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 Table of Contents  
CLINICAL STUDY
Year : 2015  |  Volume : 4  |  Issue : 4  |  Page : 212-215

Pediatric hospital admission due to adverse drug reactions: Report from a tertiary center


1 Department of Clinical Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
2 Iranian Adverse Drug Reaction Monitoring Center, Food and Drug Organization, Ministry of Health, Tehran, Iran
3 Department of Clinical Pharmacy; Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran

Date of Web Publication13-Oct-2015

Correspondence Address:
Toktam Faghihi
Department of Clinical Pharmacy; Pediatrics Center of Excellence, Children's Medical Center, Tehran University of Medical Sciences, Tehran
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2279-042X.167045

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  Abstract 

Objective: Adverse drug reactions (ADRs) are known as a cause of hospital admission. We have carried out a prospective study to characterize and assess the frequency, probability, preventability, and severity of ADRs, which lead to hospital admission in children. Methods: In a prospective observational study, a cohort of children admitted to a tertiary pediatric hospital was randomly screened to assess ADR as the cause of admission from June 2014 to January 2015. ADRs causing admissions were detected based on patients' records, interviewing their parents, and confirmation by medical team. The probability of the ADRs was assessed based on WHO criteria and Naranjo tool. The preventability assessment was performed using Schumock and Thornton questionnaire. Findings: Of the 658 evaluated emergency admissions, 27 were caused by an ADR giving an incidence of 4.1%. Among ADRs, 37.1% were estimated to be preventable. Antibiotics were the most common medication class which caused hospital admission. Conclusion: Pediatric pharmacotherapy still needs evidence-based strategies to improve child care including education, monitoring, planning for medications after ADR occurrence, and implementing preventive measures when applicable.

Keywords: Adverse drug reaction; children; hospitalization; incidence


How to cite this article:
Gholami K, Babaie F, Shalviri G, Javadi MR, Faghihi T. Pediatric hospital admission due to adverse drug reactions: Report from a tertiary center. J Res Pharm Pract 2015;4:212-5

How to cite this URL:
Gholami K, Babaie F, Shalviri G, Javadi MR, Faghihi T. Pediatric hospital admission due to adverse drug reactions: Report from a tertiary center. J Res Pharm Pract [serial online] 2015 [cited 2021 Jul 24];4:212-5. Available from: https://www.jrpp.net/text.asp?2015/4/4/212/167045




  Introduction Top


Adverse drug reactions (ADRs) are reported to be a cause of hospital admission in adult as well as pediatric population,[1],[2],[3],[4],[5],[6],[7] thus, far incurring an important public health problem. The studies in children have reported the various incidences of ADR-related hospitalizations. Moreover, various drug classes, different organ systems, and clinical presentations are frequently reported.[5],[6],[7] In light of ADR-related hospitalization incidence, a systematic review performed in 2001 elucidated weighted average of 2.09%.[8] Likewise, a systematic review in 2012 demonstrated a pooled estimate incidence of 2.9%.[9] A prospective observational study conducted in the Czech Republic illustrated an incidence of 2.2% of pediatric hospital admissions.[6] However, to the authors' knowledge, there is no study evaluating ADRs causing admission in the pediatric population in Iran. Thus, in a prospective manner, we sought to determine the frequency, preventability, severity, and causality of these reactions. The secondary outcome was to characterize the pattern of ADRs.


  Methods Top


This prospective observational study was conducted in the emergency ward of a referral tertiary level hospital, the Children's Medical Center, Tehran University of Medical Sciences between June 2014 and January 2015. A cohort of pediatric patients (≤18 years) admitted was randomly screened in order to assess ADR as the cause of admission. ADR was defined according to Edwards and Aronson.[10]

Exclusion criteria were as following: Hospitalization period <6 h, drug overdoses, and drug consumption due to suicide and hospitalization due to medication error. We excluded ADRs that resulted in patient hospitalization of <6 h according to Gallagher et al. study methodology [7],[11] in order to identify more severe reactions. Gallagher et al. illustrated incidence of admissions leading to early discharge are lower and less severe than the main ward admissions.[7],[11]

