Impact of hypoglycemia on patients with type 2 diabetes mellitus and their quality of life, work productivity, and medication adherence

Abstract

Background

The purpose of this study was to determine the characteristics of adults with type 2 diabetes mellitus (T2DM) that correlate with greater risk of hypoglycemia and determine the impact of hypoglycemia on health-related quality of life, work productivity, and medication adherence from a patient perspective.

Methods

Data from a large web-based survey were retrospectively analyzed. Adults with a diagnosis of T2DM taking antihyperglycemic agents were included in the analysis. Participants with knowledge of their hypoglycemic history were divided into three groups: those experiencing recent hypoglycemia (previous 3 months), those experiencing nonrecent hypoglycemia, and those never experiencing hypoglycemia.

Results

Of the participants with T2DM taking antihyperglycemic agents who were knowledgeable of their hypoglycemia history, 55.7% had ever experienced hypoglycemia. Of those, 52.7% had recent hypoglycemia. Compared with those who never experienced hypoglycemia, those who experienced hypoglycemia tended to: be younger; be more aware of their glycated hemoglobin (HbA_1c) levels; have higher HbA_1c levels; have a higher body mass index; have higher Charlson Comorbidity Index scores; be on insulin, sulfonylureas, and/or glucagon-like peptide-1 agonists; and be less adherent to their antihyperglycemic agents. Hypoglycemia interfered with social activities, caused more missed work (absenteeism), more impairment while at work (presenteeism), and decreased overall work productivity compared with patients who had never experienced hypoglycemia. Overall health-related quality of life, as determined by the Short Form-36 health questionnaire, was negatively impacted by hypoglycemia. Both Physical and Mental Summary scores were significantly lower for the recent hypoglycemia and nonrecent hypoglycemia groups compared with the never hypoglycemia group.

Conclusion

Hypoglycemia can negatively impact many aspects of life. Greater awareness of those who are at risk for developing hypoglycemia can lead to the development of measures (eg, patient and physician education) to prevent future hypoglycemia episodes.

Keywords:

• adherence
• survey
• patient preference
• burden
• antihyperglycemic
• low glucose effect
• hemoglobin A_1C

Introduction

Several large-scale, prospective, randomized trials have documented that lowering glycemic levels can prevent the development of microvascular disease in people with type 2 diabetes mellitus (T2DM). Consequently, T2DM management guidelines generally recommend a treatment target of glycated hemoglobin (HbA_1c) levels <7.0%, with some suggesting that even more intensive glycemic goals (<6.5%) would be beneficial.^1–3 However, one issue with intensive glycemic control is the possibility of hypoglycemic events.

Treatment-related hypoglycemia is known to occur in people with T2DM, but its impact from the individual patient’s perspective is not well characterized. Determining the impact of hypoglycemia on the lives of people with T2DM is very difficult since there is no consensus definition of hypoglycemia. This results in inconsistencies in the identification, measurement, and reporting methods across studies. The incidence and impact of hypoglycemia can be masked by factors such as age, treatment modality, duration of diabetes, body weight, and glycemic control.⁴ The acute and chronic complications of hypoglycemia invariably affect various aspects of life, including work productivity, social interactions, sleep, sexual activity, driving, sport and leisure activities, and adherence to therapy.^5,6 Acute symptoms can be mild (eg, palpitations, tremor, hunger, sweating) or severe (eg, behavioral changes, difficulty thinking, confusion, loss of consciousness). Long-term complications of hypoglycemia include cardiovascular and neurological complications, such as myocardial infarction, arrhythmias, stroke, cognitive decline, dementia, and cardiovascular death.^4,7 Health-related quality of life (HRQoL) may be affected as a result of the complications and/or effects of hypoglycemia, or as a consequence of avoidant, precautionary, or compensatory actions due to the fear of having a hypoglycemia episode.⁴ Glycemic control may be an issue since patients who experience hypoglycemia are more prone to worry about future hypoglycemic events and may maintain higher glycemic levels to avoid hypoglycemia.^5,8 Glycemic control may also suffer if health care providers delay advancement of treatment due to similar fears.⁹ The result is a negative impact on overall HRQoL, which has been well documented in studies on hypoglycemia in people with T2DM.^4,7

There are data to suggest that hypoglycemia can have a significant impact on many aspects of the lives of people with T2DM. However, there have not been any previous studies on the characterizations and impacts of hypoglycemia on HRQoL, work productivity, and medication adherence in people with T2DM purely based on the patient perspective and in a single analysis. In addition, the impact of hypoglycemia on these factors in association with glycemic control and burden of disease within the same study has not been examined. Consequently, the purpose of this study is to retrospectively analyze a large sample of people with T2DM to describe their perspectives on the impact of hypoglycemia on diabetes and related comorbidity burden, HRQoL, and work productivity, as well as the association between hypoglycemia and adherence to antihyperglycemic medication.

