Abstract
Background
Rising antibiotic resistance threatens to reverse health gains from antibiotic access, especially in low- and middle-income countries. Identifying factors influencing prescribing patterns and appropriateness is vital to optimising antibiotic use and strengthening antimicrobial stewardship. However, evidence on this in paediatric outpatient care in Ghana is limited.
Objectives
To identify patient-related and prescriber-related factors associated with antibiotic prescribing patterns and the appropriateness of antibiotic use among paediatric patients.
Methods
A retrospective review of outpatient records at the Princess Marie Louise Children’s Hospital in Ghana was conducted from 1 April to 30 June 2022. Logistic regression and generalised estimating equations analyses were used, where appropriate, to assess associations between patient age and sex, prescriber rank, prior antibiotic use, fever status and the appropriateness of antibiotic prescribing by indication, choice, dosage, duration, antibiotic tier and multiple-antibiotic use.
Results
Among 16 555 outpatient consultations, 3244 (20%) resulted in an antibiotic prescription, of which 2862 records were analysed. Most patients were male (54%). Male sex was associated with antibiotic prescribing when not indicated (p=0.007), whereas older children (p=0.030) and patients presenting with fever (p=0.036) were less frequently prescribed antibiotics when not indicated. Compared with house officers, specialised nurses and physician assistants were associated with inappropriate use of antibiotics (p<0.001 and p=0.005, respectively); however, they were less likely to prescribe multiple or higher-tier antibiotics. Medical officers and residents were associated with appropriate antibiotic dosing and duration (p=0.004 and p=0.005, respectively), and prior antibiotic use doubled the odds of receiving higher-tier antibiotics (p<0.001).
Conclusion
Patient and prescriber characteristics were significantly associated with antibiotic prescribing patterns and appropriateness. Targeted interventions leveraging these findings are needed to improve prescribing and strengthen antimicrobial stewardship.
Keywords: Children, Health Policy, Health services research, Low and Middle Income Countries, Therapeutics
WHAT IS ALREADY KNOWN ON THIS TOPIC
While patient and provider factors are known to influence prescribing patterns and appropriateness, their effects vary by context, and important evidence gaps remain in our setting. Addressing these gaps is essential for designing locally effective antimicrobial stewardship strategies.
WHAT THIS STUDY ADDS
This study reveals that prescription patterns and appropriateness are influenced by prescriber and patient characteristics, including prescriber cadre, patient age and sex, presence of fever and prior antibiotic use.
HOW THIS STUDY MIGHT AFFECT RESEARCH, PRACTICE OR POLICY
This creates a foundation for future studies, such as comparative studies and those that explore causal pathways. It supports the need for targeted antimicrobial stewardship interventions. This study offers baseline evidence to inform policy changes and improve paediatric antibiotic use.
Introduction
Antibiotics are crucial for treating and preventing bacterial diseases, playing a significant role in modern medicine. While global access to antibiotics has improved due to factors like better health insurance and rising incomes, this has also contributed to a rise in antibiotic resistance. Resistance develops when bacteria adapt and become impervious to antibiotics, making infections increasingly difficult to treat.1 Among the key factors driving resistance is inappropriate use in healthcare.2 In 2019, antimicrobial resistance (AMR) caused approximately 4.95 million deaths, particularly in Western and sub-Saharan Africa, with projections estimating 10 million deaths annually by 2050 if no action is taken.3 In sub-Saharan Africa, resistance levels to common antibiotics are alarmingly high, driven largely by misuse in both human and veterinary contexts.4 In Ghana, research shows high antibiotic usage among patients, with hospitals serving as reservoirs for resistant strains, often due to inappropriate prescribing practices.5 Due to a lack of diagnostic support (especially in primary health facilities) or preference, prescribers usually rely on symptoms for diagnosis, leading to empiric prescriptions6 7 and high rates of antibiotic use reaching 66%.8
Antimicrobial stewardship, the careful and responsible management of antimicrobials, is a key pillar in combating resistance.9–12 In line with this, the WHO advocates for rational drug use policies like treatment guidelines to minimise resistance,13 but implementation is lacking in many low- and middle-income countries,14–16 and in countries like Ghana, adherence remains voluntary and inconsistent.16 There is also a significant knowledge gap among healthcare workers regarding antibiotic prescription patterns and factors that influence nonadherence to guidelines (inappropriate use).7 Assessing antimicrobial prescriptions/utilisation patterns drives quality improvement initiatives in antimicrobial stewardship,17–20 as post-prescription reviews with feedback have been shown to effectively reduce antibiotic use.12 Several studies have reported on antibiotic prescription patterns both internationally21–23 and locally,18 24 some in outpatient and inpatient settings, but there is a paucity of data evaluating antibiotic prescriptions/utilisation in purely paediatric outpatient settings. Using the Standard Treatment Guidelines (STGs),25 this study examines factors associated with antibiotic prescribing patterns and appropriateness in paediatric outpatient care to provide feedback that can inform and strengthen antimicrobial stewardship programmes.
Materials and methods
Study design
This was a retrospective chart review involving the extraction of secondary data from patients’ electronic medical records from 1 April 2022 to 30 June 2022.
Study site
The study was conducted at Princess Marie Louise Children’s Hospital (PMLCH) in Accra, Ghana, a 110-bed specialist facility and the largest stand-alone children’s hospital in the country. It serves mostly children aged 0–18 years, with an average of 157 daily outpatient and emergency visits and about 440 admissions per month, primarily from Accra and surrounding areas.
Inclusion criteria
All children (aged 0–18 years) who visited the Outpatient Department at PMLCH between 1 April and 30 June 2022 and received only oral antibiotics were included in the study. The study focused on outpatient departments because drug use studies are generally recommended to be conducted within a single type of health facility to ensure meaningful interpretation of the findings. Although inpatient prescribing can also be evaluated, it is often more complex than outpatient prescribing. Given the specific objectives of this study, the outpatient setting was therefore more appropriate for evaluating antibiotic prescribing patterns and appropriateness.26
Exclusion criteria
Patients with incomplete medical records, diagnoses not covered by the STGs,25 or antibiotics (eg, linezolid) not listed in the STGs were excluded. Patients on anti-tuberculosis drugs and sickle cell patients on penicillin V prophylaxis were also excluded because these represent long-term treatment or prophylactic regimens rather than prescribing decisions for the presenting outpatient illness, which could bias estimates of antibiotic prescribing patterns and appropriateness.
Sampling method and sample size determination
The sampling method used was a census sampling. Thus, all Electronic Medical Records obtained within the period of the study (1 April 2022 to 30 June 2022) were considered.
Operational definition
Appropriate indication
Assessed whether the antibiotic prescribed was recommended by the STGs,25 based on the differential or provisional diagnosis recorded during the patient consultation.
