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Pragmatic and Observational Research logoLink to Pragmatic and Observational Research
. 2013 Sep 27;4:27–37. doi: 10.2147/POR.S49746

Incidence of diabetic peripheral neuropathic pain in primary care – a retrospective cohort study using the United Kingdom General Practice Research Database

Catherine Reed 1,, Jihyung Hong 2, Diego Novick 1, Alan Lenox-Smith 3, Michael Happich 4
PMCID: PMC5045014  PMID: 27774022

Abstract

Purpose

To determine the incidence of diabetic peripheral neuropathic pain (DPNP) in the United Kingdom (UK) primary care population using the General Practice Research Database (GPRD).

Patients and methods

This retrospective cohort study identified incident cases of DPNP in the UK GPRD between July 1, 2002 and June 30, 2011, using diagnostic codes. Trends in the incidence rate were examined by dividing the study period into 3-year periods: (1) July 1, 2002–June 30, 2005; (2) July 1, 2005–June 30, 2008; and (3) July 1, 2008–June 30, 2011. Patient characteristics (age, sex, comorbidities) and initial pharmacological treatment were described; the proportion of patients with incident DPNP, who had previously been screened for neuropathic symptoms, was determined.

Results

Among almost 7.5 million persons contributing 38,118,838 person-years of observations in the GPRD, 6,779 new cases of DPNP were identified (45.5%, women), giving an incidence rate of 17.8 per 100,000 person-years (95% confidence interval [CI] 17.4–18.2). The incidence of DPNP increased with age, but it was stable over the three consecutive 3-year periods: 17.9, 17.2, and 18.4 cases per 100,000 person-years. Of the 6,779 patients with incident DPNP, 15.5% had prior neuropathic screening during the study period. The majority of patients with incident DPNP (84.5%) had a treatment for pain initiated within 28 days of first diagnosis. The most common first-line treatments prescribed were tricyclic antidepressants (27.2%), anticonvulsants (17.0%), and nonsteroidal anti-inflammatory drugs (14.9%), with 26.6% of patients receiving combination therapy as their initial treatment.

Conclusion

The incidence of DPNP in UK primary care has remained steady over the past 10 years. Our results suggest that DPNP is underdiagnosed, and initial treatment prescribed does not follow clinical guidelines.

Keywords: diabetes, peripheral neuropathy, pain, incidence, primary care

Introduction

Peripheral neuropathy affects up to 50% of patients with diabetes and is characterized by pain, paresthesia, and sensory loss, increasing the risk for foot problems that can result in amputation.1 Diabetic peripheral neuropathic pain (DPNP) is generally diagnosed and managed in the primary care setting in the United Kingdom (UK), but it can be difficult for general practitioners (GPs) to recognize, because patients often do not relate pain to diabetes and, therefore, do not volunteer information on their pain symptoms during consultations.2 DPNP is associated with impaired patient functioning and quality of life, as well as higher societal and health care costs compared to patients with diabetes but without neuropathic pain.3,4

Prevalence rates of DPNP in Europe range from 8%–26% in different diabetes patient populations.511 In the UK, the prevalence of DPNP in the diabetes population ranges from 10%–26%, depending on the criteria used to assess/define DPNP and the patient population studied.57

Incidence of DPNP has been less well-studied, but it is an important measure within the general population to inform health policy for screening and detection and to plan health care resources. A study, using the UK General Practice Research Database (GPRD), estimated the incidence of DPNP at 15.3 cases per 100,000 person-years in the UK primary care population between 1992 and 2002,12 increasing to 27.2 cases per 100,000 person-years between 2002 and 2005.13

In the UK, clinical practice guidelines for patients with diabetes include annual checks for neuropathic symptoms and appropriate pain management plans to improve patient outcomes.2,14 Annual screening of all diabetes patients for neuropathy and a foot examination (including assessment of peripheral pulses and sensation) is part of the Quality Outcome Framework (QOF), a financial incentive scheme for GP practices introduced in 2004.15

Up-to-date DPNP incidence rates will inform health care providers and practitioners on the impact of clinical guidelines and neuropathic screening on the diagnosis and treatment patterns of DPNP in UK primary care; such information is captured in the GPRD.

The objectives of our study were to use the GPRD to determine the impact of the introduction of national guidelines14 on the incidence of DPNP in the UK primary care population in the last 9 years and to examine trends in the incidence rate over the study period (2002–2011). In addition, we describe the characteristics of the primary care patients with incident DPNP and their initial pharmacological treatment, and we determined the proportion of patients with incident DPNP who had previously been screened for neuropathic symptoms.

Material and methods

Data source

This study used a retrospective cohort design to identify incident cases of DPNP in the UK GPRD between July 1, 2002–June 30, 2011. GPRD records for >5 million currently registered patients meet the GPRD standards of acceptable quality for use in research, which is equivalent to approximately 8.5% of the UK population.16 Recent systematic reviews have confirmed the validity of medical diagnoses and quality of information on the GPRD.17,18

Study population and study cohort with incident DPNP

The total study population included all patients who were permanently registered at one of the GP practices contributing to the GPRD system at any time during the 9-year study period (July 1, 2002–June 30, 2011) and who provided acceptable-quality data as recorded in the GPRD. For each patient, the period of observation was from a start date to an end date. The start date was defined as the last of either: (1) the start of the study period (July 1, 2002); (2) the patient’s date of registration with the practice; or (3) the date the practice was considered “up to standard” by the GPRD. The end date was defined as the first of the following: (1) end of the study period (June 30, 2011); (2) death; (3) transfer out of the practice; or (4) the final data collection.

The study cohort with incident DPNP was identified from the total population and included those who had a GPRD record containing one of the following: a diagnosis of DPNP; a diagnosis of diabetic neuropathy with a prescription for treatment for pain current at the date of diagnosis; a diagnosis of diabetes and neuropathic pain; and a diagnosis of both diabetes and neuralgia plus a treatment for pain current on the data of the neuralgia code. Prescription for treatment for pain includes antidepressants, anticonvulsants, narcotics, nonnarcotics, and nonsteroidal anti-inflammatory drugs (NSAIDs). All diagnoses were identified based on Read codes (Table S1 and Table S2). Patients were excluded from the study cohort if they had a DPNP diagnosis in their record prior to the incident date, which was defined as the date of the first DPNP diagnosis recorded in the GPRD during the study period. They were also excluded if they had fewer than 12 months of computerized data prior to the incident date or data not considered of acceptable quality by the GPRD.

Figure 1 presents the flow chart for identification and selection of the study cohort with incident DPNP in the GPRD.

Figure 1.

Figure 1

Flow diagram of selection of patient cohort from GPRD.

Notes: aThose who had acceptable quality data and were registered at any time during the total study period (July 1, 2002–June 30, 2011); bPatients with the following conditions were removed: patients with diabetic neuropathy but no pain relief prescriptions on the date of diabetic neuropathy code; patients with neuropathic pain but no diagnosis of diabetes recorded between July 1, 2002 and June 30, 2011; patients with neuralgia but no diagnosis of diabetes recorded between July 1, 2002 and June 30, 2011 and/or no pain relief prescriptions on the data of neuralgia code.

Abbreviations: GPRD, General Practice Research Database; DPNP, diabetic peripheral neuropathic pain; n, number.

Data collected

Data on patient age and sex were collected from the GPRD for the total eligible population (n = 7,483,143) and for the study cohort with incident DPNP (n = 6,779).

