Hospitalizations and adverse drug events in the Brazilian unified health system: a ten-year retrospective analysis of routine data

Lunara Teles Silva Ana Carolina Figueiredo Modesto Rodrigo Alves de Oliveira Rita Goreti Amaral Flavio Marques Lopes About the authors

ABSTRACT

OBJECTIVE

To describe the frequency and characteristics of hospitalizations for/with adverse drug events in the Brazilian unified health system routine data.

METHODS

Nationwide retrospective study using data obtained from a period of ten years from the Brazil Hospital Information System (SIH-SUS), an administrative database that registers hospitalizations in the unified health system. We selected hospitalizations with primary and/or secondary diagnosis related to adverse drug events according to a list of validated International Classification Disease 10th edition (ICD-10) codes. These events were described according to year, age group, sex, length of hospital stay, mortality, hospital costs, Brazilian geographical region, and category of ICD-10 codes. Crude hospitalization rates of adverse drug events per 100,000 inhabitants were obtained and Joinpoint Regression was used to analyze temporal changes in these rates along the years. The most frequent ICD-10 codes were also identified.

RESULTS

Over ten years, 603,663 hospitalizations in Brazil were found in the database, out of which 2.5% of the patients died. Though 2009 had the highest prevalence of hospitalization per 100,000 inhabitants (32.57), no significant annual change in rates was found for the entire period. All age groups and sexes presented a jointpoint in temporal series; however, only women had a significative increase trend. The most frequent codes were from the chapter of mental and behavioral disorders (F19.2, F19.0, and F19.5 codes).

CONCLUSIONS

The database methodology can be useful to estimate frequencies of adverse drug events and perform characterization nationwide and to help monitor morbidity along the years.

Drug-related side effects and adverse reactions; Pharmacoepidemiology; Hospitalization; Databases, factual

INTRODUCTION

Adverse drug events (ADE) have been considered as a significant cause of hospital admission or complications during hospital stay11. Sousa-Pinto B, Marques B, Lopes F, Freitas A. Frequency and impact of adverse events in inpatients: a nationwide analysis of episodes between 2000 and 2015. J Med Syst. 2018;42(3):48. https://doi.org/10.1007/s10916-018-0898-5
https://doi.org/10.1007/s10916-018-0898-...
. ADE are estimated to occur in a mean of 21.6% of patients during hospitalization44. Laatikainen O, Miettunen J, Sneck S, Lehtiniemi H, Tenhunen O, Turpeinen M. The prevalence of medication-related adverse events in inpatients: a systematic review and meta-analysis. Eur J Clin Pharmacol. 2017;73(12):1539-49. https://doi.org/10.1007/s00228-017-2330-3
https://doi.org/10.1007/s00228-017-2330-...
. In Germany, around 5.0% of hospital admissions were related to ADE over five years55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
. ADE are also associated with increased length of hospital stay (LOS) and risk of death22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
, 66. Shamliyan TA, Kane RL. Drug-related harms in hospitalized Medicare beneficiaries: results from the Healthcare Cost and Utilization Project, 2000-2008. J Patient Saf. 2016;12(2):89-107. https://doi.org/10.1097/PTS.0000000000000106
https://doi.org/10.1097/PTS.000000000000...
. A study conducted at a university hospital found that length of stay increased in 1.13 days when an ADE was present77. Amelung S, Meid AD, Nafe M, Thalheimer M, Hoppe-Tichy T, Haefeli WE, et al. Association of preventable adverse drug events with inpatients’ length of stay: a propensity-matched cohort study. Int J Clin Pract. 2017;71(10):e12990. https://doi.org/10.1111/ijcp.12990
https://doi.org/10.1111/ijcp.12990...
. Another study estimated a 10.5% drug-related mortality in a hospital in Spain33. Pardo Cabello AJ, Del Pozo Gavilán E, Gómez Jiménez FJ, Mota Rodríguez C, Luna Del Castillo JD, Puche Cañas P. Drug-related mortality among inpatients: a retrospective observational study. Eur J Clin Pharmacol. 2016;72(6):731-6. https://doi.org/10.1007/s00228-016-2026-0
https://doi.org/10.1007/s00228-016-2026-...
. ADE also have a great economic burden – ADE-related hospitalization in the USA from 2008 to 2011 totaled $142 billion22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
.

Assessing ADE occurrence nationwide remains a challenge despite the impact of these injuries because of the difficulties of assessment in a large population, the different strategies available for event reporting, incomplete information, or underreporting11. Sousa-Pinto B, Marques B, Lopes F, Freitas A. Frequency and impact of adverse events in inpatients: a nationwide analysis of episodes between 2000 and 2015. J Med Syst. 2018;42(3):48. https://doi.org/10.1007/s10916-018-0898-5
https://doi.org/10.1007/s10916-018-0898-...
, 88. Wu TY, Jen MH, Bottle A, Molokhia M, Aylin P, Bell D, et al. Ten-year trends in hospital admissions for adverse drug reactions in England 1999–2009. R Soc Med. 2010;103(6):239-50. https://doi.org/10.1258/jrsm.2010.100113
https://doi.org/10.1258/jrsm.2010.100113...
. Administrative hospital data, which use International Classification of Diseases (ICD) codes, are being increasingly approached to assess ADE as a potential strategy to complement existing methods for ADE identification22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
, 55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
. Studies have found that ICD codes can reasonably detect ADE in hospital routine data99. Kane-Gill SL, Van Den Bos J, Handler SM. Adverse drug reactions in hospital and ambulatory care settings identified using a large administrative database. Ann Pharmacother. 2010;44(6):983-93. https://doi.org/10.1345/aph.1M726
https://doi.org/10.1345/aph.1M726...
, 1010. Kuklik N, Stausberg J, Jöckel KH. Adverse drug events in German hospital routine data: a validation of International Classification of Diseases, 10th revision (ICD-10) diagnostic codes. PLoS One. 2017;12(11):e0187510. https://doi.org/10.1371/journal.pone.0187510
https://doi.org/10.1371/journal.pone.018...
. However, research on ADE using ICD codes varies regarding which codes to use. In Brazil, Mota et al.1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
validated a list of codes stratified by groups according to their probability of indicating a real ADE. To our knowledge, however, the list has not been applied to analyze hospitalizations related to ADE. This study thus aimed to describe the frequency and characteristics of hospitalizations for/with ADE in the Brazilian unified health system routine data.