Materials and methods

Survey design

The US National Health and Wellness Survey (NHWS) is a cross-sectional, Internet-based survey of adults aged ≥18 years. Using a stratified random sampling framework, potential respondents are recruited through Internet panels such that the demographic composition of the NHWS is identical to that of the general population, as measured by the US Census. The reliability and validity of the NHWS, particularly as it relates to disease prevalence, has been assessed in prior research.^10–12 These studies have compared data collected from the NHWS and various other sources, including the US Census Bureau’s Current Population Survey, National Health Interview Survey, National Health and Nutrition Examination Survey, and the Medical Expenditure Panel Survey.^10–12

Data from the 2012 NHWS were analyzed for this descriptive analysis. The NHWS was administered to a sample of adults who were identified through a web-based consumer panel. It is a cross-sectional, self-administered, web-based survey encompassing 100 various conditions. The diabetes condition series consists of 41 questions. Survey data for this analysis were collected during the first three quarters of 2012. The projected number of US adults diagnosed with diabetes from the NHWS aligned favorably with the estimate from the National Health Interview Survey results and is thus nationally representative.¹³

Participant selection

Participants were recruited through opt-in emails, coregistration with other panels, e-newsletter campaigns, and online banner placements. The total sample size of the NHWS consisted of 71,157 participants. Participants were included in this analysis if they were adults aged 18 years or older who reported a diagnosis of T2DM. At the time of the survey, participants self-identified as taking prescription antihyperglycemic agent(s) to treat diabetes.

Participant characterization

Hypoglycemia was identified by self-report by participants in response to questions in the survey. Participants were asked if they had ever experienced hypoglycemia or low blood sugar as a result of their diabetes, with examples of symptoms of hypoglycemia provided (shakiness, nervousness, sweating, dizziness-lightheadedness, sleepiness, confusion, difficulty speaking, anxiety, weakness, fainting, crying out or having nightmares, finding clothes or sheets damp from perspiration, feeling tired, irritable, or confused after waking up). Participants were grouped into one of three potential hypoglycemia categories: those who had experienced hypoglycemia within the previous 3 months (recent hypoglycemia); those who had experienced hypoglycemia in the past, but not in the previous 3 months (nonrecent hypoglycemia); and those who had never experienced hypoglycemia (never hypoglycemia).

Race/ethnicity, degree of blood glucose control, body mass index (BMI), Charlson Comorbidity Index (CCI) scores, medication adherence, health-related HRQoL, and work productivity were determined for each hypoglycemia category. For race/ethnicity, five categories were reported, ie, White, African American, Hispanic, Asian, and American Indian. Participants with more than one race/ethnicity or who did not belong to one of the five main categories were excluded from this analysis. For the degree of blood glucose control, participants self-reported their most recent HbA_1c level by responding to the question, “What is your hemoglobin A_1c level?” They were then categorized into one of five categories: low (<7.0%), slightly elevated (≥7.0% to ≤8.5%), elevated (>8.5% to ≤11.0%), seriously elevated (>11.0%), and those who did not know their HbA_1c levels. BMI was calculated based on self-reported height and weight, then categorized into one of four categories: obese (≥30 kg/m²), overweight (25 to <30 kg/m²), normal weight (≥19 to <25 kg/m²), and underweight (<19 kg/m²). Mortality risk based on self-reported comorbid conditions was calculated using the CCI as another indicator of disease burden. Increasing CCI score has been shown to correlate with increased risk of mortality in people with T2DM.^14,15 In order to remain true to the method of identifying all conditions and diseases, diabetes remained a condition measured in the CCI and counted for one point.

