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Effect of artificial pancreas

systems on glycemic

control in patients with

type 1 diabetes

The Lancet Diabetes & Endocrinology

Take-home message

This meta-analysis of randomized controlled trials eval-

uated the efficacy of single- and dual-hormone artificial

pancreas systems compared with conventional insulin

pump therapy for glucose control in adults and children

with type 1 diabetes. The results show that time in target

glucose range was higher with artificial pancreas systems

and was highest with dual-hormone systems.

The authors concluded that, regardless of varying clinical

factors, artificial pancreas systems are superior to insulin

pump therapy in glucose control.

Abstract

BACKGROUND

Closed-loop artificial pancreas systems have been in

development for several years, including assessment in numerous var-

ied outpatient clinical trials. We aimed to summarise the efficacy and

safety of artificial pancreas systems in outpatient settings and explore

the clinical and technical factors that can affect their performance.

METHODS

We did a systematic review and meta-analysis of randomised

controlled trials comparing artificial pancreas systems (insulin only or

insulin plus glucagon) with conventional pump therapy (continuous subcu-

taneous insulin infusion [CSII] with blinded continuous glucose monitoring

[CGM] or unblinded sensor-augmented pump [SAP] therapy) in adults

and children with type 1 diabetes. We searched Medline, Embase, and

the Cochrane Central Register of Controlled Trials for studies published

from 1946, to Jan 1, 2017. We excluded studies not published in English,

those involving pregnant women or participants who were in hospital,

and those testing adjunct medications other than glucagon. The primary

outcome was the mean difference in percentage of time blood glucose

concentration remained in target range (3.9–10 mmol/L or 3.9–8 mmol/L,

depending on the study), assessed by random-effects meta-analysis.

FINDINGS

We identified984 reports; after exclusions, 27 comparisons from24

studies (23 crossover and one parallel design) including a total of 585 par-

ticipants (219 in adult studies, 265 in paediatric studies, and 101 in combined

studies) were eligible for analysis. Five comparisons assessed dual-hor-

mone (insulin andglucagon), two comparisons assessedboth dual-hormone

and single-hormone (insulin only), and 20 comparisons assessed single-hor-

mone artificial pancreas systems. Time in target was 12.59% higher with

artificial pancreas systems (95% CI 9.02–16.16; p<0.0001), from a weighted

mean of 58.21% for conventional pump therapy (I(2)=84%). Dual-hormone

artificial pancreas systems were associated with a greater improvement in

time in target range compared with single-hormone systems (19.52% [95%

CI 15.12–23.91] vs 11.06% [6.94 to 15.18]; p=0.006), although six of seven

comparisons compared dual-hormone systems to CSII with blinded CGM,

whereas 21 of 22 single-hormone comparisons had SAP as the compara-

tor. Single-hormone studies had higher heterogeneity than dual-hormone

studies (I(2) 79%vs 66%). Bias assessment characteristics were incompletely

reported in 12 of 24 studies, no studies masked participants to the inter-

vention assignment, and masking of outcome assessment was not done

in 12 studies and was unclear in 12 studies.

INTERPRETATION

Artificial pancreas systems uniformly improved glucose

control in outpatient settings, despite heterogeneous clinical and tech-

nical factors.

Effect of artificial pancreas systems on glycaemic control in patients

with type 1 diabetes: a systematic review and meta-analysis of out-

patient randomised controlled trials.

Lancet Diabetes Endocrinol

2017

May 19;[EPub Ahead of Print], A Weisman, JW Bai, M Cardinez, et al.

CONCLUSIONS AND RELEVANCE

Despite possessing health insurance, many

youths with diabetes are not receiving eye examinations by 6 years after

initial diagnosis to monitor for DR. These data suggest that adherence to

clinical practice guidelines is particularly challenging for racial minorities

and youths from less affluent families.

Ophthalmic screening patterns among youths with diabetes enrolled in a

large US Managed Care Network.

JAMA Ophthalmol

2017 Mar 23;[EPub

Ahead of Print], SY Wang, CA Andrews, TW Gardner, et al.

COMMENT

By Raza M Shah

MD

A

s a healthcare community, we’re failing our diabetics. Less

than half of diabetics are getting their annual eye exams.

For primary care providers, this means they’re failing their

Health Effectiveness Data and Information Set (HEDIS) quality

measures. For eye care providers, we’re failing to provide the

care we’ve been trained and sworn to give. For patients, we’re

falling prey to one of the leading causes of vision loss in the

United States. We can come up with many excuses…patients

aren’t following recommendations, referrals aren’t happening

soon enough, access is limited in certain areas, etc. The bot-

tom line is we can do better. We have to do better. But how?

Thankfully, an answer to our question is already here...Intelligent

Retinal Imaging Systems (IRIS). Microsoft recently awarded their

prestigious 2017 Health Innovation Award for IRIS’s diagnostic

solution. By providing the only FDA-approved system, they’ve

created a safe, noninvasive, quick, and accurate way to help

our diabetics. Essentially, they’ve created a way to integrate the

diabetic eye exam with primary care. Instantly, HEDIS measures

are met, people with previously undiagnosed disease can be

identified, and blindness can be prevented.

Diabetic screening involves taking a non-mydriatic photo in

the office and having it sent to a reading center for evaluation.

Within minutes, a report can be generated, which seamlessly

integrates with a practice’s electronic medical record (EMR).

We already know that over 99% of patients who’ve undergone

this method like it enough to recommend it to a friend or col-

league. We also know that seeing your disease with your own

eyes is much more likely to put everything in perspective and

help ensure you take an active role in fighting your disease.

As with any condition, the earlier we’re able to diagnose and treat,

the better our patients will do. As our young diabetic population

continues to skyrocket, we need to be able to keep up and even-

tually get ahead. It not only helps our patients, but can prevent the

need for later-stage, expensive treatments and surgeries that will

eventually cripple the healthcare system.

Does it mean patients don’t need their annual eye exam? Abso-

lutely not. This does not replace the skilled examinations needed

to diagnose and treat many other eye conditions. It does, how-

ever, help identify the nearly 60% of diabetics who previously

were not being seen or treated by eye care providers and help

reduce the risk of severe vision loss by nearly 90%. We owe this

to our patients.

Dr Shah is Retina Surgeon at Mid Atlantic Retina

Specialists in Maryland.

EDITOR’S PICKS

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VOL. 1 • NO. 1 • 2017