ADRs were identified by reviewing patients' records, interviewing their parents, and confirmation by treating pediatrician and the research pharmacist. Whenever an ADR was detected, the pharmacist recorded demographic data, patient diagnosis, age, gender, concurrent medications, allergies, medication history, medical history, laboratory tests, and filled the national yellow form for ADRs. Medication history comprised any medication taken within the 4 weeks prior to admission. The pharmacist also followed up the patients during hospitalization to monitor the outcome.

The severity of ADR was defined as those causing death, life-threatening, or causing hospital admission.[12] Causality assessment was performed by using Naranjo score [13] and WHO criteria for causality assessment.[12] Preventability was determined by Schumock and Thornton questionnaire.[14]


  Results Top


In total, 7909 children were admitted during 6 months study period. A total of 752 nonsuccessive admissions were evaluated, of which 658 fulfilled the eligibility criteria to be screened for ADRs as the reason of admission. Overall, 48 ADRs were seen in 27 patients including 11 females and 16 males. Two of 27 patient admissions were exposed to cancer chemotherapy (7.4%). Mean ± standard deviation age of participants was 40.6 ± 36 months.

The incidence of hospital admission due to ADRs was 4.1% (27/658). Most adverse reactions were detected in the children < 1-year old. Based on study definition, all ADRs considered to be severe because of hospital attendance; however, all patients recovered without a sequel. According to Schumock and Thornton questionnaire, 37.1% of ADRs were preventable.

The WHO causality assessment of ADRs revealed that 33.3% of ADRs were detected as certain, followed by 48.2% as probable, and 18.5% as possible. Causality assessed by Naranjo algorithm illuminated 3.7% as definite, 85.2% as probable, and 11.1% as possible.

The most frequent and the highest number of ADRs occurred with cefixime (5 patients), 9 (18.8%) of ADRs, followed by phenobarbital (4 patients), 4 (8.3%) of ADRs. Drug classes implicated in ADRs are shown in [Table 1].
Table 1: Drug classes implicated in causing ADRs in the study population

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The majority of system-organ classes are shown in [Table 2], depicting skin and appendages disorders (39.6%) and gastrointestinal systems (27.1%) being the two most frequently involved organs. Maculopapular rashes (12.5%), diarrhea (12.5%), and vomiting (10.4%) were the most frequent clinical complications.
Table 2: System-organ classes implicated in causing ADRs in the study population

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  Discussion Top


To the authors' knowledge, this is the first study reporting pediatric ADR-related admissions in Iran. In the present study, we determined to have an incidence of 4% ADR-related admissions.

A systematic review and meta-analysis of 17 prospective studies elucidated the rate of pediatric admissions due to ADRs ranges from 0.59% to 4.1% with the weighted average of 2.09%.[8] Easton et al.[15] evaluated a broader set of 8 categories of drug-related problems (DRPs), one of which included ADR. The authors reported 4.3% hospital admissions due to DRPs in children with <25% of them being ADRs.

Gallagher et al.[7] conducted a study in the UK to ascertain the occurrence of ADRs causing hospital attendance in children and illustrated an incidence of 2.9% over the 1-year period. The other study conducted earlier by Gallagher et al.[11] reported the estimated incidence of 4% hospital admissions. However, the primary outcome of the study was to develop a methodology of such trials. Langerova et al. illuminated that 2.2% of pediatric hospital admissions were caused by an ADR.[6] A systematic review in 2012 by Smyth et al. demonstrated a range of 0.4% to 10.3% incidence rate for ADRs causing hospital attendance, with a pooled estimate of 2.9%.[9] However, after excluding an outlier, Smyth et al. reported a reduction in hospital admission incidence rate to 0.4% to 4%.[9] Another trial performed by Posthumus et al.[5] reported 6.9% ADR-related acute admissions in children. Of note, the majority of the participants comprised pediatric undergoing cancer chemotherapy.[5]

Of note, exposure to cancer chemotherapy agents has been demonstrated to be a risk factor for ADR occurrence. The studies with a high proportion of oncology participants have a higher ADR incidence rate.[5],[7]

We observed an incidence of 4% ADR-related admissions. Putting together, by considering that children exposed to cancer chemotherapy agents compromised a limited number in the present study, it seems ADRs-related acute hospital admissions are in the upper limit. This high incidence calls for the need for implementation of pediatric pharmacovigilance.