Appropriate choice
For cases where an antibiotic was indicated, assessed whether the prescribed drug matched the STG recommendation for the recorded diagnosis. For cases where there were multiple diagnoses, the diagnosis closely related to the antibiotic prescribed was considered.
Appropriate duration
Assessed whether the prescribed duration matched the STG recommendation (for cases where the antibiotic was indicated and the correct drug was chosen).
Appropriate dosage
Assessed whether the prescribed dosage matched the STG recommendation (for cases where the antibiotic was indicated and the correct drug was chosen), allowing for minor adjustments to fit available formulation strengths.
Prior antibiotic exposure
Any antibiotic taken by the patient within 28 days before the consultation.27
First-line therapy
Antibiotic recommended as the first-line treatment for the recorded diagnosis according to the STG.
Higher-tier antibiotics
Antibiotics recommended as second-line or third-line treatment for the recorded diagnosis according to the STGs.
Data collection techniques and tools
Initially, a summary spreadsheet was obtained from the hospital’s Lightwave Health Information Management System. This spreadsheet had all patients who attended the outpatient department over the period under study. Additionally, a Google Forms-based data extraction tool was manually populated using data from patient folders, accessed one at a time. Data was extracted from each folder for which at least one antibiotic was prescribed (applying the inclusion and exclusion criteria). The Google Forms were divided into four sections. Section 1 collected demographic and clinical information (eg, age, sex, diagnosis, history of fever, antibiotic use, prescriber rank and indication for antibiotics). Sections 2, 3 and 4 focused on each antibiotic prescribed, including name, appropriateness in choice, duration and dosage. Where there was missing information for the history of fever and prior antibiotic use, missing data were recorded as a variable (information not available).
Data handling and analysis
Data were checked for completeness at the point of collection and analysed using Microsoft Excel and Stata V.15. Excel was used to estimate the prevalence of antibiotic use and to perform descriptive analyses, while Stata was used for inferential statistics. Patient characteristics, including sociodemographic and clinical variables, and the prescriber characteristics (prescriber rank) were summarised at the patient level. Variables, including age, sex, prescriber rank, history of fever and prior antibiotic use (independent variables), were selected a priori based on existing literature and clinical relevance. Logistic regression was used to assess the association between these and the number and highest tier of antibiotics prescribed because each consultation was treated as a single observation, irrespective of the number of antibiotics prescribed. However, when assessing the association between the independent variables and the appropriateness of antibiotic choice, dosage and duration, each prescribed antibiotic was treated as a separate observation. As a result, patients who received more than one antibiotic contributed multiple observations, resulting in repeated patient and prescriber characteristics for each antibiotic. These observations were therefore not independent. To account for this within-patient correlation, generalised estimating equations with an exchangeable working correlation structure and robust SEs, clustered by patient ID, were used. Statistical significance was set at p<0.05.
Patient and public involvement
Patients and the public were involved in the dissemination plans of this research.
Results
Sociodemographic and clinical characteristics of patients
Out of 16 555 OPD patient consultations during the study period, 3244 (20%) received antibiotics. Table 1 displays the sociodemographic and clinical characteristics of patients. Most antibiotic recipients were male (54%, n=1539) and aged 5 years or younger (78%, n=2239). The top diagnoses were pharyngitis/tonsillitis, otitis media, pneumonia, bacterial skin infections and diarrhoea/gastroenteritis, respectively. Patients who had used antibiotic(s) prior to consultation were 11.81% (n=338).
Table 1. Sociodemographic and clinical characteristics of paediatric outpatients receiving antibiotics.
| Patient characteristics | Category | Frequency (n=2862) | Percentage |
|---|---|---|---|
| Age range | |||
| 0–27 days | 5 | 0.17 | |
| 28 days to 12 months | 432 | 15.09 | |
| 13–23 months | 629 | 21.98 | |
| 2–5 years | 1173 | 40.99 | |
| 6–11 years | 511 | 17.85 | |
| 12–18 years | 112 | 3.91 | |
| Sex | |||
| Ambiguous | 2 | 0.07 | |
| Female | 1321 | 46.16 | |
| Male | 1539 | 53.77 | |
| Presence of fever | |||
| Yes | 1916 | 66.95 | |
| No | 759 | 26.52 | |
| Information not available | 187 | 6.53 | |
| Prior antibiotic use | |||
| No | 1627 | 56.85 | |
| Yes | 338 | 11.81 | |
| Information not available | 897 | 31.34 | |
| Diagnosis* | |||
| Pharyngitis/tonsillitis | 1143 | 36.00 | |
| Acute otitis media | 530 | 16.69 | |
| Pneumonia | 419 | 13.20 | |
| Bacterial skin infection | 290 | 9.13 | |
| Diarrhoea/acute gastroenteritis | 289 | 9.10 | |
| Urinary tract infection | 255 | 8.03 | |
| Mumps | 43 | 1.35 | |
| Nasopharyngitis | 33 | 1.04 | |
| Cellulitis | 22 | 0.69 | |
| Sinusitis | 20 | 0.63 | |
| Periodontal infection | 16 | 0.50 | |
| Severe acute malnutrition | 15 | 0.47 | |
| Allergic rhinitis | 12 | 0.38 | |
| Bronchiolitis | 11 | 0.35 | |
| Acute exacerbation of asthma | 8 | 0.25 | |
| Cough | 8 | 0.25 | |
| Typhoid fever | 8 | 0.25 | |
| Vomiting | 7 | 0.22 | |
| Atopic dermatitis | 7 | 0.22 | |
| Chicken pox | 6 | 0.19 | |
| scdx with voc | 6 | 0.19 | |
| Acute gastritis | 5 | 0.16 | |
| Others | 22 | 0.69 | |
Multiple diagnoses present in some cases.
Prescribing characteristics and nature of prescriptions
House officers attended to nearly half (48%) of all patients who received at least one antibiotic. First-line antibiotics were used at the highest level in 87% of consultations. Antibiotics were indicated in 95% of cases where at least one antibiotic was given. Among the prescriptions where antibiotics were indicated, the appropriate choice of antibiotic was prescribed 98% of the time, but the appropriate duration and dosage were prescribed only 40% and 85% of the time, respectively. Antibiotics used were mainly co-amoxiclav (45%), cefuroxime (16%) and amoxicillin (10%) (table 2).
