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Drug Use Evaluation of Ceftriaxone in Ras-Desta Memorial General Hospital, Ethiopia

Authors Muhammed OS , Nasir BB

Received 4 May 2020

Accepted for publication 21 August 2020

Published 10 September 2020 Volume 2020:12 Pages 161—168

DOI https://doi.org/10.2147/DHPS.S260364

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Professor Siew Siang Chua



Oumer Sada Muhammed, Beshir Bedru Nasir

Department of Pharmacology and Clinical Pharmacy, School of Pharmacy, College of Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia

Correspondence: Beshir Bedru Nasir Department of Pharmacology and Clinical Pharmacy
School of Pharmacy, College of Health Sciences, Addis Ababa University, Churchill Avenue, P.O. Box 1176, Addis Ababa, Ethiopia
Email [email protected]

Background: Ceftriaxone is one of the most commonly used antibiotics due to its availability, wide spectrum of activity and low toxicity. However, irrational use of ceftriaxone is one of the current issues in most countries, especially developing ones.
Objective: The aim of this study was to evaluate ceftriaxone utilization in different wards of Ras-Desta Memorial General Hospital (RDMGH) in Ethiopia.
Methods: An institution-based retrospective cross-sectional study was conducted on randomly selected 1,079 patients who were admitted to RDMGH from May 2017 to April 2018. A structured data abstraction format was used to collect data from patients’ medical chart. Micromedex® drug interaction checker was used to identify significant drug–drug interactions, and national and international guidelines were used to evaluate the appropriateness of ceftriaxone use. The data were analyzed by using SPSS version 20.0.
Results: Among the 1,079 patients enrolled, ceftriaxone was utilized by 601 (55.7%) patients, and these patients were considered for evaluation of appropriateness and subsequent analysis. Among 601 patients, ceftriaxone was used for therapeutic purpose in 362 (60.2%) patients; of which, 359 (99.2%) were for empiric therapy and the rest 239 (39.8%) were for prophylaxis. In the majority of the patients, the dose of ceftriaxone was 2g/day 472 (78.6%) and for a duration of 2– 7 days 409 (68.1%). Inappropriate use of ceftriaxone was observed among 237 (39.4%) patients with regard to indication, dose/frequency and duration. About half (49.3%) of the deviation from the guidelines was observed from surgical and gynecologic/obstetrics wards. Among the co-prescribed medications with ceftriaxone, ringer lactate, warfarin and heparin were found to have a significant drug–drug interaction.
Conclusion: This study revealed that inappropriate use of ceftriaxone was high in RDMGH. This may increase the emergence of resistant pathogens which may lead to treatment failure and increase cost of therapy. Therefore, adherence to current evidence-based guidelines is recommended.

Keywords: antimicrobials, ceftriaxone, drug use evaluation; DUE, Ethiopia

Introduction

Antimicrobials have played a remarkable role in public health through decreasing of morbidity and mortality.1 The 19th and 20th centuries were peculiar in that health and longevity of populations progressed as the result of substantial achievements in controlling infectious diseases. This however, was not without challenges.2

The wide spread of misuse together with the emergence of antimicrobial resistance and escalating unwanted expenditures have resulted in antimicrobials being the drug most frequently chosen for drug use evaluation (DUE) studies.3 Ceftriaxone, as the most frequently used drug among the third generations cephalosporin class with reputable broad spectrum activity and utilization in many developing countries,4 was also highly prone to such problems. Studies reported that ceftriaxone was most often prescribed before culture and sensitivity tests and accurate decision was made in the diagnosis process.5

A high rate of inappropriate use of ceftriaxone (87.9%) and impacts of antimicrobial resistance was documented in the world including the developing countries like Ethiopia.5 A high rate of ceftriaxone resistance among gram negative bacteria was also reported across the European Union member states, which resulted in extra numbers of cases of infection, deaths, and hospital days.3

Inappropriate indication, empiric or prophylactic therapy and multiple drug uses were associated with misuse of antibiotics6 and findings in German indicated a dramatic 10 fold increase in E. coli resistance to 3rd generation cephalosporin including ceftriaxone.7 Ceftriaxone resistance was also reported among E.coli (86.1%) and K. pneumonia (95.8%) in Sudanese general hospital.8