The results of our study depicted that ADRs were more detected in the children <1-year old, which is in line with the previous trials showing a higher incidence during the 1st year of life.[16]

In the present study, we detected 37.1% of ADRs as preventable. In studies on children population, preventability of ADRs has noted to be between 33% and 51.3%.[5]

To relate an ADR to a medication, it has been stated to encompass certain (definite), probable and possible probabilities into the total number of ADRs.[6] In the present study, the most of the ADRs were determined to be in the definite and probable category and all of the ADRs were in the certain (definite), probable, and possible probabilities by WHO and Naranjo algorithm as well.

In this study, anti-infective agents were the most class of drugs caused ADRs (proportion of 37%). In a systematic review by Smyth et al. in children,[9] anti-infectives determined to be the most prevalent drug class involved in the three settings: ADRs causing admission, ADRs occurring during hospital stay, and ADRs within the community. Smyth et al. reported anti-infectives were responsible for 3.5–66.6% of ADRs causing admission.[9] Anti-cancers, immunosuppressants, vaccines, anti-epileptics, and nonsteroidal anti-inflammatory drugs (NSAIDs) are also frequently reported drug classes in causing admissions, reflecting prescribing practices in various settings.[7],[9],[11] Likewise, studies in which oncology patients constituted the majority of participants,[6],[7] anti-cancer medications reported to be the most common drug class contributing to ADR-related admissions.

In the adult population, however, cardiovascular drugs and NSAIDs are commonly implicated in causing hospital admissions.[1],[2] In accordance with these results, it has been demonstrated that ADRs are different in children to those in adults in terms of drugs implicated and reactions noticed.[17]

It has been demonstrated that probiotics diminish the incidence of antibiotic-associated diarrhea in pediatrics.[18] When started with the initiation of antibiotic therapy, probiotics can prevent 1 in 7 cases of antibiotic-associated diarrhea in children.[18] Thus, based on the results of this study illuminating a major cause of hospital admission in children being a prevalent gastrointestinal adverse effect, including diarrhea associated with antibiotics use, it is worth considering use of probiotics for prevention of antibiotic-associated diarrheas.

Pediatric pharmacotherapy still needs evidence-based strategies to improve child care including education, monitoring, planning for medications after ADR occurrence, and implementing prophylactic measures when applicable. Pharmacist and clinical pharmacists should have a definite role.


  Authors' Contribution Top


Kheirollah Gholami has proposed the concept, designed the study, defined the intellectual content, edited and reviewed the manuscript. Fatemeh Babaie was responsible for literature review and data collection. Gloria Shalviri has designed the study, defined the intellectual content, edited and reviewed the manuscript and controlled study progress. Mohammad Reza Javadi has designed the study, edited and reviewed the manuscript. Toktam Faghihi has designed the study, defined the intellectual content, done literature research, prepared, edited and reviewed the manuscript.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.