Table 2. Prescribing characteristics and nature of prescriptions for paediatric outpatients who received antibiotics.
| Prescribing characteristics | Category | Frequency (n=2862) | Percentage |
|---|---|---|---|
| Rank of prescriber | |||
| House officer | 1371 | 47.90 | |
| Medical officer | 902 | 31.52 | |
| Nurse | 252 | 8.81 | |
| Physician assistant | 259 | 9.05 | |
| Resident | 55 | 1.92 | |
| Specialist (paediatrician) | 23 | 0.80 | |
| Number of antibiotics | |||
| One | 2754 | 96.23 | |
| Two | 108 | 3.77 | |
| Highest antibiotic category prescribed | |||
| First-line | 2503 | 87.46 | |
| Second-line | 312 | 10.90 | |
| Third-line | 47 | 1.64 | |
| Indication for antibiotics* | |||
| Yes | 2719 | 95.00 | |
| No | 143 | 5.00 | |
| Prescriptions† | (n=2824) | ||
| Right choice | 2765 | 97.91 | |
| Wrong choice | 59 | 2.09 | |
| (n=2765) | |||
| Right duration | 1097 | 39.67 | |
| Wrong duration | 1668 | 60.33 | |
| (n=2765) | |||
| Right dosage | 2353 | 85.10 | |
| Wrong dosage | 412 | 14.90 | |
| Antibiotics prescribed† | (n=2967) | ||
| Co-amoxiclav | 1344 | 45.30 | |
| Amoxicillin | 307 | 10.35 | |
| Cefuroxime | 462 | 15.57 | |
| Flucloxacillin | 285 | 9.61 | |
| Azithromycin | 268 | 9.03 | |
| Ciprofloxacin | 133 | 4.48 | |
| Ciprofloxacin+Tinidazole | 1 | 0.03 | |
| Erythromycin | 75 | 2.53 | |
| Metronidazole | 59 | 1.99 | |
| Clindamycin | 28 | 0.94 | |
| Doxycycline | 3 | 0.10 | |
| Nitrofurantoin | 1 | 0.03 | |
| Secnidazole | 1 | 0.03 | |
Patient-level characteristics used.
Some patients received multiple antibiotic prescriptions; therefore, each antibiotic was counted as a separate entry.
Patient and prescriber characteristics associated with appropriateness of antibiotic prescriptions
Male sex was associated with antibiotic prescribing when not indicated (adjusted OR (aOR) 1.64, 95% CI 1.14 to 2.34), whereas older age (12–18 years) (aOR 0.25, 95% CI 0.07 to 0.88) and a history of fever (aOR 0.76, 95% CI 0.51 to 1.15) were associated with fewer antibiotic prescriptions when not indicated. Compared with house officers, specialised nurses and physician assistants were associated with antibiotic prescribing when not indicated (specialised nurses: aOR 4.08, 95% CI 2.55 to 6.53; physician assistants: aOR 2.19, 95% CI 1.27 to 3.76) (table 3).
Table 3. Univariable and multivariable generalised estimating equations analyses of factors associated with antibiotic prescribing when not indicated.
| Variable | OR (95% CI) | P value (OR) | aOR (95% CI) | P value (aOR) |
|---|---|---|---|---|
| Age | ||||
| 28 days to 12 months | Ref | Ref | ||
| 0–27 days | Non-estimable | Non-estimable | ||
| 13–23 months | 0.57 (0.33 to 0.99) | 0.045* | 0.58 (0.33 to 1.02) | 0.057 |
| 2–5 years | 0.77 (0.49 to 1.21) | 0.262 | 0.70 (0.44 to 1.12) | 0.139 |
| 6–11 years | 0.64 (0.36 to 1.12) | 0.115 | 0.62 (0.35 to 1.11) | 0.109 |
| 12–18 years | 0.36 (0.11 to 1.21) | 0.099 | 0.25 (0.07 to 0.88) | 0.030* |
| Sex | ||||
| Female | Ref | Ref | ||
| Male | 1.64 (1.15 to 2.33) | 0.006* | 1.64 (1.14 to 2.34) | 0.007* |
| Ambiguous | Non-estimable | Non-estimable | ||
| Rank of prescriber | ||||
| House officer | Ref | Ref | ||
| Specialised nurse | 4.75 (3.04 to 7.40) | <0.001* | 4.08 (2.55 to 6.53) | <0.001* |
| Physician assistant | 2.47 (1.47 to 4.14) | 0.001 | 2.19 (1.27 to 3.76) | 0.005* |
| Medical officer | 0.90 (0.57 to 1.43) | 0.666 | 0.87 (0.54 to 1.38) | 0.546 |
| Resident | 0.48 (0.07 to 3.58) | 0.478 | 0.46 (0.06 to 3.36) | 0.459 |
| Specialist (paediatricians) | 1.23 (0.16 to 9.31) | 0.841 | 1.18 (0.17 to 8.35) | 0.868 |
| History of fever | ||||
| No | Ref | Ref | ||
| Yes | 0.66 (0.46 to 0.95) | 0.026* | 0.76 (0.51 to 1.15) | 0.036* |
| Information not available | 0.98 (0.51 to 1.88) | 0.943 | 0.84 (0.42 to 1.68) | 0.661 |
| Prior antibiotics given | ||||
| No | Ref | Ref | ||
| Yes | 1.16 (0.64 to 2.10) | 0.631 | 1.05 (0.57 to 1.92) | 0.791 |
| Information not available | 2.27 (1.59 to 3.24) | <0.001* | 1.41 (0.93 to 2.13) | 0.009* |
P value <0.05.
aOR, adjusted OR.
No significant associations were observed between appropriate antibiotic choice and age, sex, prescriber rank, history of fever or prior antibiotic use (online supplemental table 1). However, medical officers were associated with correct antibiotic dosing compared with house officers (aOR 1.45, 95% CI 1.12 to 1.86). Additionally, a history of fever was associated with correct antibiotic dosing (aOR 1.28, 95% CI 1.01 to 1.62) (table 4).
Table 4. Univariable and multivariable generalised estimating equations analyses of factors associated with appropriate dosage of antibiotics.
