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Insulin infusion and glucose monitoring: a guideline for

diabetes technologies

Comment by Jennifer Sherr,

MD, PhD

In this modern day of diabetes management, healthcare providers are faced with a vast array of tools to assist our patients

as we strive to help themmeet prescribed glycaemic targets. Yet, determination of who would benefit from the application

of diabetes technologies to their regimens is, at times, less clear.

T

o help address this question,

the Endocrine Society ap-

pointed a Task Force of seven

experts, a methodologist, and a

medical writer. Use of two diabe-

tes technologies was considered:

continuous subcutaneous insulin

infusions (insulin pumps) and real-

time continuous glucose monitors

(RT-CGM). To quantify the degree

with which the task force endorsed a

certain recommendation, the terms

“we recommend” was indicative of

a strong recommendation, whereas

a weak recommendation was identi-

fied by the phrase “we suggest.”

For those with type 1 diabetes

(T1D), the guidelines recommend

consideration of pump use in those

who have not achieved their A1c

goal and in those who have reached

target but experience severe hypo-

glycaemia or high glucose variability.

Both of these recommendations

were qualified by the statement that

the patient needed to be “willing and

able to use the device.”

Most individuals living with T1D

would fall into one of these two

categories, and thus be considered

a candidate for pump therapy. Pump

use was suggested to be considered

in those with type 2 diabetes (T2D)

who failed to achieve targeted gly-

caemic control despite adherence

to a prescribed medical regimen, in-

cluding glucose monitoring, lifestyle

modifications, and use of intensive

insulin therapy in conjunction with

oral or injectable agents. Addition-

ally, continuation of pumps during

hospitalisation is also feasible, as

long as a protocol for this and safety

measures are in place.

In the case of RT-CGM, for those

with T1D, the same criteria for the

use of pumps was applied to sensor

use contingent on the patient being

willing to use the device on a nearly

daily basis. However, in those with

T2D, only short-term, intermittent

use of these devices for those with

A1c >7% was suggested.

Educating patients on the various

features that pumps and RT-CGM

is essential. Indeed, the guidelines

highlight that the use of bolus cal-

culators is suggested for those on

pump therapy. Only by educating

our patients on pump features (bo-

lus calculators, advanced boluses,

the ability to have multiple basal

rates, temporary basal rates, etc) and

RT-CGM features (real time alarms

and retrospective review of reports),

can we expect them to reap the full

benefit of these technologies. If one

were to merely manually bolus with

an insulin pump, it would be like

using a smartphone simply to make

calls.

Determination of who would be

an acceptable candidate and thus

benefit from these technologies is

essential, especially due to the cost

associated with their use. Impor-

tantly, based on the guidelines it

seems most adults with T1D who

are motivated and willing to use

them would be candidates for both

pump and RT-CGM use. Preparing

patients by integrating use of these

technologies into their daily lives

now will be critical as we move to-

wards the marriage of these devices

through closed loop insulin delivery

systems.

Dr Sherr is Instructor, Pediatrics

(Endocrinology), Yale University

School of Medicine, New

Haven, Connecticut.

JOURNAL SCAN

Increased mortality in people with impaired glucose tolerance after the onset of diabetes

Diabetes Care

Take-home message

This study included 542 patients with impaired glucose tolerance participating in a lifestyle diabetes prevention trial who were

followed for 23 years. Of these patients, 174 died during follow-up. The overall death rate was 15.9/1000 person-years, with age-

adjusted death rates of 11.1/1000 person-years before development of type 2 diabetes and 19.4/1000 person-years after diabetes

development. An adjusted, time-dependent multivariate analysis revealed that development of type 2 diabetes was associated

with a 73% increased risk of death.

This study demonstrates that a large portion of the increased mortality risk in patients with impaired glucose tolerance is attribut-

able to development of type 2 diabetes.

Abstract

OBJECTIVE

People with impaired glucose tolerance (IGT) have in-

creased risk of mortality and a high risk of progression to diabetes,

but the extent that the excess mortality is associated with IGT per se

or is the result of subsequent diabetes is unclear.