METHODS

Study Design and Database

A retrospective study was conducted to describe ADE using data from the Sistema de Informação Hospitalar (SIH-SUS – Hospital Information System), an administrative database that registers hospitalizations in the Brazilian unified health system (used by more than 70% of the population) since 1992 and records a mean of 11 million registries per year for reimbursement. The database is maintained by the Departamento de Informática do Sistema Único de Saúde (DATASUS – Information Technology Department of the Brazilian Unified Health System), a service of the Ministry of Health.

The SIH-SUS collects information from the Autorização de Internação Hospitalar (AIH – Inpatient Hospital Authorization), which describes some characteristics of the hospital stay. AIH dataset is available for download and contains patients’ socioeconomic data (age, sex, and race) and clinical characteristics (LOS, costs incurred, and type of admission). It also includes information of patients’ primary and secondary diagnoses using the ICD-10 codes. Data from AIH are registered by coders in each public hospital after discharge and then sent to authorities. When a patient is admitted, an AIH number is generated for the new hospitalization, representing a line in the dataset. If the patient’s length of stay is prolongated, the hospital creates another AIH with the same number of the original. In this case, a new line is added in the dataset and the type of hospitalization changes from new AIH to prolongation AIH1212. Cerqueira DRC, Alves PP, Coelho DSC, Reis MVM, Lima AS. Uma análise da Base de Dados do Sistema de Informação Hospitalar entre 2001 e 2018: dicionário dinâmico, disponibilidade dos dados e aspectos metodológicos para a produção de indicadores sobre violência. Rio de Janeiro: Instituto de Pesquisa Econômica Aplicada; 2019. .

Definitions

ADE is defined as “harm experienced by a patient as a result of exposure to a drug” and it involves, for example, anaphylaxis to penicillin or major hemorrhage from overdose of heparin1313. Agency for Healthcare Research and Quality, Patient Safety Network- PSNet. Medication errors and adverse drug events. Rockville, MD: AHRQ; 2019 [cited 2020 Mar 16]. Available from: https://psnet.ahrq.gov/primer/medication-errors-and-adverse-drug-events
https://psnet.ahrq.gov/primer/medication...
. This study considered two main categories as ADE: (1) adverse drug reaction (ADR) and (2) drug poisoning. ADR are classically defined as harms caused by the use of a drug in a recommended manner, being usually described in ICD as “adverse effects” or with the terms “due to a drug”, “drug-induced”, and “secondary to drugs”1313. Agency for Healthcare Research and Quality, Patient Safety Network- PSNet. Medication errors and adverse drug events. Rockville, MD: AHRQ; 2019 [cited 2020 Mar 16]. Available from: https://psnet.ahrq.gov/primer/medication-errors-and-adverse-drug-events
https://psnet.ahrq.gov/primer/medication...
, 1414. World Health Organization. International Statistical Classification of Diseases and Related Health Problems - 10th revision; version 2019. Geneva (CH): WHO; 2019 [cited 2020 Mar 16]. Available from: https://icd.who.int/browse10/2019/en
https://icd.who.int/browse10/2019/en...
. Vaccines were not included in this category. Drug poisoning was considered as unintentional or undetermined cause of poisoning or toxic effect by medication1414. World Health Organization. International Statistical Classification of Diseases and Related Health Problems - 10th revision; version 2019. Geneva (CH): WHO; 2019 [cited 2020 Mar 16]. Available from: https://icd.who.int/browse10/2019/en
https://icd.who.int/browse10/2019/en...
. Hospitalizations with codes of intentional poisoning as the external cause were not included despite their other codes. “ADE” was the preferable term used in this paper and “hospitalization” was chosen for ADE related to hospital admissions and/or ADE occurring during inpatient treatment.

ADE Identifications and Data Processing

Hospitalization data were collected from a period of ten years (2009 to 2018) from SIH-SUS, in which hospitalizations with at least one ICD-10 code related to ADE as primary and/or secondary diagnosis were identified as cases. Cases in this study thus include hospitalization that ends in discharge, death, or change in number of the AIH with the ICD-10 codes predefined1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
. If a unique hospitalization had more than one line, data was gathered in a single line. If a patient identified more than one code, their hospitalization was counted only once.

In total, 618 ICD-10 codes were extracted and classified according a list previously validated by Mota et al.1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
The classification divides the ICD-10 codes into five categories based on the validity of each one as an indicator of event: Certain (A1 – adverse reaction caused by drug and B1 – poisoning by drugs), Probable (A2 – adverse reaction caused by drug or other causes and B2 – poisoning caused by drug or other causes), Possible (C – adverse event possibly expected by drug), and Occasional (D – adverse event occasionally expected by drug).1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
Supporting information summarizes the codes and categories.