For the study cohort, information was collected on the most common diabetes-related comorbidities (cardiovascular disease, cerebrovascular and peripheral vascular disease, retinopathy, hypoglycemic event, other metabolic diseases, skin problems, nephropathy, obesity, and anxiety) and pain-related comorbidities (lower back pain, osteoarthritis, fibromyalgia syndrome, migraine, psoriatic arthropathy, and rheumatoid arthritis). Items from the Charlson Comorbidity Index (CCI) were identified using 17 previously defined categories of comorbid conditions based on Read codes.19 The frequency and percentage of these comorbidities in the 12 months before the incident date were estimated; and the CCI score, a summary measure of index that represents the 1-year mortality for patients based on their history of a range of comorbid conditions, was calculated for each patient.

Information on initial treatment for DPNP was collected within 28 days of the first record of the DPNP diagnosis (incident date) during the study period for: tricyclic antidepressants (TCAs); selective serotonin reuptake inhibitors (SSRIs); serotonin norepinephrine reuptake inhibitors (SNRIs); other antidepressants; anticonvulsants; opioids; nonnarcotics; and NSAIDs. The frequency and percentage of each type of drug were estimated. If more than one pharmacotherapy was prescribed on the same day, the initial treatment was considered to be a combination of these therapies.

The frequency and percentage of patients who underwent screening for neuropathic symptoms during the study period were determined by examining Read codes for diabetic peripheral neuropathy screening and diabetic foot examination/screen (Table S3). The number/percentage of patients diagnosed with DPNP after neuropathic screening during the study period was calculated.

Analysis

To replicate the methodology of Hall et al,12 the incidence rate of DPNP per 100,000 person-years of observation was calculated for the total study period and for the three 3-year subperiods: (1) July 1, 2002–June 30, 2005; (2) July 1, 2005–June 30, 2008; and (3) July 1, 2008–June 30, 2011. The incidence of DPNP was also estimated by sex and age groups (0–14, 15–29, 30–44, 45–59, 60–74, 75+ years). The age group for each patient was determined using a reference year, which was either the start of the study period (2002 for the total study period as well as the first subperiod; 2005 for subperiod 2; and 2008 for subperiod 3), or the date of entry into the GPRD if this occurred later than the start of the study period. Confidence intervals (95% CI) for incidence rates were calculated based on Poisson exact CI. The incidence rates of DPNP for the three subperiods were compared using a Poisson regression model for each age group. The number of DPNP cases was the dependent variable, and the period indicator was included as an independent variable. Total years of observations were included as time of exposure. Results of patient characteristics, comorbidities, and medication are based on nonmissing data. All data analyses were carried out using SAS software version 9.2 (SAS Institute Inc., Cary, NC, USA).

Results

The total study population eligible for analysis was almost 7.5 million patients (Figure 1), providing approximately 38.1 million (38,118,838) person-years of observation. Of this total population, 50.9% were female, and the mean age was 35.3 years (standard deviation 23.5).

From the total study population, 6,779 patients were identified as having incident DPNP during the study period (Figure 1), and Table 1 summarizes the characteristics of this patient cohort.

Table 1.

Characteristics of patient cohort with incident DPNP

Characteristic n (%) or mean (SD)
Number of patients with incident DPNP during total study period 6,779
Sex, n (%)
 Female 3,083 (45.5)
 Male 3,696 (54.5)
Age, mean (SD) years at DPNP incidence 65.5 (12.9)
 Females 66.0 (13.5)
 Males 65.0 (12.4)
Diabetes-related comorbidities*, n (%)
 Cardiovascular disease 453 (6.7)
 Cerebrovascular and peripheral vascular disease 595 (8.8)
 Retinopathy 484 (7.1)
Pain-related comorbidities*, n (%)
 Lower back pain 431 (6.4)
 Osteoarthritis 362 (5.3)
CCI score, mean (SD) 0.97 (1.01)

Notes:

*

Comorbidities occurring in >5% of patients in the 12 months prior to diagnosis of DPNP. Other diabetes-related comorbidities examined included hypoglycemic events, other metabolic diseases, skin problems, nephropathy, obesity and anxiety. Other pain-related comorbidities examined included fibromyalgia syndrome, migraine, psoriatic arthropathy, and rheumatoid arthritis.

Abbreviations: DPNP, diabetic peripheral neuropathic pain; SD, standard deviation; CCI score, Charlson Comorbidity Index score; n, number.

The overall incidence of newly diagnosed DPNP during the whole study period was 17.8 per 100,000 person-years (95% CI = 17.4–18.2). Table 2 shows that the incidence of DPNP increased with age among both men and women, but it did not change significantly over the three subperiods, except among women aged 60–74 years, where the incidence decreased in the period 2008–2011 compared with the two earlier periods (P = 0.001).

Table 2.

Incidence of DPNP per 100,000 person-years (95% CI) by sex, age group, and time period

Subperiod 1
July 1, 2002–June 30, 2005
Subperiod 2
July 1, 2005–June 30, 2008
Subperiod 3
July 1, 2008–June 30, 2011
Total 17.9 (17.1–18.6) 17.2 (16.5–17.9) 18.4 (17.7–19.2)
Female
 0–14 years
 15–29 years 0.6 (0.2–1.3) 0.9 (0.4–1.7) 1.2 (0.7–2.1)
 30–44 years 6.4 (5.2–7.9) 5.1 (4.0–6.4) 5.3 (4.1–6.7)
 45–59 years 20.4 (18.0–23.1) 19.1 (16.8–21.6) 20.5 (18.1–23.2)
 60–74 years 48.7 (44.2–53.5) 47.9 (43.6–52.5) 38.7 (34.8–42.8)*
 75+ years 48.6 (43.1–54.6) 41.2 (36.2–46.7) 50.2 (44.5–56.4)
Male
 0–14 years
 15–29 years 0.7 (0.3–1.3) 0.6 (0.2–1.3) 1.1 (0.6–1.9)
 30–44 years 6.1 (4.9–7.5) 5.4 (4.3–6.7) 5.4 (4.2–6.8)
 45–59 years 26.8 (24.0–29.7) 25.1 (22.5–27.9) 28.4 (25.5–31.5)
 60–74 years 61.9 (56.6–67.5) 61.7 (56.6–67.1) 64.1 (58.9–69.5)
 75+ years 69.9 (61.2–79.4) 67.1 (59.0–76.1) 76.3 (67.5–85.9)

Notes: Poisson exact CI (95%) are given in brackets.

*

P = 0.001 from Poisson regression for trend of incidence rates.

Abbreviations: DPNP, diabetic peripheral neuropathic pain; CI, confidence interval.

During the whole study period, 90,162 patients in the total study population underwent neuropathic screening. Of these patients, 3,152 (3.5%) had a diagnosis of DPNP after neuropathic screening (but were not necessarily an incident case); and 1,053 (1.2%) were identified with incident DPNP. Of the 6,779 patients in the study cohort with incident DPNP, 1,053 (15.5%) had prior neuropathic screening during the study period (n = 109 for subperiod 1, n = 388 for subperiod 2, and n = 556 for subperiod 3).

A treatment for DPNP was initiated for 5,767 (85.1%) of the patients with incident DPNP within 28 days of diagnosis, and Table 3 summarizes the initial pharmacological treatment prescribed for these patients. Over the total study period, the most common single first-line treatments were TCAs (27.2%), anticonvulsants (17.0%), and NSAIDs (14.9%), with combination therapy being prescribed as the initial treatment for 26.6% of patients. There was little change in first-line medication use across the three subperiods, except for a slight decrease in the use of opioids and NSAIDs, and a very small increase in the use of SNRIs (Table 3). The most common combinations prescribed within 28 days of first diagnosis during the total study period were NSAIDs plus opioids (10.3%); TCAs, plus NSAIDs (9.6%); and TCAs plus opioids (8.6%).

Table 3.

