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Translation and validation into portuguese Language of the Medication Regimen Complexity Index

Abstracts

BACKGROUND: The complexity of pharmacotherapy is a result of a multiplicity of prescribed regimen factors, including the number of different drugs in the regimen, the number of dosage units per dose, the total number of prescribed doses per day and administration instructions. The Medication Regimen Complexity Index (MRCI) is a specific, reliable and valid tool used to measure the complexity of pharmacotherapy, originally developed in English language. OBJECTIVE: Transcultural translation and validation of this tool into Brazilian Portuguese. METHODS: A cross-sectional study was developed with 95 type-2 diabetes patients, receiving multiple medications. The validation process included translation into Portuguese, back-translation and pre-test of the tool, creating a new version called the Pharmacotherapy Complexity Index (PCI). The psychometric parameters were assessed, including convergent validity, discriminant validity and reliability (interclass and test-retest correlation). RESULTS: The complexity of pharmacotherapy measured by the MRCI-Brazil had an average score of 15.7 points (SD=8.36). MRCI-Brazil showed significant correlation with the number of medications (r=0.86; p<0.001) and age of patients (r=0.28, p=0.005). Interrater reliability analysis found an intra-class correlation (ICC) of 0.99 (p<0.001) and test-retest correlation was of 0.997 (p<0.001). CONCLUSION: The results have shown that the Brazilian version of the MRCI presents adequate validity and reliability, and may be useful in clinical practice and research involving the analysis of the drug regimen complexity.

Drug therapy; patient compliance; guidelines


FUNDAMENTO: A complexidade da farmacoterapia consiste de múltiplas características do regime prescrito, incluindo o número de diferentes medicações no esquema, o número de unidades de dosagem por dose, o número total de doses por dia e os cuidados na administração dos medicamentos. O Medication Regimen Complexity Index (MRCI) é um instrumento específico, validado e utilizado para medir a complexidade da farmacoterapia, desenvolvido originalmente em língua inglesa. OBJETIVO: Tradução transcultural e validação desse instrumento para o português do Brasil. MÉTODOS: Foi desenvolvido um estudo transversal envolvendo 95 pacientes com diabete do tipo 2 utilizando múltiplas medicações. O processo de validação teve início pela tradução, retrotradução e pré-teste do instrumento, gerando uma versão adaptada chamada Índice de Complexidade da Farmacoterapia (ICFT). Em seguida foram analisados parâmetros psicométricos, incluindo validade convergente, validade divergente, confiabilidade entre avaliadores e teste-reteste. RESULTADOS: A complexidade da farmacoterapia medida pelo ICFT obteve média de 15,7 pontos (desvio padrão = 8,36). O ICFT mostrou correlação significativa com o número de medicamentos em uso (r = 0,86; p < 0,001) e a idade dos pacientes (r = 0,28; p = 0,005). A confiabilidade entre avaliadores obteve correlação intraclasse igual a 0,99 (p < 0,001) e a confiabilidade teste-reteste obteve correlação de 0,997 (p < 0,001). CONCLUSÃO: Os resultados demonstraram que o ICFT apresenta bom desempenho de validade e confiabilidade, podendo ser utilizado como ferramenta útil na prática clínica e em pesquisas envolvendo análise da complexidade da terapia.

Quimioterapia; cooperação do paciente; diretrizes


ORIGINAL ARTICLE

Translation and validation into portuguese language of the medication regimen complexity index

Ana Carolina MelchiorsI; Cassyano Januário CorrerI; Fernando Fernández-LlimosII

IUniversidade Federal do Paraná, Curitiba, PR – Brasil

IIFaculdade de Farmácia - Universidade de Lisboa, Lisboa – Portugal

Mailing address Mailing address: Cassyano Januário Correr Pinheiro Guimarães, 420/444 80330-250 - Curitiba, PR - Brazil E-mail: cassyano@ufpr.br

SUMMARY

BACKGROUND: The complexity of pharmacotherapy is a result of a multiplicity of prescribed regimen factors, including the number of different drugs in the regimen, the number of dosage units per dose, the total number of prescribed doses per day and administration instructions. The Medication Regimen Complexity Index (MRCI) is a specific, reliable and valid tool used to measure the complexity of pharmacotherapy, originally developed in English language.

