Skip to main content

Antimicrobial use by WHO methodology at primary health care centers: a cross sectional study in Punjab, Pakistan



To investigate the antimicrobial (AM) use and prescribing patterns at primary health care centers (PHCCs) in Punjab, Pakistan.


A cross-sectional study was designed according to the World Health Organization (WHO) methodology for AM usage from January, 2017 to June, 2017. Standard data collection forms designed by the WHO were used to collect the data from 32 PHCCs (16 rural healthcare centers (RHCs) and 16 basic health units (BHUs)) in Punjab province of Pakistan. PHCCs were randomly selected from 8 main cities. The study sample consisted of prescription records of 6400 outpatients (200 prescriptions records from each PHCC) and 800 inpatients (25 inpatient records from each PHCC). Data of the year 2016 were collected retrospectively by using systematic random sampling technique and analyzed through SPSS.


Among the hospital indicators, standard treatment guidelines (STGs) regarding the infectious diseases were not available in PHCCs. Number of days during which key AMs were out of stock was 12.1 days per month (range = 3.1–19.2). Out of total PHCC medicines costs, expenditures on AMs were 26.2% (range = 17.1–39.0). In case of prescribing indicators, the average number of AMs per prescription was 1.4 (range = 1.1–1.7), percentage of prescriptions prescribed with AMs was 81.5% (range = 68.9–89.1) and duration of AM treatment on average was 5.1 days per patient (range = 3.3–6.4). Average cost of prescribed AMs per patient was 1.3 USD (range = 0.6–4.3). The PHCCs prescribed a median of 5 (range = 3–9) types of AMs, including 10 (range = 5–15) individual agents. Out of 79.3% prescriptions of outpatients prescribed with AMs, only 16.4% were properly prescribed. Out of 100% prescriptions of inpatients prescribed with AMs, 12.1% were properly prescribed. Out of all the AM prescriptions 23.6% contained penicillins, 20.1% contained cephalosporins and 19.4% contained fluoroquinolones Metronidazole (18.0%), ciprofloxacin (16.5%) and co-amoxiclav (14.3%) were most commonly prescribed AMs.


In PHCCs, AMs were prescribed more frequently. However large proportions of these prescriptions were inappropriate. Continuous education and training of medical staff and cost effective policies could play an important role in promotion of rational use of AMs.

Peer Review reports


Antimicrobial resistance (AMR) has emerged as a global issue and presents a major challenge regarding the treatment options of infectious diseases [1]. AMR result in decreased potency of antimicrobials (AMs) against causative microbes, unnecessary health costs and ultimately leads to failure of therapy. Various studies reported different factors causing the AMR but inappropriate or excessive prescribing of AMs and unnecessary usage of broad spectrum AMs were the main factors [2,3,4]. According to a study, AMs accounts for more than 30% of total hospital budget as one third to half of hospitalized patients receive at least one AM [5, 6]. Out of total use of AMs, 20–50% is not proper [2, 7, 8] leading to decreased quality of patient care, increased cost of therapy and prevalence of adverse drug effects [9].

AMR has emerged widely but developing countries are more affected by this issue due to lack of proper health care facilities and high rate of infections [10, 11]. In Pakistan, most of the physicians in government hospitals tend to prescribe those AMs that are not effective against majority of the causative microbes [12].

In Pakistan, hospitals are classified as primary, secondary and tertiary care hospitals. Primary health care centers (PHCCs) [RHCs = Rural health centers and BHUs = Basic health units] are small clinical set ups, providing limited medical facilities. Secondary care hospitals are county hospitals, while the tertiary care hospitals offer vast medical and clinical facilities and mostly located in big cities. Survey reports of AMs in secondary and tertiary care hospitals showed high prescribing rates of AMs as 48.9%, [13] 51.5%, [14] 52%, [15] and 52.4% [14] but there is unavailability of any data regarding prescribing trend of AMs in PHCCs with special reference to the World Health Organization (WHO) AM use indicators. Availability of this data is very important as majority of Pakistani population avails medical services at PHCCs, therefore understanding of AMs use in PHCCs and promotion of rational use of AMs is crucial.

The purpose of this study was to investigate the usage and prescribing patterns of AMs at 32 selected PHCCs in Punjab, Pakistan. AM usage was compared among RHCs and BHUs, outpatients and inpatients as well as in surgical and nonsurgical patients.