Adherence characterization

Adherence to antidiabetic medications was determined using the Morisky Medication Adherence Scale (MMAS). The MMAS is a structured, self-reported measure with higher scores representing higher medication adherence. The English version of the eight-item MMAS (MMAS-8) has not been validated in patients with T2DM, but has been validated in hypertensive patients taking antihypertensive medications.¹⁶ The Malaysian version of the MMAS-8 and the four-item MMAS (MMAS-4) have been validated in patients with T2DM.¹⁷ The MMAS-8 has been assessed for its reliability and congruence with the MMAS-4 in T2DM patients taking antidiabetic medications which has shown that increased scores in the MMAS-4 are significantly associated with decreasing HbA_1c levels.^17–20 In this analysis, the eight-item questionnaire was truncated to seven items, eliminating the question “Do you sometimes forget to take your pills?” The question was removed to prevent confusion for those participants on insulin and other injectable medications in order to preserve their inclusion in the study. From a reliability assessment, the developer of the scale assessed the internal consistency of the seven-item scale and it did not significantly differ for reliability; removing the question decreases the internal consistency (Cronbach’s α) of the MMAS-8 from 0.83 to 0.78.¹⁶ A MMAS score of 7 is categorized as high adherence, 5–6 is medium adherence, and <5 is low adherence.

Health-related quality of life

Quality of life was determined using the Short Form-36 health survey (SF-36), version 2,²¹ and specific questions from the NHWS (eg, interference with normal social activities due to physical health or emotional problems, whether patients feel hassled about taking their antihyperglycemic medications, whether the participant had symptoms that required assistance from a health care practitioner). Physical and mental summary scores were derived based on scores from the eight domains of the SF-36 (physical functioning, role-physical, bodily pain, general health perceptions, vitality, social functioning, role-emotional, and mental health).

Work productivity

Work productivity was determined by absenteeism and presenteeism based on self-reported days/hours missed from work. Absenteeism is defined as the percentage of work time missed due to hypoglycemia-related health issues. Presenteeism is defined as the percentage of overall work impaired by hypoglycemia-related health issues. Overall work productivity impairment is defined as the percentage of time missed due to either absenteeism or presenteeism.

Statistical analysis

Statistical analyses were conducted with IBM SPSS Data Collection Quantum Version 5.8.1 (IBM Corp, Armonk, NY, USA). Group comparisons were performed using unpaired t-tests or analysis of variance for continuous variables and chi-square analysis for categorical variables.

Results

A total of 7,239 participants reported a diagnosis of T2DM (Table 1). Of those, 6,065 were treated with antihyperglycemic agents (oral and injectable agents). The mean age was 60.6 years and the majority (60.3%) was male. A large proportion of participants (36.0%) did not know their HbA_1c levels. In those who reported HbA_1c, mean levels were 6.9%. Over 60% of participants had hypertension and/or high cholesterol.

Table 1 Characteristics of survey participants with T2DM who were treated with antihyperglycemic agents

	n (%)
Participants reporting a diagnosis of T2DM	7,239
Treated participants xwith T2DM	6,065 (100.0)
Demographics
Mean age (years ± SD)	60.6±11.5
Sex
Male	3,655 (60.3)
Female	2,410 (39.7)
Race/ethnicity
White	4,658 (76.8)
African American	693 (11.4)
Hispanic	400 (6.6)
Asian	128 (2.1)
American Indian	92 (1.5)
Clinical characteristics
HbA1c(%)
Low (<7.0%)	2,163 (35.7)
Slightly elevated (≥7.0% and ≤8.5%)	1,299 (21.4)
Elevated (>8.5% to ≤11.0%)	247 (4.1)
Seriously elevated (>11.0%)	55 (0.9)
Don’t know	2,186 (36.0)
Mean ± SD	6.9±1.3
Mean BMI (kg/m^2 ± SD)	33.8±7.7
Ever experienced high cholesterol	3,784 (62.4)
Ever experienced hypertension	3,867 (63.8)
Antihyperglycemic agents
Insulin	1,742 (28.7)
Metformin	3,176 (57.3)
Sulfonylureas	2,101 (37.9)
DPP-4 inhibitors	572 (10.3)
GLP-1 agonists	323 (5.8)
Thiazolidinediones	530 (9.6)

Abbreviations: HbA_1c, glycated hemoglobin; BMI, body mass index; DPP-4, dipeptidyl peptidase-4; GLP-1, glucagon-like peptide-1; SD, standard deviation; T2DM, type 2 diabetes mellitus.