OBJECTIVE: Transcultural translation and validation of this tool into Brazilian Portuguese.

METHODS: A cross-sectional study was developed with 95 type-2 diabetes patients, receiving multiple medications. The validation process included translation into Portuguese, back-translation and pre-test of the tool, creating a new version called the Pharmacotherapy Complexity Index (PCI). The psychometric parameters were assessed, including convergent validity, discriminant validity and reliability (interclass and test-retest correlation).

RESULTS: The complexity of pharmacotherapy measured by the MRCI-Brazil had an average score of 15.7 points (SD=8.36). MRCI-Brazil showed significant correlation with the number of medications (r=0.86; p<0.001) and age of patients (r=0.28, p=0.005). Interrater reliability analysis found an intra-class correlation (ICC) of 0.99 (p<0.001) and test-retest correlation was of 0.997 (p<0.001).

CONCLUSION: The results have shown that the Brazilian version of the MRCI presents adequate validity and reliability, and may be useful in clinical practice and research involving the analysis of the drug regimen complexity.

Key words: Drug therapy/utilization/economics; patient compliance; guidelines.

Introduction

The pharmacotherapy represents the main therapeutic resource to cure and control diseases. Among the determinant factors of the extension of medication use by the population is the constant development of new drugs, the use of drugs allied to clinical directive recommendations and the population’s demand for drug consumption. Additionally, the changes in the epidemiological profile and predominance of chronic diseases have increased the need for multiple treatments, a phenomenon known as polypharmacy. The result for the patients is the existence of higher-complexity therapies1.

Several studies have identified the complexity of pharmacotherapy as one of the main factors for non-compliance to treatment2-6. In hypertensive and diabetic patients, for instance, the number of medications7 or the dosage frequency8 have been associated to lower treatment compliance and worse blood pressure or metabolic control. Treatment compliance can be defined as the "The extent to which a person’s behaviour – taking medication, following a diet, and/or executing lifestyle changes, corresponds with agreed recommendations from a health care provider"9.

Several definitions of the complexity of pharmacotherapy can be found in the literature. Some are simple, involving only the number of medications and/or daily doses1,5 and others are more comprehensive, such as the one performed by Stone et al6. In general, it is accepted that the complexity of pharmacotherapy consists of multiple characteristics of the prescribed regimen, including at least the number of different drugs in the regimen, the number of daily doses, the number of dosage units per dose, the total number of daily doses and associations between dose and diet6,10.

Studies carried out in recent years have evaluated the complexity of pharmacotherapy in a wide array of diseases, such as epilepsy5, schizophrenia11, hypertension12, type-2 diabetes13, HIV/AIDS3,6 and specific population groups such as the elderly14-16, polymedicated patients1 and renal transplanted patients17. Some of these studies have demonstrated that the critical points of the complexity of pharmacotherapy can vary depending on the patients’ characteristics, such as, for instance, the use of 12 or more doses of medications per day in elderly patients15 or the dietary restrictions imposed by the administration of the medications in HIV-positive patients6.

This variety of definitions and interpretations can impair the uniformity of the measurement of this parameter. Important aspects, such as special use instructions (for instance, take it with food) or required medication management actions (take half a pill or crush the pill before taking it) can be ignored in the calculation of the complexity of pharmacotherapy5, making the comparison and generalization of scientific studies difficult.

Considering the importance of the relation of the complexity of pharmacotherapy with treatment compliance and the difficulty in standardizing the measurement of this parameter, George et al18 developed an index, called Medication Regimen Complexity Index (MRCI). The MRCI is a tool used to measure the complexity of pharmacotherapy of an individual patient, which is divided in three sections: A, B and C. Section A corresponds to the information on dosage forms, section B corresponds to the information on dose frequency and Section C corresponds to additional information, such as drug specific time and concomitant use with food, among others. Each section is scored based on the analysis of the patient’s pharmacotherapy and the complexity index is obtained by adding the points (scores) of the three sections18.