 
  References Top

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Hopf Y, Watson M, Williams D. Adverse-drug-reaction related admissions to a hospital in Scotland. Pharm World Sci 2008;30:854-62.  Back to cited text no. 1
    
2.
Pirmohamed M, James S, Meakin S, Green C, Scott AK, Walley TJ, et al. Adverse drug reactions as cause of admission to hospital: Prospective analysis of 18 820 patients. BMJ 2004;329:15-9.  Back to cited text no. 2
    
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van der Hooft CS, Dieleman JP, Siemes C, Aarnoudse AJ, Verhamme KM, Stricker BH, et al. Adverse drug reaction-related hospitalisations: A population-based cohort study. Pharmacoepidemiol Drug Saf 2008;17:365-71.  Back to cited text no. 3
    
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Easton-Carter KL, Chapman CB, Brien JE. Emergency department attendances associated with drug-related problems in paediatrics. J Paediatr Child Health 2003;39:124-9.  Back to cited text no. 4
    
5.
Posthumus AA, Alingh CC, Zwaan CC, VanGrootheest KK, Hanff LL, Witjes BB, et al. Adverse drug reaction-related admissions in paediatrics, a prospective single-center study. BMJ Open 2012;2:E000934.  Back to cited text no. 5
    
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Langerova P, Vrtal J, Urbanek K. Adverse drug reactions causing hospital admissions in childhood: A prospective, observational, single-center study. Basic Clin Pharmacol Toxicol 2008;102:408-11.  Back to cited text no. 6
    
7.
Gallagher RM, Mason JR, Bird KA, Kirkham JJ, Peak M, Williamson PR, et al. Adverse drug reactions causing admission to a paediatric hospital. PLoS One 2012;7:e50127.  Back to cited text no. 7
    
8.
Impicciatore P, Choonara I, Clarkson A, Provasi D, Pandolfini C, Bonati M. Incidence of adverse drug reactions in paediatric in/out-patients: A systematic review and meta-analysis of prospective studies. Br J Clin Pharmacol 2001;52:77-83.  Back to cited text no. 8
    
9.
Smyth RM, Gargon E, Kirkham J, Cresswell L, Golder S, Smyth R, et al. Adverse drug reactions in children – A systematic review. PLoS One 2012;7:e24061.  Back to cited text no. 9
    
10.
Edwards IR, Aronson JK. Adverse drug reactions: Definitions, diagnosis, and management. Lancet 2000;356:1255-9.  Back to cited text no. 10
    
11.
Gallagher RM, Bird KA, Mason JR, Peak M, Williamson PR, Nunn AJ, et al. Adverse drug reactions causing admission to a paediatric hospital: A pilot study. J Clin Pharm Ther 2011;36:194-9.  Back to cited text no. 11
    
12.
World Health Organization. Safety Monitoring of Medical Products, Guidelines for Setting up and Running a Pharmacovigilance Centre. Uppsala Monitoring Centre: World Health Organization; 2000.  Back to cited text no. 12
    
13.
Naranjo CA, Busto U, Sellers EM, Sandor P, Ruiz I, Roberts EA, et al. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther 1981;30:239-45.  Back to cited text no. 13
    
14.
Schumock GT, Thornton JP. Focusing on the preventability of adverse drug reactions. Hosp Pharm 1992;27:538.  Back to cited text no. 14
    
15.
Easton KL, Chapman CB, Brien JA. Frequency and characteristics of hospital admissions associated with drug-related problems in paediatrics. Br J Clin Pharmacol 2004;57:611-5.  Back to cited text no. 15
    
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Martínez-Mir I, García-López M, Palop V, Ferrer JM, Rubio E, Morales-Olivas FJ. A prospective study of adverse drug reactions in hospitalized children. Br J Clin Pharmacol 1999;47:681-8.  Back to cited text no. 16
    
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Blake KV, Zaccaria C, Domergue F, Mache EL, Saint-Raymond A, Hidalgo-Simon A. Comparison between paediatric and adult suspected adverse drug reactions reported to the European medicines agency: Implications for pharmacovigilance. Pediatr Drugs 2014;16:309-19.  Back to cited text no. 17
    
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Thomas DW, Greer FR, American Academy of Pediatrics Committee on Nutrition, American Academy of Pediatrics Section on Gastroenterology, Hepatology, and Nutrition. Probiotics and prebiotics in pediatrics. Pediatrics 2010;126:1217-31.  Back to cited text no. 18
    



 
 
    Tables

  [Table 1], [Table 2]


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