Of the participants who were treated with antihyperglycemic agents (n=6,065), 5,756 (94.9%) knew their hypoglycemia status (Figure 1). Approximately 56% of participants who knew their hypoglycemia status had experienced hypoglycemia in the past (n=3,204). Approximately 29% (n=1,688) of those who knew their hypoglycemia status reported experiencing recent hypoglycemia. Over half (53%) of the participants with recent hypoglycemia required assistance from another person (data not shown). Of the participants who had recent hypoglycemia and self-managed their episodes, 57% had hypoglycemia episodes monthly (data not shown). In participants who had recent hypoglycemia and needed assistance from another person, 43% had episodes 2–6 times a year (data not shown).

Figure 1 Description of population.

Abbreviations: HG, hypoglycemia; T2DM, type 2 diabetes mellitus; AHA, antihyperglycemic agent.

Table 2 describes the demographic profile according to hypoglycemia group. Participant mean age ranged from 59.2 years to 61.3 years. The recent hypoglycemia group had a lower proportion of male participants (55.8%) compared with the nonrecent hypoglycemia (59.4%, P<0.05) and never hypoglycemia (63.8%, P<0.05) groups. The race/ethnicity distributions were similar among the hypoglycemia groups.

Table 2 Hypoglycemic episodes by demographic profile in participants treated with antihyperglycemic agents

	Recent HG (n=1,688)	Nonrecent HG (n=1,516)	Never HG (n=2,552)
Age, years
18–44	212 (12.5%)a	132 (8.7%)	234 (9.2%)
45–54	324 (19.2%)c	271 (17.9%)	416 (16.3%)
55–64	490 (29.0%)	444 (29.3%)	694 (27.2%)
65+	662 (39.2%)a	669 (44.1%)c	1,208 (47.3%)
Mean (years ± SD)	59.2±11.9a	60.9±10.9	61.3±11.5
Sex
Male	941 (55.8%)a	901 (59.4%)	1,629 (63.8%)
Female	747 (44.3%)a	615 (40.6%)c	923 (36.2%)
Race/ethnicity
White	1,296 (76.8%)	1,154 (76.1%)	1,965 (77.0%)
African American	168 (10.0%)b	196 (12.9%)	301 (11.8%)
Hispanic	118 (7.0%)	104 (6.9%)	159 (6.2%)
Asian	31 (1.8%)	22 (1.5%)c	67 (2.6%)
Native American	42 (2.5%)a	17 (1.1%)	28 (1.1%)

Notes:

a P<0.05 versus both nonrecent HG and never HG groups;

b P<0.05 versus nonrecent HG group only;

c P<0.05 versus never HG group only.

Abbreviations: HG, hypoglycemia; SD, standard deviation; T2DM, type 2 diabetes mellitus.

Table 3 describes the incidence of hypoglycemia according to diabetes-related clinical characteristics. The mean HbA_1c levels were 7.1% in the recent hypoglycemia group, 7.0% in the nonrecent hypoglycemia group, and 6.8% in the never hypoglycemia group. A larger percentage of participants in the never hypoglycemia group (40.9%) did not know their HbA_1c status compared with the recent hypoglycemia and nonrecent hypoglycemia groups (27.0% and 34.3%, respectively, P<0.05). A higher percentage of participants in the recent hypoglycemia group (29.5%) had slightly elevated HbA_1c levels (≥7.0% to ≤8.5%) compared with the nonrecent hypoglycemia group (23.2%, P<0.05), both of which were significantly higher than the never hypoglycemia group (16.5%, P<0.05 for both). Due to the variability between groups in the percentage of participants who did not know or did not report their HbA_1c values, glycemic control was also examined only in the participants who reported their HbA_1c values (Table 4). In the total population, there were no significant between-group differences in the percentage of participants with low HbA_1c (<7.0%). However, in those who reported their HbA_1c values, a significantly lower percentage of those in the recent hypoglycemia group had low HbA_1c (50.0%) compared with the nonrecent hypoglycemia group (55.2%, P<0.05), both of which were significantly lower than the never hypoglycemia (64.3%) group (P<0.05 for both). The relationship between hypoglycemia and the percentage of participants with slightly elevated HbA_1c was similar to that of the total population.

