| Literature DB >> 27583362 |
David Flood1,2, Sandy Mux1, Boris Martinez1, Pablo García1,3, Kate Douglas1, Vera Goldberg1,4, Waleska Lopez1, Peter Rohloff1,5.
Abstract
BACKGROUND: The burden of chronic, non-communicable diseases such as diabetes is growing rapidly in low- and middle-income countries. Implementing management programs for diabetes and other chronic diseases for underserved populations is thus a critical global health priority. However, there is a notable dearth of shared programmatic and outcomes data from diabetes treatment programs in these settings. PROGRAM DESCRIPTION: We describe our experiences as a non-governmental organization designing and implementing a type 2 diabetes program serving Maya indigenous people in rural Guatemala. We detail the practical challenges and solutions we have developed to build and sustain diabetes programming in this setting.Entities:
Mesh:
Year: 2016 PMID: 27583362 PMCID: PMC5008811 DOI: 10.1371/journal.pone.0161152
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Challenges, Opportunities, and Solutions for Implementation of Diabetes Programs in Guatemala.
| Challenge | Opportunities | Solution |
|---|---|---|
| Cultural and linguistic barriers to biomedical care for indigenous Maya population | Rising number of educated young Maya professionals experienced in issues related to language, cultural, and health advocacy | Employ exclusively native speakers of Mayan languages as front-line health providers |
| Low physician density | Large labor pool of indigenous nurses | Nurse-driven diabetes protocols |
| High cost of diabetes medications | Dynamic generics industry in Guatemala | Limited formulary of locally purchased generic drugs |
| Low availability of laboratory diagnostics | Validated point-of-care tests available on the local market | Use of point-of-care laboratory testing for hemoglobin A1C |
| Patients live in rural, difficult-to-access villages | • Availability of open-source electronic medical record platforms | Deployment of smart-phone-based data entry and open-source electronic medical record |
| Low levels of education and health literacy | • Patients often work from home or return to home during day | Home visit program by diabetes educator using locally adapted curriculum |
| Patients present late in disease course, often with significant end-organ damage | Excellent subspecialty care available in capital city | Centralized case management system to coordinate referrals from rural health workers to pre-selected subspecialty clinics |
| Chronic disease care is expensive and requires long-term commitments to beneficiaries | Blended financing models are emerging in global health | • Crowdfunding provides funding for extraordinary and catastrophic care |
Demographic profile of Type 2 Diabetes Cohort.
| Characteristic | Value |
|---|---|
| 56.1 ± 11.8 | |
| 80.3 | |
| Kaqchikel Mayan | 50.8 |
| Spanish | 37.7 |
| K’iche’ Mayan | 11.5 |
| Grades completed, median (IQR) | 2 (0–4) |
| Completed primary school–% | 20.8 |
| Median (IQR) | 7 (4–12) |
| 47.2 ± 11.7 | |
| Median (IQR) | 2.5 (1.3–3.8) |
For continuous variables with normal distribution, values are given as mean ± standard deviation. For continuous variables with nonnormal distribution, median and interquartile range (IQR) are specified. Some non-clinical data including preferred language, years with diabetes, and education attained were not available for all patients, as indicated by n in parentheses.
Clinical profile of Type 2 Diabetes Cohort.
| Clinical Characteristic | Value |
|---|---|
| 8.1 ± 2.1 | |
| Diagnosis of hypertension–% | 45.8 |
| Systolic BP, mean–mmHg | 121.8 ± 20.4 |
| Diastolic BP, mean–mmHg | 74.9 ± 10.2 |
| Mean | 28.0 ± 5.0 |
| BMI ≥ 25 –% | 70.8 |
| BMI ≥ 30 –% | 30.8 |
| GFR 30–60 –% | 40.1 |
| GFR ≤ 30 –% | 3.5 |
| Proteinuria–% | 33.6 |
| On dialysis–% | 2.1 |
| Metformin | 85.9 |
| Sulfonylurea | 44.4 |
| Insulin NPH | 25.4 |
| Insulin regular | 2.8 |
| No insulin or oral anti-diabetic agent | 5.0 |
| ACE inhibitor | 43.7 |
| Median | 11.5 |
| Interquartile range | 8–15 |
BP, blood pressure; BMI, body mass index, GFR, glomerular filtration rate.
a GFR was estimated from clinical variables using the CKD-EPI equation.
Cross-sectional outcomes indicators for Type 2 Diabetes Cohort.
| % | |
| At least one measurement of hemoglobin A1C | 99.3 |
| Comprehensive foot evaluation | 98.6 |
| Measurement of creatinine and rate of glomerular filtration | 90.1 |
| Four or more clinical encounters during year | 95.1 |
| Diabetes self-care education provided in home visit | 50 |
| Overweight/obese (BMI ≥25 kg/m2) patients with hemoglobin A1C ≥ 6.5 who received metformin, unless contraindicated (n = 66) | 98.8 |
| Patients with hemoglobin A1C ≥ 8% who received insulin (n = 64) | 37.5 |
| Patients with hypertension receiving inhibitors of angiotensin converting enzyme or angiotensin-receptor blocker, unless contraindicated (n = 65) | 95.4 |
| Hemoglobin A1C < 8% in last measurement (n = 142) | 54.9 |
| Blood pressure <140/90 mmHg in last 3 measurements (n = 139) | 59.0 |
| Hemoglobin A1C < 8% in last measurement and blood pressure <140/90 mmHg in last 3 measurements (n = 139) | 29.5 |
Longitudinal outcomes indicators for Type 2 Diabetes Cohort.
| Characteristic (n = 142) | Initial | Last | p-value |
|---|---|---|---|
| Hemoglobin A1C –% | 9.2 ± 2.4 | 8.1 ± 2.1 | 0.00 |
| Systolic BP–mmHg | 124.3 ± 20.0 | 121.8 ± 20.4 | 0.17 |
| Diastolic BP–mmHg | 77.6 ± 11.2 | 74.9 ± 10.2 | 0.02 |
| Percent of patients with hemoglobin A1C < 8% | 38.0 | 54.9 | 0.001 |
| Percent of patients with blood pressure <140/90 mmHg | 69.7 | 73.2 | 0.46 |
| Percent of patients with hemoglobin A1C <8% and blood pressure <140/90 mmHg | 25.4 | 38.0 | 0.01 |
BP, blood pressure.