| Variable | OR (95% CI) | P value (OR) | aOR (95% CI) | P value (aOR) |
|---|---|---|---|---|
| Age | ||||
| 28 days to 12 months | Ref | Ref | ||
| 0–27 days | 0.87 (0.10 to 7.88) | 0.900 | 1.02 (0.12 to 8.91) | 0.985 |
| 13–23 months | 1.37 (0.97 to 1.94) | 0.072 | 1.36 (0.96 to 1.92) | 0.082 |
| 2–5 years | 1.47 (1.08 to 2.01) | 0.015* | 1.48 (1.08 to 2.02) | 0.014* |
| 6–11 years | 0.95 (0.67 to 1.34) | 0.754 | 0.98 (0.69 to 1.39) | 0.906 |
| 12–18 years | 1.40 (0.77 to 2.54) | 0.271 | 1.41 (0.76 to 2.61) | 0.279 |
| Sex | ||||
| Female | Ref | Ref | ||
| Male | 0.93 (0.75 to 1.15) | 0.504 | 0.92 (0.74 to 1.14) | 0.433 |
| Ambiguous | Non-estimable | Non-estimable | ||
| Rank of prescriber | ||||
| House officer | Ref | Ref | ||
| Specialised nurse | 1.34 (0.87 to 2.05) | 0.185 | 1.30 (0.82 to 2.04) | 0.264 |
| Physician assistant | 0.88 (0.61 to 1.26) | 0.476 | 0.86 (0.60 to 1.24) | 0.417 |
| Medical officer | 1.45 (1.13 to 1.86) | 0.004* | 1.45 (1.12 to 1.86) | 0.004* |
| Resident | 1.32 (0.59 to 2.95) | 0.506 | 1.31 (0.58 to 2.99) | 0.514 |
| Specialist (paediatricians) | 1.98 (0.46 to 8.52) 0.361 | 2.19 (0.52 to 9.13) 0.283 | ||
| History of fever | ||||
| No | Ref | Ref | ||
| Yes | 1.31 (1.04 to 1.65) | 0.025* | 1.28 (1.01 to 1.62) | 0.044* |
| Information not available | 0.96 (0.62 to 1.50) | 0.866 | 0.89 (0.57 to 1.39) | 0.613 |
| Prior antibiotics given | ||||
| No | Ref | Ref | ||
| Yes | 0.78 (0.56 to 1.07) | 0.126 | 0.80 (0.58 to 1.11) | 0.188 |
| Information not available | 0.98 (0.77 to 1.24) | 0.844 | 1.01 (0.78 to 1.29) | 0.965 |
P value <0.05. Analysis was restricted to prescriptions with an appropriate indication and antibiotic choice.
aOR, adjusted OR.
The odds of receiving the correct duration of antibiotic decreased among children aged 2–5 years and 6–11 years compared with those aged 28 days to 12 months. Relative to house officers, residents were associated with correct antibiotic duration (aOR 2.36, 95% CI 1.29 to 4.31), while specialised nurses (aOR 0.51, 95% CI 0.36 to 0.72) and physician assistants (aOR 0.72, 95% CI 0.53 to 0.97) were associated with incorrect antibiotic duration. Also, the presence of fever decreased the odds of prescribing the correct antibiotic duration (aOR 0.38, 95% CI 0.32 to 0.46) (table 5).
Table 5. Univariable and multivariable generalised estimating equations analyses of factors associated with appropriate duration of antibiotics.
| Variable | OR (95% CI) | P value (OR) | aOR (95% CI) | P value (aOR) |
|---|---|---|---|---|
| Age | ||||
| 28 days to 12 months | Ref | Ref | ||
| 0–27 days | 5.10 (0.57 to 46.10) | 0.147 | 2.83 (0.30 to 26.57) | 0.363 |
| 13–23 months | 0.96 (0.74 to 1.24) | 0.747 | 1.00 (0.77 to 1.29) | 0.978 |
| 2–5 years | 0.69 (0.55 to 0.88) | 0.002* | 0.69 (0.54 to 0.87) | 0.002* |
| 6–11 years | 0.83 (0.63 to 1.09) | 0.181 | 0.73 (0.55 to 0.97) | 0.029* |
| 12–18 years | 1.31 (0.85 to 2.01) | 0.217 | 1.14 (0.72 to 1.79) | 0.584 |
| Sex | ||||
| Female | Ref | Ref | ||
| Male | 0.84 (0.72 to 0.98) | 0.026* | 0.85 (0.73 to 1.00) | 0.052 |
| Ambiguous | Non-estimable | Non-estimable | ||
| Rank of prescriber | ||||
| House officer | Ref | Ref | ||
| Specialised nurse | 0.59 (0.43 to 0.81) | 0.001* | 0.51 (0.36 to 0.72) | <0.001* |
| Physician assistant | 0.74 (0.55 to 0.99) | 0.043* | 0.72 (0.53 to 0.97) | 0.031* |
| Medical officer | 1.00 (0.84 to 1.19) | 0.972 | 0.97 (0.81 to 1.16) | 0.746 |
| Resident | 2.26 (1.29 to 3.97) | 0.004* | 2.36 (1.29 to 4.31) | 0.005* |
| Specialist (paediatricians) | 2.57 (1.07 to 6.16) | 0.035* | 2.15 (0.88 to 5.24) | 0.093 |
| History of fever | ||||
| No | Ref | Ref | ||
| Yes | 0.38 (0.32 to 0.46) | <0.001* | 0.38 (0.32 to 0.46) | <0.001* |
| Information not available | 1.00 (0.71 to 1.40) | 1.000 | 0.99 (0.70 to 1.40) | 0.954 |
| Prior antibiotics given | ||||
| No | Ref | Ref | ||
| Yes | 1.61 (1.26 to 2.05) | <0.001* | 1.56 (1.20 to 2.02) | 0.001* |
| Information not available | 1.14 (0.96 to 1.36) | 0.136 | 1.14 (0.94 to 1.37) | 0.179 |
P value <0.05. Analysis was restricted to prescriptions with an appropriate indication and antibiotic choice.
aOR, adjusted OR.
Older age was associated with receiving multiple antibiotics. Compared with children aged 28 days to 12 months, the odds of receiving multiple antibiotics increased progressively with age: aOR 2.46 (95% CI 1.15 to 5.26) for children aged 2–5 years, 2.58 (95% CI 1.14 to 5.81) for those aged 6–11 years and 4.58 (95% CI 1.69 to 12.43) for those aged 12–18 years. Relative to house officers, the odds of prescribing multiple antibiotics were reduced among specialised nurses (aOR 0.12, 95% CI 0.03 to 0.52), physician assistants (aOR 0.39, 95% CI 0.15 to 0.98), and medical officers (aOR 0.55, 95% CI 0.35 to 0.87) (online supplemental table 2).
Compared with house officers, the odds of prescribing higher-tier antibiotics were reduced among specialised nurses (aOR 0.35, 95% CI 0.20 to 0.61), physician assistants (aOR 0.26, 95% CI 0.14 to 0.47) and medical officers (aOR 0.65, 95% CI 0.51 to 0.85). Additionally, prior antibiotic use was associated with increased odds of prescribing higher-tier antibiotics (aOR 2.12, 95% CI 1.56 to 2.86) (online supplemental table 3).
Discussion
The overall prevalence of antibiotic use in our outpatient department (20%) was well within the local and WHO targets of 20% and 30%,28 respectively, possibly due to recent antimicrobial stewardship campaigns and awareness.29–31 However, the prevalence was substantially lower than that reported in China (63.8%)32 and India (36.8%),33 but was similar to that reported in Madagascar, Senegal and Cambodia (29.3%).34
While a meta-analysis from high-income countries found that females generally received more antibiotics,35 the opposite pattern was observed in this low-income and middle-income paediatric setting. Males received more antibiotics, consistent with findings by Mandal et al33 and Young et al,36 and were 1.6 times more likely to receive antibiotics when not indicated, as also reported in Uganda.37 Limited diagnostic access in these settings may encourage reliance on symptom severity,38 which may be greater in males because of biological and hormonal differences.39 Stewardship interventions addressing symptom-based prescribing and promoting the appropriate use of diagnostic investigations could therefore reduce unnecessary antibiotic use, particularly among boys.
