84.0% for amikacin and meropenem, results that were consistent with previous studies where they presented (9, 8) percentages greater than 60.0%9and 100%8.

Likewise, there were isolates of K. pneumoniae with higher resistance levels for ampicillin/sulbactam, ceftazidime and trimethoprim/sulfamethoxazole compared to those found in studies carried out in Arequipa12and Colombia8,15. ESBL production constitutes the most frequent mechanism that confers resistance to cephalosporins and other beta-lactams, except carbapenems, in the Klebsiella as shown in this research16.

Between 75.9% and 91.9% of A. baumannii complex were resistant to amikacin, gentamicin, tobramycin and trimethoprim/sulfamethoxazole, values of lower than 100% resistance for these drugs in a study conducted in Colombia17. Carbapenem resistance rates for A. baumannii complex have increased dramatically worldwide, making the antibiotic arsenal more restricted, and clinical practice shifting toward agents such as colistin18.

The resistance results obtained in the study of P. aeruginosa for cefepime were lower than the results from Arequipa12and Colombia8. For carbapenems such as meropenem and imipenem, results were well below those obtained in Arequipa12and India7. 53.3% of the isolates were resistant to ciprofloxacin, unlike the high resistance that exists in India7and Arequipa12. Finally, 61.1% were resistant to piperacillin/tazobactam, while in India and Colombia the values were lower with 30.0%7and 50.0%8, respectively. While a study in Arequipa observed a higher resistance12.

P. aeruginosa has a high level of intrinsic resistance to various antibiotics and is also capable of acquiring or inducing new resistance, significantly reducing therapeutic options. Intrinsic resistance contributes to resistance to penicillin, aminopenicillins (including combinations with β-inhibitors). lactamases),first, second and third generation cephalosporins, chloramphenicol, nitrofurantoin, sulfonamides, trimethoprim, tetracycline, and ertapenem19; however, the available therapeutic options are still effective in our environment.

Being a retrospective study, the limitations that exist are the measurement bias where the data was already measured and recorded by the microbiology laboratory service of the hospital under study. Likewise, the results have limited external validity due to the access restrictions of other hospitals that have intensive care units. However, it provides findings that will allow the initiation of new and larger studies on the subject.

CONCLUSION

In conclusion, the bacteria most frequently isolated from cultures from HRL critical care units in 2019 to 2020 were A. baumannii complex, P. aeruginosa, E. coli and K. pneumoniae. The antimicrobial susceptibility prole of A. baumannii complex showed high resistance to carbapenems and aminoglycosides, but they were sensitive to colistin, as was P. aeruginosa. Meanwhile, E. coli and K. pneumoniae were ESBL in half of their isolates, and showed high sensitivity to amikacin and meropenem.

Acknowledgments:

The authors of this manuscript thank the doctor Tony Farías Rodríguez and the microbiologist Abdías Clayton Martínez Estela, for being part of the data collection of this research.

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Funding sources: Self-funded.

Received: September 26, 2021; Accepted: March 01, 2022

Correspondence: Marco Antonio Chilon Chavez Address: Alfonso Ugarte 1650, Chiclayo. Telephone number: +51 945072038 E-mail:chilonchavezmarco@gmail.com

Authorship contributions: The authors conceived and designed the study; They also managed the permits and obtained the data to carry out the statistical analysis. They analyzed and interpreted the data and wrote the manuscript. All authors participated in the critical review of the article, approval of the nal version and assume responsibility for the content of the article.

Conflicts of interest: The authors declare that they have no conicts of interest to carry out this study.

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