Since the discovery of antimicrobials in the late 1920s, they have been seen as a miracle treatment for infectious diseases and their usage has grown tremendously.1 Since then antimicrobial resistance (AMR) has slowly and steadily emerged and progressed to the point where infection with AMR has led to serious illnesses, prolonged hospital admissions, increased healthcare costs, higher costs in second-line drugs, and treatment failures.2 The situation has inflated to the point where antimicrobials may be causing more harm than good.3
The global problem of AMR is particularly pressing in developing countries, where the infectious disease burden is high and cost constraints prevent the widespread application of newer, more expensive agents.4 In these countries AMR is driven by the high incidence of infectious diseases,2 inappropriate use of antimicrobials in treatment,5 use of antimicrobials as growth promoters6, and lack or poor implementation of legislation to AMR.7 AMR is, nevertheless, a global issue of public health concern.
Infection is the most common presentation among hospitalized patients in intensive care unit (ICU), and in many instances, is a determining factor for patient outcomes.8,9 Antimicrobials have become an essential part of treatment in all spectrums of critically ill patients. Stronger antimicrobials are particularly used in critical care.7 This may have escalated antimicrobial resistance to a newer dimension. Hence, ICUs are now often recognized as the epicenter of infections in the hospital.10
The situation in Nepal is comparable. There has been an increasing burden of antimicrobial resistance (AMR) in Nepal over the last two decades.11–15 However, there is a lack of data on antimicrobial use in ICUs of Nepal. This data is important to help develop pertinent strategies to improve the future use of antimicrobials in hospitals as part of the National Action Plan for Containment of Antimicrobial Resistance 2016.16 We intend to conduct a point prevalence survey to characterize and quantify the antimicrobial utilization in level III ICUs of Nepal. This study will inform, at the policy level, the strategies to implement antimicrobial stewardship programs and develop antimicrobial guidelines in Nepal.
A multicentre quantitative cross-sectional study was conducted in various ICUs in Nepal. The study was conducted for one month after getting ethical approval from Nepal Health Research Council. WHO methodology for PPS and the global point prevalence survey method were adopted, which are standardized methods for surveillance of antibiotic use and validated tools to assess the quality of antibiotic prescribing. Antibiotics studied in this study were classified according to the Anatomic Therapeutic Chemical (ATC) methodology developed by the WHO Collaborating Center for Drug Statistics Methodology in Oslo, Norway. Only antibiotics listed in Annex XI of the referred document and administered through oral, parenteral, rectal, or inhalation routes were included in the survey. For example, topical applications, eye drops, ear drops, and vaginal suppositories were excluded.
As per WHO methodology and Global-PPS form, all the adult patients (>18 yr) admitted to the participating ICUs as an inpatient at or before 08:00 were included in the survey irrespective of whether they were receiving antibiotic treatment or not. All inpatients admitted in the ICU at 8 o’clock in the morning on the day of survey were counted in the denominator. All inpatients “on antibiotic agents” at 8 o’clock in the morning on the day of survey were included in the numerator. All daycare hospitalizations, all patients admitted after 8 a.m. on the day of the survey, and all patients who received surgical prophylaxis after 8 a.m. on the day of the PPS were excluded. Definition of “on antibiotic agents”: A patient receiving an antibiotic eg every 48 hours but not receiving this antibiotic on the survey day must be included = ongoing antibiotic treatment. An antibiotic prescribed at one o’clock (during the ward round or when results become available or for surgical prophylaxis) in the afternoon on the day of the survey must not be included (not active or ongoing at 8 o’clock in the morning). For patients receiving surgical prophylaxis, the administration of antibiotic prophylaxis should be checked in the previous 24 hours in order to encode the duration of prophylaxis as either one dose, one day (=multiple doses given in one day), or >1 day. This means that patients who received the surgical prophylaxis ‘before’ 8 a.m. on the day of the PPS will be included in the survey.
The sampling technique recommended by WHO Methodology for Point Prevalence Survey on Antimicrobial Use in Hospitals Version 1.1 was utilized as follows: All the ICU patients fulfilling the inclusion criteria were included in the studies from all the involved hospitals.
Convenience sampling techniques were used for both hospitals and patient-level sampling. The sampling was done in each ICU on the day of the survey. The data collector prepared a list of all eligible patients according to the inclusion criteria. The list was ordered alphabetically according to patients’ surnames (not by bed or patient number).
Data was collected using three Google forms, one for hospital level and two ward-level and one for patient-level data, as described in the Global-PPS method. The principal source for completing data collection was through a review of the patient’s medical records. The treating physician was interviewed when needed for clarification. Patient’s prescriptions and files were accessed at 2.00 p.m.. However, information was collected only up to 8:00 a.m. in the morning of the same day and further changes beyond that time were excluded.
Before initiating the full survey, a pilot study was also conducted in one of the participating hospitals by, for example, reviewing clinical notes for up to 10 patients involving the whole investigator team.