Variables

The main outcome measure was the detection of ADE related to hospitalizations identified by ICD-10 codes. Secondary outcomes were: year of hospitalization, age group (≤ 4; 5–14; 15–24; 25–34; 35–44; 45–54; 55–64; 65–74; ≥ 75), sex (female and male), LOS, death in hospital, costs of the AIH (in dollars, costs in Brazilian reais were converted to US dollar before the publication of the dataset), geographical region, level of service complexity (moderate or high), and ICD-10 code category (A1/A2/B1/B2/C/D).

Statistical Analysis

The data were managed and analyzed with software R 3.6.3 (The R Foundation for Statistical Computing, 2019). Overall frequencies of hospitalizations with ADE were calculated by year, age group, sex, deaths, level of complexity, and geographical region. Median costs of the AIH and LOS were calculated overall and by year. Mean/median and standard deviation/interquartile range were computed when possible.

The annual prevalence of hospitalizations (per 100,000 inhabitants) was estimated overall and by sex, age group, and region of Brazil. The number of hospitalizations with at least one ADE code was used as the numerator whereas the population obtained from a Brazilian census projection was the denominator. Temporal trends in rates in the studied period were estimated using the Joinpoint Regression Program Version 4.8.0.1 (Statistical Research and Applications Branch, National Cancer Institute). This method identifies trend changes and describes the joinpoint model using annual percentage change (APC) during a particular trend and average annual percentage change (AAPC) for the entire period1515. National Cancer Institute, Division of Cancer Control & Population Sciences. Surveillance Research Program. The Joinpoint Regression Program, Version 4.8.0.1. Rockville, MD: NCI; 2020 [cited 2020 July 20]. Available from: https://surveillance.cancer.gov/joinpoint/
https://surveillance.cancer.gov/joinpoin...
.

The ADE frequencies were estimated by each ICD-10 code category regarding sex, age, age group, LOS, AIH costs, and deaths. Since some hospitalizations were registered with two or more ICD-10 codes included in different categories (A1/A2/B1/B2/C/D), the number of hospitalizations with at least one ADE was lower than the sum of identified episodes by each ICD category. The most frequent ICD-10 codes by year, sex, age group, and geographical region were identified. Moreover, ICD-10 codes from categories A1 and B1 were categorized by drug classes and costs of the AIH were studied.

Ethical Aspects

Data used in this study are public and accessible by all those interested. Nevertheless, the study was approved by the Research Ethics Committee of the Universidade Federal de Goiás - UFG (CAEE 32355720.9.0000.5083).

RESULTS

Overall and Ten-Year Trends in Hospitalizations Related to ADE

From 2009 to 2018, 607,663 hospitalizations had at least one ICD-10 related to ADE in the Brazilian unified health system. The mean of hospitalizations by year was 60,280.8. Table 1 summarizes the baseline characteristics of the study population. The median age of all patients was 31.0 (IQT: 22.0–44.0) and 33.9% of the patients were women. By age group, was observed in patients aged 25 to 34 years had the highest number of adverse events. Patients were hospitalized for more than 11 days in 39.9% of the cases. ADE accounted for 9,558,623 hospital-bed days during the studied period. The median of health care cost of hospitalizations per year was US$ 25,995,036. In total, 15,486 (2.5%) patients died during hospitalization. Regarding discharge status, most patients were discharged after improving and 6.6% were discharged at their own request.

Table 1
Characteristics of the hospitalizations with ICD-10 codes related to adverse drug event in the Brazilian Unified Health System.

Table 2 describes crude rates of hospitalizations related to ADE per 100,000 inhabitants in Brazil and the trends in rates according to the joinpoints (i.e., a trend change). During the studied period, the highest rate of hospitalization for ADE was registered in Brazil in 2009 (32.57 per 100,000 inhabitants). Men and the age group 25 to 34 years old presented higher rates of ADE. A joinpoint was identified in rates by overall hospitalizations in 2016, leading to two periods with different trends: a decrease followed by an increase. The same occurred between the rates in women and men, but only women had a significant annual increase (1.4%) during the period. All age groups presented a joinpoint in time series; however, only segments represented by APC were significant. No joinpoints were found in the analysis of rates according to Brazilian regions, that is, APC equals AAPC, and only two regions showed a significant decrease in rates. The inpatient mortality rate related to ADE per 100,000 inhabitants showed a joinpoint in 2013, with 9.8% increase from 2013 to 2018 (data not shown in Table 2 ).

Table 2
Hospitalization in the Brazilian Unified Health System with ICD-10 codes of adverse drug event per 100,000 inhabitants (crude rates).

Overall Description of the ICD-10 Codes

In total, 638,685 ICD-10 codes were assigned to hospitalizations related to ADE in the Brazilian unified health system. Codes from the category “certain” (A1 and B1) were found in 90,452 (14.9%) hospitalizations. Cases from this category accounted for 404,821 hospital-bed days. Around 9.3% of all costs were related to hospitalizations with codes of the category “certain”. Codes from the category “probable” (A2 and B2) appeared in 70.6% of cases ( Table 3 ). Supporting information has the frequencies of hospitalizations with each ICD-10 code.

Table 3
Distribution of hospitalizations in the Brazilian Unified Health System related to adverse drug event by ICD-10 codes category (A1/A2/B1/B2/C/D).

The three most common ICD-10 codes in numbers were those from chapter V (mental and behavioral disorders), F19.2 (187,130; 29.3%), F19.0 (45,635; 7.1%), and F19.5 (30,756; 4.8%), followed by the code of poisoning by unspecified substance T50.9 (27,873; 4.3%) and the code D70 (agranulocytosis) (23,813; 3.7%). Figure A shows the ten codes most related to ADE in each of the ten years analyzed. These codes represent more than 57% of all events in each age group. Figure B shows the distribution of the most prevalent codes except for F19.2, which had higher prevalence (43.5; 50.0%) than other principal codes in all years studied. Codes from chapter V appeared at least five times among the first ten most frequent codes in all years.