The MRCI is the only currently validated tool found in literature used to measure the complexity of pharmacotherapy, which was originally written in the English language. The validation of this tool for our country can help the studies involving therapy compliance and strategies for its improvement, allowing a better standardization of methodology and result comparison. The aim of this study is the adaptation and validation of the Medication Regimen Complexity Index tool into Brazilian Portuguese.

Methods

A transversal study was carried out between October and December 2005. Pharmacotherapeutic files of 105 patients with type 2 diabetes who were using oral antihyperglycemic agents or insulin were analyzed and were participating in a clinical study on pharmaceutical concern in community pharmacies in the city of Curitiba, Paraná. The use of medication was analyzed for each patient in its totality, including prescribed anti-diabetic medication and drugs used for other conditions, such as hypertension and dyslipidemia. The medications used for acute conditions or used when necessary were also taken into account. For each patient, the first constant pharmacotherapeutic regimen was considered from the date the patient was included in the study. This study was developed by the Department of Pharmacy of the Federal University of Paraná, being approved by the Research Ethics Committee of Hospital das Clinicas, protocol # CEP-HC n. 092ext046/2003-08. All patients gave their written informed consent prior to study enrollment.

Transcultural translation - The process of translation and validation followed international recommendations19,20 and considered studies that had used the tool for Brazilian patients21. The tool was submitted to two translators who were fluent in the English language, who knew the underlying objectives and concepts of the study and whose mother language was Portuguese. The two translations were compared, generating a consensual version, which was called "Version 1".

At the second phase, the Version 1 of the tool was submitted to back-translation into the English language. It was carried out by a translator who was fluent in the English language and did not know the underlying objectives and concepts of the study. This new English version was compared to the original tool and the correction of the casual discrepancies originated a new version, called "Version 2".

At the third phase, an evaluation committee that consisted of three healthcare professionals who were bilingual revised all parts of the tool Version 2, checking semantic, idiomatic, cultural and conceptual equivalence. After this phase, the third version of the tool, called Version 3, was generated. The latter was then submitted to a pre-test, using a fictitious patient presented to three clinical pharmacists who had not taken part in the prior phases of the study. They described their main doubts and difficulties in using the tool and their assessments were based on the validity of the content and face validity. The final version was attained after the committee’s assessment and index adjustments, based on the proposed modifications.

Validation - The tool was used together with the patients’ files by two separate researchers. After applying the tool, psychometric analyses were carried out aiming at assessing its validity and reliability. Test selection was based on the normal distribution of data confirmed by the Komolgorov-Smirnov test. The construct validity was analyzed by the convergent validity, checking the correlation between the total score of the index and the number of medications of the treatment, using Pearson’s correlation coefficient.

The discriminant validity was analyzed from the correlation between the total score of the complexity and independent variables. The body mass index (BMI) was used with Pearson’s correlation coefficient and differences in scores between genders were used with Student’s t test.

To estimate reliability, the inter-rater reliability was assessed by comparing the results from two different and independent users and the test-retest reliability was assessed by having the same user repeat the filling out of the index twice during a thirty-day interval, for all patients.

The reliability analyses used the intraclass correlation coefficient (ICC)(95%CI). The database was organized by double-typing the measured results and statistical tests were carried out through the SPSS v.12.0 software. Significance was set at p<0.05.

Results

Of the 105 patients that participated in the study, 10 were excluded from the validation study. The reasons for the exclusion were the failure in using antihyperglycemic agents (3 cases) or absent data from the medical files, which prevented the adequate use of the measurement tool (7 cases). A total of 95 patients were included in the study (90.4%).