In Ethiopia, though there were no comprehensive nationwide studies to demonstrate the magnitude and direction of the problem, a few fragmented studies have documented the threatening incidences of inappropriate use of ceftriaxone. It was reported that there was an increasing rate of ceftriaxone utilization with a high rate of inappropriate use with regard to indication, presence of drug interaction, absence of lab investigation, duration of treatment and dosage regimen.5,9,10 This in turn was also associated with fueling an ever-increasing need for a newer antibiotics. Therefore, prudent prescribing of antimicrobial drugs is essential as it may reduce incidences of antimicrobial drug resistance.11

The literature review showed that the previous findings of ceftriaxone utilization in Ethiopia were a small sample size, in limited clinical settings, and evaluated the appropriateness against the Ethiopian standard treatment guideline developed for general hospitals. So, the use of a more rigorous evaluation tool, displaying the magnitude of the problem in a large sample size involving all clinical departments in a facility level is more reliable. Therefore, the objective of this study was to evaluate ceftriaxone utilization in different wards of Ras-Desta Memorial General Hospital (RDMGH), Addis Ababa, Ethiopia.

Materials and Methods

Study Setting

The study was conducted in RDMGH which is one of the state owned public hospitals in the capital city of Ethiopia. The hospital provides a comprehensive medical service with its 550 staff, consisting of 246 medical staff and social workers, 98 technical and 206 administrative staff. The hospital has 168 beds in 5 inpatient wards (37 in gynecological and obstetric, 39 in surgical, 33 in medical, 19 in pediatric and 40 in adult and neonatal intensive care unit [ICU] wards).

Study Design

An institution-based retrospective cross sectional study design was employed to evaluate ceftriaxone utilization by reviewing medical records of patients who received ceftriaxone during May 1, 2017 to April 30, 2018. The DUE was made against the criteria of the currently developed protocol regarding the rational use of ceftriaxone. The treatment protocol was prepared by compiling current evidence-based recommendations regarding the use of ceftriaxone from WHO guidelines, Ethiopian standard treatment guideline for general hospital (STG 2014)12 and Infectious Disease Society of America (IDSA). STG 2014, which is a comprehensive guideline, used in Ethiopian general hospitals for the management of majority of diseases including surgical prophylaxis was extensively used for the protocol preparation. WHO guidelines (classification and management of childhood pneumonia13 and prevention of surgical site infection14 and IDSA practice guideline 2017 that includes several documents like management of infective endocarditis, meningitis and sepsis were also used. Micromedex® (Micromedex 2.0). Truven Health Analytics Inc) drug interaction checker was used to identify drug interactions. It is online application that provides evidence-based medical information including drug–drug interaction.

Source and Study Population

All patients admitted to RDMGH constituted the source population. The study population was all patients admitted to RDMGH during the study period and prescribed with at least 1 dose of ceftriaxone.

Sample Size Determination and Sampling Procedure

Because 385 is a minimum samples which is commonly considered using single population proportion formula with a proportion of 50% of inappropriate ceftriaxone utilization and confidence level of 95% with a z-value of 1.96 (P=0.05).15 Large samples of 1,079 patients’ medical charts were reviewed to get the assumed minimum samples that used ceftriaxone. However, among 1,079 medical charts reviewed 601 (55.7%) were found to use ceftriaxone and considered for evaluation ceftriaxone use appropriateness and subsequent analysis. Systematic random sampling was used to employ the sample from a total of 3024 patients who were admitted during the data collection period (May 1, 2017 to April 30, 2018). Sampling fraction (K) was calculated by dividing the total number of patients admitted in the study period (3,024) by the estimated sample for the study (601) that results 5. The first patients’ medical chart was selected using simple random sampling technique then every 5th chart was selected until the desired sample size was reached.