Table 3 Diabetes-related clinical characteristics by hypoglycemia category in participants treated with antihyperglycemic agents

n (%)	Recent HG (n=1,688)	Nonrecent HG (n=1,516)	Never HG (n=2,552)
HbA1c
Low (<7.0%)	607 (36.0%)	533 (35.2%)	933 (36.6%)
Slightly elevated (≥7.0% to ≤8.5%)	498 (29.5%)a	351 (23.2%)c	420 (16.5%)
Elevated (>8.5% to ≤11.0%)	96 (5.7%)c	65 (4.3%)c	78 (3.1%)
Seriously elevated (>11.0%)	14 (0.8%)	17 (1.1%)	21 (0.8%)
Do not know	456 (27.0%)a	520 (34.3%)c	1,043 (40.9%)
Mean (% ± SD)	7.1±1.3c	7.0±1.3c	6.8±1.3
Antihyperglycemic agentsd
Insulin	777 (46.0%)a	491 (32.4%)c	433 (17.0%)
Metformin	790 (54.8%)c	772 (56.7%)	1,436 (58.8%)
Sulfonylureas	674 (46.7%)a	582 (42.7%)c	748 (30.6%)
DPP-4 inhibitors	135 (9.4%)b	163 (12.0%)	248 (10.2%)
GLP-1 agonists	126 (8.7%)a	87 (6.4%)c	98 (4.0%)
Thiazolidinediones	147 (10.2%)	156 (11.5%)c	206 (8.4%)
BMI (kg/m^2)
Obese (≥30)	1,111 (67.3%)c	984 (66.7%)c	1,545 (61.9%)
Overweight (≥25 to <30)	410 (24.8%)c	375 (25.4%)c	725 (29.0%)
Normal (≥19 to <25)	125 (7.6%)	111 (7.5%)	223 (8.9%)
Underweight (<19)	5 (0.3%)	5 (0.3%)	4 (0.2%)
Mean ± SD	34.0±7.7c	34.0±7.7c	33.3±7.6
CCI score
1	1,004 (59.5)c	947 (62.5)c	1,820 (71.3)
2	317 (18.8)c	287 (18.9)c	392 (15.4)
3	184 (10.9)c	166 (11.0)c	219 (8.6)
4+	183 (10.8)a	116 (7.7)c	121 (4.7)
Mean ± SD	1.88±1.49a	1.72±1.22c	1.52±1.05

Notes:

a P<0.05 versus both nonrecent HG and never HG groups;

b P<0.05 versus nonrecent HG group only;

c P<0.05 versus never HG group only;

d antihyperglycemic agents are not mutually exclusive regimens.

Abbreviations: HbA_1c, glycated hemoglobin; BMI, body mass index; CCI, Charlson Comorbidity Index; DPP-4, dipeptidyl peptidase-4; GLP-1, glucagon-like peptide-1; HG, hypoglycemia; SD, standard deviation; T2DM, type 2 diabetes mellitus.

Table 4 HbA_1c levels by hypoglycemia category in participants who reported HbA_1c levels

n (%)	Recent HG (n=1,215)	Nonrecent HG (n=966)	Never HG (n=1,452)
Low (<7.0%)	607 (50.0%)a	533 (55.2%)b	933 (64.3%)
Slightly elevated (≥7.0% to ≤8.5%)	498 (41.0%)a	351 (36.3%)b	420 (28.9%)
Elevated (>8.5% to ≤11.0%)	96 (7.9%)b	65 (6.7%)	78 (5.4%)
Seriously elevated (>11.0%)	14 (1.2%)	17 (1.8%)	21 (1.5%)
Mean (% ± SD)	7.05±1.27b	6.98±1.27b	6.78±1.26

Notes:

a P<0.05 versus both nonrecent HG and never HG groups;

b P<0.05 versus never HG group only.

Abbreviations: HbA_1c, glycated hemoglobin; HG, hypoglycemia; SD, standard deviation.