Study settings

The study was conducted in Punjab province of Pakistan, which have a population of 110,012,442 according to the census of 2017 [16]. The total PHCCs existing in 8 main cities of Punjab (Lahore, Faisalabad, Bahawalpur, Multan, Dera Ghazi Khan, Sargodha, Rawalpindi, and Gujranwala) are 128 (43 RHCs and 85 BHUs). 4 PHCCs (2 RHCs and 2BHUs) were randomly selected from the peripheries of each selected city so total 32 PHCCs (16 RHCs and 16 BHUs) were selected for this study. These selected PHCCs cover 14.3% of the total population of the Punjab i.e., 15,731,779. The characteristics of the selected PHCCs are summarized in Table 1.

Table 1 Characteristics of the selected primary health care centers, median (range)

Study design and outcome variables

It was an observational and cross-sectional study, designed according to the objectives of the study. The outcome indicators were related to two general areas of AMs usage i.e., hospital indicators and prescribing indicators. The AMs usage patterns in terms of frequency and percentages were also determined. The Anatomical Therapeutic Chemical (ATC) classification system [17] was used for the coding of AMs.

Study inclusion / exclusion criteria

The inclusion criteria were based on the time period of study, health status (acute and chronic illness), annual bulk purchase data and duration of treatment, whereas records of pre-existing infections, multiple and local purchase data were excluded from the study (Additional file 1).

Sampling and data collection

The standard indicator forms were used to collect the data. Reliability of the data was assured by adhering to WHO guidelines and methods [10, 18]. The data were collected from January, 2017 to June, 2017. Two investigators (Pharm.D students) were assigned to each PHCC; all investigators received the same training prior to the survey for the collection and validation of data. During the survey, one investigator filled out the investigational forms while the other reviewed the data. All data were checked for completeness and logicality.

The data of hospital indicators were collected over a period of 1 year (January, 2016 to December, 2016). Most recent copies of formulary list/essential medicines list (FL/EML), key AMs and STGs were obtained from the Pharmacy Departments of the PHCCs.

Out of the total 921,311 outpatient prescriptions and 25,184 inpatient prescriptions, a retrospective selection of 6400 outpatient and 800 inpatient prescription records (200 outpatients and 25 inpatients per PHCC) was made over a period of 1 year i.e., from January, 2016 to December, 2016. To minimize the selection bias, prescription records written for the prescribed time period in each of the selected PHCCs were divided into four quarters and from each quarter 50 outpatient and 6 inpatient prescription records were selected by using systematic random sampling technique [19]. From these prescription records, the WHO prescribing indicators and prescribing patterns of AMs were determined.

AMs prescription was judged according to “WHO prescribing and hospital indicators” [18, 20], “Infectious Diseases Society of Pakistan (IDSP) guidelines for AMs use” [21] and “American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults” [22]. The expert opinion was taken from the local team of consultant pharmacists, microbiologists and the physicians having specialization in infectious diseases. The discrepancy between investigators regarding assessment of appropriateness of AMs therapy was also resolved by consulting the aforementioned team of consultants. The AMs usage was considered to be proper (correct decision) if it contained the standard treatment regimen and duration that was indicated for the patient’s symptoms of infection or prophylaxis. AMs usage was considered improper if clinical condition of the patient did not justify use of AMs for either treatment or prophylaxis (incorrect/missing data and incorrect decision) [21, 23, 24].

Data analysis

Statistical Package for Social Sciences (IBM Corp. Released 2012. IBM SPSS Statistics for Windows Version 21.0. Armonk, NY: IBM Corp.) and Microsoft Excel (MS Office 2010) were used for data analysis. Kolmogorov-Smirnov and Shapiro-Wilks tests were carried out to test the normality of the data. Median was used, when the data showed non-normal distribution. Independent Samples Mann-Whitney U Test was employed to assess the difference among the PHCCs, and a p-value < 0.05 was used for statistical significance of differences.