Children aged 5 years or younger accounted for most antibiotic prescriptions, consistent with findings from Finland40 and India,33 likely because of their greater burden of infectious diseases.41 However, many of these infections are viral and do not require antibiotics.42 These children were also more likely to receive antibiotics when not indicated, as reported in the USA.43 This may reflect clinicians’ perception that younger children are more vulnerable or caregiver pressure to prescribe antibiotics.44 Antimicrobial stewardship programmes that educate caregivers of younger children about the signs and symptoms of viral infections and equip clinicians to manage caregiver pressure for unnecessary antibiotic prescribing could reduce inappropriate antibiotic use in this age group.45 Children aged 6–11 years were less likely to receive the correct antibiotic duration than infants, consistent with findings from Ethiopia, where inappropriate antibiotic use was also common in this age group.46 This may be explained by the higher frequency of conditions such as acute pharyngitis/tonsillitis and acute otitis media (AOM) among them,47 for which penicillin was often prescribed for shorter durations than recommended. For example, although Ghana’s STGs recommend a 10-day course of antibiotics for AOM across all age groups, nearly three-quarters of patients received only 5–7 days. This suggests that prescribing practices may not fully align with national guidelines and may instead reflect international trends, as similar deviations have been reported in the USA.48 Qualitative studies exploring prescribers’ views and reasons for deviating from recommended treatment durations could provide further insight into this issue and inform improvements in treatment guidelines, antibiotic formulations and prescribing practices. Our study also found that older children were more likely to be prescribed multiple antibiotics than infants, despite infants being more vulnerable to severe infections.49 This is worrisome, as Obakiro et al found that health workers were less likely to adhere to guidelines when prescribing antibiotics in combination.37 This pattern may stem from diagnostic uncertainty or overestimation of infection complexity in older children.50 Addressing this issue will require further investigation into the underlying causes of these prescribing practices and a stronger focus on evidence-based guidelines to ensure appropriate antibiotic use across all age groups.
The majority (67%) of patients who received antibiotics in our study complained of fever, which aligns closely with findings from Opoku et al, who reported a 70.1% prevalence of antibiotic prescriptions among febrile patients in outpatient departments in Ghana.41 This suggests fever is a common trigger for antibiotic use, often due to concerns about underlying infections. However, they were less likely to receive the correct duration of antibiotics. This may indicate that fever, while often seen as a key indicator for antibiotic treatment, does not always result in appropriate or guideline-adherent prescribing practices. Symptom-based antimicrobial stewardship interventions targeting fever, including guidelines,51 clinical flowcharts and diagnostic tools such as C reactive protein testing52 to differentiate viral from bacterial causes of fever, could reduce inappropriate antibiotic use.
Patients who had received antibiotics before presentation had double the odds of being prescribed a higher-tier antibiotic than those who had not. Higher-tier antibiotics are broad-spectrum and often prescribed when initial treatments fail or when there are concerns about resistant infections.53 Inappropriate use of higher-tier antibiotics is dangerous, as these antibiotics are our only defence against resistant strains. Lack of clinical improvement following initial first-line antibiotic therapy should prompt prescribers to consider alternative explanations, including substandard or falsified medicines, poor adherence, viral infections or an incorrect diagnosis, rather than automatically escalating to higher-tier antibiotics. Antimicrobial stewardship programmes should therefore train prescribers to systematically evaluate these factors before prescribing higher-tier antibiotics.
Our study found that 87% of antibiotic prescriptions were first-line, exceeding the recommended 80% benchmark.54 This is encouraging, as unnecessary broad-spectrum antibiotic use promotes AMR.53 Antibiotics most commonly prescribed included co-amoxiclav, cefuroxime and amoxicillin, consistent with other findings.21 55 Despite this positive trend, antibiotic overuse was evident. Antibiotics were prescribed at the first visit for 75% of children with pharyngitis and 74% of children with AOM, although the vast majority of cases are caused by viruses.56 Also, 18% of children with acute diarrhoea received antibiotics despite WHO recommendations for ORS and zinc as mainstays and antibiotics only for bloody diarrhoea, suspected cholera with severe dehydration and serious non-intestinal infections.57 Since bacterial causes like bloody diarrhoea are uncommon (2.2%)58 and no cholera cases were reported, this suggests unnecessary prescribing, consistent with prior reports of up to 40% antibiotic use for non-bacterial cases.59 This may reflect the lack of WHO-recommended clinical decision-support tools in Ghana’s STGs, such as clinical severity scoring systems and guidance on watchful waiting for mild cases.25 56 Updating the guidelines to incorporate these approaches and align more closely with the WHO AWaRe guidelines56 could therefore reduce unnecessary antibiotic use.60
Prescribers’ years of experience have been found to have an effect on treatment decisions,61 and house officers (who have <3 years of experience) accounted for the majority of antibiotic prescriptions. This was inconsistent with findings by Opoku et al that found prescribers with more years of experience (>5 years) being more likely to prescribe antibiotics compared with those with fewer years (<3 years).41 This was likely because house officers constituted the largest proportion of prescribers at PMLCH. House officers were also more likely to prescribe multiple or select higher-tier antibiotics than specialised nurses, physician assistants and medical officers, possibly reflecting more cautious prescribing practices due to their limited clinical experience.62 Compared with house officers, medical officers and residents were more likely to prescribe the correct antibiotic dosage and duration, respectively, probably reflecting greater clinical experience and familiarity with treatment guidelines. House officer orientation should therefore include training on STGs, exposure to antimicrobial stewardship initiatives and mentorship from senior clinicians (residents and medical officers). In contrast, specialised nurses and physician assistants were more likely to prescribe antibiotics when not indicated, consistent with findings from Uganda, where clinical officers with similar roles also tended to prescribe antibiotics unnecessarily.63 Similar observations have been reported elsewhere, with less-qualified healthcare providers more likely to prescribe antibiotics,64 possibly because of professional culture, diagnostic uncertainty50 or limited familiarity with clinical guidelines. Strengthening formal and continuous medical training for physician assistants and specialised nurses may improve diagnostic confidence, encourage consideration of alternative management strategies and reduce inappropriate antibiotic prescribing.65
Limitations
This study was limited to enteral antibiotics, excluding parenteral formulations commonly used in inpatient settings and for certain conditions such as STIs in older adolescents. Most diagnoses were provisional rather than microbiologically confirmed, and cases outside the STGs were excluded. As with all retrospective studies, the findings were subject to incomplete or inaccurate clinical documentation, which may lead to misclassification of antibiotic appropriateness, and also does not allow for causal inference. In addition, the observed association between sex and antibiotic indication may reflect unmeasured differences in underlying diagnoses. Only prescriber rank was available as a prescriber-related characteristic; other characteristics, such as sex, age, years of experience and AMS training, could not be assessed because they were not routinely recorded in the electronic medical records.