Conversely, the percentage of participants experiencing hypoglycemia was examined based on HbA_1c group (Table 5). A significantly lower proportion of participants in the low HbA_1c group reported recent hypoglycemia (29.3%) compared with both the slightly elevated HbA_1c (39.2%) and elevated HbA_1c (40.2%) groups (P<0.05 for both). This corresponded to a significantly higher proportion of participants reporting never hypoglycemia (45.0%) compared with the slightly elevated HbA_1c (33.1%) and elevated HbA_1c (32.6%) groups (P<0.05 for both). In participants who reported not knowing their HbA_1c levels (n=2,019), the percentage that reported experiencing a recent hypoglycemia (22.6%) was significantly lower than for the low, slightly elevated, and elevated HbA_1c groups (P<0.05 for all). The percentage of participants who did not know their HbA_1c levels and reported never experiencing hypoglycemia (51.7%) was significantly higher than in the low, slightly elevated, and elevated HbA_1c groups (P<0.05 for all).

Table 5 Percentage of participants reporting hypoglycemia by HbA_1c level

n (%)	Low (<7.0%) n=2,073	Slightly elevated (≥7% to ≤8.5%) n=1,269	Elevated (>8.5% to ≤11.0%) n=239	Seriously elevated (>11.0%) n=52	Do not know n=2,019
Recent HG	607 (29.3)a	498 (39.2)	96 (40.2)	14 (26.9)	456 (22.6)b
Nonrecent HG	533 (25.7)	351 (27.7)	65 (27.2)	17 (32.7)	520 (25.8)
Never HG	933 (45.0)a	420 (33.1)	78 (32.6)	21 (40.4)	1,043 (51.7)b

Notes:

a P<0.05 versus the slightly elevated, elevated, and do not know groups;

b P<0.05 versus the low, slightly elevated, and elevated groups.

Abbreviations: HbA_1c, glycated hemoglobin; HG, hypoglycemia.

The never hypoglycemia group had the lowest use of insulin (17.0%) compared with the nonrecent hypoglycemia (32.4%) and recent hypoglycemia (46%) groups (P<0.05 in both). The never hypoglycemia group also had the lowest use of sulfonylurea and glucagon-like peptide-1 agonists (Table 3).

The mean BMI was 33.3 kg/m² in the never hypoglycemia group and 34.0 kg/m² in both the recent and nonrecent hypoglycemia groups (Table 3). More than 60% of participants were overweight or obese. Diabetes disease burden was higher in participants with hypoglycemia. The mean CCI score was highest in those with recent hypoglycemia (1.88) compared with those with nonrecent hypoglycemia (1.72; P=0.05 versus recent hypoglycemia) and never hypoglycemia (1.52; P<0.05 versus both the recent hypoglycemia and nonrecent hypoglycemia groups).

Of all participants taking antihyperglycemic agents, 52% reported medium to low adherence with their medications, a quarter of whom had low adherence. The recent hypoglycemia group had the highest proportion of medium or low adherence followed by the nonrecent hypoglycemia and never hypoglycemia groups (Table 6).

Table 6 Morisky Medication Adherence Scale scores in participants taking antihyperglycemic agents

Adherence score	Recent HG (n=1,688)	Nonrecent HG (n=1,516)	Never HG (n=2,552)
High (7)	660 (39.1%)a	691 (45.6%)b	1,411 (55.3%)
Medium (5–6)	733 (43.4%)b	607 (40.0%)b	901 (35.3%)
Low (<5)	295 (17.5%)a	218 (14.4%)b	240 (9.4%)

Notes:

a P<0.05 versus both nonrecent HG and never HG groups;

b P<0.05 versus never HG group only.

Abbreviation: HG, hypoglycemia.

Hypoglycemia had significant impact on participants’ lives. A larger proportion of participants in the recent hypoglycemia and nonrecent hypoglycemia groups reported moderately to extreme interference with social activities compared with the never hypoglycemia group (Table 7). Work productivity was also impacted. Those with recent hypoglycemia had significantly higher absenteeism (7.6%), presenteeism (21.3%), and total work productivity impairment (25.5%) due to health compared with those with nonrecent hypoglycemia (4.4%, 15.1%, and 18.0%, respectively; P<0.05 for all comparisons) or never hypoglycemia (3.5%, 14.0%, and 16.3%, respectively; P<0.05 for all comparisons; Figure 2). Overall, recent hypoglycemia episodes contributed to lower HRQoL. General health summary scores across all domains of the SF-36, physical and mental, were significantly lower in participants with recent hypoglycemia compared with those with nonrecent hypoglycemia or never hypoglycemia (P<0.05 for all comparisons; Figure 3).

Figure 2 Work productivity in participants taking antihyperglycemic agents.