Hospital indicators

In all PHCCs, the Drug and Therapeutic Committee (DTC) was working on regular basis and a FL/EML was available that contains 15 generics of AMs. 15 AMs listed in FL/EML were available in 22 different dosage forms. Out of these 22 dosage forms, an average of 15 dosage forms (68.2%, range = 7–22) were available in the stock at the day of data collection. Average number of days during which a set of key AMs was out of stock in all PHCCs was found to be 12.1 (3.1–19.2) days per month for the 15 AMs. The difference among the PHCCs was statistically significant for 6─10 hospital indicators (Table 2). The results of the hospital indicators are summarized in Table 2.

Table 2 WHO hospital indicators at the selected primary health care centers

Prescribing indicators

The percentage of prescriptions with at least one AMs prescribed was 81.5% (range = 68.9–89.1) and from these patients, average number of AMs per prescription was 1.4 (range = 1.1–1.7). The difference among the PHCCs was statistically significant for 1st, 2nd, 4th, and 5th prescribing indicator (Table 3). Results regarding prescribing indicators in the selected PHCCs are summarized in Table 3.

Table 3 WHO prescribing indicators at the selected primary health care centers

Antimicrobial use in outpatients and inpatients

In all PHCCs 79.2% (76.7% in RHCs and 81.8% in BHUs) of outpatient prescriptions contained one or more AMs, out of which 22.1% in RHCs, 11.9% in BHUs and 16.4% in all PHCCs were proper. 100% of inpatient prescriptions contained one or more AMs, out of which 14.3% in RHCs, 11.6% in BHUs and 12.1% in all PHCCs were proper. Out of the 436 surgical inpatient prescriptions, 13.1% in RHCs, 11.7% in BHUs and 11.9% in all PHCCs were proper and of the 364 nonsurgical inpatient prescriptions, 15.1% in RHCs, 11.3% in BHUs and 12.9% in all PHCCs were proper (Table 4).

Table 4 Antimicrobial use in Outpatients and Inpatients

Prescribing patterns of antimicrobials

81.5% (n = 5868) prescriptions were prescribed with a total of 8236 AMs especially in gastrointestinal tract (GIT) infections (16.4%, n = 1182), urinary tract infections (UTIs) (13%, n = 937) and acute bronchitis (11%, n = 801) (Additional file 2). Overall Penicillins (23.6%, n = 1944), cephalosporins (20.1%, n = 1658) and fluoroquinolones (19.4%, n = 1594) were the most frequently prescribed AM classes at the selected PHCCs (Additional file 3). But in comparison of BHUs with RHCs, penicillins (25.3%, n = 1143) and fluoroquinolones (22.8%, n = 1030) were mostly prescribed in BHUs while cephalosporins (22.3%, n = 829) in RHCs. Metronidazole (18.0%, n = 1480), ciprofloxacin (16.5%, n = 1357) and co-amoxiclav (a combination of amoxicillin and clavulanic acid) (14.3%, n = 1176) were the most frequently prescribed AMs at the selected PHCCs (Table 5).

Table 5 Antimicrobial agents being prescribed at the selected primary health care centers


Irrational use of AMs is spreading over the globe as an international public health threat. But this problem is more prevalent in the developing countries due to scarcity of resources, higher rates of infections and less availability of medical facilities [10, 11]. This study targeted 32 PHCCs in which the practices regarding AMs usage had been the core objective of investigation. Results of this study could be used by policy makers to assess and improve AMs usage along with the promotion of rational use of AMs in Pakistan. AMs usage was very high in inpatients as well as in outpatients. In prescriptions of patients, there was evidence of AMs usage without clear indications and observance of many errors. Moreover, unnecessary prescribing pattern of the broad spectrum AMs, multiple combinations, prolonged usage and intravenous administration of AMs were also observed in this study.

Hospital indicators

The presence of STGs and FL/EML in health care facilities represents provision of good quality patient care and promotion of rational use of medicines [10]. All PHCCs contained EML that had 15 generic AMs. The Drug and Therapeutic Committee (DTC) functions in an ongoing basis in the study settings and consequently the EML was revised, updated and approved annually by the administration of the PHCCs. None of the PHCCs had STGs for infectious diseases. Due to this reason, prescribers do not have any STGs for prescribing and this obstacles rational prescribing of AMs. Ultimately quality of patient care was compromised [10].