Initial treatment prescribed for incident DPNP by type of medication and study period

Medication Subperiod 1
July 1, 2002–June 30, 2005 (n = 1,871)
Subperiod 2
July 1, 2005–June 30, 2008 (n = 1,940)
Subperiod 3
July 1, 2008–June 30, 2011 (n = 1,956)
Total study period
July 1, 2002–June 30, 2011 (n = 5,767)
n % n % n % n %
Nonopioid analgesics 47 2.5 38 2.0 46 2.4 131 2.3
Opioid 192 10.3 170 8.8 142 7.3 504 8.7
NSAIDs 354 18.9 297 15.3 210 10.7 861 14.9
Anticonvulsants 266 14.2 366 18.9 350 17.9 982 17.0
TCAs 505 27.0 490 25.3 574 29.4 1,569 27.2
SSRIs 28 1.5 31 1.6 31 1.6 90 1.6
SNRIs* 1 0.1 5 0.3 78 4.0 84 1.5
Duloxetine 0 0 4 0.2 75 3.8 79 1.4
Other antidepressants 2 0.1 2 0.1 7 0.4 11 0.2
Combination therapy 476 25.4 541 27.9 518 26.5 1,535 26.6

Notes: Data presented are number and percentage of initial prescriptions by type of medication within 28 days of first diagnosis of DPNP for the total study period and each subperiod.

*

SNRIs consist of duloxetine and venlafaxine. Duloxetine is also listed separately as it is the only SNRI recommended for DPNP. Combination therapy is defined as more than one pharmacotherapy prescribed on the same day.

Abbreviations: DPNP, diabetic peripheral neuropathic pain; NSAIDs, nonsteroidal anti-inflammatory drugs; TCA, tricyclic antidepressant; SSRIs, selective serotonin reuptake inhibitors; SNRI, serotonin norepinephrine reuptake inhibitor; n, number.

Discussion

In this study, the overall incidence rate of DPNP in the UK primary care population using the GPRD was 17.8 cases per 100,000 person-years over the 9-year study period from 2002–2011. This is consistent with the previously reported DPNP incident rate of 15.3 cases per 100,000 person-years for 1992–2002,12 where the number of incident cases (per 100,000 person-years) increased over time from 12.9 for 1992–1994, to 14.4 for 1995–1997, to 19.0 for 1998–2001, to 27.2 for 2002–2005. In contrast to the previous studies by Hall et al,12,13 we found little change over time in the incidence of DPNP; the number of incident cases per 100,000 person-years was stable over the three consecutive 3-year periods (17.9, 17.2, and 18.4, respectively).

The total incident cases of DPNP (n = 6,779) during 2002–2011 out of 7.5 million primary care patients can be translated into a crude prevalence rate of 0.5% in the general population, based on the assumption that prevalence is approximately the product of disease incidence and average disease duration, using an assumed duration of DPNP of 5 years.20 Although there is little information on the natural history of DPNP, it is generally believed that painful symptoms resolve or become less prominent over time while the neuropathy continues to progress.21,22 As of 2011, a total of 2.9 million people in the UK have been diagnosed with diabetes, giving an average diabetes prevalence rate of 4.5%.23 Using this diabetes prevalence rate – and assuming that DPNP occurs in 21.0% of people with diabetes based on recent data from >15,000 UK patients with diabetes5 – would provide a DPNP prevalence rate of 0.9% in the general population. While the estimates from our study do not provide a definitive indication of DPNP prevalence rates in the UK, they suggest that DPNP is being underdiagnosed in UK primary care. The results of our study also indicate that general practitioners (GPs) are not prescribing first-line treatments for neuropathic pain as recommended by clinical guidelines,14,24 suggesting that other factors are being taken into consideration when selecting treatment for DPNP.

In clinical practice, DPNP is diagnosed based on clinical signs and symptoms, such as the type of pain, time of pain occurrence, and abnormal sensations; therefore, an accurate diagnosis relies on the patient’s description of pain.22,25 However, patients often do not link pain to diabetes or find it difficult to describe the symptoms they are experiencing and, therefore, may not report their pain symptoms to the doctor.2,6,22 This could be one reason for the underdiagnosis of DPNP in primary care, and highlights the need for physicians to gather information on pain by prompting patients for relevant information, potentially using a simple screening form.26 The annual foot examination and/or test for neuropathy in patients with diabetes is an ideal opportunity to diagnose DPNP, and is part of the QOF scheme for GP practices in the UK, which provides a financial incentive to complete these assessments.6 However, the annual foot screen does not include specific screening questions on pain; there is no financial incentive for providing any diagnosis (including that of DPNP) arising from the assessment. Unexpectedly, we found that only 15.5% of patients with incident DPNP had a previous diabetic peripheral neuropathy screen or foot examination recorded in GPRD. This raises questions about how accurately screening is recorded in GPRD and whether it fully captures the QOF annual screening program, although a recent survey conducted by Diabetes UK found that a quarter of patients with diabetes could not recall having had an annual foot screen.27 Our finding that more than one-half of the incident DPNP cases with prior neuropathic screening occurred in the last subperiod (2008–2011) suggests that diagnosis of DPNP may be improving and that the QOF scheme (introduced in 2004) may be helping. However, as screening was checked for during the total study period (2002–2011), patients identified with DPNP in subperiod 3 had a longer time for screening to be recorded than the patients in subperiod 1. Nevertheless, rates of screening are low and further research over the next few years should make this clearer.

There was a low frequency (<10%) of diabetes- and pain-related comorbidities in the 12 months before DPNP diagnosis, and the most common comorbidities were consistent with those reported previously in a retrospective database study of >11,000 patients with DPNP.28 Some diabetes-related comorbidities (neuropathy, obesity, low levels of high-density lipoprotein cholesterol, and high levels of triglycerides) have been identified as independent risk factors for DPNP.9

In our study, the majority (85.1%) of patients with incident DPNP started pain-relief medication within 28 days. The most commonly used first-line medications were TCAs, anticonvulsants, and NSAIDs – despite a lack of evidence for NSAID efficacy in DPNP. SNRIs, such as duloxetine, were rarely prescribed as initial treatment. These findings are consistent with other studies in patients with DPNP.3,9,12,20 Interestingly, treatment patterns at the time of first diagnosis of DPNP do not seem to have changed over the 9-year study period and, even in the last 3-year period (2008–2011), only 4.0% of patients received an SNRI as their initial medication. This indicates that patients are not being treated according to current clinical guidelines, which recommend duloxetine as first-line treatment for people with painful diabetic neuropathy, or amitriptyline, if duloxetine is contraindicated.14 It is possible that patients are being prescribed TCAs (alone, or in combination with NSAIDs or opioids) because GPs are unsure of the diagnosis, and these antidepressants are known to be cheap and effective for the treatment of many painful conditions.

This study has several limitations. First, patients with incident DPNP were identified in the GPRD using multiple diagnostic codes covering diabetes, neuropathy, and neuropathic pain, together with prescription of pain relief medication. Although this was relatively straightforward and consistent with a previous publication,12 more accurate data collection would be achieved if there was a consistent and clear definition of DPNP, and a diagnostic code that is uniformly used to record its presence. Second, because of the inclusion criteria, patients with diabetic neuropathy or diabetes plus neuralgia and taking medication for depression or another painful condition may be included, resulting in an overestimation of the incidence of DPNP. Third, our study cohort of patients with incident DPNP does not include patients with impaired glucose tolerance (prediabetes) that may have peripheral neuropathy and/or neuropathic pain.29 Fourth, we were not able to assess pain severity in the GPRD, which may influence the diagnosis of DPNP and prescription of pain medication. Many patients with DPNP report having severe pain,7 and those with severe pain are more likely to receive pain treatment.10 Increasing pain severity is also associated with poorer patient outcomes and increased health care resource use and related costs.30

The strengths of our study include the large sample of primary care patients from the GPRD, which is representative of the UK population and utilizes real-life data that is routinely collected and recorded during primary care consultations. Importantly, as DPNP is typically diagnosed and managed in primary care, GPRD is the most appropriate data source available in the UK. Other strengths of this study are that we used similar methodology to Hall et al,12 and the incidence of DPNP during the 9-year study period was well-defined.