Notes: Absenteeism refers to mean percentage of work time missed due to health (currently employed full-time people); presenteeism refers to mean percentage impairment while working due to health (currently employed full-time people); work productivity impairment refers to mean overall work impairment due to health. ^aP<0.05 versus nonrecent HG. ^bP<0.001 versus never HG. ^cP=0.001 versus nonrecent HG.
Abbreviation: HG, hypoglycemia.

Figure 3 General health summary scores (Short Form-36) in participants taking antihyperglycemic agents who know their hypoglycemic status.

Abbreviations: PF, physical functioning; RP, role-physical; BP, body pain; GH, general health; VT, vitality; SF, social functioning; RE, role-emotional; MH, mental health; HG, hypoglycemia.

Table 7 Extent of interference with social activities in the previous 4 weeks in participants taking antihyperglycemic agents by HG experience

Frequency	Recent HG (n=1,688)	Nonrecent HG (n=1,516)	Never HG (n=2,552)
Not at all	615 (36.4%)a	691 (45.6%)	1,437 (56.3%)
Slightly	433 (25.7%)b	349 (23.0%)	537 (21.0%)
Moderately	319 (18.9%)b	255 (16.8%)b	342 (13.4%)
Quite a bit	235 (13.9%)a	166 (11.0%)b	176 (6.9%)
Extremely	86 (5.1%)a	55 (3.6%)b	60 (2.4%)

Notes:

a P<0.05 versus both nonrecent HG and never HG groups;

b P<0.05 versus never HG group only.

Abbreviation: HG, hypoglycemia.

Discussion

Studies have shown that glycemic control deteriorates progressively over time, necessitating increased use of insulin therapy. Although this approach may lessen the deterioration, it may come at the expense of significant weight gain and hypoglycemia.²² Despite newer antihyperglycemic agent treatment options, such as the dipeptidylpeptidase-4 inhibitors and glucagon-like peptide-1 agonists, a large proportion of people with T2DM still report experiencing hypoglycemia. To our knowledge, this is the first large-scale study to characterize the impact of hypoglycemia on diabetes burden, HRQoL, and work productivity from the patient perspective in a single analysis. The results of this study offer insight into the demographics and clinical characteristics of survey participants who experienced hypoglycemia (recent or nonrecent) or never experienced hypoglycemia. In addition, the results show that hypoglycemia negatively impacts social function, overall HRQoL, work productivity, and medication adherence.

The results suggest that adults with T2DM who experience hypoglycemia tend to be younger, be more aware of their HbA_1c levels and have higher HbA_1c levels, have higher BMIs, have higher CCI scores, be treated with insulin, sulfonylureas, or glucagon-like peptide-1 agonists, and be less adherent to their antihyperglycemic agents compared with those who never experience hypoglycemia. The impact appears even greater in those experiencing recent hypoglycemia. Although we did not expect the never hypoglycemia group to have an older mean age than the nonrecent hypoglycemia or recent hypoglycemia groups, and we really do not know the reason behind these findings, we can speculate that older patients may be more prone to recall bias and other limitations inherent with surveys. Also, we may expect the risks of hypoglycemia to increase with advancing age, but the recognition of hypoglycemia signs may decrease.

The association of hypoglycemia with poor glycemic control is consistent with the notion that the fear of hypoglycemia leads to maintenance of higher glycemic levels, although there is little evidence in the literature to support this.^5,8 The results of this study would add support, as almost twice the percentage of those with recent hypoglycemia (29.5%) had slightly elevated HbA_1c levels (7.0%–8.5%) compared with those who never had hypoglycemia (16.5%). The association between hypoglycemia and poor medication adherence is consistent with other observations in the literature. A database analysis using the 2006–2008 NHWS found a significant association between the number of tolerability issues (hypoglycemia, constipation/diarrhea, headaches, weight gain, and water retention) and medication nonadherence in participants with T2DM. Each additional tolerability issue was associated with a 28% greater likelihood of medication nonadherence.²³ A European study in people with T2DM that added a sulfonylurea or a thiazolidinedione to ongoing metformin therapy reported that those with hypoglycemia were significantly more likely to report barriers to adherence.²⁴ A study drawing on a large administrative database of managed care plans (Impact database; Ingenix) showed that in people with T2DM on one or more oral antihyperglycemic agents, having one or more hypoglycemic events within a 6-month interval was significantly associated with treatment discontinuation over this period and the subsequent 6-month interval.²⁵ There has been an association observed between better medication adherence and better glycemic control in people with T2DM.^20,26 The results of this study show that hypoglycemia may be a significant factor in medication adherence and glycemic control, given that both were poorer in those having nonrecent hypoglycemia compared with those never having hypoglycemia, and were even worse in those with recent hypoglycemia compared with those with nonrecent hypoglycemia.