Along with the provision of STGs, there must be sufficient availability of key AMs at all the time in PHCCs. There was 100% availability of key AMs on the day of study. This result is comparable to a study from Ethiopia that reported 90.1% availability of key AMs in the stock [25]. Stock maintenance of health care facility can be determined by the number of days during which there is an unavailability of AMs. Resulting value of this indicator was 12.1 days per month for 15 key AMs, making it higher than Afghanistan (8.7 days per month for 15 key AMs) [26] and Ethiopia (15–45 days over a 12-months period) [25]. Findings revealed that 60.8% key AMs were in stock. Unavailability of key AMs could be the reason for; patients not treated with drug of choice, financial burden and treatment failure. This noncompliance may lead to an increase in rates of morbidity and mortality [10].

Due to irrational and excessive use of AMs, expenditures on single class of drugs are on boom. Indicator 5 records the cost of antimicrobials and demonstrates it as percentage of total hospital medicines costs. This study showed that expenditure on AMs (annual bulk purchase data only) was 26.2% of the total annual budget (Table 3). This is the cause of financial burden; hence patient treatment protocols are compromised.

Prescribing indicators

Extent of AMs prescribing in health care facilities was determined by the Indicator 6. In this study the percentage of prescriptions containing AMs was 81.5% (Table 4). This value was lower than that reported from Afghanistan (90%) [26] and Nepal (93%) [27], whereas higher than Ethiopia (79.8%) [25], Thailand (44%) [28], Tanzania (35.4%) [29], Brazil (28.8%) [30] and Bangladesh (25%) [31]. Inpatients may receive more than one AMs depending upon health condition but could further lead to irrational use, inappropriate combination therapy and unnecessary changes in dosage regimen [10]. In this study, the average number of AMs per prescription was 1.4 and this value was lower than that reported in Ethiopia (1.2) [25] and higher than Afghanistan (1.7) [26] and Nepal (2.4) [27]. Treatment duration with AMs for infectious diseases is 7–10 days but some advance infectious diseases require longer duration such as osteomyelitis and meningitis [10]. Average duration of prescribed AMs treatment in PHCCs was 5.1 days and comparable to study from Afghanistan that reported it to be 5 days [26].

The WHO recommended prescribing of medicines by their generic names. Study showed that percentage of AMs prescribed by generic names was100%. This value was higher than the studies conducted in Thailand (87%) [28] and Afghanistan (88%) [26]. Prescribing of AMs by the brand names may lead to increase risks of morbidity and mortality along with financial burdens on health care budgets [32].

AMs may contribute towards financial burden due to irrational prescribing as they contribute more than 30% of the total hospital budget [5]. The results of current study revealed that the average cost of AMs prescribed per patient was 1.3 USD. Though this cost is 5 folds less as compared to the cost of AMs prescribed per patient in Nigeria but still it poses huge financial encumbrance on healthcare sector of Pakistan [33]. In public sector hospitals of Pakistan, government is solely responsible to bear health care costs and unfortunately no proper health insurance schemes have been developed till date. This is the main reason of limited stock and unavailability of AMs and essential medicines in government hospitals.

STGs are the main pillar to be relied upon for the promotion of rational prescribing of AMs. It is also necessary to follow the STGs for proper treatment of pneumonia and other infections [26]. Unavailability of STGs is the leading cause of irrational prescribing, prolong hospital stay and increase cost of therapy. The adherence of prescribers to the hospital’s STGs depends upon two factors; prescribing only those AMs listed in STGs; prescribing doses mentioned in the STGs [10] Results of the current study concluded that none of the pneumonia patients received AMs in accordance with the WHO AM use indicators, IDSP guidelines and American Thoracic Society Consensus Guidelines on the Community-acquired Pneumonia in Adults. Due to the absence of STGs in PHCCs previously published guidelines mentioned in the literature were used as a reference [22]. These results were in accordance with a similar study from Afghanistan in which none of the patients received treatment in accordance to STGs [26].

Prescribing patterns of antimicrobials

According to a study 35–60% of the patients were prescribed with AMs and less than 20% were prescribed properly [34]. In current study, 81.5% of the prescriptions had one or more AMs especially in GIT infections (16.4%), UTI (13%) and acute bronchitis (11%). GIT infections (bacterial and viral origin) are prevailing in Pakistan because of unhygienic sanitary conditions, contaminated water and edibles. AMs, especially fluoroquinolones, are frequently prescribed in GIT infections (bacterial origin) to lessen the severity of infection and to minimize other symptoms [35]. Patients suffering from UTI are frequently prescribed with cephalosporins and penicillins [36]. Acute bronchitis is mostly caused by bacteria and viruses and AMs are prescribed to reduce the duration of cough and other symptoms [37].