Conclusion

In conclusion, our study provides up-to-date information on the incidence rate of DPNP in the UK primary care population. The incidence of DPNP increases with age and more commonly affects men, but it has remained relatively stable over the past 9 years. However, our results suggest that DPNP is underdiagnosed in UK primary care and that treatment on diagnosis does not follow clinical guidelines, indicating the need for improved awareness and education about DPNP. If GPs can provide an early and confident diagnosis of DPNP, they may be more likely to implement treatments that reflect current clinical guideline recommendations, thereby improving patient care and reducing the burden of this disease.

Supplementary tables

Table S1.

Read codes for diabetes

Medcode Read code Read term
1038 C100011 IDDM
15690 C103.00 DM with ketoacidotic coma
46963 C108000 IDDM with renal complications
57621 C108D00 IDDM with nephropathy
4513 C109.00 NIDDM
55842 C109200 NIDDM with neurological complications
17262 C109600 NIDDM with retinopathy
33343 C10y.00 DM with other specified manifestation
1682 C101.00 DM with ketoacidosis
53200 C101000 DM, juvenile type, with ketoacidosis
42505 C101z00 DM NOS with ketoacidosis
7795 C106.12 DM with neuropathy
59365 C109C00 NIDDM with nephropathy
63371 C10y100 DM, adult + other specified manifestation
13279 C104y00 Other specified DM with renal complications
56448 C108A00 IDDM without complication
9013 66AJ.11 Unstable diabetes
14889 C100111 Maturity onset diabetes
41389 C105100 DM, adult onset + ophthalmic manifestation
32556 C107.12 Diabetes with gangrene
1647 C108.00 IDDM
40401 C109500 NIDDM with gangrene
2471 K01x100 Nephrotic syndrome in DM
506 C100112 NIDDM
16491 C106.13 DM with polyneuropathy
67853 C106000 DM, juvenile + neurological manifestation
49276 C108100 IDDM with ophthalmic complications
26855 C108400 Unstable IDDM
6509 C108700 IDDM with retinopathy
52303 C109000 NIDDM with renal complications
62146 C109300 NIDDM with multiple complications
34912 C109400 NIDDM with ulcer
63762 C10z100 DM, adult onset + unspecified complication
64357 C10zz00 DM NOS with unspecified complication
50609 L180600 Preexisting DM, noninsulin-dependent
24490 C100000 DM, juvenile type, no mention of complications
52283 C108200 IDDM with neurological complications
29979 C109900 NIDDM without complication
40023 C102000 DM, juvenile type, with hyperosmolar coma
35105 C104100 DM, adult onset, with renal manifestation
35107 C104z00 DM with nephropathy NOS
32403 C107.11 DM with gangrene
17858 C108.12 Type 1 DM
52104 C108300 IDDM with multiple complications
6791 C108800 IDDM – poor control
66675 C10A000 Malnutrition-related DM with coma
31790 F372.00 Polyneuropathy in diabetes
22967 2BBF.00 Retinal abnormality – diabetes-related
711 C10.00 DM
14803 C100100 DM, adult onset, no mention of complications
35399 C107.00 DM with peripheral circulatory disorder
63357 C107100 DM, adult + peripheral circulatory disorder
18505 C108.11 IDDM
45467 C109B00 NIDDM with polyneuropathy
52236 C10A.00 Malnutrition-related DM
52212 Cyu2.00 [X] DM
34528 3882.00 Diabetes well-being questionnaire
50972 C100z00 DM NOS with no mention of complications
16502 C104.00 DM with renal manifestation
33807 C107200 DM, adult with gangrene
5884 C109.11 NIDDM
72320 C109A00 NIDDM with mononeuropathy
45491 C10z.00 DM with unspecified complication
17067 F171100 Autonomic neuropathy due to diabetes
55431 L180X00 Preexisting DM, unspecified
13069 66A8.00 Has seen dietitian – diabetes
54856 C101100 DM, adult onset, with ketoacidosis
21482 C102.00 DM with hyperosmolar coma
69748 C105000 DM, juvenile type + ophthalmic manifestation
34283 C105z00 DM NOS with ophthalmic manifestation
65025 C107z00 DM NOS with peripheral circulatory disorder
17859 C109.12 Type 2 DM
50429 C109100 NIDDM with ophthalmologic complications
38986 C100.00 DM with no mention of complications
43139 C102100 DM, adult onset, with hyperosmolar coma
72345 C102z00 DM NOS with hyperosmolar coma
68843 C103100 DM, adult onset, with ketoacidotic coma
33254 C105.00 DM with ophthalmic manifestation
16230 C106.00 DM with neurological manifestation
39317 C106100 DM, adult onset + neurological manifestation
44443 C108500 IDDM with ulcer
60499 C108600 IDDM with gangrene
31310 C108900 IDDM maturity onset
41716 C108C00 IDDM with polyneuropathy
8403 C109700 NIDDM, poor control
50960 L180500 Preexisting DM, insulin-dependent
24423 C108.13 Type 1 DM
18219 C109.13 Type 2 DM
24458 C109711 Type 2 DM, poor control
42729 C108E11 Type 1 DM with hypoglycemic coma
63017 C108911 Type 1 DM maturity onset
44440 C108E00 IDDM with hypoglycemic coma
62107 C109511 Type 2 DM with gangrene
55075 C109411 Type 2 DM with ulcer
62352 C108H11 Type 1 DM with arthropathy
42762 C109612 Type 2 DM with retinopathy
44779 C109E12 Type 2 DM with diabetic cataract
10642 ZC2C800 Dietary advice for DM
44260 C108F00 IDDM with diabetic cataract
46850 C108811 Type 1 DM, poor control
58604 C109611 Type 2 DM with retinopathy
47409 C109B11 Type 2 DM with polyneuropathy
17545 C108F11 Type 1 DM with diabetic cataract
64571 C109C11 Type 2 DM with nephropathy
65616 C108H00 IDDM with arthropathy
41049 C108712 Type 1 DM with retinopathy
66965 C109H12 Type 2 DM with neuropathic arthropathy
60699 C109F12 Type 2 DM with peripheral angiopathy
45914 C108812 Type 1 DM, poor control
56268 C109D11 Type 2 DM with hypoglycemic coma
50225 C109011 Type 2 DM with renal complications
18278 C109 J00 Insulin-treated Type 2 DM
48192 C109E11 Type 2 DM with diabetic cataract
24836 C109C12 Type 2 DM with nephropathy
37648 C109J11 Insulin-treated NIDDM
24693 C109G00 NIDDM with arthropathy
45919 C109212 Type 2 DM with neurological complications
66872 C108D11 Type 1 DM with nephropathy
70316 C109112 Type 2 DM with ophthalmic complications
60107 C108411 Unstable type 1 DM
45913 C109712 Type 2 DM, poor control
47816 C109H11 Type 2 DM with neuropathic arthropathy
18209 C109012 Type 2 DM with renal complications
61344 C108011 Type 1 DM with renal complications
65704 C109412 Type 2 DM with ulcer
43785 C109D00 NIDDM with hypoglycemic coma
18264 C109 J12 Insulin-treated Type 2 DM