Data collected after surveying each hospital were sorted and organized to prevent mix-up during data entry. All the data collected in the study were entered into a Google Form and exported into MS-Excel/SPSS for analyses.
Total of 98 patients, from 12 ICUs of 11 hospitals, were enrolled in the study. Of all the patients included in the study, the majority (54.08%) were from private-for-profit institutes. Among these patients, 63 (64.28%) were undergoing treatment for a medical cause (Table 1).
Table 1.
Patient and hospital characteristics
| Variable | N | Mean ± SD OR % | |
|---|---|---|---|
| Patient age | 13–39 yrs | 28 | 53.66 ± 20.92 |
| 40–64 yrs | 38 | ||
| >65 yrs | 32 | ||
| Gender | Male | 57 | 58.16% |
| Female | 41 | 41.83% | |
| Type of treatment | Medical | 63 | 64.28% |
| Surgical | 35 | 35.71% | |
| Antibiotics use | On Antibiotics | 91 | 92.85% |
| NOT on Antibiotics | 7 | 7.14% | |
| Hospital ownership | Public | 45 | 45.92% |
| Private not for profit | – | – | |
| Private for profit | 53 | 54.08% | |
In total, 91 (92.85%) patients were on at least one antibiotic at the time of the PPS. 56 patients (34.78%) were on two antibiotics, 13 patients (8.07%) were on three antibiotics and one patient (0.62%) was on more than 3 antibiotics. Total number of antibiotics received by all 98 patients combined was 160. The most common indication for the use of antibiotics was surgical prophylaxis (36.25%), followed by community-acquired infection (32.50%) and healthcare-associated infection (20%) (Figure 1).
Respiratory system was the commonest body system (40.70%) for which antibiotics were being prescribed and this was followed by Central Nervous System (CNS) (14.30%), Gastrointestinal system (14.30%), and Skin, soft tissue, bone, and joint (13.2 %) (Figure 2).
Piperacillin was the most commonly used antibiotic and was used in 35.16% of all patients receiving antibiotics. This was closely followed by Meropenem (22.2%) and Ceftriaxone (17.8%). Polymyxin B was prescribed in 8.9%, Linezolid in 7.8% and Vancomycin was used in 6.7% of all patients receiving antibiotics. Piperacillin was the most commonly used antibiotic for both community-acquired infections and surgical prophylaxis, while Meropenem was the most commonly used antibiotic for hospital-acquired infections (Figure 3).
Of all the antibiotic prescriptions (160), 108 (67.5%) were empirical therapy and 49 (30.6%) were targeted (3 patients had missing data). Of all these prescriptions, most didn’t have a stop or review date mentioned nor were compliant with local guidelines. Use of biomarkers to start or change antibiotics was low (35.16%) (Table 2).
Table 2.
Prescribing practice
| Practice | N/Total (%) |
|---|---|
| Stop/review date recorded | 23/160 (14.37%)a |
| Use of biomarkers to start or change Antibiotics | 32/91 (35.16%) |
| Compliant to local guidelines | 44/160 (27.50%)a |
| Cultures sent to document Infection | 56/91 (61.53 %) |
| Cultures sent prior to starting or changing Antibiotics | 31/160 (34.4%) |
a Total number of antibiotics received by all 98 patients combined was 160.
Of all the patients on antibiotics (91), cultures were sent to 56 patients (61.53%). Among these 56 patients, cultures were sent before starting antibiotics in 31 patients (55.36%). Total of 112 samples were sent for culture. Majority of the samples were Blood (35), Sputum/bronchial aspirate (35), and Urine (34).
Of all the cultures sent, the majority (56.25%) were negative for any growth, and 26.78% of the samples grew an organism (Table 3). Among the cultured organisms, Klebsiella pneumoniae was the most common, appearing in 5 instances across various samples. Citrobacter freundii followed closely with 4 occurrences. Escherichia coli and Staphylococcus aureus were each found 3 times. Notably, 12 of the cultured organisms (40%) were isolated from sputum/ bronchial aspirate samples.
Table 3.
Microbiological diagnosis
| Variable | N (%) |
|---|---|
| Sample collected for microbiological workup | |
| Yes | 56/91 |
| No | 35/91 |
| Samples sent before starting/changing antibiotics | |
| Yes | 31/56 |
| No | 25/56 |
| Specimen type | |
| Blood | 35/112 |
| Sputum/bronchial aspirate | 35/112 |
| CSF | 3/112 |
| Urine | 34/112 |
| BAL | 1/112 |
| Wound | 4/112 |
| Other | – |
| Culture results | |
| Positive | 30/112 (26.78%) |
| Negative | 63/112 (56.25%) |
| Awaited/unknown | 19/112 (16.96%) |
Piperacillin was the most commonly used antibiotic (35.6%), followed by Meropenem (22.2%) and Ceftriaxone (17.8%). It was observed that 60% of the positive cultures exhibited resistance to Amoxicillin, while 50% of the positive cultures showed resistance to Carbapenem. (Figure 4).