Recommendations
Policymakers and clinicians should adopt a multifaceted approach to antibiotic use surveillance and antimicrobial stewardship, as inappropriate prescribing may persist despite achieving current antibiotic prescribing targets. Future research should standardise this surveillance approach and evaluate whether WHO targets should be expanded to include measures of prescribing quality (eg, indication, antibiotic choice, dosage and duration).
Conclusion
The prevalence of antibiotic prescribing among paediatric outpatients was within national and WHO targets, with high adherence to first-line antibiotic prescribing. However, inappropriate prescribing remained evident, particularly among males, younger children, patients presenting with fever and certain diagnoses. One prescriber group was more likely to prescribe multiple and higher-tier antibiotics, practices that could promote AMR. Strengthening antimicrobial stewardship through improved diagnostic support, updated clinical guidelines, targeted prescriber training and mentorship, and caregiver education could further optimise antibiotic use and help mitigate AMR.
Supplementary material
Acknowledgements
We would like to express our sincere appreciation to Dr Faye BoamahMensah, the medical staff at the hospital and all other stakeholders who supported this study. We also acknowledge Professor Charlene Rodrigues of the London School of Hygiene and Tropical Medicine, our mentor, for her encouragement and guidance throughout the study. In addition, we acknowledge the Fleming Fund for sponsoring training in data analysis, which proved vital to the preparation of this manuscript.
Footnotes
Funding: This research was funded by Princess Marie Louise Children’s Hospital, Ghana Health Service.
Provenance and peer review: Not commissioned; externally peer reviewed.
Patient consent for publication: Not applicable.
Data availability free text: The data used in this study are owned by Princess Marie Louise Children’s Hospital, part of the Ghana Health Service. Access to the data is available upon request to researchers who meet the criteria for confidential data access. Requests should be directed to AKA at adufulabena32@gmail.com. All data requests must include a clear description of the intended use and comply with the Ethical Review Committee’s requirements of the Ghana Health Service. The data will only be provided for the purposes outlined in the request or research protocol.
Patient and public involvement: Patients and/or the public were involved in the design, or conduct, or reporting, or dissemination plans of this research. Refer to the Methods section for further details.
Ethics approval: The study was conducted with permission from management and ethical approval from the Ghana Health Service Ethics Review Committee (GHS-ERC: 025/08/22).
Data availability statement
Data are available upon reasonable request.
References
- 1.Habboush Y, Guzman N. StatPearls. StatPearls Publishing; 2024. Antibiotic resistance.http://www.ncbi.nlm.nih.gov/books/NBK513277/ Available. [Google Scholar]
- 2.Salam MdA, Al-Amin MdY, Salam MT, et al. Antimicrobial Resistance: A Growing Serious Threat for Global Public Health. Health Care (Don Mills) 2023;11:1946. doi: 10.3390/healthcare11131946. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Antimicrobial Resistance Collaborators Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet. 2019;399:629–55. doi: 10.1016/S0140-6736(21)02724-0. https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(21)02724-0/fulltext?ref=healthtips.kr Available. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hussein HA, Abdi SM, Ahad AA. Factors and challenges contributing to antimicrobial resistance in East African pastoral settings and importance of One Health approach. CABI One Health. 2023 doi: 10.1079/cabionehealth.2023.0025. [DOI] [Google Scholar]
- 5.Labi A-K, Obeng-Nkrumah N, Nartey ET, et al. Antibiotic use in a tertiary healthcare facility in Ghana: a point prevalence survey. Antimicrob Resist Infect Control. 2018;7:15. doi: 10.1186/s13756-018-0299-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Do NTT, Ta NTD, Tran NTH, et al. Point-of-care C-reactive protein testing to reduce inappropriate use of antibiotics for non-severe acute respiratory infections in Vietnamese primary health care: a randomised controlled trial. Lancet Glob Health. 2016;4:e633–41. doi: 10.1016/S2214-109X(16)30142-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Nahar P, Unicomb L, Lucas PJ, et al. What contributes to inappropriate antibiotic dispensing among qualified and unqualified healthcare providers in Bangladesh? A qualitative study. BMC Health Serv Res. 2020;20:656. doi: 10.1186/s12913-020-05512-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Labi A-K, Kartey BS, Hedidor GK, et al. Antibiotic consumption trends in Ghana: analysis of six-years pharmacy issue data from a secondary healthcare facility. JAC Antimicrob Resist . 2023;5:dlad025. doi: 10.1093/jacamr/dlad025. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Hersh AL, De Lurgio SA, Thurm C, et al. Antimicrobial stewardship programs in freestanding children’s hospitals. Pediatrics. 2015;135:33–9. doi: 10.1542/peds.2014-2579. [DOI] [PubMed] [Google Scholar]
- 10.Sefah IA, Chetty S, Yamoah P, et al. An Assessment of the Current Level of Implementation of the Core Elements of Antimicrobial Stewardship Programs in Public Hospitals in Ghana. Hosp Pharm. 2024;59:367–77. doi: 10.1177/00185787231224066. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Shrestha J, Zahra F, Cannady J. StatPearls. StatPearls Publishing; 2026. Antimicrobial stewardship.http://www.ncbi.nlm.nih.gov/books/NBK572068/ Available. [PubMed] [Google Scholar]
- 12.Zaffagnini A, Rigotti E, Opri F, et al. Enforcing surveillance of antimicrobial resistance and antibiotic use to drive stewardship: experience in a paediatric setting. J Hosp Infect. 2024;144:14–9. doi: 10.1016/j.jhin.2023.12.001. [DOI] [PubMed] [Google Scholar]
- 13.World Health Organization . World Health Organization - Regional Office for the Eastern Mediterranean; 2011. [3-Oct-2024]. Regulate and promote rational use of medicines, including in animal husbandry, and ensure proper patient care.http://www.emro.who.int/world-health-days/2011/regulate-and-promote-rational-use-of-medicines-including-in-animal-husbandry-and-ensure-proper-patient-care.html Available. Accessed. [Google Scholar]