Figure
Most frequent ICD-10 codes related to hospitalization and adverse drug events in the Brazilian unified health system by year, sex, age group and geographical region. Continue

The database analysis identified 97,604 ICD-10 codes from category “certain”. The main codes from category A1 were O89.4 (spinal and epidural anesthesia-induced headache during the puerperium) (10,724; 1.7%), Y42.5 (events by estrogens and progestogens) (4,052; 0.6%), and Y57.8 (events by other drugs and medicaments) (3,895; 0.6%). In category B1, the most poisonings by unintentional or undetermined cause were T42.4 (benzodiazepines) (4,632; 0.7%), T36.9 (systemic antibiotic, unspecified) (4,236; 0.7%), and T45.5 (anticoagulants) (3,543; 0.6%).

The ten most frequent codes between sexes were almost equal except for O89.4 (spinal and epidural anesthesia-induced headache during the puerperium) and G95.8 (other specified diseases of spinal cord), which appeared only in women, and F19.1 (mental and behavioral disorders, harmful use) and F19.3 (mental and behavioral disorders, withdrawal state), which appeared only in men (Figures C and D). The five codes most prevalent among age groups were analyzed. None of the codes was repeated in any age group (Figures E and F). Four codes were most common in the five regions of Brazil: T50.9, K25.0, F19.5, F19.0, and F19.9 (Figures G and H).

Table 4 provides an overview of the most common classes of substances associated with ADE from codes of the category “certain” (A1 and B1). The most frequent drugs from category A1 were anesthetics and therapeutic gases and hormones (including synthetic substitutes and antagonists). In category B1, the two main classes related to drug poisoning were (1) systemic anti-infectives and (2) antiepileptics, antiparkinsonism drugs, sedatives-hypnotics and antianxiety drugs.

Table 4
Description of codes related to adverse drug events according to drug class and costs related to hospitalization with at least one code from the class.

DISCUSSION

Our study provided a comprehensive, population-level assessment of the impact of adverse drug events in Brazil’s unified health system. From 2009 to 2018, 607,663 hospitalizations were registered with at least one ICD-10 code related to ADE, out of which 2.5% patients died. Our results show that, overall, these rates of hospitalizations per 100,000 inhabitants had a pattern of decrease followed by an increase during the ten years in two temporal segments. Several studies show a yearly increasing trend in the prevalence and rates of ADE-related hospitalizations22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
, 66. Shamliyan TA, Kane RL. Drug-related harms in hospitalized Medicare beneficiaries: results from the Healthcare Cost and Utilization Project, 2000-2008. J Patient Saf. 2016;12(2):89-107. https://doi.org/10.1097/PTS.0000000000000106
https://doi.org/10.1097/PTS.000000000000...
, 1616. Santos GAS, Boing AC. [Hospitalizations and deaths from drug poisoning and adverse reactions in Brazil: an analysis from 2000 to 2014]. Cad Saude Publica. 2018;34(6):e00100917l. Portuguese. https://doi.org/10.1590/0102-311X00100917
https://doi.org/10.1590/0102-311X0010091...
, 1717. Miguel A, Marques B, Freitas A, Lopes F, Azevedo L, Pereira AC. Detection of adverse drug reactions using hospital databases: a nationwide study in Portugal. Pharmacoepidemiol Drug Saf. 2013;22(8):907-13. https://doi.org/10.1002/pds.3468
https://doi.org/10.1002/pds.3468...
. Santos and Boing1616. Santos GAS, Boing AC. [Hospitalizations and deaths from drug poisoning and adverse reactions in Brazil: an analysis from 2000 to 2014]. Cad Saude Publica. 2018;34(6):e00100917l. Portuguese. https://doi.org/10.1590/0102-311X00100917
https://doi.org/10.1590/0102-311X0010091...
showed that hospitalizations caused by ADE in Brazil increased 1.6 times over 15 years. Cases of ADE are expected to increase with time considering the number of drugs that enter the market every year, the prescription/use of many drugs, and improvements in database registrations1717. Miguel A, Marques B, Freitas A, Lopes F, Azevedo L, Pereira AC. Detection of adverse drug reactions using hospital databases: a nationwide study in Portugal. Pharmacoepidemiol Drug Saf. 2013;22(8):907-13. https://doi.org/10.1002/pds.3468
https://doi.org/10.1002/pds.3468...
. In recent years, national ADE patterns – as described by our results – have been addressed with greater awareness about patient safety and continuously improving pharmacovigilance practices, as seen with the Third Global Patient Safety Challenge: Medication Without Harm, launched in 20171818. Donaldson LJ, Kelley ET, Dhingra-Kumar N, Kieny MP; Sheikh A. Medication Without Harm: WHO’s Third Global Patient Safety Challenge. Lancet. 2017;389(10080):1680-1. https://doi.org/10.1016/S0140-6736(17)31047-4
https://doi.org/10.1016/S0140-6736(17)31...
.