Antimicrobial resistance is a global issue and the burden is high and increasing.17,18 In this study we found that the antibiotic prescribing rate was very high in ICUs of Nepal. 92.85% of patients in ICU were on antibiotics, and surgical prophylaxis continued in ICU was the commonest reason for prescribing antibiotics (36%). Prolonged surgical prophylaxis, sometimes continued up to the time the patient gets discharged, is a concerning issue for all Low-and-middle income countries (LMICs).19 This could be an area when stewardship programs could improve antibiotic utilization.
We also aimed to see the prescribing practices of Antibiotics. We found that 67.5% of all antibiotic prescriptions were for empirical therapy. In a study done in Vietnam, 63.6% of the patients in critical care units were on empiric antibiotic therapy.20 Prescribing practices were poor with poor practice of defining the duration of therapy (14.37%), poor use of guidelines of therapy (27.5%), and poor utilization of biomarkers to start/change antibiotics (35.16%). Practice of sending cultures to document infection was also poor (61.1%). And cultures were sent only 34.4% of all the times when antibiotics were started or changed. Among all the cultures sent, only 26.78% had positive reports. This could also indicate that there might have been no infection in most cases.
In >50% of these, either Piperacillin/Tazobactam or Meropenem was used. This indicates most clinicians use broad-spectrum antibiotics even for surgical prophylaxis or community-acquired infections. AMR was also high with Penicillin, cephalosporins, and carbapenem groups all having resistance in > = 50% of the available culture/sensitivity reports. A good antibiotic stewardship program could decrease the misuse of these antibiotics.21
This study underscores the urgent need for effective antimicrobial stewardship programs in ICUs of Nepal. The high rate of antibiotic prescription, the prevalent use of broad-spectrum antibiotics even for surgical prophylaxis or community-acquired infections, and the poor adherence to guidelines and best practices highlight areas that require immediate attention. The high resistance observed against commonly used antibiotics further emphasizes the gravity of the situation.
Implementing robust antimicrobial stewardship programs could help optimize antibiotic utilization, improve patient outcomes, and ultimately combat the global threat of antimicrobial resistance. Future research should focus on developing and evaluating interventions tailored to the unique challenges faced by low and middle-income countries like Nepal. This study serves as a stepping stone towards understanding and improving antibiotic prescribing practices in ICUs of Nepal.
In conclusion, there was an overprescription of broad-spectrum antibiotics for all causes of admission to ICUs. It is now crucial to establish and implement protocols/guidelines for empirical antibiotic therapy and also start to implement the surveillance of antibiotic use in ICUs of Nepal.
Our study had some limitations. One of the major limitations was that all ICUs in Nepal could not be involved. Being a PPS, the population captured might have been small and might not have reflected the real patient combination. Future consideration could be to design a new study with involvement of more ICUs in Nepal and design a longer-duration longitudinal study. There were also no follow-ups to know the exact duration of treatment, escalation/de-escalation based on microbiology reports, etc. Additionally, the majority of initial diagnosis of infection were made clinically, partly related to the lack of rapid diagnostics whilst the empirical antibiotic prescribing decisions were influenced by doctors’ experiences and by the level of the hospitals.
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Abstract
Objective: This study aimed to investigate the prevalence and practices of antibiotic use in intensive care units (ICUs) in Nepal and to identify potential areas for implementing antimicrobial stewardship programs. Design: A point prevalence survey was conducted to characterize and quantify the antimicrobial utilization in level III ICUs of Nepal. Methods: Data on antibiotic prescription rates, reasons for prescribing antibiotics, and prescribing practices were collected and analyzed. The prevalence of antimicrobial resistance was also assessed. Results: The antibiotic prescribing rate was found to be very high, with 92.85% of patients in ICU on antibiotics. Prolonged surgical prophylaxis was the most common reason for prescribing antibiotics. Empirical therapy accounted for 67.5% of all antibiotic prescriptions. Prescribing practices were poor, with low adherence to guidelines and best practices. Broad-spectrum antibiotics were commonly used even for surgical prophylaxis or community-acquired infections. High resistance was observed against commonly used antibiotics. Conclusions: The study underscores the urgent need for effective antimicrobial stewardship programs in ICUs of Nepal. Implementing robust stewardship programs could help optimize antibiotic utilization, improve patient outcomes, and combat the global threat of antimicrobial resistance. The findings serve as a stepping stone toward understanding and improving antibiotic prescribing practices in ICUs of Nepal.
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Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Hospital for Advanced Medicine and Surgery (HAMS), Kathmandu, Nepal
2 Nepal Intensive Care Research Foundation, Kathmandu, Nepal
3 John H. Stroger Jr. Cook County Hospital, Chicago, IL, USA
4 National Academy of Medical Sciences (NAMS), Bir Hospital, Kathmandu, Nepal