51957 C108511 Type 1 DM with ulcer
38161 C108711 Type 1 DM with retinopathy
67905 C109211 Type 2 DM with neurological complications
61071 C109D12 Type 2 DM with hypoglycemic coma
18230 C108 J12 Type 1 DM with neuropathic arthropathy
49146 C108211 Type 1 DM with neurological complications
36633 C109K00 Hyperosmolar nonketotic state in type 2 DM
1549 C10E.00 Type 1 DM
758 C10F.00 Type 2 DM
12640 C10FC00 Type 2 DM with nephropathy
1407 C10FJ00 Insulin-treated Type 2 DM
18387 C10E700 Type 1 DM with retinopathy
21983 C108012 Type 1 DM with renal complications
69278 C109E00 NIDDM with diabetic cataract
18642 C10EH00 Type 1 DM with arthropathy
35385 C10FH00 Type 2 DM with neuropathic arthropathy
54899 C109F11 Type 2 DM with peripheral angiopathy
10418 C10ED00 Type 1 DM with nephropathy
25041 ZC2CA00 Dietary advice for type 2 diabetes
18496 C10F600 Type 2 DM with retinopathy
47954 C10F900 Type 2 DM without complication
32359 ZRbH.00 Perceived control of insulin-dependent diabetes
18390 C10FM00 Type 2 DM with persistent microalbuminuria
50813 C109A11 Type 2 DM with mononeuropathy
10692 C10EM00 Type 1 DM with ketoacidosis
39070 C10EE00 Type 1 DM with hypoglycemic coma
70766 C108E12 Type 1 DM with hypoglycemic coma
62674 C10FA00 Type 2 DM with mononeuropathy
47582 C10E000 Type 1 DM with renal complications
40837 C10EN00 Type 1 DM with ketoacidotic coma
32627 C10FN00 Type 2 DM with ketoacidosis
26054 C10FL00 Type 2 DM with persistent proteinuria
35288 C10E800 Type 1 DM, poor control
37806 C10FF00 Type 2 DM with peripheral angiopathy
40682 C10E900 Type 1 DM maturity onset
47649 C10E100 Type 1 DM with ophthalmic complications
34268 C10F200 Type 2 DM with neurological complications
44982 C10FE00 Type 2 DM with diabetic cataract
25627 C10F700 Type 2 DM, poor control
43921 C10E400 Unstable type 1 DM
49074 C10F400 Type 2 DM with ulcer
30294 C10EL00 Type 1 DM with persistent microalbuminuria
18777 C10F000 Type 2 DM with renal complications
12736 C10F500 Type 2 DM with gangrene
18683 C10E500 Type 1 DM with ulcer
36695 C10D.00 DM autosomal dominant type 2
46301 C10EC00 Type 1 DM with polyneuropathy
18425 C10FB00 Type 2 DM with polyneuropathy
61829 C108212 Type 1 DM with neurological complications
30323 C10EK00 Type 1 DM with persistent proteinuria
46624 C10C.11 Maturity onset diabetes in youth
54008 C10EJ00 Type 1 DM with neuropathic arthropathy
25591 C10FQ00 Type 2 DM with exudative maculopathy
51756 C10FP00 Type 2 DM with ketoacidotic coma
46917 C10FD00 Type 2 DM with hypoglycemic coma
22871 C10EP00 Type 1 DM with exudative maculopathy
62209 C10EM11 Type 1 DM with ketoacidosis
42831 C10E200 Type 1 DM with neurological complications
51697 C10G.00 Secondary pancreatic DM
47321 C10F100 Type 2 DM with ophthalmic complications
49949 C10E411 Unstable type 1 DM
49554 C10EF00 Type 1 DM with diabetic cataract
18143 C109G11 Type 2 DM with arthropathy
49869 C109G12 Type 2 DM with arthropathy
69043 ZC2C900 Dietary advice for type 1 diabetes
65267 C10F300 Type 2 DM with multiple complications
59253 C10FG00 Type 2 DM with arthropathy
51261 C10E.12 IDDM
69993 C10E600 Type 1 DM with gangrene
22884 C10F.11 Type 2 DM
60796 C10FL11 Type 2 DM with persistent proteinuria
47650 C10E300 Type 1 DM with multiple complications
59725 C109111 Type 2 DM with ophthalmic complications
12455 C10E.11 Type 1 DM
69676 C10EA00 Type 1 DM without complication
68105 C10EB00 Type 1 DM with mononeuropathy
64668 C10FJ11 Insulin-treated type 2 DM
55239 C10EQ00 Type 1 DM with gastroparesis
57278 C10F011 Type 2 DM with renal complications
49655 C10F611 Type 2 DM with retinopathy
63690 C10FR00 Type 2 DM with gastroparesis
47315 C10F711 Type 2 DM, poor control
54600 C10E412 Unstable IDDM
93468 C10EG00 Type 1 DM with peripheral angiopathy
53392 C10F911 Type 2 DM without complication
43227 C10F311 Type 2 DM with multiple complications
50527 C10FB11 Type 2 DM with polyneuropathy
45276 C10E312 IDDM with multiple complications
66145 C10EN11 Type 1 DM with ketoacidotic coma
72702 C10E812 IDDM, poor control
96506 C10G000 Secondary pancreatic DM without complication
66475 66Ak.00 Diabetic monitoring, lower risk albumin excretion
69163 8HTi.00 Referral to multidisciplinary diabetic clinic
62613 C10EA11 Type 1 DM without complication
57382 7272600 Laser photocoagulation to lesion of retina NEC
95813 9N1o.00 Seen in multidisciplinary diabetic clinic
61021 68AB.00 Diabetic digital retinopathy screening offered
72827 7P17100 Insulin secretion glucagon test
64142 8Hl1.00 Referral for diabetic retinopathy screening
84142 44V6.00 Extended glucose tolerance test
91164 ZRB4.11 CSQ, Diabetes clinic satisfaction questionnaire
82474 8Hl4.00 Referral to community diabetes specialist nurse
83532 66Ao.00 Diabetes type 2 review
83485 66Am.00 Insulin dose changed
85660 66An.00 Diabetes type 1 review
91646 C10F411 Type 2 DM with ulcer
91942 C10E311 Type 1 DM with multiple complications
91943 C10EC11 Type 1 DM with polyneuropathy
85336 7P17.00 Diagnostic endocrinology
90301 66Ag.00 Insulin needles changed daily
85991 C10FM11 Type 2 DM with persistent microalbuminuria
93380 C10N100 Cystic fibrosis-related DM
92979 7P17z00 Diagnostic endocrinology NOS
93390 9OLH.00 Attended DAFNE diabetes-structured education program
93491 9OLJ.00 DAFNE diabetes structured education program completed
93657 8Hj4.00 Referral to DESMOND diabetes structured education program
93631 9OLL.00 XPERT diabetes-structured education program completed
93704 8Hj3.00 Referral to DAFNE diabetes structured education program
93727 C10FE11 Type 2 DM with diabetic cataract
93854 9OLM.00 Diabetes-structured education program declined
93870 8Hj5.00 Referral to XPERT diabetes-structured education program
93875 C10E712 IDDM with retinopathy
93878 C10E511 Type 1 DM with ulcer

Abbreviations: IDDM, insulin dependent diabetes mellitus; CSQ, (Diabetes) clinic satisfaction questionnaire; DM, diabetes mellitus; NEC, not elsewhere classified; NOS, not otherwise specified; NIDDM, noninsulin dependent diabetes mellitus; DAFNE, Dose Adjustment For Normal Eating; DESMOND, Diabetes Education and Self-Management for Ongoing and Newly Diagnosed.

Table S2.

