<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JDM</journal-id><journal-title-group><journal-title>Journal of Diabetes Mellitus</journal-title></journal-title-group><issn pub-type="epub">2160-5831</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jdm.2019.93013</article-id><article-id pub-id-type="publisher-id">JDM-94526</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Effectiveness of Clinical Pharmacist Directed-Diabetes Management
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Neha</surname><given-names>Farheen Tabassum</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>N.</surname><given-names>Himanandini</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manaal</surname><given-names>Fathima</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>M.</surname><given-names>Sankeerthna</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nikhil</surname><given-names>Kumar Vanjari</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Siva</surname><given-names>Subrahmanyam Bandaru</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Vaageswari College of Pharmacy, Karimnagar, Telangana, India</addr-line></aff><aff id="aff2"><addr-line>Department of Pharmacy Practice, Vaageswari College of Pharmacy, Karimnagar, Telangana, India</addr-line></aff><aff id="aff3"><addr-line>Sri Bhadrakali Diabetes Care Centre, Warangal, Telangana, India</addr-line></aff><pub-date pub-type="epub"><day>09</day><month>08</month><year>2019</year></pub-date><volume>09</volume><issue>03</issue><fpage>137</fpage><lpage>145</lpage><history><date date-type="received"><day>11,</day>	<month>May</month>	<year>2019</year></date><date date-type="rev-recd"><day>19,</day>	<month>August</month>	<year>2019</year>	</date><date date-type="accepted"><day>22,</day>	<month>August</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Objective: The main aim of the study is predominately utilizing clinical pharmacist in the provision of continuing diabetic education programs to emphasize and re-emphasize the importance of risk factors, prevention, adherence to medication and behavioral changes to prevent recurrences of the disease, their progression, and ultimately minimize hospitalization. Specific goals are to improve clinical outcomes for patients with diabetes—to maintain optimal plasma glucose concentrations Fasting, Postprandial Plasma Glucose, and Glycated Hemoglobin. 
  Study design: A prospective interventional study in the Outpatient General Medicine Department, for a period of six months from October 2018 to March 2019. 
  Results: HbA1c levels were reduced from baseline by 
  &amp;minus;1.107 &#177; 0.8634, Fasting Plasma Glucose levels and Postprandial blood glucose levels were reduced from baseline by 
  &amp;minus;24.2218 &#177; 5.70352 and 
  &amp;minus;30.1891 &#177; 1.40592 respectively. 
  Conclusion: A trained clinical pharmacist by providing diabetes education and care can significantly reduce hyperglycemia, thereby improving the quality of life in diabetes patients and ultimately reducing health care costs associated with these morbidities.
 
</p></abstract><kwd-group><kwd>Diabetes Mellitus</kwd><kwd> Clinical Pharmacist</kwd><kwd> Glycated Hemoglobin</kwd><kwd> Fasting Plasma Glucose</kwd><kwd> Post-Prandial Blood Glucose</kwd><kwd> Diabetes Care and Management</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Diabetes mellitus is a chronic progressive metabolic disorder characterized by hyperglycemia with impaired metabolism of carbohydrate, protein, and fat resulting from absolute Type 1 Diabetes Mellitus or relative Type 2 Diabetes Mellitus deficiency of insulin or both. Diabetes has leaped from 108 million in 1980 to 422 million patients in 2014. From 4.7% in 1980, the global incidence in the ages above 18 years has uprisen to 8.5% in 2014 [<xref ref-type="bibr" rid="scirp.94526-ref1">1</xref>]. Hyperglycaemia over a long period of time can lead to metabolic disturbances and virtually affects every system of the human body particularly the blood vessels and nerves leading to diabetes mellitus associated macrovascular &amp; microvascular complications, diabetic foot ulcer and recurrent infections [<xref ref-type="bibr" rid="scirp.94526-ref2">2</xref>]. The essential element in the management of diabetes mellitus includes therapeutic management, self-care management, patient adherence to the prescribed medication and lifestyle modifications. Though the diabetic patients are managed by the physicians, clinical inertia and limited time with patients hamper efforts to meet treatment goals. So, to have an effective delivery in achieving the goal of therapy, it requires a partnership between people and healthcare providers. With the intimate understanding of how medications work and patient care, clinical pharmacist brings a unique and valuable perspective to diabetes care even as the population of patients with diabetes continues to grow [<xref ref-type="bibr" rid="scirp.94526-ref3">3</xref>]. As a vital members of the healthcare team, pharmacist has a significant impact on diabetes care and education by screening patients at high risk for diabetes, setting and monitoring diabetic treatment goals, assessing patient’s health status, home glucose meter training, performed physical assessment of patient’s feet, skin, blood pressure and weight, blood pressure &amp; lipid management education and adherence to standards of care [<xref ref-type="bibr" rid="scirp.94526-ref4">4</xref>]. Alterations in behavior to ameliorate plasma glucose levels were observed when interventions were made by a healthcare provider in diabetic patients [<xref ref-type="bibr" rid="scirp.94526-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.94526-ref6">6</xref>] and adequate intake of fat, protein, and carbohydrate controls metabolism which minimizes the hospitalizations and deaths owing to diabetes [<xref ref-type="bibr" rid="scirp.94526-ref7">7</xref>].