Patients’ mean age was 58.5 yrs (SD=11.2; ranging from 31-88 yrs), with 63.2% of them being females. The patients were characterized regarding time of diagnosis, access to healthcare services, time since the last medical appointment, schooling, body mass index (BMI), waist circumference, glycated hemoglobin (HbA1) levels, fasting glycemia levels and blood pressure. The patients were also evaluated regarding Charlson’s comorbidity Index, which evaluates patients’ comorbidity load, allowing an estimate of the ten-year mortality risk22. The index presents a linearity between 0-5 points, with 0 corresponding to 99% of chance of survival and 5 to 34% of chance of survival in a ten-year period. The data are summarized in Table 1.

The mean number of medications per patient was 4.5 (SD=2.5). Most of the patients used only oral antihyperglycemic agents (84.3%); 49.4% used antihypertensive drugs, 18% used hypolipemiant drugs and 34.8% used platelet antiaggregant agents. These conditions were taken into account as they are clinically significant for diabetic patients and the ones that are most often observed23,24. The most frequently used medications for these conditions are summarized in Table 2.

The transcultural adaptation process resulted in the Portuguese version of the tool, called Índice de Complexidade da Farmacoterapia – ICFT. The translated tool includes instructions for its use and maintains the same presentation of the original version.

The complexity of pharmacotherapy measured in the population by the ICFT obtained a score of 15.7 points (SD=8.36). The maximum score obtained was 45.5 at a treatment that included 12 medications and the minimum score was 4, in a treatment that consisted of only one pill a day. There was a significant correlation between the number of medications and the ICFT obtained (r=0.86; p<0.001), showing a convergence between these parameters.

Additionally, there was a difference regarding the ICFT scores among patients using the same number of medications, demonstrating the significance of other factors in the calculation of the index. The mean of the ICFT and its dispersion considering a 95%CI shows an overlap of results and dispersion increase with the increase of the total of medications. These results are show in details in Table 3.

Specifically regarding the antidiabetic treatment, the addition of insulin to the oral antihyperglycemic agents was associated with a significant increase in the therapy complexity, with a mean increase of 10 points at the ICFT (p=0.003).

The ICFT also showed a significant correlation with age (r=0.28, p=0.005), specifically in Section A (dosage forms) and Section B (dosage frequency). The exception was Section C of the tool, which deals with the additional information on the medications and was not significantly correlated with age (r=0.18; p=0.08).

The divergent validity analysis between the ICFT score and BMI reached r=0.02 (p=0.790), showing a low correlation among the variables. No significant difference was found between ICFT scores for men and women (15.5±7.1 vs. 15.8±8.9; p=0.873). The patients who were followed exclusively at the Public Health Service presented treatment with similar complexity (ICFT=16.0, SD=9.4) when compared to those followed exclusively at private healthcare services (ICFT=15.2, SD=6.7; p=0.709).

No significant correlation results were observed between the ICFT and clinical parameters such as HbA1 (r=0.06; p=0.56) and fasting glycemia (r=-0.15; p=0.14). The correlation results between ICFT and the main independent variables are shown in Table 4.

Regarding reliability, a high correlation was observed between the results of the ICFT applied by two different raters to the same sample of patients. The interrater ICC was 0.99 (p<0.001) for the total ICFT and showed results > 0.98 among the three sections. The test-retest reliability reached a correlation (ICC) of 0.997 and 1.00, 0.99 and 0.99 for sections A, B and C, respectively. The means of the ICFT results at the test-retest were not significantly differently either (15.7±8.3 versus 15.6±8.1; p=0.32).

Discussion

The ICFT is a tool that measures the complexity of pharmacotherapy regardless of socioeconomic, pharmacological or clinical variables. This tool is based solely on the necessary actions for the drug administration, i.e., which is the pharmaceutical form, frequency and other additional information that must be taken into account by the patient for the correct administration of the medication. This tool can be useful in clinical research and practice, as it provides valuable information on the elements that constitute the complexity of pharmacotherapy, allowing an estimate of the degree of difficulty in therapy compliance exhibited by the patient. In order to use it, however, it is necessary to have an adequate version that has been validated into our language and a system of clinical data registry.