Read codes for DPNP

Medcode Read code Read term
1. Painful diabetic neuropathy
48078 F372000 Acute painful diabetic neuropathy
35785 F372100 Chronic painful diabetic neuropathy
2. Diabetic neuropathy (+ pain medication)
2342 F372.12 Diabetic neuropathy
5002 F372.11 Diabetic polyneuropathy
16230 C106.00 DM with neurological manifestation
16491 C106.13 DM with polyneuropathy
17247 F35z000 Diabetic mononeuritis NOS
18056 2G5C.00 Foot abnormality, diabetes-related
18230 C108J12 Type 1 DM with neuropathic arthropathy
22573 C106z00 DM NOS with neurological manifestation
24694 C108B00 IDDM with mononeuropathy
27921 2G51000 Foot abnormality, diabetes-related
31790 F372.00 Polyneuropathy in diabetes
41716 C108C00 IDDM with polyneuropathy
42831 C10E200 Type 1 DM with neurological complications
43227 C10F311 Type 2 DM with multiple complications
44033 F345000 Diabetic mononeuritis multiplex
45276 C10E312 IDDM with multiple complications
45467 C109B00 NIDDM with polyneuropathy
45919 C109212 Type 2 DM with neurological complications
47409 C109B11 Type 2 DM with polyneuropathy
47650 C10E300 Type 1 DM with multiple complications
34152 G73y000 Diabetic peripheral angiopathy
34268 C10F200 Type 2 DM with neurological complications
35385 C10FH00 Type 2 DM with neuropathic arthropathy
37315 F3y0.00 Diabetic mononeuropathy
39317 C106100 DM, adult onset + neurological manifestation
39809 C108J00 IDDM with neuropathic arthropathy
54899 C109F11 Type 2 DM with peripheral angiopathy
55842 C109200 NIDDM with neurological complications
60208 C108J11 Type 1 DM with neuropathic arthropathy
60699 C109F12 Type 2 DM with peripheral angiopathy
72320 C109A00 NIDDM with mononeuropathy
91942 C10E311 Type 1 DM with multiple complications
7795 C106.12 DM with neuropathy
11663 M271100 Neuropathic diabetic ulcer – foot
61523 C106y00 Other specified DM with neurological comps
61829 C108212 Type 1 DM with neurological complications
65267 C10F300 Type 2 DM with multiple complications
67853 C106000 DM, juvenile + neurological manifestation
67905 C109211 Type 2 DM with neurological complications
98616 C10F211 Type 2 DM with neurological complications
99231 C108B11 Type 1 DM with mononeuropathy
101735 C10E212 IDDM with neurological comps
49146 C108211 Type 1 DM with neurological complications
50813 C109A11 Type 2 DM with mononeuropathy
52283 C108200 IDDM with neurological comps
54212 C109F00 NIDDM with peripheral angiopathy
3. Neuropathic (pain + diabetes)
35537 Fyu7C00 [X] Polyneuropathy, unspecified
2790 F367.00 Peripheral neuropathy
3958 F366.00 Polyneuropathy
97306 Fyu7200 [X] Other specified polyneuropathies
55076 Fyu7.00 [X] Polyneuropathies and other disorder of peripheral nervous system
24226 F37z.11 Polyneuropathy unspecified
4. Neuralgia (+ diabetes + pain medication)
2284 N242000 Neuralgia unspecified
54992 N242.00 Neuralgia, neuritis, and radiculitis unspecified
23839 N242z00 Neuralgia, neuritis, or radiculitis NOS

Note: [X] Cross referenced to specific ICD-10 codes (other READ terms relate to ICD-9).

Abbreviations: DPNP, diabetic peripheral neuropathic pain; DM, diabetes mellitus; IDDM, insulin-dependent diabetes mellitus; NIDDM, noninsulin-dependent diabetes mellitus.

Table S3.

Read codes for DPNP screening

Medcode Read code Read term
1. Painful diabetic neuropathy
10977 66Ac.00 Diabetic peripheral neuropathy screening
12247 8I6G.00 Diabetic foot examination not indicated
22823 66Ab.00 Diabetic foot examination
95994 66Aq.00 Diabetic foot screen

Abbreviation: DPNP, diabetic peripheral neuropathic pain.

Acknowledgments

The authors would like to acknowledge Deirdre Elmhirst for medical writing assistance, which was funded by Eli Lilly and Company.

Footnotes

Disclosure

This study was funded by Eli Lilly and Company Limited. Catherine Reed, Diego Novick, Alan Lenox-Smith, and Michael Happich are employees of Eli Lilly and Company Limited. Jihyung Hong is a consultant for Eli Lilly and Company Limited. The authors report no other conflicts of interest in this work.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Table S1.