Data Collection and Analysis

Data was collected by 2 trained pharmacists through patients’ medical chart review by using patient data abstraction tool. The content of the data collection tool was designed to record patient information, disease condition, working diagnosis, abnormal laboratory tests, abnormal diagnostic results, culture and sensitivity results, information regarding administration of ceftriaxone including its indication, dose, frequency of administration, duration of therapy, and information regarding co-administered medications. Five criteria, namely indication for use, dose, frequency of administration, duration of treatment, and drug interaction were used to evaluate appropriateness of ceftriaxone utilization based on the prepared protocol. After checking the completeness and appropriateness, the data was entered and analyzed by using Statistical Package for Social Science (SPSS) version 20.0. Descriptive statistics such as frequency distribution and percentages were performed to summarize the result. Mean with standard deviation was used to report continuous variables.

Ethics Approval

The study was approved by Department of Pharmacy, Faculty of Medical Sciences, Alkan Health Science, Business and Technology College (AHSBTC, ref 02/18). Confidentiality of the collected data was maintained throughout the study. Data was analyzed and reported in aggregate and all patient identifiers were avoided during data collection process.

Results

Socio-Demographic Characteristics and Clinical Information of Patients

Among the 1,079 patients enrolled, ceftriaxone was utilized in 601 (55.7%) patients and these patients were considered for evaluation of appropriateness and subsequent analysis. The mean ±SD age of the study participants was 35.0 ± 17.7 years ranging from 3 months to 89 years. The majority (55.7%) of the patients were male and more than two thirds (71.1%) did not have any chronic co-morbidities. Among the study participants, 581 (96.7%) had at least one type of routine investigation which was done before or during ceftriaxone therapy. Hematologic test 483 (80.4%) was the most frequently conducted investigation followed by gram stain 66 (11%).

Among 9 blood cultures tested, only 3 of them showed growth of a specific microorganism (E.coli). The remaining 6 patients whose culture did not show any microbial growth were treated empirically. Among 601 patients, ceftriaxone was used for therapeutic purpose in 362 (60.2%) patients with (99.2%) empiric therapy and the rest 239 (39.8%) was used for prophylaxis. The prophylaxis uses were commonly for surgical prophylaxis but it was also used among a few patients who had soft tissue injuries.

The mean duration of ceftriaxone treatment was 5.2 ± 3.8 days (ranging from stat to 50 days). Majority (68.1%) of the patients were treated for 2–7 days and 18 (3%) took ceftriaxone for more than 14 days. For the majority (472; 78.6%) of the patients, the dose of ceftriaxone was 2g/day (50 mg/kg/day for pediatric age groups), followed by 2g-4g/day among 112 (18.6%) patients (Table 1).

Table 1 Socio-Demographic Characteristics and Clinical Information of Patients in RDMGH, June, 2018 (n=601)

Maintenance fluid, diclofenac, and metronidazole were the top 3co-medications prescribed among 290 (48.2%), 220 (36.6%) and 74 (12.3%) patients respectively (Table 2).

Table 2 Top 10 Drugs Frequently Co-Prescribed with Ceftriaxone in RDMGH, June 2018 (n=601)

Indication of Ceftriaxone Use and Compliance to National and International Guidelines

Regarding compliance to guidelines on ceftriaxone utilization, 364 (60.6%) of the samples were found to agree with the recommendations set in the guidelines. The rest (237; 39.4%) of the ceftriaxone use was not consistent with the guidelines. Among the top 10 indications for which ceftriaxone was prescribed, pre-operative prophylaxis 239 (39.4%) was the most common. Other indications for ceftriaxone use were pneumonia (149; 24.5%), acute febrile illness (AFI) (33; 5.4%) and urinary tract infection (UTI) (30; 4.9%) (Table 3). Ceftriaxone was prescribed for AFI, AGE, wound, bronchial asthma, stroke and peptic ulcer disease which were not recommended by the guidelines as eligible indication. Noncompliance to guidelines was observed in 120 (50.2%) of pre-operative uses; 3 (20%) of sepsis; and 2 (20%) of cellulitis treatment.