Our results on the frequencies of hospitalizations related to ADE were different from those of other authors. Two studies conducted in a Germany database found higher annual frequencies than our analysis55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
, 1919. Stausberg J. International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA. BMC Health Serv Res. 2014;14:125. https://doi.org/10.1186/1472-6963-14-125
https://doi.org/10.1186/1472-6963-14-125...
; one of them identified 775,959 inpatient stays with ICD-10 codes related to ADE in a year1919. Stausberg J. International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA. BMC Health Serv Res. 2014;14:125. https://doi.org/10.1186/1472-6963-14-125
https://doi.org/10.1186/1472-6963-14-125...
. Differences in frequencies and rates among studies can be partially explained by aspects such as the lack of standardization, especially regarding ADE definitions and ICD coding framework. We defined ADE as “any harm experienced as the result of drug exposure” and included ICD-10 codes of “adverse effects” and “poisoning of unintentional/undetermined cause” previously validated for the Brazilian reality for a wide approach of types of drug harm1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
. Other aspects that can contribute to differences between studies are the structure of the population involved – such as a higher presence of older age groups –, differences in prescribing standards, polypharmacy, as well as differences in documentation and database types1919. Stausberg J. International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA. BMC Health Serv Res. 2014;14:125. https://doi.org/10.1186/1472-6963-14-125
https://doi.org/10.1186/1472-6963-14-125...
, 2020. Patel H, Bell D, Molokhia M, Srishanmuganathan J, Patel M, Car J, et al. Trends in hospital admissions for adverse drug reactions in England: analysis of national hospital episode statistics 1998–2005. BMC Clin Pharmacol. 2007;7:9. https://doi.org/10.1186/1472-6904-7-9
https://doi.org/10.1186/1472-6904-7-9...
.

Codes associated with ADE-related hospitalizations usually vary between countries, although specific codes are common across studies. As an example, the codes T50.9 and D70 appeared both in our study and in a German study as two of the ten most frequent codes found in primary diagnosis55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
. In studies using Brazilian databases, codes related to “other and unspecified drugs” were common in national registries of hospitalizations, in which the most frequent code was T50.92121. Paula TC, Bochner R, Montilla DER. Clinical and epidemiological analysis of hospitalizations of elderly due to poisoning and adverse effects of medications, Brazil from 2004 to 2008. Rev Bras Epidemiol. 2010;15(4):828-44. https://doi.org/10.1590/s1415-790x2012000400014
https://doi.org/10.1590/s1415-790x201200...
, 2222. Lessa MA, Bochner R. Analysis of hospitalizations of children under one year of age due to drug intoxication and adverse events in Brazil. Rev Bras Epidemiol. 2008;11(4):660-74. https://doi.org/10.1590/S1415-790X2008000400013
https://doi.org/10.1590/S1415-790X200800...
. On the other hand, in analyses of databases from Germany, England, and the USA, the most frequent ADE was enterocolitis caused by Clostridium difficile (code A04.7)1919. Stausberg J. International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA. BMC Health Serv Res. 2014;14:125. https://doi.org/10.1186/1472-6963-14-125
https://doi.org/10.1186/1472-6963-14-125...
. Codes from chapter V (mental and behavioral disorders) were 52% of all codes studied, where F19.2 alone corresponded to 29.3% of the codes in our results. In Brazil, Chile, and England, F19 codes were one of the two main causes of events1616. Santos GAS, Boing AC. [Hospitalizations and deaths from drug poisoning and adverse reactions in Brazil: an analysis from 2000 to 2014]. Cad Saude Publica. 2018;34(6):e00100917l. Portuguese. https://doi.org/10.1590/0102-311X00100917
https://doi.org/10.1590/0102-311X0010091...
, 1717. Miguel A, Marques B, Freitas A, Lopes F, Azevedo L, Pereira AC. Detection of adverse drug reactions using hospital databases: a nationwide study in Portugal. Pharmacoepidemiol Drug Saf. 2013;22(8):907-13. https://doi.org/10.1002/pds.3468
https://doi.org/10.1002/pds.3468...
, 2020. Patel H, Bell D, Molokhia M, Srishanmuganathan J, Patel M, Car J, et al. Trends in hospital admissions for adverse drug reactions in England: analysis of national hospital episode statistics 1998–2005. BMC Clin Pharmacol. 2007;7:9. https://doi.org/10.1186/1472-6904-7-9
https://doi.org/10.1186/1472-6904-7-9...
, 2323. Collao JF, Favereau R, Miranda R, Aceitón C. [Drug related harm in Chilean hospitals: prevalence analysis 2010-2017]. Rev Med Chile. 2019;147(4):416-25. Spanish. https://doi.org/10.4067/S0034-98872019000400416
https://doi.org/10.4067/S0034-9887201900...
, 2424. Waller P, Shaw M, Ho D, Shakir S, Ebrahim S. Hospital admissions for ‘drug-induced’ disorders in England: a study using the Hospital Episodes Statistics (HES) database. Br J Clin Pharmacol. 2005;59(2):213-9. https://doi.org/10.1111/j.1365-2125.2004.02236.x
https://doi.org/10.1111/j.1365-2125.2004...
.

By analyzing codes from the category “certain” only, we found that about 15% of hospitalizations were related to this category. These codes allow identifying a drug as the only one responsible for ADE, excluding confounding factors1111. Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
https://doi.org/10.1590/1413-81232018239...
. A German study, for example, found less cases of hospitalizations related to ADE with codes A1 and B1 (almost half of what we found)55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
. Moreover, “systemic anti-infectives” and “anesthetics and therapeutic gases” were the two main classes of drugs analyzed from codes of the “certain” category. Similarly to other studies22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
, 2525. Parikh S, Christensen D, Stuchbery P, Peterson J, Hutchinson A, Jackson T. Exploring in-hospital adverse drug events using ICD-10 codes. Aust Health Rev. 2014;38(4):454-60. https://doi.org/10.1071/AH13166
https://doi.org/10.1071/AH13166...
, our results reported anti-infectives as one of the most prevalent classes – likely because antibiotics are drugs commonly used in inpatient hospitalization. A study from the Johns Hopkins Hospital showed that 20% of hospitalized patients receiving antibiotics for at least one day developed an ADE2626. Tamma PD, Avdic E, Li DX, Dzintars K, Cosgrove SE. Association of adverse events with antibiotic use in hospitalized patients. JAMA Intern Med. 2017;177(9):1308-15. https://doi.org/10.1001/jamainternmed.2017.1938
https://doi.org/10.1001/jamainternmed.20...
. Medications are currently not included in hospital routine data although some ICD-10 codes cover such information, including T36-T50 “poisoning” and Y40-Y59 “adverse effects”. Identifying similarities between causative medications could guide further investigation of underlying reasons for particular types of ADE.