Read codes for diabetes

Medcode Read code Read term
1038 C100011 IDDM
15690 C103.00 DM with ketoacidotic coma
46963 C108000 IDDM with renal complications
57621 C108D00 IDDM with nephropathy
4513 C109.00 NIDDM
55842 C109200 NIDDM with neurological complications
17262 C109600 NIDDM with retinopathy
33343 C10y.00 DM with other specified manifestation
1682 C101.00 DM with ketoacidosis
53200 C101000 DM, juvenile type, with ketoacidosis
42505 C101z00 DM NOS with ketoacidosis
7795 C106.12 DM with neuropathy
59365 C109C00 NIDDM with nephropathy
63371 C10y100 DM, adult + other specified manifestation
13279 C104y00 Other specified DM with renal complications
56448 C108A00 IDDM without complication
9013 66AJ.11 Unstable diabetes
14889 C100111 Maturity onset diabetes
41389 C105100 DM, adult onset + ophthalmic manifestation
32556 C107.12 Diabetes with gangrene
1647 C108.00 IDDM
40401 C109500 NIDDM with gangrene
2471 K01x100 Nephrotic syndrome in DM
506 C100112 NIDDM
16491 C106.13 DM with polyneuropathy
67853 C106000 DM, juvenile + neurological manifestation
49276 C108100 IDDM with ophthalmic complications
26855 C108400 Unstable IDDM
6509 C108700 IDDM with retinopathy
52303 C109000 NIDDM with renal complications
62146 C109300 NIDDM with multiple complications
34912 C109400 NIDDM with ulcer
63762 C10z100 DM, adult onset + unspecified complication
64357 C10zz00 DM NOS with unspecified complication
50609 L180600 Preexisting DM, noninsulin-dependent
24490 C100000 DM, juvenile type, no mention of complications
52283 C108200 IDDM with neurological complications
29979 C109900 NIDDM without complication
40023 C102000 DM, juvenile type, with hyperosmolar coma
35105 C104100 DM, adult onset, with renal manifestation
35107 C104z00 DM with nephropathy NOS
32403 C107.11 DM with gangrene
17858 C108.12 Type 1 DM
52104 C108300 IDDM with multiple complications
6791 C108800 IDDM – poor control
66675 C10A000 Malnutrition-related DM with coma
31790 F372.00 Polyneuropathy in diabetes
22967 2BBF.00 Retinal abnormality – diabetes-related
711 C10.00 DM
14803 C100100 DM, adult onset, no mention of complications
35399 C107.00 DM with peripheral circulatory disorder
63357 C107100 DM, adult + peripheral circulatory disorder
18505 C108.11 IDDM
45467 C109B00 NIDDM with polyneuropathy
52236 C10A.00 Malnutrition-related DM
52212 Cyu2.00 [X] DM
34528 3882.00 Diabetes well-being questionnaire
50972 C100z00 DM NOS with no mention of complications
16502 C104.00 DM with renal manifestation
33807 C107200 DM, adult with gangrene
5884 C109.11 NIDDM
72320 C109A00 NIDDM with mononeuropathy
45491 C10z.00 DM with unspecified complication
17067 F171100 Autonomic neuropathy due to diabetes
55431 L180X00 Preexisting DM, unspecified
13069 66A8.00 Has seen dietitian – diabetes
54856 C101100 DM, adult onset, with ketoacidosis
21482 C102.00 DM with hyperosmolar coma
69748 C105000 DM, juvenile type + ophthalmic manifestation
34283 C105z00 DM NOS with ophthalmic manifestation
65025 C107z00 DM NOS with peripheral circulatory disorder
17859 C109.12 Type 2 DM
50429 C109100 NIDDM with ophthalmologic complications
38986 C100.00 DM with no mention of complications
43139 C102100 DM, adult onset, with hyperosmolar coma
72345 C102z00 DM NOS with hyperosmolar coma
68843 C103100 DM, adult onset, with ketoacidotic coma
33254 C105.00 DM with ophthalmic manifestation
16230 C106.00 DM with neurological manifestation
39317 C106100 DM, adult onset + neurological manifestation
44443 C108500 IDDM with ulcer
60499 C108600 IDDM with gangrene
31310 C108900 IDDM maturity onset
41716 C108C00 IDDM with polyneuropathy
8403 C109700 NIDDM, poor control
50960 L180500 Preexisting DM, insulin-dependent
24423 C108.13 Type 1 DM
18219 C109.13 Type 2 DM
24458 C109711 Type 2 DM, poor control
42729 C108E11 Type 1 DM with hypoglycemic coma
63017 C108911 Type 1 DM maturity onset
44440 C108E00 IDDM with hypoglycemic coma
62107 C109511 Type 2 DM with gangrene
55075 C109411 Type 2 DM with ulcer
62352 C108H11 Type 1 DM with arthropathy
42762 C109612 Type 2 DM with retinopathy
44779 C109E12 Type 2 DM with diabetic cataract
10642 ZC2C800 Dietary advice for DM
44260 C108F00 IDDM with diabetic cataract
46850 C108811 Type 1 DM, poor control
58604 C109611 Type 2 DM with retinopathy
47409 C109B11 Type 2 DM with polyneuropathy
17545 C108F11 Type 1 DM with diabetic cataract
64571 C109C11 Type 2 DM with nephropathy
65616 C108H00 IDDM with arthropathy
41049 C108712 Type 1 DM with retinopathy
66965 C109H12 Type 2 DM with neuropathic arthropathy
60699 C109F12 Type 2 DM with peripheral angiopathy
45914 C108812 Type 1 DM, poor control
56268 C109D11 Type 2 DM with hypoglycemic coma
50225 C109011 Type 2 DM with renal complications
18278 C109 J00 Insulin-treated Type 2 DM
48192 C109E11 Type 2 DM with diabetic cataract
24836 C109C12 Type 2 DM with nephropathy
37648 C109J11 Insulin-treated NIDDM
24693 C109G00 NIDDM with arthropathy
45919 C109212 Type 2 DM with neurological complications
66872 C108D11 Type 1 DM with nephropathy
70316 C109112 Type 2 DM with ophthalmic complications
60107 C108411 Unstable type 1 DM
45913 C109712 Type 2 DM, poor control
47816 C109H11 Type 2 DM with neuropathic arthropathy
18209 C109012 Type 2 DM with renal complications
61344 C108011 Type 1 DM with renal complications
65704 C109412 Type 2 DM with ulcer
43785 C109D00 NIDDM with hypoglycemic coma
18264 C109 J12 Insulin-treated Type 2 DM
51957 C108511 Type 1 DM with ulcer
38161 C108711 Type 1 DM with retinopathy
67905 C109211 Type 2 DM with neurological complications
61071 C109D12 Type 2 DM with hypoglycemic coma
18230 C108 J12 Type 1 DM with neuropathic arthropathy
49146 C108211 Type 1 DM with neurological complications
36633 C109K00 Hyperosmolar nonketotic state in type 2 DM
1549 C10E.00 Type 1 DM
758 C10F.00 Type 2 DM
12640 C10FC00 Type 2 DM with nephropathy
1407 C10FJ00 Insulin-treated Type 2 DM
18387 C10E700 Type 1 DM with retinopathy
21983 C108012 Type 1 DM with renal complications
69278 C109E00 NIDDM with diabetic cataract
18642 C10EH00 Type 1 DM with arthropathy
35385 C10FH00 Type 2 DM with neuropathic arthropathy
54899 C109F11 Type 2 DM with peripheral angiopathy
10418 C10ED00 Type 1 DM with nephropathy
25041 ZC2CA00 Dietary advice for type 2 diabetes
18496 C10F600 Type 2 DM with retinopathy
47954 C10F900 Type 2 DM without complication
32359 ZRbH.00 Perceived control of insulin-dependent diabetes
18390 C10FM00 Type 2 DM with persistent microalbuminuria
50813 C109A11 Type 2 DM with mononeuropathy
10692 C10EM00 Type 1 DM with ketoacidosis
39070 C10EE00 Type 1 DM with hypoglycemic coma
70766 C108E12 Type 1 DM with hypoglycemic coma
62674 C10FA00 Type 2 DM with mononeuropathy
47582 C10E000 Type 1 DM with renal complications
40837 C10EN00 Type 1 DM with ketoacidotic coma
32627 C10FN00 Type 2 DM with ketoacidosis
26054 C10FL00 Type 2 DM with persistent proteinuria
35288 C10E800 Type 1 DM, poor control
37806 C10FF00 Type 2 DM with peripheral angiopathy
40682 C10E900 Type 1 DM maturity onset
47649 C10E100 Type 1 DM with ophthalmic complications
34268 C10F200 Type 2 DM with neurological complications
44982 C10FE00 Type 2 DM with diabetic cataract
25627 C10F700 Type 2 DM, poor control
43921 C10E400 Unstable type 1 DM
49074 C10F400 Type 2 DM with ulcer
30294 C10EL00 Type 1 DM with persistent microalbuminuria
18777 C10F000 Type 2 DM with renal complications
12736 C10F500 Type 2 DM with gangrene
18683 C10E500 Type 1 DM with ulcer
36695 C10D.00 DM autosomal dominant type 2
46301 C10EC00 Type 1 DM with polyneuropathy
18425 C10FB00 Type 2 DM with polyneuropathy
61829 C108212 Type 1 DM with neurological complications
30323 C10EK00 Type 1 DM with persistent proteinuria
46624 C10C.11 Maturity onset diabetes in youth
54008 C10EJ00 Type 1 DM with neuropathic arthropathy
25591 C10FQ00 Type 2 DM with exudative maculopathy
51756 C10FP00 Type 2 DM with ketoacidotic coma
46917 C10FD00 Type 2 DM with hypoglycemic coma
22871 C10EP00 Type 1 DM with exudative maculopathy
62209 C10EM11 Type 1 DM with ketoacidosis
42831 C10E200 Type 1 DM with neurological complications
51697 C10G.00 Secondary pancreatic DM
47321 C10F100 Type 2 DM with ophthalmic complications
49949 C10E411 Unstable type 1 DM
49554 C10EF00 Type 1 DM with diabetic cataract
18143 C109G11 Type 2 DM with arthropathy
49869 C109G12 Type 2 DM with arthropathy
69043 ZC2C900 Dietary advice for type 1 diabetes
65267 C10F300 Type 2 DM with multiple complications
59253 C10FG00 Type 2 DM with arthropathy
51261 C10E.12 IDDM
69993 C10E600 Type 1 DM with gangrene
22884 C10F.11 Type 2 DM
60796 C10FL11 Type 2 DM with persistent proteinuria
47650 C10E300 Type 1 DM with multiple complications
59725 C109111 Type 2 DM with ophthalmic complications
12455 C10E.11 Type 1 DM
69676 C10EA00 Type 1 DM without complication
68105 C10EB00 Type 1 DM with mononeuropathy
64668 C10FJ11 Insulin-treated type 2 DM
55239 C10EQ00 Type 1 DM with gastroparesis
57278 C10F011 Type 2 DM with renal complications
49655 C10F611 Type 2 DM with retinopathy
63690 C10FR00 Type 2 DM with gastroparesis
47315 C10F711 Type 2 DM, poor control
54600 C10E412 Unstable IDDM
93468 C10EG00 Type 1 DM with peripheral angiopathy
53392 C10F911 Type 2 DM without complication
43227 C10F311 Type 2 DM with multiple complications
50527 C10FB11 Type 2 DM with polyneuropathy
45276 C10E312 IDDM with multiple complications
66145 C10EN11 Type 1 DM with ketoacidotic coma
72702 C10E812 IDDM, poor control
96506 C10G000 Secondary pancreatic DM without complication
66475 66Ak.00 Diabetic monitoring, lower risk albumin excretion
69163 8HTi.00 Referral to multidisciplinary diabetic clinic
62613 C10EA11 Type 1 DM without complication
57382 7272600 Laser photocoagulation to lesion of retina NEC
95813 9N1o.00 Seen in multidisciplinary diabetic clinic
61021 68AB.00 Diabetic digital retinopathy screening offered
72827 7P17100 Insulin secretion glucagon test
64142 8Hl1.00 Referral for diabetic retinopathy screening
84142 44V6.00 Extended glucose tolerance test
91164 ZRB4.11 CSQ, Diabetes clinic satisfaction questionnaire
82474 8Hl4.00 Referral to community diabetes specialist nurse
83532 66Ao.00 Diabetes type 2 review
83485 66Am.00 Insulin dose changed
85660 66An.00 Diabetes type 1 review
91646 C10F411 Type 2 DM with ulcer
91942 C10E311 Type 1 DM with multiple complications
91943 C10EC11 Type 1 DM with polyneuropathy
85336 7P17.00 Diagnostic endocrinology
90301 66Ag.00 Insulin needles changed daily
85991 C10FM11 Type 2 DM with persistent microalbuminuria
93380 C10N100 Cystic fibrosis-related DM
92979 7P17z00 Diagnostic endocrinology NOS
93390 9OLH.00 Attended DAFNE diabetes-structured education program
93491 9OLJ.00 DAFNE diabetes structured education program completed
93657 8Hj4.00 Referral to DESMOND diabetes structured education program
93631 9OLL.00 XPERT diabetes-structured education program completed
93704 8Hj3.00 Referral to DAFNE diabetes structured education program
93727 C10FE11 Type 2 DM with diabetic cataract
93854 9OLM.00 Diabetes-structured education program declined
93870 8Hj5.00 Referral to XPERT diabetes-structured education program
93875 C10E712 IDDM with retinopathy
93878 C10E511 Type 1 DM with ulcer