Rate of AMs usage in PHCCs in Pakistan is comparable to China (75.9%) [1], India (78%) [38], Indonesia (84%) [39] and Jordan (85%) [40]. AMs usage in Pakistan was exceeded as compared to developed countries like the United States (63.7%) [41] and Sweden (30%) [42].

In Pakistan, India and China the most commonly prescribed AMs were penicillins, fluoroquinolones (in BHUs) and cephalosporins (in RHCs). Contrary to European countries, most commonly used AMs for outpatients were tetracyclines, benzylpencillins and sulfonamides [38, 42]. The results of the current study revealed that most frequently prescribed AMs included metronidazole (18.0%), ciprofloxacin (16.5%) and co-amoxiclav (14.3%). Higher prescribing rates of AMs may be due to better clinical outcomes, stock availability or excessive marketing campaigns. A study performed in Ethiopia revealed that the most frequently prescribed AMs were penicillin G (28.4%), ceftriaxone (24.9%) and cloxacillin (12.8%) [25]. Indian study showed that the highest prescribed AMs were levofloxacin (25.8%), metronidazole (14.8%) and ceftriaxone (12.7%). Treatment duration for most of the infections extends to few days but complicated and severe infectious cases may require multiple AMs usage for extended period of time. [43,44,45] These multiple AMs treatments are usually considered to provide broad AMs spectrum [46].

This study revealed that 12.1% of inpatients and 16.4% of outpatients were prescribed properly. Contributing factors towards inappropriate use of AMs in PHCCs in Pakistan could be lack of medical facilities and health experts. In both the RHCs and BHUs, medical staff was not skilled properly but in RHCs physicians having specialization degrees are working as compared to BHUs which is under the supervision of medical officer (bachelor’s degree holder). This might be the reason that our findings showed proper usage more in RHCs than in BHUs. Medical facilities are more directed towards secondary and tertiary care hospitals in cities further limiting exposure and training opportunities of PHCCs staff. Lack of proper medical facilities and unavailability of STGs lead to irrational prescribing of broad-spectrum AMs, use of multiple AMs in different combinations, excessive AMs use in prophylaxis for surgical patients and longer duration of therapy. The findings of the current study could be used as a baseline for further follow-up for quality of AMs usage in the future. Furthermore these findings will also help the policy makers to implement appropriate interventions designed to improve rational use of AMs at PHCCs of Pakistan in specific and globally at large.

Strengths and limitations of the study

To the author’s best knowledge, there is no previously published data available (neither in Asian region nor in African region) on the WHO AM use indicators with special focus on current practices in PHCCs regarding AM use. This study enlightens the path of future researchers, policy makers and stakeholders in Pakistan.

This study has some limitations. First, the daily doses of AMs were not measured. Second, the study was conducted in a single province of Pakistan so results could not be generalizable to entire country. However, the condition of healthcare sector is similar across the country and similar findings are expected nationwide. Last, the reasons accountable for irrational prescribing were not inquired. Future studies should focus on these aspects.


The results of the current study highlighted irrational AMs utilization patterns concerning availability of STGs, AMs stock shortage days, and percentage of AMs prescribing. Substantial improper AMs use occurs in PHCCs in Pakistan, probably because of the inadequate education and skill levels of professional staff, and weak oversight. To overcome these shortcomings, DTC should develop and implement the STGs for infectious diseases at the PHCCs. Pharmacists (having specialty in infectious diseases) should be appointed because these professionals can play critical role in improving the current scenario by developing and implementing surveillance system in the hospital; searching and providing data about the most common strains of microbes in Punjab and promoting rational prescribing trend among prescribers on continuous basis. Furthermore, prime focus must be given to prescriber’s training regarding rational use of AMs and the development of cost-effective interventions by the health authorities and the policy makers respectively.