</p></sec><sec id="s2"><title>2. Aim and Objectives</title><p>The main aim of the study is predominately utilizing clinical pharmacist in the provision of Continuous education programs and counseling helps Diabetic patients to emphasize and re-emphasize the importance of risk factors, prevention, adherence to medication and behavioral changes to prevent recurrences of the disease, their progression, and ultimately minimize hospitalization. Specific goals are to improve clinical outcomes for patients with diabetes—to maintain optimal plasma glucose concentrations Fasting, Post-prandial Plasma Glucose, and Glycated Hemoglobin.</p></sec><sec id="s3"><title>3. Materials and Methods</title><p>Patients were enrolled in the study if they were with type 2 diabetes mellitus who were treated with either oral agents or insulin and had an HbA1C concentration &gt; 7%. Patients are referred to the program by the primary care physician for various indications, such as newly diagnosed diabetes, poor glycemic control, poor adherence, or a combination of these. In addition, the patient was included based on an HbA1C concentration &gt; 7% and the primary care provider’s overall judgment that the patient required additional time at follow-up visits for intensive patient education and monitoring, once enrolled in the study, Each visit is individualized based on patient-specific needs; patients were scheduled to meet with the pharmacist every 4-weeks for approximately 30 minutes. Patients were followed in the clinic for at least 3 - 4 months. Follow-up is conducted through a combination of telephone appointments and clinic visits. All pharmacists managing patients in this study are clinically trained under Diabetic Educator, bilingual and had spent at least one clinical rotation (6 months) during their Pharm.D course in the Hospital. During clinic appointments, the pharmacist provided diabetes education, medication counseling, monitoring, and management.</p></sec><sec id="s4"><title>4. Study Design</title><p>A prospective interventional study was carried out in the Sri Bhadrakali Diabetes Clinic, Warangal, Telangana, India. The study was carried out for a period of Six months from October 2018 to March 2019.</p><p>Patients with diabetes mellitus with or without co-morbidities visiting the outpatient general medicine department were included in the study. Pregnant women, mentally challenged patients, and critically ill patients were excluded from the study. Patient’s demographic details including past medical and medication history, current drug treatment and laboratory values were collected in the data sheet designed as per the need of the study. Educational materials (validated patient information leaflets) and medication counseling were given to the interventional group by the study pharmacist during various follow-up visits.</p></sec><sec id="s5"><title>5. Statistical Analysis</title><p>Data is collected using a self-designed collection form and analyzed using GraphPad Prism 8. Demographic data values are presented in mean with standard deviation. A confidence level of 99% is employed and the test results are statistically significant if the P-value is &lt;0.001. A One-way ANOVA of repeated measures and Student’s paired t-test were applied to Fasting/Post-prandial plasma glucose and Glycated hemoglobin respectively.</p></sec><sec id="s6"><title>6. Results</title><p>Clinical characteristics: Of the initial 608 Type 2 Diabetic patients who were given Diabetic Education based on patient-specific needs., 401 patients were lost for follow-up and 207 patients were followed up for HbA1c, Fasting Plasma Glucose, and Postprandial Plasma Glucose. A correlation test was also performed to evaluate the relationship between Fasting plasma glucose and Glycated Hemoglobin, both at baseline and 12-weeks (<xref ref-type="table" rid="table1">Table 1</xref>) (<xref ref-type="fig" rid="fig1">Figure 1</xref>) (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>47% were males and 53% were females from a total of 207 diabetic patients (<xref ref-type="table" rid="table2">Table 2</xref>). The mean age was 48.99091 &#177; 12.27377 and 52.94845 &#177; 9.790982 in</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Correlation of HbA1c &amp; Fasting Plasma Glucose</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characterstic</th><th align="center" valign="middle" >Correlation Coeficent</th><th align="center" valign="middle" >Interpretation</th></tr></thead><tr><td align="center" valign="middle" >Baseline FPG &amp; HbA1c</td><td align="center" valign="middle" >r = 0.4372</td><td