Abbreviations: IDDM, insulin dependent diabetes mellitus; CSQ, (Diabetes) clinic satisfaction questionnaire; DM, diabetes mellitus; NEC, not elsewhere classified; NOS, not otherwise specified; NIDDM, noninsulin dependent diabetes mellitus; DAFNE, Dose Adjustment For Normal Eating; DESMOND, Diabetes Education and Self-Management for Ongoing and Newly Diagnosed.

Table S2.

Read codes for DPNP

Medcode Read code Read term
1. Painful diabetic neuropathy
48078 F372000 Acute painful diabetic neuropathy
35785 F372100 Chronic painful diabetic neuropathy
2. Diabetic neuropathy (+ pain medication)
2342 F372.12 Diabetic neuropathy
5002 F372.11 Diabetic polyneuropathy
16230 C106.00 DM with neurological manifestation
16491 C106.13 DM with polyneuropathy
17247 F35z000 Diabetic mononeuritis NOS
18056 2G5C.00 Foot abnormality, diabetes-related
18230 C108J12 Type 1 DM with neuropathic arthropathy
22573 C106z00 DM NOS with neurological manifestation
24694 C108B00 IDDM with mononeuropathy
27921 2G51000 Foot abnormality, diabetes-related
31790 F372.00 Polyneuropathy in diabetes
41716 C108C00 IDDM with polyneuropathy
42831 C10E200 Type 1 DM with neurological complications
43227 C10F311 Type 2 DM with multiple complications
44033 F345000 Diabetic mononeuritis multiplex
45276 C10E312 IDDM with multiple complications
45467 C109B00 NIDDM with polyneuropathy
45919 C109212 Type 2 DM with neurological complications
47409 C109B11 Type 2 DM with polyneuropathy
47650 C10E300 Type 1 DM with multiple complications
34152 G73y000 Diabetic peripheral angiopathy
34268 C10F200 Type 2 DM with neurological complications
35385 C10FH00 Type 2 DM with neuropathic arthropathy
37315 F3y0.00 Diabetic mononeuropathy
39317 C106100 DM, adult onset + neurological manifestation
39809 C108J00 IDDM with neuropathic arthropathy
54899 C109F11 Type 2 DM with peripheral angiopathy
55842 C109200 NIDDM with neurological complications
60208 C108J11 Type 1 DM with neuropathic arthropathy
60699 C109F12 Type 2 DM with peripheral angiopathy
72320 C109A00 NIDDM with mononeuropathy
91942 C10E311 Type 1 DM with multiple complications
7795 C106.12 DM with neuropathy
11663 M271100 Neuropathic diabetic ulcer – foot
61523 C106y00 Other specified DM with neurological comps
61829 C108212 Type 1 DM with neurological complications
65267 C10F300 Type 2 DM with multiple complications
67853 C106000 DM, juvenile + neurological manifestation
67905 C109211 Type 2 DM with neurological complications
98616 C10F211 Type 2 DM with neurological complications
99231 C108B11 Type 1 DM with mononeuropathy
101735 C10E212 IDDM with neurological comps
49146 C108211 Type 1 DM with neurological complications
50813 C109A11 Type 2 DM with mononeuropathy
52283 C108200 IDDM with neurological comps
54212 C109F00 NIDDM with peripheral angiopathy
3. Neuropathic (pain + diabetes)
35537 Fyu7C00 [X] Polyneuropathy, unspecified
2790 F367.00 Peripheral neuropathy
3958 F366.00 Polyneuropathy
97306 Fyu7200 [X] Other specified polyneuropathies
55076 Fyu7.00 [X] Polyneuropathies and other disorder of peripheral nervous system
24226 F37z.11 Polyneuropathy unspecified
4. Neuralgia (+ diabetes + pain medication)
2284 N242000 Neuralgia unspecified
54992 N242.00 Neuralgia, neuritis, and radiculitis unspecified
23839 N242z00 Neuralgia, neuritis, or radiculitis NOS

Note: [X] Cross referenced to specific ICD-10 codes (other READ terms relate to ICD-9).

Abbreviations: DPNP, diabetic peripheral neuropathic pain; DM, diabetes mellitus; IDDM, insulin-dependent diabetes mellitus; NIDDM, noninsulin-dependent diabetes mellitus.

Table S3.

Read codes for DPNP screening

Medcode Read code Read term
1. Painful diabetic neuropathy
10977 66Ac.00 Diabetic peripheral neuropathy screening
12247 8I6G.00 Diabetic foot examination not indicated
22823 66Ab.00 Diabetic foot examination
95994 66Aq.00 Diabetic foot screen

Abbreviation: DPNP, diabetic peripheral neuropathic pain.


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