Antimicrobial Resistance




Anatomical therapeutic chemical classification system


Basic health units


Formulary list/Essential medicines list


Primary health care centers


Rural health centers


Statistical packages for social sciences


Standard treatment guidelines


World Health Organization


  1. Wang J, Wang P, Wang X, Zheng Y, Xiao Y. Use and prescription of antibiotics in primary health care settings in China. JAMA Intern Med. 2014;174(12):1914–20.

    Article  Google Scholar 

  2. Cizman M. The use and resistance to antibiotics in the community. Int J Antimicrob Agents. 2003;21(4):297–307.

    Article  CAS  Google Scholar 

  3. Levy SB, Marshall B. Antibacterial resistance worldwide: causes, challenges and responses. Nat Med. 2004;10(12 Suppl):S122–9.

    Article  CAS  Google Scholar 

  4. Okeke IN, Klugman KP, Bhutta ZA, Duse AG, Jenkins P, O'Brien TF, Pablos-Mendez A, Laxminarayan R. Antimicrobial resistance in developing countries. Part II: strategies for containment. Lancet Infect Dis. 2005;5(9):568–80.

    Article  Google Scholar 

  5. Vlahovic Palcevski V, Morovic M, Palcevski G. Antibiotic utilization at the university hospital after introducing an antibiotic policy. Eur J Clin Pharmacol. 2000;56(1):97–101.

    Article  CAS  Google Scholar 

  6. Atif M, Azeem M, Saqib A, Scahill S. Investigation of antimicrobial use at a tertiary care hospital in southern Punjab, Pakistan using WHO methodology. Antimicrob Resist Infect Control. 2017;6(1):41.

    Article  Google Scholar 

  7. Mora Y, Avila-Agüero ML, Umaña MA, Jiménez AL, París MM, Faingezicht I. Epidemiologic observations of the judicious use of antibiotics in a pediatric teaching hospital. Int J Infect Dis. 2002;6(1):74–7.

    Article  Google Scholar 

  8. Gottlieb T, Nimmo GR. Antibiotic resistance is an emerging threat to public health: an urgent call to action at the antimicrobial resistance summit 2011. Med J Aust. 2011;194(6):281–3.

    PubMed  Google Scholar 

  9. Beringer PM, Wong-Beringer A, Rho JP. Economic aspects of antibacterial adverse effects. PharmacoEconomics. 1998;13(1 Pt 1):35–49.

    Article  CAS  Google Scholar 

  10. How to Investigate Antimicrobial Use in Hospitals: Selected Indicators []. Accessed 12 Sept 2017.

  11. Okeke IN, Laxminarayan R, Bhutta ZA, Duse AG, Jenkins P, O'Brien TF, Pablos-Mendez A, Klugman KP. Antimicrobial resistance in developing countries. Part I: recent trends and current status. Lancet Infect Dis. 2005;5(8):481–93.

    Article  CAS  Google Scholar 

  12. Howard DH, Scott DR. The economic burden of drug resistance. Clin Infect Dis. 2005;41(Suppl 4):S283–6.

    Article  Google Scholar 

  13. Atif M, Sarwar MR, Azeem M, Naz M, Amir S, Nazir K. Assessment of core drug use indicators using WHO/INRUD methodology at primary healthcare centers in Bahawalpur, Pakistan. BMC Health Serv Res. 2016;16(1):684.

    Article  Google Scholar 

  14. Atif M, Sarwar MR, Azeem M, Umer D, Rauf A, Rasool A, Ahsan M, Scahill S. Assessment of WHO/INRUD core drug use indicators in two tertiary care hospitals of Bahawalpur, Punjab, Pakistan. J Pharm Policy Pract. 2016;9(1):27.

    Article  Google Scholar 

  15. Hafeez A, Kiani AG, ud Din S, Muhammad W, Butt K, Shah Z, Mirza Z. Prescription and dispensing practices in public sector health facilities in Pakistan: survey report. JPMA J Pak Med Assoc. 2004;54(4):187–91.

    CAS  PubMed  Google Scholar 

  16. Pakistan Bureau of Statistics. Provincial summary results of 6th population and housing census-2017.

  17. World Health Organization. The anatomical therapeutic chemical classification system with defined daily doses (ATC/DDD). Oslo: WHO; 2006.

    Google Scholar 

  18. How to investigate drug use in health facilities: selected drug use indicators []. Accessed 12 Sept 2017.

  19. Akl OA, El Mahalli AA, Elkahky AA, Salem AM. WHO/INRUD drug use indicators at primary healthcare centers in Alexandria, Egypt. J Taibah Univ Med Sci. 2014;9(1):54–64.