- 14.Ahiabu MA, Tersbøl BP, Biritwum R, et al. A retrospective audit of antibiotic prescriptions in primary health-care facilities in Eastern Region, Ghana. Health Policy Plan. 2016;31:250–8. doi: 10.1093/heapol/czv048. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Holloway KA, Rosella L, Henry D. The Impact of WHO Essential Medicines Policies on Inappropriate Use of Antibiotics. PLoS One. 2016;11:e0152020. doi: 10.1371/journal.pone.0152020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Sefah IA, Essah DO, Kurdi A, et al. Assessment of adherence to pneumonia guidelines and its determinants in an ambulatory care clinic in Ghana: findings and implications for the future. JAC-Antimicrob Resist. 2021;3:dlab080. doi: 10.1093/jacamr/dlab080. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Agiri O, Osena G, Bahati F, et al. Knowledge, attitudes and practices survey on antimicrobial resistance and stewardship among pharmacy healthcare workers in 28 African countries. BMJ Glob Health. 2025;10 doi: 10.1136/bmjgh-2025-019151. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Agyare E, Acolatse JEE, Dakorah MP, et al. Antimicrobial stewardship capacity and antibiotic utilisation practices in the Cape Coast Teaching Hospital, Ghana: A point prevalence survey study. PLoS One. 2024;19 doi: 10.1371/journal.pone.0297626. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Gobezie MY, Tesfaye NA, Faris AG, et al. Surveillance of antimicrobial utilization in Africa: a systematic review and meta-analysis of prescription rates, indications, and quality of use from point prevalence surveys. Antimicrob Resist Infect Control. 2024;13:101. doi: 10.1186/s13756-024-01462-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Shah P, Maheshwari T, Patel D, et al. An overview: Implementation and core elements of antimicrobial stewardship programme. Clin Epidemiol Glob Health. 2024;29:101543. doi: 10.1016/j.cegh.2024.101543. [DOI] [Google Scholar]
- 21.Abubakar FI, Ahmed HK, Akintunde OO, et al. Pattern and appropriateness of antibiotic therapy for acute respiratory tract infection among under-five children accessing care in a tertiary facility, Sokoto, Nigeria. BMJ Paediatr Open . 2025;9:e003468. doi: 10.1136/bmjpo-2025-003468. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Alekaw H, Derebe D, Melese WM, et al. Antibiotic Prescription Pattern, Appropriateness, and Associated Factors in Patients Admitted to Pediatric Wards of Tibebe Ghion Specialized Hospital, Bahir Dar, North West Ethiopia. Infect Drug Resist. 2022;15:6659–69. doi: 10.2147/IDR.S380897. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Demoz GT, Kasahun GG, Hagazy K, et al. Prescribing Pattern of Antibiotics Using WHO Prescribing Indicators Among Inpatients in Ethiopia: A Need for Antibiotic Stewardship Program. Infect Drug Resist. 2020;13:2783–94. doi: 10.2147/IDR.S262104. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Darkwah TO, Afriyie DK, Sneddon J, et al. Assessment of prescribing patterns of antibiotics using National Treatment Guidelines and World Health Organization prescribing indicators at the Ghana Police Hospital: a pilot study. Pan Afr Med J. 2021;39:222. doi: 10.11604/pamj.2021.39.222.29569. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Ministry of Health Ghana-standard treatment guidelines-2017. 2017
- 26.World Health Organization How to investigate drug use in health facilities: selected drug use indicators. [23-Jun-2024]. https://iris.who.int/handle/10665/60519 Available. Accessed.
- 27.Ingelbeen B, Koirala KD, Verdonck K, et al. Antibiotic use prior to seeking medical care in patients with persistent fever: a cross-sectional study in four low- and middle-income countries. Clin Microbiol Infect. 2021;27:1293–300. doi: 10.1016/j.cmi.2020.11.003. [DOI] [PubMed] [Google Scholar]
- 28.Ofori-Asenso R. A closer look at the World Health Organization’s prescribing indicators. J Pharmacol Pharmacother. 2016;7:51–4. doi: 10.4103/0976-500X.179352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Koduah A, Gyansa-Lutterodt M, Hedidor GK, et al. Antimicrobial resistance national level dialogue and action in Ghana: setting and sustaining the agenda and outcomes. One Health Outlook . 2021;3:18. doi: 10.1186/s42522-021-00051-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Kpokiri EE, Ladva M, Dodoo CC, et al. Knowledge, Awareness and Practice with Antimicrobial Stewardship Programmes among Healthcare Providers in a Ghanaian Tertiary Hospital. Antibiotics (Basel) 2021;11:6. doi: 10.3390/antibiotics11010006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Sneddon J, Cooper L, Afriyie DK, et al. Supporting antimicrobial stewardship in Ghana: evaluation of the impact of training on knowledge and attitudes of healthcare professionals in two hospitals. JAC Antimicrob Resist . 2020;2:dlaa092. doi: 10.1093/jacamr/dlaa092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Guo S, Sun Q, Zhao X, et al. Prevalence and risk factors for antibiotic utilization in Chinese children. BMC Pediatr. 2021;21:255. doi: 10.1186/s12887-021-02706-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Mandal P, Asad M, Kayal A, et al. Assessment of use of World Health Organization access, watch, reserve antibiotics and core prescribing indicators in pediatric outpatients in a tertiary care teaching hospital in Eastern India. Perspect Clin Res. 2023;14:61–7. doi: 10.4103/picr.picr_22_22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Ardillon A, Ramblière L, Kermorvant-Duchemin E, et al. Inappropriate antibiotic prescribing and its determinants among outpatient children in 3 low- and middle-income countries: A multicentric community-based cohort study. PLoS Med. 2023;20:e1004211. doi: 10.1371/journal.pmed.1004211. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Schröder W, Sommer H, Gladstone BP, et al. Gender differences in antibiotic prescribing in the community: a systematic review and meta-analysis. J Antimicrob Chemother. 2016;71:1800–6. doi: 10.1093/jac/dkw054. [DOI] [PubMed] [Google Scholar]
- 36.Young EH, Strey KA, Lee GC, et al. National Disparities in Antibiotic Prescribing by Race, Ethnicity, Age Group, and Sex in United States Ambulatory Care Visits, 2009 to 2016. Antibiotics . 2022;12:51. doi: 10.3390/antibiotics12010051. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Obakiro SB, Napyo A, Wilberforce MJ, et al. Are antibiotic prescription practices in Eastern Uganda concordant with the national standard treatment guidelines? A cross-sectional retrospective study. J Glob Antimicrob Resist. 2022;29:513–9. doi: 10.1016/j.jgar.2021.11.006. [DOI] [PubMed] [Google Scholar]