Table 3 Common Conditions for Which Ceftriaxone Was Prescribed and Respective Compliance to the Guidelines in RDMGH, June 2018 (n=601)

The highest proportion of ceftriaxone use was observed in internal medicine ward accounting for 290 (48.3%) of the cases followed by 152 (25.2%) in surgical, 91 (15.1%) in gynecologic/obstetrics, 40 (6.7%) in pediatrics and 28 (4.7%) in emergency wards. Noncompliance to the guidelines was mainly identified from the emergency department (19; 66.7% out of 28 cases), followed by surgical ward (84; 55.6%), and gynecology/obstetrics ward (37; 40.7%) (Figure 1). Compared to the internal medicine ward the rate of inappropriate ceftriaxone utilization was significantly higher in the emergency and surgery wards by 4.22 and 2.6 times (AOR=4.22, 95% CI [1.80–12.24] and AOR=2.60, 95% CI [1.44–7.82]), respectively.

Figure 1 Compliance of ceftriaxone utilization to the guidelines in each department of RDMGH, June 2018 (n=601).

About half (49.3%) of noncompliance to the guidelines was found from surgical and gynecologic/obstetrics wards due to either longer duration of therapy or wrong timing of ceftriaxone use in surgical prophylaxis. Similarly, incorrect indications and unacceptable duration of therapy for certain diagnosis composed the subsequent higher rate of the noncompliant cases (88; 36.9% and 20; 7.6%). Regarding the general categories of inappropriate ceftriaxone use, unaccepted use for prophylaxis (120; 50%) and wrongly indicated (87; 36.7%) were the major problems identified in this study (Figure 2).

Figure 2 Categories inappropriate ceftriaxone utilization in RDMGH, June 2018 (n=237).

Potential Drug–Drug Interaction Among Drugs Co-Prescribed with Ceftriaxone

Among total of 46 drugs checked for potential drug–drug interactions with ceftriaxone, 4 drugs were shown to have amoderate interaction that needs monitoring. The drug interactions were identified among 54 (9%) of the participants with ringer lactate 21 (3.5%), doxycycline 16 (2.7%), heparin 13 (2.2%), and warfarin 4 (0.7%).

Discussion

This study was designed to evaluate the appropriateness of ceftriaxone utilization in RDMGH. The current study revealed that a high rate (55.7%) of ceftriaxone utilization was observed. Similar findings of high rate of ceftriaxone utilization (58%) was reported in a study conducted in Tikur Anbessa specialized hospital, Ethiopia.5 High rate ceftriaxone utilization was also reported by other studies and the reasons might be attributed to its availability, effectiveness, broad spectrum and low toxicity rates.8 In Ethiopia ceftriaxone is the cheapest and commonly available parenteral antibiotics.

The mean duration of treatment in this study was 5.2 days (ranging from stat to 50 days) in fact more than two thirds (68.1%) of the patients were treated for 2–7 days. The duration was lower than the findings reported from Ayder referral hospital 7.2 days8 and Tikur Anbessa specialized hospital.5 The shorter duration of therapy in this study might be due to this study included patients in surgery ward that needs short duration of therapy for prophylaxis and a more frequent step down switch of ceftriaxone (intravenous) to other (oral) antimicrobials. The median duration treatment in Victorian hospitals was also found to be only 3 days19 which is shorter than the median of the present study. The discrepancy could be attributed to difference in treated disease conditions and hospitals’ protocols used to switch intravenous antibiotic to oral. Generally shorter duration of intravenous therapy would be desirable in most cases to reduce hospital stay and cost.20 However, severity and site of infection, numbers of comorbidities and patients’ response to alternative oral regimens are important before making the decision.

In this study, the most common indications of ceftriaxone use were preoperative prophylaxis (39.8%) and pneumonia (24.8%). Similarly, preoperative prophylaxis and pneumonia were the common indication of ceftriaxone use in the findings of Ayder referral hospital10 and Dessie referral hospital.21

In this study, the most frequent daily dose of ceftriaxone was 2g (78.6%) which is in line with the finding of Ayder referral hospital.10 However, a higher rate of dose of 2g/day was reported from a study in Tikur Anbessa hospital (88.9%).5 The discrepancy could be due to the latter study did not include pediatric patients in which a lower daily dose of ceftriaxone was used. This dose was commonly used in Ethiopia for most cases and empiric therapy except for diseases that requires a higher dose, such as meningitis and infective endocarditis.