    Google Scholar 

  20. World Health Organization. How to Investigate Antimicrobial Use in Hospitals: Selected Indicators. 2nd ed; 2012. p. 79.

    Google Scholar 

  21. The Infectious Diseases Society of Pakistan: Guidelines for the use of antmicrobials. In. Pakistan; 2007.

  22. Mandell LA, Wunderink RG, Anzueto A, Bartlett JG, Campbell GD, Dean NC, Dowell SF, File TM Jr, Musher DM, Niederman MS. Infectious Diseases Society of America/American Thoracic Society consensus guidelines on the management of community-acquired pneumonia in adults. Clin Infect Dis. 2007;44(Supplement_2):S27–72.

    Article  CAS  Google Scholar 

  23. Gyssens IC, Van Den Broek PJ, Kullberg B-J, Hekster YA, Van Der Meer JW. Optimizing antimicrobial therapy. A method for antimicrobial drug me evaluation. J Antimicrob Chemother. 1992;30(5):724–7.

    Article  CAS  Google Scholar 

  24. Willemsen I, Groenhuijzen A, Bogaers D, Stuurman A, van Keulen P, Kluytmans J. Appropriateness of antimicrobial therapy measured by repeated prevalence surveys. Antimicrob Agents Chemother. 2007;51(3):864–7.

    Article  CAS  Google Scholar 

  25. Woldu MA, Suleman S, Workneh N, Berhane H. Retrospective study of the pattern of antibiotic use in Hawassa University referral hospital pediatric Ward, southern Ethiopia. J Applied Pharm Sci. 2013;3(2):93.

    Google Scholar 

  26. Green T, Omari M, Siddiqui AZ, Anwari J, Noorzaee A. Afghanistan medicine use study: a survey of 28 health facilities in 5 provinces. In.: submitted to the US Agency for international development by the strengthening pharmaceutical systems (SPS) program. Arlington: Management Sciences for Health; 2010.

    Google Scholar 

  27. Palikhe N. Prescribing pattern of antibiotics in pediatric hospital of Kathmandu valley. J Nepal Health Res Counc. 2004;2(1):6–12.

  28. Aswapokee N, Vaithayapichet S, Heller RF. Pattern of antibiotic use in medical wards of a university hospital, Bangkok, Thailand. Review Infect Dis. 1990;12(1):136–41.

    Article  CAS  Google Scholar 

  29. Massele A, Nsimba S, Rimoy G. Prescribing habits in church-owned primary health care facilities in Dar Es Salaam and other Tanzanian coast regions. East Afr Med J. 2001;78(10):510–4.

    Article  CAS  Google Scholar 

  30. Holloway KA, Henry D. WHO essential medicines policies and use in developing and transitional countries: an analysis of reported policy implementation and medicines use surveys. PLoS Med. 2014;11(9):e1001724.

    Article  Google Scholar 

  31. Guyon AB, Barman A, Ahmed J, Ahmed A, Alam M. A baseline survey on use of drugs at the primary health care level in Bangladesh. Bull World Health Organ. 1994;72(2):265.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Promoting rational use of medicines: core components - WHO policy perspectives on medicines []. Accessed 12 Sept 2017.

  33. Akande T, Ologe M, Medubi G. Antibiotic prescription pattern and cost at University of Ilorin teaching hospital, Ilorin, Nigeria. Int J Trop Med. 2009;4(2):50–4.

    Google Scholar 

  34. Interventions and strategies to improve the use of antimicrobials in developing countries. Drug Management Program []. Accessed 12 Sept 2017.

  35. Aarestrup FM, Wiuff C, Mølbak K, Threlfall EJ. Is it time to change fluoroquinolone breakpoints for Salmonella spp.? Antimicrob Agents Chemother. 2003;47(2):827–9.

    Article  CAS  Google Scholar 

  36. Jafri SA, Qasim M, Masoud MS, Rahman MU, Izhar M, Kazmi S. Antibiotic resistance of E. coli isolates from urine samples of urinary tract infection (UTI) patients in Pakistan. Bioinformation. 2014;10(7):419–22.