align="center" valign="middle" >Moderate Correlation</td></tr><tr><td align="center" valign="middle" >12-Week FPG &amp; HbA1c</td><td align="center" valign="middle" >r = 0.2431</td><td align="center" valign="middle" >Low Correlation</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Age and Gender Distribution</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Sample Size</th><th align="center" valign="middle" >n = 207</th></tr></thead><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" >Males: 47% Females: 53%</td></tr><tr><td align="center" valign="middle" >Age in years</td><td align="center" valign="middle" >Males: 48.99091 &#177; 12.27377 Females: 52.94845 &#177; 9.790982</td></tr></tbody></table></table-wrap><p>males and females respectively. Changes in Glycemic control from baseline to 12-weeks is represented in tabulated form (<xref ref-type="table" rid="table3">Table 3</xref>). The mean HbA1c levels at the beginning of the study were 9.417341 &#177; 1.821157. At the end of the study, HbA1c levels were reduced from baseline by −1.107 &#177; 0.8634 with a P value &lt; 0.0001 (<xref ref-type="fig" rid="fig3">Figure 3</xref>). The mean Fasting Plasma Glucose levels at the beginning of the study was 173.072 &#177; 61.49741. At the end of the study, Fasting Plasma Glucose</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Changes in Glycemic control from baseline to 12-weeks</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Characteristics</th><th align="center" valign="middle" >Baseline (Mean &#177; SD)</th><th align="center" valign="middle" >8 Weeks (Mean &#177; SD)</th><th align="center" valign="middle" >12 Weeks (Mean &#177; SD)</th><th align="center" valign="middle" >Changes from Baseline Mean difference &#177; SD</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >HbA1C%</td><td align="center" valign="middle" >9.417341 &#177; 1.821157</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >8.44372 &#177;1.406647</td><td align="center" valign="middle" >−1.107 &#177; 0.8634</td><td align="center" valign="middle" >˂0.0001</td></tr><tr><td align="center" valign="middle" >Fasting plasma glucose (mg/dl)</td><td align="center" valign="middle" >173.072 &#177;61.49741</td><td align="center" valign="middle" >162.9614 &#177; 61.15363</td><td align="center" valign="middle" >148.8502 &#177; 55.79389</td><td align="center" valign="middle" >−24.2218 &#177; 5.70352</td><td align="center" valign="middle" >˂0.0001</td></tr><tr><td align="center" valign="middle" >Postprandial plasma glucose (mg/dl)</td><td align="center" valign="middle" >245.2222 &#177; 74.15605</td><td align="center" valign="middle" >230.8357 &#177; 73.15527</td><td align="center" valign="middle" >215.0331 &#177; 72.75013</td><td align="center" valign="middle" >−30.1891 &#177;1.40592</td><td align="center" valign="middle" >˂0.0001</td></tr></tbody></table></table-wrap><p>levels were reduced from baseline by −24.2218 &#177; 5.70352 with a P value &lt; 0.0001 (<xref ref-type="fig" rid="fig4">Figure 4</xref>). The mean Fasting Plasma Glucose levels at the beginning of the study were 173.072 &#177; 61.49741. At the end of the study, Fasting Plasma Glucose levels were reduced from baseline by-30.1891 &#177; 1.40592 with a P value &lt; 0.0001 (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p></sec><sec id="s7"><title>7. Discussion</title><p>Several studies have acknowledged the importance of pharmacist provided counseling in diabetes patients. In the present study, 207 patients were followed up for HbA1c, Fasting Plasma Glucose and Postprandial Plasma Glucose. At the end of the study, HbA1c levels were reduced from baseline by −1.107 &#177; 0.8634 with a P value &lt; 0.0001, Fasting Plasma Glucose levels were reduced by −24.2218 &#177; 5.70352 with a P value &lt; 0.0001, Postprandial Plasma Glucose levels were reduced by −30.1891 &#177; 1.40592 with a P value &lt; 0.0001. Clinically significant improvements are reported.</p><p>The efficacy of Diabetic Pharmaceutical care was conducted for a period of 12 months by the Fremantle Study. Patients were counseled for lifestyle changes, use of daily medication, Dietary pattern and were assessed at baseline, 6 months and 12 months. The main outcome measure was changed in HbA1C. The study concluded that the 12-month PC program in type 2 diabetes reduced glycemia and blood pressure. Pharmacist involvement contributed to improvement in HbA1c independently of pharmacotherapeutic changes [<xref ref-type="bibr" rid="scirp.94526-ref8">8</xref>]. Cioffi et al. conducted the study to determine the effect of a clinical pharmacist directed diabetes</p><p>management clinic on glycemic control and cardiovascular and renal parameters in patients with type 2 diabetes. The primary endpoint was the impact of 9 - 12 months of participation in the clinic on HbA1C. The study demonstrated that a clinical pharmacist can effectively care for patients with diabetes referred by their primary care provider because of poor glycemic control [<xref ref-type="bibr" rid="scirp.94526-ref9">9</xref>]. Gerber et al. conducted a study to assess the impact on healthcare utilization and costs of pharmacist consultations provided to patients with diabetes. The study suggested that pharmacist consultations provided to