Poor medication adherence and glycemic control in people with T2DM with hypoglycemia may be a result of the additional burden caused by fear of hypoglycemia and the need to manage it. Diabetes is a chronic disease that involves constant monitoring of behaviors and habits (eg, eating, social activities, exercise) in order to maintain proper glycemic control, and hypoglycemia appears to add to these burdens. Study participants who had a previous hypoglycemia reported feeling more “hassled” about taking their antihyperglycemic agents compared with participants who had never had hypoglycemia (data not reported). Increased interference with social activities, missed work, and work impairment were also reported in those with hypoglycemia and more so in those with recent hypoglycemia. Thus, it is no surprise that overall HRQoL decreased in those with nonrecent hypoglycemia and decreased further in those with recent hypoglycemia.

Hypoglycemia is associated with significant morbidity and mortality, which further adds to the burden for people with T2DM.²⁷ In this study, mean CCI scores were highest in participants with recent hypoglycemia, followed by those who had nonrecent hypoglycemia and those who never had hypoglycemia. The higher disease burden and risk of mortality in those with hypoglycemia is consistent with observations that hypoglycemia may increase morbidity and mortality in people with T2DM. In a post-hoc analysis of the ADVANCE (Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified-Release Control Evaluation) trial, severe hypoglycemia was associated with significant increases in the risks of major microvascular and macrovascular events and deaths.²⁸ In the ACCORD (Action to Control Cardiovascular Risk in Diabetes) and ADVANCE trials, patients with a history of severe hypoglycemia events had approximately a 1.4-fold to 3-fold higher risk of mortality, with one-third to one-half of all deaths being cardiovascular in nature. However, it is not known if severe hypoglycemia contributes to adverse outcomes or if it is a marker of vulnerability to these events.^28,29

Because this analysis is based on a patient survey, there are caveats to keep in mind when interpreting its findings. The data collected are subject to recall bias, missing values, and variability in the interpretation of questions. Certain characteristics such as BMI and CCI were based on patient self-reported information and, thus, may be susceptible to bias. In addition, due to limitations regarding how the data were collected and the descriptive nature of the study, there were no adjustments for factors such as severity of hypoglycemia and unknown HbA_1c levels. The descriptive nature of the study also precludes any definitive conclusions regarding causality being made in any of the observed relationships. Furthermore, the survey depended on participant interpretation and reporting of hypoglycemia episodes as opposed to biochemical documentation with a glucose reading. Finally, the survey was Internet-based, and so may not be fully representative of the entire population with T2DM given that it only includes participants who have computer access and a degree of computer literacy. Thus, although certain demographic characteristics (eg, sex, age, region) approximate the US census population, this survey sample may not be completely generalizable to the entire population with T2DM.

Conclusion

The results of this study highlight the significant burden of hypoglycemia from a patient perspective and its impact on HRQoL, work productivity, and medication adherence. The causes of hypoglycemia are likely multifactorial. Patient education regarding hypoglycemia early in the disease course may be helpful, since the fear of future hypoglycemia events may result in poor medication adherence and glycemic control that could lead to the development of long-term T2DM-associated complications. Another important consideration is the selection of antihyperglycemic treatment, given that certain classes of medications are associated with higher risks of hypoglycemia. This analysis focused on patients’ perspectives of hypoglycemia, but it is also important to consider the impact of hypoglycemia in other areas. From the perspectives of the health care provider, payer, and employer, increasing attention towards hypoglycemia in people with T2DM may increase work productivity and decrease health care utilization. These results support the need for multi-modal approaches, including careful selection of medication regimens, to minimize the risk and burden of hypoglycemia.

Acknowledgments

The authors would like to thank Kenneth Chiang and ECIR Medical Communications for writing and editorial support.

Disclosure

JMSL, RAB, and MFTR are employees of Janssen Pharmaceuticals, Inc. KA is an employee of Kantar Health. DEM reports no conflicts of interest.