During the studied period, registered ADE amounted to US$ 259.9 million in hospitalization costs and 9.5 million hospital-bed days. Considerable costs such as those described are generally associated with hospitalizations related to ADE. In Spain, ADR alone cost health systems around €1.533 billion for over six years2727. Carrasco-Garrido P, Andrés LA, Hernámdez Barrera V, Miguel GA, Jiménez-García R. Trends of adverse drug reactions related-hospitalizations in Spain (2001-2006). BMC Health Serv Res. 2010;10:287. https://doi.org/10.1186/1472-6963-10-287
https://doi.org/10.1186/1472-6963-10-287...
. The US, in turn, had US$ 1,851.43 of additional costs from ADE-related hospitalization22. Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
https://doi.org/10.1002/pds.4184...
. The economic burden to the health system is thus related to the allocation of resources for symptoms diagnosis and treatment.

Studies using administrative databases generally report lower ADE frequencies than studies using intensive monitoring and higher frequencies than spontaneous reporting2727. Carrasco-Garrido P, Andrés LA, Hernámdez Barrera V, Miguel GA, Jiménez-García R. Trends of adverse drug reactions related-hospitalizations in Spain (2001-2006). BMC Health Serv Res. 2010;10:287. https://doi.org/10.1186/1472-6963-10-287
https://doi.org/10.1186/1472-6963-10-287...
, 2828. Scripcaru G, Mateus C, Nunes C. Adverse drug events: analysis of a decade. A Portuguese case-study, from 2004 to 2013 using hospital database. PLoS One. 2017;12(6):e0178626. https://doi.org/10.1371/journal.pone.0178626
https://doi.org/10.1371/journal.pone.017...
. In African hospitals, the median of patients with ADE during hospital stay was 8.4% whereas the median of patients admitted for ADE was 2.8% considering studies that used record review, clinical examination, or interview2929. Mekonnen AB, Alhawassi TM, McLachlan AJ, Brien JE. Adverse drug events and medication errors in African hospitals: a systematic review. Drugs Real World Outcomes. 2018;5(1):1-24. https://doi.org/10.1007/s40801-017-0125-6
https://doi.org/10.1007/s40801-017-0125-...
. Nevertheless, large health databases are great sources of real-world data regarding drug safety which allow characterizing ADE nationwide and indicating critical points1717. Miguel A, Marques B, Freitas A, Lopes F, Azevedo L, Pereira AC. Detection of adverse drug reactions using hospital databases: a nationwide study in Portugal. Pharmacoepidemiol Drug Saf. 2013;22(8):907-13. https://doi.org/10.1002/pds.3468
https://doi.org/10.1002/pds.3468...
, 3030. Chan EW, Liu KQL, Chui CSL, Sing CW, Wong LYL, Wong ICK. Adverse drug reactions – examples of detection of rare events using databases. Br J Clin Pharmacol. 2015;80(4):855-61. https://doi.org/10.1111/bcp.12474
https://doi.org/10.1111/bcp.12474...
. The increasing availability of large databases offers opportunities to investigate several ADE and detect signals as a complement of spontaneous reporting55. Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
https://doi.org/10.1186/1472-6963-11-134...
.

Our study provides evidence regarding the use of health system routine data to estimate the main features of hospitalizations for ADE during a decade in Brazil, showing increasing trends in hospitalizations and deaths. The study also showed that ICD-10 codes in the “certain” category of validity (A1 and B1) as ADE indicators were partly responsible for the costs of hospitalizations. Anti-infectives and anesthetics and therapeutic gases were the drugs most frequently involved in cases with “certain” codes, but ICD-10 codes related to unspecified drugs were prevalent overall. While this assessment focuses on frequency and tendency over time, future studies should determine patients at risk of hospitalization related to ADE nationwide for additional policy recommendations.

Strengths and Limitations

This study has strengths, including the assessment of a period of ten years within a nationwide scope; in fact, one of the advantages of using administrative databases to study ADE is the possibility of efficiently assessing large populations over long periods of time. Moreover, the list of codes applied was previous validated and includes several situations related to drug use. However, the study has limitations. The use of ICD-10 codes and administrative databases, including the SIH-SUS dataset, to identify potential ADE themselves has limitations. Firstly, regarding the database, factors such as incompleteness, misclassification, and variation among codifiers must be emphasized even with coding-quality monitoring. In this study, we could not estimate error caused by biases2323. Collao JF, Favereau R, Miranda R, Aceitón C. [Drug related harm in Chilean hospitals: prevalence analysis 2010-2017]. Rev Med Chile. 2019;147(4):416-25. Spanish. https://doi.org/10.4067/S0034-98872019000400416
https://doi.org/10.4067/S0034-9887201900...
,36. Secondly, regarding ICD-10 codes, we were careful to exclude cases which might be related to drug abuse, use of illicit substance, and intentional overdose; however, we used some codes that include both illicit and licit drugs, which might be confounding.