The process of validation of the original tool included phases of design and the comparison of its results with the analysis made by the specialists’ committee18. Starting from the original study, ours analyzed the characteristics of reproducibility, validity and reliability of the tool in Brazilian Portuguese. In order to do so, we chose to use the methodology for translation and validation of tools that is internationally accepted and broadly utilized19,20.

As in the original tool (MRCI), the ICFT in Brazilian Portuguese has three sections, being divided as follows: section A: dosage forms; section B: dosage frequency and section C: additional information. As the tool is to be filled out by the healthcare professional and not by the patient, its system allows several medications and additional information to be included into the assessment, making it broader.

Some tools published in the literature do not allow a complete evaluation of the complexity1 or assess other concepts rather than the complexity of pharmacotherapy17.

The content and face validity were analyzed by the evaluation and pre-test committees, respectively, as established in the methodology of translation by Guillemin et al19. In the pre-test phase, there were difficulties concerning the understanding of some instructions of the ICFT, which were modified to facilitate the understanding of the healthcare professional at the moment of filling it out. One of the suggestions made by the pre-test pharmacists was to create an electronic tool using the ICFT, in order to shorten the time needed for filing it out and make its use helpful in clinical practice.

The main reported difficulties regarding the use of the instrument during the pre-test were related to the registry of the additional pharmacotherapy instructions. The main divergent points were those regarding the need of taking some medications with food, which were solved with the literature, use at specific times, considered even when the frequency is fixed (i.e., every 12 hrs) and the use of insulin, considered as multiple units at the same time.

The number of medications used by the patient greatly influences complexity, but it cannot be considered the only factor1,6. The results showed that the ICFT is capable of differentiating the complexity of treatments with the same number of medications, corroborating the concept that simply counting the number of medications does not correspond to the complexity.

The divergent validity was demonstrated by comparing the results of the ICFT between genders and BMI. Considering that these factors do not have direct influence on the complexity of treatment itself, the low correlation found is within the expected and demonstrates the absence of influence of external factors on the index calculation.

At the calculation of the tool reliability, the test-retest was carried out, which demonstrated a high correlation of the total ICFT as well as of the its sections, applied before and after 1 month, and the intra-class reliability that also showed high correlation between the raters. The data obtained at this phase is similar to that of the original ICFT18.

This validated tool allows the development of new research on the association between therapy compliance and therapy complexity, including the possible definition of ICFT cutoffs from which the compliance presents significant decreases or increases. Such studies can be quite useful in generating strategies to stimulate compliance directed at the reduction of therapy complexity in polypharmacy and multidiagnosis conditions and numerous clinical practice scenarios (outpatient clinic, healthcare units, and community pharmacies). Additionally, the association between therapy complexity and the occurrence of favorable or undesirable clinical outcomes can collaborate in the optimization of pharmacological treatments.

Although this study was carried out in type 2-diabetic patients, the ICFT can be used with any type of patients or pharmacological treatment.

Conclusions

The translated version into Brazilian Portuguese of the Medication Regimen Complexity Index (MRCI), which was called Pharmacotherapy Complexity Index (PCI) demonstrated an adequate psychometric quality and can be used to compare not only groups of patients, but also individual patients. Its usefulness in clinical practice and research is due to the analysis of the compliance determinants as well as the effects of health interventions on the complexity of pharmacotherapy.

Acknowledgements

The authors wish to thank the Professors and Clinical Pharmacists of the Pharmacy Service and the Pharmaceutical Care of Centro Universitário Positivo (UNICENP), for their willing collaboration in the validation of this tool: Paula Rossignoli, Renata B. Schulz and Rodrigo A. de Paula e Souza.

References

Manuscript received October 16, 2006; revised manuscript received February 12, 2007; accepted February 12, 2007.

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  • Mailing address:

    Cassyano Januário Correr
    Pinheiro Guimarães, 420/444
    80330-250 - Curitiba, PR - Brazil
    E-mail:
  • Publication Dates

    • Publication in this collection
      18 Apr 2008
    • Date of issue
      Oct 2007

    History

    • Accepted
      12 Feb 2007
    • Reviewed
      12 Feb 2007
    • Received
      16 Oct 2006
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