RESEARCH DESIGN AND METHODS

We compared mortality before and

after the development of diabetes among 542 persons with IGT

initially who participated in a 6-year lifestyle diabetes prevention

trial and were followed-up from 1986 to 2009.

RESULTS

During the 23-year follow-up, 174 (32.1%) died, with an overall

death rate of 15.9/1,000 person-years. The majority of deaths (74.7%;

130 of 174) occurred after progression to type 2 diabetes, with age-

adjusted death rates of 11.1/1,000 person-years (95% CI 8.2–12.0)

before and 19.4/1,000 person-years (95% CI 11.9–23.3) after the de-

velopment of type 2 diabetes. The cumulative mortality was 37.8%

(95% CI 33.1–42.2%) in participants who developed type 2 diabetes

during first 10 years of follow-up, 28.6% (95% CI 21.6–35.0%) in those

who progressed to type 2 diabetes in 10–20 years, and 13.9% (95%

CI 7.0–20.3%) in those who did not develop to type 2 diabetes within

20 years. Time-dependent multivariate Cox proportional hazards

analyses, with adjustment for baseline age, sex, intervention, and

other potential confounding risk factors, showed that the development

of type 2 diabetes was associated with a 73% higher risk of death

(hazard ratio 1.73 [95% CI 1.18–2.52]).

CONCLUSIONS

As elsewhere, IGT is associated with increased risk of

mortality in China, but much of this excess risk is attributable to the

development of type 2 diabetes.

Changes in mortality in people with IGT before and after the

onset of diabetes during the 23-year follow-up of the Da Qing

Diabetes Prevention Study

Diabetes Care

2016;39:1550-1555,

Gong Q, Zhang V, Wang J, et al.

Diabetes technology – continuous subcutaneous

insulin infusion therapy and continuous glucose

monitoring in adults: an Endocrine Society

clinical practice guideline

The Journal of Clinical Endocrinology and Metabolism

Take-home message

Current treatments such as continuous subcutaneous insulin infusion and

continuous glucose monitoring play an important part in the manage-

ment of diabetes. This evidence-based, clinical practice guideline offers

a literature review and recommendations for use in adult patients.

Data on the use of medical devices are limited. However, current studies

do support the use of technology for the treatment of diabetes.

Abstract

OBJECTIVE

To formulate clinical practice

guidelines for the use of continuous

glucose monitoring and continuous

subcutaneous insulin infusion in adults

with diabetes.

PARTICIPANTS

The participants include

an Endocrine Society-appointed Task

Force of seven experts, a methodolo-

gist, and a medical writer. The Ameri-

can Association for Clinical Chemistry,

the American Association of Diabetes

Educators, and the European Society

of Endocrinology co-sponsored this

guideline.

EVIDENCE

The Task Force developed

this evidence-based guideline using

the Grading of Recommendations, As-

sessment, Development, and Evalua-

tion system to describe the strength

of recommendations and the quality

of evidence. The Task Force commis-

sioned one systematic review and

used the best available evidence from

other published systematic reviews

and individual studies.

CONSENSUS PROCESS

One group meet-

ing, several conference calls, and

e-mail communications enabled con-

sensus. Committees and members of

the Endocrine Society, the American

Association for Clinical Chemistry, the

American Association of Diabetes

Educators, and the European Society

of Endocrinology reviewed and com-

mented on preliminary drafts of these

guidelines.

CONCLUSIONS

Continuous subcutane-

ous insulin infusion and continuous

glucose monitoring have an important

role in the treatment of diabetes. Data

from randomized controlled trials are

limited on the use of medical devices,

but existing studies support the use of

diabetes technology for a wide variety

of indications. This guideline presents

a review of the literature and practice

recommendations for appropriate

device use.

J Clin Endocrinol Metab

2016 Sep

02;[Epub ahead of print], Peters AL,

Ahmann AJ, Battelino T, et al.

DIABETES

PRACTICEUPDATE ENDOCRINOLOGY

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