REFERENCES

  • 1
    Sousa-Pinto B, Marques B, Lopes F, Freitas A. Frequency and impact of adverse events in inpatients: a nationwide analysis of episodes between 2000 and 2015. J Med Syst. 2018;42(3):48. https://doi.org/10.1007/s10916-018-0898-5
    » https://doi.org/10.1007/s10916-018-0898-5
  • 2
    Poudel DR, Acharya P, Ghimire S, Dhital R, Bharati R. Burden of hospitalizations related to adverse drug events in the USA: a retrospective analysis from large inpatient database. Pharmacoepidemiol Drug Saf. 2017;26(6):635-41. https://doi.org/10.1002/pds.4184
    » https://doi.org/10.1002/pds.4184
  • 3
    Pardo Cabello AJ, Del Pozo Gavilán E, Gómez Jiménez FJ, Mota Rodríguez C, Luna Del Castillo JD, Puche Cañas P. Drug-related mortality among inpatients: a retrospective observational study. Eur J Clin Pharmacol. 2016;72(6):731-6. https://doi.org/10.1007/s00228-016-2026-0
    » https://doi.org/10.1007/s00228-016-2026-0
  • 4
    Laatikainen O, Miettunen J, Sneck S, Lehtiniemi H, Tenhunen O, Turpeinen M. The prevalence of medication-related adverse events in inpatients: a systematic review and meta-analysis. Eur J Clin Pharmacol. 2017;73(12):1539-49. https://doi.org/10.1007/s00228-017-2330-3
    » https://doi.org/10.1007/s00228-017-2330-3
  • 5
    Stausberg J, Hasford J. Drug-related admissions and hospital-acquired adverse drug events in Germany: a longitudinal analysis from 2003 to 2007 of ICD-10-coded routine data. BMC Health Serv Res. 2011;11:134. https://doi.org/10.1186/1472-6963-11-134
    » https://doi.org/10.1186/1472-6963-11-134
  • 6
    Shamliyan TA, Kane RL. Drug-related harms in hospitalized Medicare beneficiaries: results from the Healthcare Cost and Utilization Project, 2000-2008. J Patient Saf. 2016;12(2):89-107. https://doi.org/10.1097/PTS.0000000000000106
    » https://doi.org/10.1097/PTS.0000000000000106
  • 7
    Amelung S, Meid AD, Nafe M, Thalheimer M, Hoppe-Tichy T, Haefeli WE, et al. Association of preventable adverse drug events with inpatients’ length of stay: a propensity-matched cohort study. Int J Clin Pract. 2017;71(10):e12990. https://doi.org/10.1111/ijcp.12990
    » https://doi.org/10.1111/ijcp.12990
  • 8
    Wu TY, Jen MH, Bottle A, Molokhia M, Aylin P, Bell D, et al. Ten-year trends in hospital admissions for adverse drug reactions in England 1999–2009. R Soc Med. 2010;103(6):239-50. https://doi.org/10.1258/jrsm.2010.100113
    » https://doi.org/10.1258/jrsm.2010.100113
  • 9
    Kane-Gill SL, Van Den Bos J, Handler SM. Adverse drug reactions in hospital and ambulatory care settings identified using a large administrative database. Ann Pharmacother. 2010;44(6):983-93. https://doi.org/10.1345/aph.1M726
    » https://doi.org/10.1345/aph.1M726
  • 10
    Kuklik N, Stausberg J, Jöckel KH. Adverse drug events in German hospital routine data: a validation of International Classification of Diseases, 10th revision (ICD-10) diagnostic codes. PLoS One. 2017;12(11):e0187510. https://doi.org/10.1371/journal.pone.0187510
    » https://doi.org/10.1371/journal.pone.0187510
  • 11
    Mota DM, Vigo A, Kuchenbecker RS. Recomendações de códigos da CID-10 para vigilância de reações adversas e intoxicações a medicamentos. Cienc Saude Colet. 2018;23(9):3041-54. https://doi.org/10.1590/1413-81232018239.20692016
    » https://doi.org/10.1590/1413-81232018239.20692016
  • 12
    Cerqueira DRC, Alves PP, Coelho DSC, Reis MVM, Lima AS. Uma análise da Base de Dados do Sistema de Informação Hospitalar entre 2001 e 2018: dicionário dinâmico, disponibilidade dos dados e aspectos metodológicos para a produção de indicadores sobre violência. Rio de Janeiro: Instituto de Pesquisa Econômica Aplicada; 2019.
  • 13
    Agency for Healthcare Research and Quality, Patient Safety Network- PSNet. Medication errors and adverse drug events. Rockville, MD: AHRQ; 2019 [cited 2020 Mar 16]. Available from: https://psnet.ahrq.gov/primer/medication-errors-and-adverse-drug-events
    » https://psnet.ahrq.gov/primer/medication-errors-and-adverse-drug-events
  • 14
    World Health Organization. International Statistical Classification of Diseases and Related Health Problems - 10th revision; version 2019. Geneva (CH): WHO; 2019 [cited 2020 Mar 16]. Available from: https://icd.who.int/browse10/2019/en
    » https://icd.who.int/browse10/2019/en
  • 15
    National Cancer Institute, Division of Cancer Control & Population Sciences. Surveillance Research Program. The Joinpoint Regression Program, Version 4.8.0.1. Rockville, MD: NCI; 2020 [cited 2020 July 20]. Available from: https://surveillance.cancer.gov/joinpoint/
    » https://surveillance.cancer.gov/joinpoint/