- 38.Blandhol C, Sautmann A. Gender Differences in Children’s Antibiotic Use and Adherence. The World Bank; 2021. https://hdl.handle.net/10986/35134 Available. [Google Scholar]
- 39.Muenchhoff M, Goulder PJR. Sex Differences in Pediatric Infectious Diseases. J Infect Dis. 2014;209:S120–6. doi: 10.1093/infdis/jiu232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Parviainen S, Saastamoinen L, Lauhio A, et al. Outpatient antibacterial use and costs in children and adolescents: a nationwide register-based study in Finland, 2008-16. J Antimicrob Chemother. 2019;74:2426–33. doi: 10.1093/jac/dkz208. [DOI] [PubMed] [Google Scholar]
- 41.Opoku MM, Bonful HA, Koram KA. Antibiotic prescription for febrile outpatients: a health facility-based secondary data analysis for the Greater Accra region of Ghana. BMC Health Serv Res. 2020;20:978. doi: 10.1186/s12913-020-05771-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Fink G, D’Acremont V, Leslie HH, et al. Antibiotic exposure among children younger than 5 years in low-income and middle-income countries: a cross-sectional study of nationally representative facility-based and household-based surveys. Lancet Infect Dis. 2020;20:179–87. doi: 10.1016/S1473-3099(19)30572-9. [DOI] [PubMed] [Google Scholar]
- 43.Grammatico-Guillon L, Shea K, Jafarzadeh SR, et al. Antibiotic Prescribing in Outpatient Children: A Cohort From a Clinical Data Warehouse. Clin Pediatr (Phila) 2019;58:681–90. doi: 10.1177/0009922819834278. [DOI] [PubMed] [Google Scholar]
- 44.Lucas PJ, Cabral C, Hay AD, et al. A systematic review of parent and clinician views and perceptions that influence prescribing decisions in relation to acute childhood infections in primary care. Scand J Prim Health Care. 2015;33:11–20. doi: 10.3109/02813432.2015.1001942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Farley E, Stewart A, Davies M-A, et al. Antibiotic use and resistance: Knowledge, attitudes and perceptions among primary care prescribers in South Africa. S Afr Med J . 2018;108:763. doi: 10.7196/SAMJ.2018.v108i9.12933. [DOI] [PubMed] [Google Scholar]
- 46.Yehualaw A, Taferre C, Bantie AT, et al. Appropriateness and Pattern of Antibiotic Prescription in Pediatric Patients at Adigart General Hospital, Tigray, Ethiopia. Biomed Res Int. 2021;2021:6640892. doi: 10.1155/2021/6640892. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Alasmari NSH, Bamashmous ROM, Alshuwaykan RMA. Causes and Treatment of Tonsillitis. Egyptian J Hosp Med. 2017;69:2975–80. doi: 10.12816/0042838. [DOI] [Google Scholar]
- 48.Katz SE, Jenkins TC, Stein AB, et al. Durations of Antibiotic Treatment for Acute Otitis Media and Variability in Prescribed Durations Across Two Large Academic Health Systems. J Pediatric Infect Dis Soc. 2024;13:455–65. doi: 10.1093/jpids/piae073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.UNICEF Childhood diseases | UNICEF. 2024. https://www.unicef.org/health/childhood-diseases Available.
- 50.Wang D, Liu C, Zhang X, et al. Does diagnostic uncertainty increase antibiotic prescribing in primary care? NPJ Prim Care Respir Med. 2021;31:17. doi: 10.1038/s41533-021-00229-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Green C, Krafft H, Guyatt G, et al. Symptomatic fever management in children: A systematic review of national and international guidelines. PLoS One. 2021;16:e0245815. doi: 10.1371/journal.pone.0245815. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Saha SK, Muleme M, Hecke OV, et al. Feasibility of C-reactive protein point-of-care testing for antibiotic stewardship in rural GP-pharmacy settings. Antimicrob Steward Healthc Epidemiol . 2026;6:e148. doi: 10.1017/ash.2026.10401. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Hersh AL, Kronman MP. Inappropriate Antibiotic Prescribing: Wind at Our Backs or Flapping in the Breeze? Pediatrics. 2017;139:e20170027. doi: 10.1542/peds.2017-0027. [DOI] [PubMed] [Google Scholar]
- 54.Palms DL, Hicks LA, Bartoces M, et al. First-Line Antibiotic Selection in Outpatient Settings. Antimicrob Agents Chemother. 2019;63:01060–19. doi: 10.1128/AAC.01060-19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Lehrer BJ, Mutamba G, Thure KA, et al. Optimal Pediatric Outpatient Antibiotic Prescribing. JAMA Netw Open . 2024;7:e2437409. doi: 10.1001/jamanetworkopen.2024.37409. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.WHO The WHO AWaRE (access, watch, reserve) antibiotic book - infographics. 2022. [19-Sep-2025]. https://www.who.int/publications/i/item/WHO-MHP-HPS-EML-2022.02 Available. Accessed.
- 57.WHO Pocket book of hospital care for children| guidelines for the management of common childhood illnesses. 2013. [1-Jan-2025]. https://www.who.int/publications/i/item/9789241548373 Available. Accessed. [PubMed]
- 58.Asamoah A, Ameme DK, Sackey SO, et al. prevalence of bloody diarrhoea in Ghana - Google Search. 2016. [DOI]
- 59.Afum T, Asandem DA, Asare P, et al. Diarrhea-Causing Bacteria and Their Antibiotic Resistance Patterns Among Diarrhea Patients From Ghana. Front Microbiol. 2022;13 doi: 10.3389/fmicb.2022.894319. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Aduful AK, Nyarko MY, Neizer M, et al. Implementing the WHO AWaRe Antibiotic Guidelines for Pediatric Pharyngitis/Tonsilitis in Ghana: An Implementation Research Approach. London School of Hygiene & Tropical Medicine. 2026:1–15. doi: 10.17037/PUBS.04677993. [DOI] [Google Scholar]
- 61.Rahbi FA, Salmi IA, Khamis F, et al. Physicians’ attitudes, knowledge, and practices regarding antibiotic prescriptions. J Glob Antimicrob Resist. 2023;32:58–65. doi: 10.1016/j.jgar.2022.12.005. [DOI] [PubMed] [Google Scholar]
- 62.Gulnaz H, Zaidi SHR, Khan RA. Preparedness of house officers for independent clinical practice: are we there yet? BioMedica . 2022;38:70–6. doi: 10.51441/BioMedica/5-552. [DOI] [Google Scholar]
- 63.Tusubira B, Mukisa LN, Okuuny V, et al. Antibiotic prescription among children with common cold at a district hospital in Uganda. Afr J Prim Health Care Fam Med. 2023;15:e1–7. doi: 10.4102/phcfm.v15i1.4106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Liu C, Liu C, Wang D, et al. Intrinsic and external determinants of antibiotic prescribing: a multi-level path analysis of primary care prescriptions in Hubei, China. Antimicrob Resist Infect Control. 2019;8:132. doi: 10.1186/s13756-019-0592-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Pulcini C, Gyssens IC. How to educate prescribers in antimicrobial stewardship practices. Virulence. 2013;4:192–202. doi: 10.4161/viru.23706. [DOI] [PMC free article] [PubMed] [Google Scholar]