In this study, culture and sensitivity was done only for 9 (0.8%) of the patients in which 3 of them showed bacterial growth and were sensitive to ceftriaxone. This is negligible as compared to studies conducted in India (25.4%),2 Tikur Anbessa hospital, Ethiopia (22.4%),5 Nepal (47.4%),22 and Bangladesh (77%).23 The reason of limited culture and sensitivity test in the current study might be due to lack of equipped microbiology laboratory and unaffordability among majority of the patients that leads to empiric therapy for almost all patients. However, a high rate of resistance to ceftriaxone was reported in Ethiopia in Tikur Anbessa specialized hospital (62.5%)5 that needs due attention.

The inappropriate use of ceftriaxone in this study was found to be 39.6%. This finding was with inline Dessie Referral Hospital 46.2%,21 but lower than the findings of Tikur Anbessa specialized hospital (87.9%),5 in Iran (85.3%),20 and Ayder Referral Hospital (64.2%).10 The discrepancy of the findings might be attributed to a retrospective nature of the present study and the differences in the guidelines used to conduct the DUE. The other reason could be that, unlike this study, the above studies were conducted in referral hospitals in which treatment is complicated with several possible inappropriate medication uses. In addition, drug interaction in this study was not considered as inappropriate utilization that will lower the rate of inappropriate ceftriaxone utilization.

The highest proportion of ceftriaxone use 276 (48.3%) was found in the medical wards followed by surgical wards (25.2%). In contrary, inappropriate ceftriaxone use was frequently observed in emergency wards and the least in the medical ward. Compared to internal medicine wards a higher rate of inappropriate ceftriaxone utilization was observed in emergency and surgery wards by 4.22 and 2.6 times, respectively. Most of the deviations from the guidelines in the emergency ward were due to the overuse of antibiotics without optimal investigations and appropriate diagnosis. In addition, ceftriaxone was utilized for conditions without clear indications like patients diagnosed with AFI, wound, AGE, and bronchial asthma which were not supported in the guidelines. Surgical wards were the other areas with frequent inappropriate use of ceftriaxone for pre-operative prophylaxis. Similar finding was reported from the study of Ayder referral hospital.10 Though cefazolin is the recommended antibiotic pre-operative prophylaxis for most surgeries, ceftriaxone was used for almost all surgery cases in the current study area. Furthermore, timing of initiation and longer duration of ceftriaxone prophylaxis was frequently observed in the present study.

Maintenance fluid, diclofenac, and metronidazole were the 3 commonly co-administered medication with ceftriaxone. Among drugs concomitantly administered with ceftriaxone, ringer lactate(21; 3.5%) (16; 2.7%), heparin (13; 2.2%), and warfarin (4; 0.7%) had a potential drug–drug interaction. Co-administration with heparin and warfarin may increase the risk of bleeding. Similar studies were reported in a study conducted in Tikur Anbessa specialized hospital.5

Limitation of the Study

Despite the large sample size in most departments, it was a retrospective cross-sectional study that may under estimate the rate of inappropriate use of ceftriaxone. In addition, the evaluation was relied merely on the patients’ medical records for which practices might have actually been different.

Conclusion

The majority (55.7%) of patients admitted to RDMGH utilized ceftriaxone commonly for empiric therapy and prophylaxis purpose. Inappropriate use of ceftriaxone with regard to indication, dose/frequency and duration remains significant. This may increase the emergence of resistant pathogens which leads to treatment failure and increased cost of therapy. Therefore, adherence to current evidence-based guidelines is recommended. Few medications were also found to have a significant drug–drug interaction that requires a close monitoring or avoiding the concomitant administration.

Abbreviations

RDMGH, Ras-Desta Memorial General Hospital; AFI, acute febrile illness; UTI, urinary tract infection; STI, sexually transmitted infection; UGIB, upper gastrointestinal bleeding.

Data Sharing Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Acknowledgments

We would like to express our deepest gratitude to all staff members of RDMGH for their unlimited support. We would also like to extend our sincere gratitude to the data collectors for their support throughout the study period and Dr. Abdurahman Ahmed for his support in language editing.

Author Contributions

Both authors made substantial contributions to conception and design, analysis and interpretation of data, took part in revising the article critically for important intellectual content, gave final approval of the version to be published and agrees to be accountable for all aspects of the work.

Funding

The authors received no specific funding for this work.

Disclosure

The authors report no conflicts of interest in this work.

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