  • 16
    Santos GAS, Boing AC. [Hospitalizations and deaths from drug poisoning and adverse reactions in Brazil: an analysis from 2000 to 2014]. Cad Saude Publica. 2018;34(6):e00100917l. Portuguese. https://doi.org/10.1590/0102-311X00100917
    » https://doi.org/10.1590/0102-311X00100917
  • 17
    Miguel A, Marques B, Freitas A, Lopes F, Azevedo L, Pereira AC. Detection of adverse drug reactions using hospital databases: a nationwide study in Portugal. Pharmacoepidemiol Drug Saf. 2013;22(8):907-13. https://doi.org/10.1002/pds.3468
    » https://doi.org/10.1002/pds.3468
  • 18
    Donaldson LJ, Kelley ET, Dhingra-Kumar N, Kieny MP; Sheikh A. Medication Without Harm: WHO’s Third Global Patient Safety Challenge. Lancet. 2017;389(10080):1680-1. https://doi.org/10.1016/S0140-6736(17)31047-4
    » https://doi.org/10.1016/S0140-6736(17)31047-4
  • 19
    Stausberg J. International prevalence of adverse drug events in hospitals: an analysis of routine data from England, Germany, and the USA. BMC Health Serv Res. 2014;14:125. https://doi.org/10.1186/1472-6963-14-125
    » https://doi.org/10.1186/1472-6963-14-125
  • 20
    Patel H, Bell D, Molokhia M, Srishanmuganathan J, Patel M, Car J, et al. Trends in hospital admissions for adverse drug reactions in England: analysis of national hospital episode statistics 1998–2005. BMC Clin Pharmacol. 2007;7:9. https://doi.org/10.1186/1472-6904-7-9
    » https://doi.org/10.1186/1472-6904-7-9
  • 21
    Paula TC, Bochner R, Montilla DER. Clinical and epidemiological analysis of hospitalizations of elderly due to poisoning and adverse effects of medications, Brazil from 2004 to 2008. Rev Bras Epidemiol. 2010;15(4):828-44. https://doi.org/10.1590/s1415-790x2012000400014
    » https://doi.org/10.1590/s1415-790x2012000400014
  • 22
    Lessa MA, Bochner R. Analysis of hospitalizations of children under one year of age due to drug intoxication and adverse events in Brazil. Rev Bras Epidemiol. 2008;11(4):660-74. https://doi.org/10.1590/S1415-790X2008000400013
    » https://doi.org/10.1590/S1415-790X2008000400013
  • 23
    Collao JF, Favereau R, Miranda R, Aceitón C. [Drug related harm in Chilean hospitals: prevalence analysis 2010-2017]. Rev Med Chile. 2019;147(4):416-25. Spanish. https://doi.org/10.4067/S0034-98872019000400416
    » https://doi.org/10.4067/S0034-98872019000400416
  • 24
    Waller P, Shaw M, Ho D, Shakir S, Ebrahim S. Hospital admissions for ‘drug-induced’ disorders in England: a study using the Hospital Episodes Statistics (HES) database. Br J Clin Pharmacol. 2005;59(2):213-9. https://doi.org/10.1111/j.1365-2125.2004.02236.x
    » https://doi.org/10.1111/j.1365-2125.2004.02236.x
  • 25
    Parikh S, Christensen D, Stuchbery P, Peterson J, Hutchinson A, Jackson T. Exploring in-hospital adverse drug events using ICD-10 codes. Aust Health Rev. 2014;38(4):454-60. https://doi.org/10.1071/AH13166
    » https://doi.org/10.1071/AH13166
  • 26
    Tamma PD, Avdic E, Li DX, Dzintars K, Cosgrove SE. Association of adverse events with antibiotic use in hospitalized patients. JAMA Intern Med. 2017;177(9):1308-15. https://doi.org/10.1001/jamainternmed.2017.1938
    » https://doi.org/10.1001/jamainternmed.2017.1938
  • 27
    Carrasco-Garrido P, Andrés LA, Hernámdez Barrera V, Miguel GA, Jiménez-García R. Trends of adverse drug reactions related-hospitalizations in Spain (2001-2006). BMC Health Serv Res. 2010;10:287. https://doi.org/10.1186/1472-6963-10-287
    » https://doi.org/10.1186/1472-6963-10-287
  • 28
    Scripcaru G, Mateus C, Nunes C. Adverse drug events: analysis of a decade. A Portuguese case-study, from 2004 to 2013 using hospital database. PLoS One. 2017;12(6):e0178626. https://doi.org/10.1371/journal.pone.0178626
    » https://doi.org/10.1371/journal.pone.0178626
  • 29
    Mekonnen AB, Alhawassi TM, McLachlan AJ, Brien JE. Adverse drug events and medication errors in African hospitals: a systematic review. Drugs Real World Outcomes. 2018;5(1):1-24. https://doi.org/10.1007/s40801-017-0125-6
    » https://doi.org/10.1007/s40801-017-0125-6
  • 30
    Chan EW, Liu KQL, Chui CSL, Sing CW, Wong LYL, Wong ICK. Adverse drug reactions – examples of detection of rare events using databases. Br J Clin Pharmacol. 2015;80(4):855-61. https://doi.org/10.1111/bcp.12474
    » https://doi.org/10.1111/bcp.12474

Publication Dates

  • Publication in this collection
    10 Oct 2022
  • Date of issue
    2022

History

  • Received
    30 May 2021
  • Accepted
    12 Dec 2021
Faculdade de Saúde Pública da Universidade de São Paulo São Paulo - SP - Brazil
E-mail: revsp@org.usp.br