- Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
Background: Medication therapy management (MTM) services is a method that can effectively improve patients’ conditions, but the efficacy of economic and humanistic outcomes remain unclear. This systematic review and meta-analysis aim to use economic, clinical and humanistic outcomes to evaluate the multi-benefits of MTM services.
Method: A systematic review and meta-analysis was conducted by retrieving PubMed, EMBASE, the Cochrane Library and ClinicalTrial.gov from the inception to April 2022. There were two reviewers screening the records, extracting the data, and assessing the quality of studies independently.
Results: A total of 81 studies with 60,753 participants were included. MTM services were more effective in clinical outcomes with decreasing the rate of readmission (OR: 0.78; 95% CI: 0.73 to 0.83; I2 = 56%), emergency department visit (OR: 0.88; 95% CI: 0.81 to 0.96; I2 = 32%), adverse drug events (All-cause: OR: 0.68; 95% CI: 0.56 to 0.84; I2 = 61%; SAE: OR: 0.51; 95% CI: 0.33 to 0.79; I2 = 35%) and drug-related problems (MD: −1.37; 95% CI: −2.24 to −0.5; I2 = 95%), reducing the length of stay in hospital (MD: −0.74; 95% CI: −1.37 to −0.13; I2 = 70%), while the economic and humanistic outcomes were less effective.
Conclusion: Our systematic review and meta-analysis demonstrated that MTM services had great ability to improve patients’ clinical conditions while the efficacy of economic and humanistic outcomes, with some of the outcomes showing high degree of heterogeneity and possible publication bias, required more future studies to provide stronger evidence.
Systematic Review Registration: [https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=349050], identifier [CRD42022349050].
1 Introduction
Medication therapy management (MTM) services encompass multiple medical services delivered by pharmacists. Since the concept of MTM was first proposed in the 1990s (Hepler and Strand, 1990), this novel and integrated strategy to improve patients’ quality of life attracted widespread attention. The MTM services were strongly supported by the US government to facilitate the development of an integrated healthcare system—known as Fairview Health Services, which helped millions of patients over the years (Burns, 2008). A meta-analysis in 2014 concluded that MTM services helped patients to reduce drug-related problems, decrease healthcare utilities, and cut down the cost of healthcare, while the evidence supporting the improvement in health outcomes was insufficient (Viswanathan et al., 2015). This meta-analysis investigated the efficacy of MTM services. The results indicated that the development of MTM services was hindered by the lack of strong evidence and suggested the need for comprehensive and rigorous studies in the future.
Economic, Clinical and Humanistic Outcomes (ECHO) is a model used to provide an omnidirectional view of medications and medical interventions (Reeder, 1995). It depicts the importance of pharmaceutical services combined with traditional clinical outcomes based on more contemporary measures of economic efficiency and quality (Kozma et al., 1993). According to the model, economic, clinical and humanistic outcomes are used to comprehensively analyze the efficacy of medical intervention. Although several studies comprehensively evaluated patient’s burden and medical interventions using the ECHO model, such as refill adherence measures and STOPP/START criteria (Reeder et al., 2000; Jeremy et al., 2011; Hill-Taylor et al., 2013; Zhao et al., 2019; Chua et al., 2020), few studies evaluated the efficacy of MTM services with full ECHO model. Despite descriptive studies demonstrating that MTM services improved patients’ clinical conditions, quality of life and potentially reduced healthcare disparities (Bunting and Cranor, 2006; Shrestha et al., 2022), studies analyzed the three parts of ECHO model in one assessment was little (Singhal et al., 1999; Cheng et al., 2013; Johnson et al., 2018). The incompleteness of the analysis may result in superficial conclusions and less precise outcomes.
Leveraging the ECHO model, our meta-analysis divided outcomes into economic, clinical and humanistic outcomes to evaluate the efficacy of MTM services. The goal of our study was to elucidate the benefits of MTM services and to provide robust evidence supporting the efficacy of MTM services.
2 Methods
This systematic review and meta-analysis followed the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) 2020 statement (Page et al., 2021). The study protocol (Deng et al., 2022) was registered on PROSPERO 2022 (Registered ID: CRD42022349050).
2.1 Database search
MTM services-related studies were retrieved systematically from several mainstream databases and websites (PubMed, The Cochrane Library, Embase and ClinicalTrial.gov) using comprehensive search strategies (Table 1). To ensure compatibility with the requirements of each database, one experienced researcher (WAH) reviewed and refined the search terms. The main key words used in search terms included: “medication therapy management,” “MTM,” “medication reconciliation” and “drug therapy management”. Two researchers (PSS and CJ) conducted the search independently. The final search was conducted on 16 April 2022.
2.2 Inclusion and exclusion criteria
Studies included met the following criteria:
1) Predesigned of studies including RCTs and non-randomized studies.
2) Participants: Adults requiring MTM services.
3) Interventions: Containing MTM services administered by pharmacists.
4) Outcomes: At least one of the outcomes we interested in should be reported in the study, including clinical, economic, and humanistic outcomes.
Studies with following criteria were excluded:
1) Studies without control group.
2) Studies published in languages other than English.
3) Animal experiments.
4) Pilot studies and feasibility studies.
5) Studies comparing the efficacy between different MTM interventions.
2.3 Definition of outcomes
Basing on the definition from ECHO model for the clinical, economic and humanistic outcomes (Cheng et al., 2013; Shrestha et al., 2022; Gunter., 2023), the definition of outcomes included in our study was confirmed.
Clinical outcomes: Clinical outcomes were defined as medical events that occurred as a result of MTM services, including rate of readmission, emergency department visit, mortality, adverse drug events (including all-cause and serious adverse events), and so on.
Economic outcomes: Based on the definitions of direct and indirect cost in ECHO model, we defined the economic outcomes as measures of medical resource utilization such as hospitalization and medication costs. Indirect costs, such as evaluations of reduced productivity and lost work days, could be assessed if adequate studies results included in.
Humanistic outcomes: Humanistic outcomes were defined as the consequences of disease or treatment on patient functional status or quality of life, including physical function, social function, general health and wellbeing, and life satisfaction. Consequently, our study included life quality scales and evaluations of adherence as part of our assessment of humanistic outcomes.
2.4 Definition of intervention and comparison
Intervention: To be eligible for inclusion criteria in our meta-analysis, studies needed to involve the administration of MTM services. To avoid omission of studies and based on the definition of MTM services, medication reconciliation and drug therapy management were also included.
Comparison: The control interventions consisted of usual care or other standard therapies depending on the participants’ diseases. These usual care and standard therapies did not involve any additional medication administration or other therapies when compared with the intervention arm.
2.5 Study selection and data extraction
Two researchers (DZJ and GL) independently assessed the studies with eligibility criteria. The data of all included studies were extracted according to a predesigned format by two independent researchers. Any deviation from this approach was resolved by consensus or consultation with a third expert. The following data were extracted: 1) basic information (title, first author, year of publication, type of study, and location of study); 2) study population (age, sample size, detailed description of participants, and diseases); 3) details of interventions and comparison; 4) outcomes and 5) the length of follow-up time.
2.6 Quality assessment
The risk of bias of RCTs and non-randomized studies was evaluated by two independent researchers using Risk of Bias 2 tool (Hastert and Denni, 2003; Sterne et al., 2019) and ROBINS-I tool (Sterne et al., 2016), as recommended by Cochrane Handbook for Systematic Reviews of Interventions (version 6.3) (Cochrane, 2022), respectively. Any disagreement was resolved by consensus or consultation with a third expert.
2.7 Statistical analysis
All the data were imported and analyzed by RevMan (ver. 5.4). Outcomes including 3 studies or above were synthesized as the results. We used odds ratios (ORs) and 95% confidence intervals (CIs) to measure dichotomous variables, and mean differences (MDs) with 95% CIs for continuous variables. To synthesize the results with different scales involving the same outcomes, such as EQ-5D-3L and 5L, SF-12 and 36, and potential huge variance of unit in the cost in different studies, standard mean differences (SMDs) were calculated as effect measures to eliminate possible discrepancies in different scales. All the outcomes were applied with random-effects model. Heterogeneity was calculated using Chi-squared and I2. Results with an I2 value greater than 50% were deemed to have a high potential for heterogeneity.
Subgroup analysis was performed to detect the sources of heterogeneity. Type of studies (RCTs/No-randomized studies), district of studies (US/Non-US), and type of diseases (chronic disease/non-chronic disease/undefined) were predetermined as subgroups to analyze the outcomes. Additionally, the robustness of results was evaluated via sensitivity analysis—using the method that eliminated one study in the outcome at a time to synthesize the results of remaining studies. Publication bias was assessed via funnel plots and Egger’s test using RevMan (ver. 5.4) and STATA (ver. 16), respectively.
3 Results
3.1 Study selection
A PRISMA flow diagram was used to illustrate our process in study selection (Figure 1). A total of 2,550 records were identified in our initial search with comprehensive search strategies (Table 1). Finally, our quantitative analysis encompassed 81 studies, consisting of 66 RCTs and 15 non-randomized studies (included 10 NRCTs and 5 cohort studies). These studies were conducted across various countries and covered a range of diseases.
3.2 Study characteristics
According to the baseline table, 81 studies involved a total of 60,753 participants, with 29,587 in the intervention group and 31,166 in the control group. Aside from 30 studies conducted in the US, the remaining studies were conducted across various countries such as China, Japan, Australia, and England. In summary, 25 studies were conducted in Europe, 13 in the Aisa and 13 in other locations. This distribution of location roughly showed an overview of development of MTM services in the world, which means the US and Europe was advanced to other countries. Regarding research type, 66 studies were designed as RCT, 15 as non-randomized studies (including 10 NRCTs and 5 cohort studies). Furthermore, among the included studies, 16 studies distinctly focused on patients with chronic diseases, 5 studies included non-chronic disease patients, and 30 studies included patients with no specific definition of diseases. These findings highlight the need to pay more attention to non-chronic diseases and emphasize that MTM services could benefit various kinds of patients, not only those with chronic diseases. Besides, the follow-up time of these studies varied from 30 to 780 days, indicating that MTM services could cover both short-term and long-term care. A baseline table was formulated for the detail characteristics of included studies (Supplementary Table S1).
The evaluation of risks of bias showed that RCTs had lower risks of bias than non-randomized studies (Figures 2, 3). In RCT studies, the most critical factor leading to bias was randomization process with 28 studies having some concern and 7 having high risk in this domain. In the results of ROBINS-I, confounding had a higher risk of bias than other domains, indicating that many of the included non-randomized studies had less control over confounding factors.
3.3 Clinical outcomes
Seven clinical outcomes were analyzed including: rate of readmission, emergency department (ED) visit, mortality, adverse drug event (ADE) which included all-cause ADE and serious adverse event (SAE), the length of stay (LoS) in hospital, drug-related problems (DRPs) and medication appropriateness index (MAI) (Figure 4). Most outcomes demonstrated significant improvement in patient condition with MTM services, though some of them showed high degree of heterogeneity (Figure 2). MTM services effectively reduced the rate of readmission (OR: 0.77; 95% CI: 0.73 to 0.82; I2 = 55%), ED visit (OR: 0.88; 95% CI: 0.81 to 0.96; I2 = 32%), ADE (All-cause: OR: 0.68; 95% CI: 0.56 to 0.84; I2 = 61%; SAE: OR: 0.51; 95% CI: 0.33 to 0.79; I2 = 35%), the number of DRPs (MD: −1.37; 95% CI: −2.24 to −0.5; I2 = 95%) and MAI (MD: −2.11; 95% CI: −3.74 to −0.48; I2 = 98%). Also, the LoS in hospital was significantly shortened (MD: −0.74; 95% CI: −1.37 to −0.13; I2 = 70%). However, the mortality rate (OR: 0.91; 95% CI: 0.83 to 1.01; I2 = 1%) was not affected by MTM services. The subgroup analysis showed that the disease type was associated with a high possibility of high heterogeneity. For example, based on the results of readmission, three groups of diseases showed huge heterogeneity (chronic disease: OR: 0.82; 95% CI: 0.72 to 0.93; I2 = 70%; non-chronic disease: OR: 0.96; 95% CI: 0.69 to 1.34; I2 = 0%; undefined: OR: 0.75; 95% CI: 0.7 to 0.81; I2 = 41%). All the results of subgroup analysis are presented in Supplementary Figures S16–S39.
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FIGURE 4. Results of clinical outcomes. (A) Readmission; (B) ED visit; (C) Mortality; (D) All cause ADE; (E) SAE; (F) LoS; (G) DRPs; (H) MAI; (I) Summary of clinical outcomes.
3.4 Economic outcomes
Our results showed that the total cost (SMD: −0.1; 95% CI: −0.3 to 0.09; I2 = 87%) and the cost of hospitalization (SMD: −0.01; 95% CI: −0.25 to 0.22; I2 = 91%) were not reduced, while the medication cost was significantly decreased (SMD: −0.19; 95% CI: −0.37 to −0.01; I2 = 90%) (Figure 5). District of study was inferred as a high possibility source of heterogeneity in medication cost. (US: SMD: −0.37; 95% CI: −0.74 to 0.00; I2 = 92%; Non-US: SMD: 0.00; 95% CI: −0.14 to 0.15; I2 = 69%). The results of subgroup analysis are presented in the Supplementary Figures S40–S48.
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FIGURE 5. Results of economic outcomes. (A) Total cost; (B) Medication cost; (C) Cost of hospitalization (D) Summary of economic outcomes.
3.5 Humanistic outcomes
Humanistic outcomes included quality of life and patient’s adherence (Figure 6). The subgroup analysis is presented in the Supplementary Figures S49–S60.
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FIGURE 6. Results of humanistic outcomes. (A) EQ-5D; (B) SF-Physical outcomes; (C) SF-Mental outcomes; (D) Adherence; (E) Summary of humanistic outcomes.
The quality of life was measured using EQ-5D (3L and 5L) and SF (12D and 36D) scales. The patient’s quality of life based on EQ-5D was not increased by MTM services (SMD: 0.15; 95% CI: −0.01 to 0.31; I2 = 69%). The SF scale evaluated the quality of life based on physical and mental outcomes. Notably, MTM services effectively improved physical outcomes (SMD: 0.26; 95% CI: 0.03 to 0.5; I2 = 88%), while negligible effect was observed in mental outcomes (SMD: 0.05; 95% CI: −0.02 to 0.12; I2 = 43%).
In the analysis of patient’s adherence, the proportion of days covered of medication and the MMAS8 scale were both used as the method to evaluate patient’s adherence in medication administration. The results showed that MTM services had no effect on promoting adherence during the therapy (SMD: 0.47; 95% CI: −0.01 to 0.95; I2 = 96%).
3.6 Publication bias and sensitivity analysis
Publication bias was assessed by funnel plots and Egger’s test respectively. And according to the Egger’s test, ED visit and medication cost may have the potential of publication bias. Funnel plots were presented in Supplementary Figures S61-S75 and results of Egger’s test were in Supplementary Table S2.
The results of sensitivity analysis indicated that some outcomes, such as mortality, adherence, MAI, medication cost and cost of hospitalization, might have problems of robustness of results. For example, in results of cost of hospitalization, the elimination of Cowper et al.’s (Cowper et al., 1998) study changed the result from negative to positive. However, this change might be attributed to the old year of study. All the results of sensitivity analysis are presented in the Supplementary Figures S76–S90.
4 Discussion
Our meta-analysis evaluated the impact of MTM services with ECHO model on multiple outcomes in one assessment. The pooled analysis of 81 studies demonstrated the significant clinical efficacy of MTM services. However, due to limited study numbers and high degree of heterogeneity brought by methodological variations in measuring the economic and humanistic outcomes, the efficacy in economic and humanistic outcomes requires further investigation through additional studies.
4.1 Clinical outcomes
Collectively, our meta-analysis demonstrated that MTM services were effective in improving clinical outcomes by decreasing the risks of readmission, ED visit after discharge, lowering the rate of ADE, the numbers of DRPs, shortening the LoS in the hospital and lowering the score of MAI. These results of clinical outcomes were consistent with the results of previous meta-analysis in 2014 (Viswanathan et al., 2015). Other studies also confirmed the clinical efficacy of MTM services, like reducing return visits to emergency department (Hayes et al., 2012) and improving short-term outcomes of patients with diabetes and cardiovascular conditions (Babar et al., 2018). Further, data from Minnesota’s Fairview Health System revealed that about 85% of patients had at least 1 DRP, while the health conditions of 55% of patients improved after receiving comprehensive medication management (McFarland et al., 2021). Despite the remarkable efficacy of MTM services in improving patients’ near-term conditions, the effectiveness of MTM services at usance, as the result of mortality in our meta-analysis showed, was not significant. Some of RCTs and reviews attributed the unsignificant results of reducing the rate of mortality to the inadequate follow-up time (Christensen and Lundh, 2016; Lea et al., 2020) while our meta-analysis, which was larger than previous studies, included more studies with a follow-up time greater than 1 year, yielded the same non-significant results. The primary objective of MTM services was to facilitate patients’ self-managing their health conditions, rather than directly curing the disease and extending their lifetime expectancy. Consequently, the MTM services were more effective in improving patients’ near-term conditions, with limited long-term effects beyond a year.
4.2 Economic outcomes
In terms of economic outcomes, the MTM services reduced the need for additional medication, thereby decreasing the medication cost directly. The intervention reduced ADEs, facilitated adherence to evidence-based guidelines, timely implemented medication therapies, and increased the use of cost-effective drug therapies (Morgan et al., 2018). MTM services significantly reduced the rates of readmission and ED visits, which benefit-cost ratio of MTM services was reported that ranged from 2.1:1 to 2.6:1 by another review (Moczygemba et al., 2019). A prospective study demonstrated that MTM services contributed to a 57.9% reduction in facility costs and an 11.1% reduction in professional claims, despite a 19.7% increase in prescription drug expenditures (Isetts et al., 2008). Though many same conclusions were reported to demonstrate the efficacy of saving partial cost by MTM services (Campbell et al., 2018; Ni et al., 2018; Chung et al., 2020; Bezerra et al., 2022), several other costs apart from the medication cost might be increased by delivering MTM services, which diluted the efficacy in reducing total cost.
4.3 Humanistic outcomes
The results of humanistic outcomes showed that MTM services were more effective in improving physical outcomes like SF in the physical outcome compared with mental results, such as adherence and SF in the mental outcome. This result indicated that MTM services focused more on the patients’ physical condition and less on the mental condition. Numerous studies had reported similar results, suggesting the need for further research with greater methodological rigor to obtain evidence supporting mental health (Finley et al., 2003; Rubio-Valera et al., 2014; Hattingh et al., 2016; Silva et al., 2018). In contrast to a Cochrane review assessing multiple pharmaceutical interventions in elders and reporting little or slight effects on improving patients’ adherence, appropriateness of polypharmacy and quality of life (Rankin et al., 2018), our meta-analysis demonstrated some efficacy of MTM services in humanistic outcomes. While this Cochrane review focused on elders receiving polypharmacy, our meta-analysis was not restricted to a specific population, which enhances the generalizability of our results. Besides, as a general instrument involving the general population (Rabin and de Charro, 2001), EQ-5D might result in a less precise evaluation of a patient’s condition with a specific disease. A combination of this general instrument and disease-specific scales, such as the global registry of acute coronary events (GRACE) risk score, would be more beneficial for a comprehensive analysis. These considerations highlight the necessity for improved measures to evaluate patients’ quality of life. In adherence outcomes, due to differences in the definition of “adherent” and the lack of diagnostic gold standard, the rate of adherence in a patient with chronic conditions was reported to range between 43% and 78% (Osterberg and Blaschke, 2005) as a result. However, patients receiving multiple pharmaceutical care have a higher rate of adherence, reported to be approximately 72% (DiMatteo, 2004). Thus, despite the results of negative adherence and high levels of heterogeneity in our meta-analysis, the efficacy of MTM services for improving patients’ adherence was undeniable.
4.4 Prospects and limitations
Our meta-analysis also provided the idea that more studies need to focus on economic and humanistic outcomes to provide more comprehensively perspective of MTM services. Although MTM services could provide continuous support to patients with chronic conditions for a prolonged period, the identified disparities, according to our results, between the near-term and long-term outcomes of MTM services underscore the need for more targeted and precise research for long-term studies. Based on the results of risks of bias assessment, both RCT studies and non-randomized studies face challenges in controlling bias. To further enhance the quality of evidence generated from future studies, the adoption of the Grading of Recommendations, Assessment, Development and Evaluations (GRADE) framework (Guyatt et al., 2008) could be considered to provide a comprehensive assessment of the evidence quality and ensure the validity of the evidence generated. As MTM services are an intervention designed to guide patients in developing self-management (Burns, 2008), a lot of anthropic factors and confounding factors makes trials more difficulty to control the bias, especially in the non-randomized studies. Though subgroup analysis indicated that there was little heterogeneity in results between RCTs and non-randomized studies, future study design should be more cautious in controlling for bias and clarifying confounding factors to enhance the confidence of study results. The subgroup analysis also reveals the differences in the efficacy of MTM services between the US and other countries. These findings can be further explored to understand the variations in the more developed MTM services system in the US compared to other countries that are relatively new to this field.
Several limitations exist in this meta-analysis. First, despite the best possible search of databases, the omission of studies was inevitable, including grey articles and ongoing clinical trials. Second, though the extensive outcomes including the evaluation of the ECHO model leading to comprehensive conclusions, the meta-analysis is limited by the inadequate number of studies for every outcome analyzed. Several outcomes were predesigned in our protocol, while some of them were eventually excluded in our meta-analysis after retrieving studies. Third, the results of sensitivity analysis and publication bias showed that several outcomes, like cost of hospitalization, medication cost, mortality, and MAI, involved unstable results or publication bias. Finally, although a subgroup analysis was performed to identify the sources of heterogeneity, it was difficult to explain all the reasons underlying the high degree of heterogeneity.
The RCTs, with more rigorous inclusion and exclusion criteria, could generate more robust findings than non-randomized studies, while these restrictions limited generalizability of RCT results to real-world settings compared to non-randomized studies. And some studies reported that these two types of studies might induce the heterogeneity (Mekonnen et al., 2016; Ahmed et al., 2022). Based on these facts, we supposed that if both types of studies showed consistent tendencies of results in terms of specific outcomes, the combination analysis of these two types of studies would be more considered valid. The second one of possible source of heterogeneity was the type of diseases. Subgroup analysis revealed that MTM services were more effective in studies including patients with chronic diseases. This result was consistent with the results of other studies assessing chronic conditions (Hohmeier et al., 2019; Thompson et al., 2020; Wang et al., 2021). But limited studies showed the efficacy of MTM services in patients with non-chronic conditions, like cancer (Dürr et al., 2021) and acute coronary syndrome (Kang et al., 2018). These results showed possibility of heterogeneity in the type of diseases and indicated the need for additional evidence to support the efficacy of MTM services for managing patients with non-chronic disease. The development level and different work model of MTM services system in different countries was another main factor being considered. MTM services in the US, for instance, developed over the years and the fees were covered by American healthcare (H.R.1–108th Congress (2003-2004): Medicare Prescription Drug, Improvement, and Modernization Act of 2003, 2019), while other countries such as China offered similar MTM services free of charge. These discrepancies between different countries led to large disparities in medical expenses and healthcare use (Khalil et al., 2017; Maria et al., 2021), resulting in a high degree of heterogeneity. As a review resulted that the impact of the payment model on healthcare spending and utilization was found to vary considerably across studies (Agarwal et al., 2020), this difference might also be a source of heterogeneity. Furthermore, it is important to acknowledge that in addition to the factors mentioned, there might be other potential sources of heterogeneity such as variations between urban and rural patients, differences between those with medical insurance and those without, and variances in MTM services provided by a medical team versus those solely delivered by pharmacists. However, due to limited studies including these facts, the conduction of these analysis required more future studies focusing on them.
5 Conclusion
The results of our meta-analysis provide some evidence demonstrating the effectiveness of MTM services across multiple outcome measures. The findings suggest that MTM services are beneficial in improving short-term patient outcomes. However, due to high heterogeneity and unstable results observed in some economic and humanistic outcomes, additional studies are necessary to establish their efficacy in reducing patient costs and enhancing their quality of life. Further evaluation and standardization of economic outcome measures are necessary for a more effective analysis. Moreover, the humanistic outcomes should underscore the importance of mental healthcare in promoting patients’ overall wellbeing.
Data availability statement
The raw data supporting the conclusion of this article will be made available by the authors, without undue reservation.
Author contributions
Conception and design: A-HW, Administrative support: Y-FD, Provision of study materials or patients: LG and JC, Collection and assembly of data: Z-JD, S-SP, and LG, Data analysis and interpretation: Z-JD, A-HW, and JC, Manuscript writing: All authors, Final approval of manuscript: All authors.
Funding
Supported by grants from the National Natural Science Foundation of China (No. 81803841).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2023.1143444/full#supplementary-material
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Keywords: medication therapy management, economic, clinical, humanistic, systematic review
Citation: Deng Z-J, Gui L, Chen J, Peng S-S, Ding Y-F and Wei A-H (2023) Clinical, economic and humanistic outcomes of medication therapy management services: A systematic review and meta-analysis. Front. Pharmacol. 14:1143444. doi: 10.3389/fphar.2023.1143444
Received: 13 January 2023; Accepted: 27 March 2023;
Published: 05 April 2023.
Edited by:
Hao Li, Shanghai Jiao Tong University, ChinaReviewed by:
Chris Gillette, Wake Forest University, United StatesPengxiang Zhou, Peking University Third Hospital, China
Copyright © 2023 Deng, Gui, Chen, Peng, Ding and Wei. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yu-Feng Ding, yfding463@163.com; An-Hua Wei, ahwei0716@163.com