patients with diabetes can decrease total healthcare costs in a health maintenance organization [<xref ref-type="bibr" rid="scirp.94526-ref10">10</xref>]. Cranor et al., assessed 5 years outcome after the initiation of community-based pharmaceutical care services for diabetic patients. A Quasi-experimental, cohort study, longitudinal pre-post was conducted in twelve community pharmacies in Asheville, N.C. The study concluded that patients with diabetes who received ongoing pharmaceutical care services maintained improvement in HbA1c over time, and employers experienced a decline in mean total direct medical costs [<xref ref-type="bibr" rid="scirp.94526-ref11">11</xref>]. The impact of a specially designed education program, diabetes-related knowledge, and compliance of insulin-dependent diabetic patients were investigated by Powell et al. The program was successful in producing improvements in both compliance and knowledge but a need for individualization of patient education efforts was indicated [<xref ref-type="bibr" rid="scirp.94526-ref12">12</xref>]. Odegard et al. studied the effect of intervention by a pharmacist on improving glycemic control; secondary endpoints were medication appropriateness and self-reported adherence. Seventy-seven subjects, were randomized to receive a pharmacist intervention (n = 43) or usual care (n = 34) for 6 months, followed by a 6-month usual-care observation period for both groups. The study concluded that pharmacist intervention did allow for similar HbA1C control with fewer physician visits but did not significantly improve glycemic control. Medication appropriateness and self-reported adherence compared with usual care in individuals with poorly controlled diabetes were not changed [<xref ref-type="bibr" rid="scirp.94526-ref13">13</xref>]. Kiel and McCord evaluated the changes in clinical outcomes for patients enrolled in a pharmacist-coordinated diabetes management program. Data collection included baseline and follow-up values for HbA1C and lipids as well as the frequency of adherence to preventive care, including annual foot and eye examinations and daily aspirin therapy. The study concluded that for enrolled patients, pharmacist-coordinated diabetes supervision was effective in improving clinical laboratory tests. Significant improvements were observed in HbA1C and LDL values as well as the frequency of adherence to preventive care [<xref ref-type="bibr" rid="scirp.94526-ref14">14</xref>].</p></sec><sec id="s8"><title>8. Conclusions</title><p>The observed results might find new insights into diabetes management differently by using clinical pharmacists rather than focusing in addition to next line therapy of the hypoglycemic agents. Further acceptance of efforts of clinical pharmacists by diabetic patients may lead to the establishment of Diabetic care centers in developing countries, which leads to improvement of glycemic control, decreased rate of complications, decreased economic burden, hospitalizations and deaths. Over and above that, setting up federal mechanisms to prevent risk factors for diabetes, evaluating key hurdles in identification, management, glycemic control, diabetes prevention from primary care level and aid in the collection, analyzing of diabetic patient data on a periodic basis could promote the health and well-being of the nation.</p><p>In our study, we conclude that a trained clinical pharmacist by providing diabetes education and care can significantly reduce hyperglycemia, thereby improving the quality of life in diabetes patients. Pharmacists are in a major position to make certain that the use of medications is appropriate and safe. Patient counseling on medication, dietary pattern, physical exercises, regular monitoring of plasma glucose and annual, semi-annual Diabetes, cardiovascular and other body systems functioning tests could keep diabetic patients healthy. Providing general diabetes education, designing individual dietary instructions, regular laboratory monitoring parameters exercise decrease microvascular and macrovascular complications and ultimately reduce health care costs associated with these morbidities. To be an effective counselor, the pharmacist should update his knowledge regarding the latest developments and should possess adequate verbal and non-verbal communication skills. It is important that pharmacists’ document evidence shows positive outcomes in the management of patients with diabetes. Dissemination of this information would be valuable because it could raise the awareness of other healthcare professionals regarding pharmacists as effective clinicians in the care of patients with diabetes. This increased awareness could elevate the profile of pharmacists. Limitations of the study include a lack of control group and the small number of patients, further studies focusing on pharmacist’s efficacy in diabetic complications rather than glycemic control alone are valued.</p></sec><sec id="s9"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s10"><title>Cite this paper</title><p>Tabassum, N.F., Himanandini, N., Fathima, M., Sankeerthna, M., Vanjari, N.K. and Bandaru, S.S. (2019) Effectiveness of Clinical Pharmacist Directed-Diabetes Management. 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