    Article  Google Scholar 

  37. Smith SM, Fahey T, Smucny J, Becker L. Antibiotics for acute bronchitis. Jama. 2014;312(24):2678–9.

    Article  CAS  Google Scholar 

  38. Sharma M, Eriksson B, Marrone G, Dhaneria S, Lundborg CS. Antibiotic prescribing in two private sector hospitals; one teaching and one non-teaching: a cross-sectional study in Ujjain, India. BMC Infect Dis. 2012;12(1):155.

    Article  Google Scholar 

  39. Hadi U, Duerink DO, Lestari ES, Nagelkerke NJ, Keuter M, Huis In't Veld D, Suwandojo E, Rahardjo E, van den Broek P, Gyssens IC, et al. Audit of antibiotic prescribing in two governmental teaching hospitals in Indonesia. Clin Microbiol Infect. 2008;14(7):698–707.

    Article  CAS  Google Scholar 

  40. Al-Niemat SI, Aljbouri TM, Goussous LS, Efaishat RA, Salah RK. Antibiotic prescribing patterns in outpatient emergency clinics at queen Rania Al Abdullah II Children's hospital, Jordan, 2013. Oman Med J. 2014;29(4):250.

    Article  Google Scholar 

  41. Polk RE, Hohmann SF, Medvedev S, Ibrahim O. Benchmarking risk-adjusted adult antibacterial drug use in 70 US academic medical center hospitals. Clin Infect Dis. 2011;53(11):1100–10.

    Article  Google Scholar 

  42. Goossens H, Ferech M, Vander Stichele R, Elseviers M, Group EP. Outpatient antibiotic use in Europe and association with resistance: a cross-national database study. Lancet. 2005;365(9459):579–87.

    Article  Google Scholar 

  43. Rao GG, Patel M. Urinary tract infection in hospitalized elderly patients in the United Kingdom: the importance of making an accurate diagnosis in the post broad-spectrum antibiotic era. J Antimicrob Chemother. 2009;63(1):5–6.

    CAS  Google Scholar 

  44. Nicolle L. Complicated urinary tract infection in adults. Can J Infect Dis Med Microbiol. 2005;16(6):349–60.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Woodford HJ, George J. Diagnosis and management of urinary infections in older people. Clin Med. 2011;11(1):80–3.

    Article  Google Scholar 

  46. Ejim L, Farha MA, Falconer SB, Wildenhain J, Coombes BK, Tyers M, Brown ED, Wright GD. Combinations of antibiotics and nonantibiotic drugs enhance antimicrobial efficacy. Nat Chem Biol. 2011;7(6):348–50.

    Article  CAS  Google Scholar 

Download references


We would like to appreciate the help of the PHCCs staff for their help in data retrieving. A note of thanks to all pharmacy students served as data collectors.


No funding was involved in the preparation of this manuscript or in the decision to submit it for publication.

Availability of data and materials

The raw data on which conclusions of this manuscript rely is available upon request. Please contact Muhammad Rehan Sarwar at

Author information

Authors and Affiliations



MRS and AS conceptualized and designed the study. TS and SI analyzed and interpreted the data. MRS, TS and AS drafted the manuscript. SI and MRS critically revised the manuscript. All authors read and approved final version of the manuscript.

Corresponding author

Correspondence to Muhammad Rehan Sarwar.

Ethics declarations

Ethics approval and consent to participate

Ethical approval was obtained from the Pharmacy Research Ethics Committee (PREC) at the Akhtar Saeed College of Pharmaceutical Sciences, ACPS (Reference: 12–2016/PREC, dated December 22, 2016). The permission to conduct this study was also obtained from the administrators of the PHCCs. Furthermore, this was a retrospective study so consent of participants was not required.

Consent for publication

Not applicable

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional files

Additional file 1:

Study inclusion/exclusion criteria. (DOCX 16 kb)

Additional file 2:

Conditions in which antimicrobials being prescribed at the selected primary health care centers. (DOCX 16 kb)

Additional file 3:

Antimicrobial classes being prescribed at the selected primary health care centers. (DOCX 15 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sarwar, M.R., Saqib, A., Iftikhar, S. et al. Antimicrobial use by WHO methodology at primary health care centers: a cross sectional study in Punjab, Pakistan. BMC Infect Dis 18, 492 (2018).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: