Evidence map›Paper›PMID 23602044›Full record

ReviewDiabetes, obesity & metabolism2013

A review of artificial pancreas technologies with an emphasis on bi-hormonal therapy.

P A Bakhtiani, L M Zhao, J El Youssef, J R Castle, W K Ward

Open access · bronzeAbstract readReview
In one paragraph

Review in Diabetes, obesity & metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
5.3field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Current status and issues of the artificial pancreas: abridged English translation of a special issue in Japanese.Journal of artificial organs : the official journal of the Japanese Society for Artificial Organs · 2018
    Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Immune interventions to preserve β cell function in type 1 diabetes.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2016
    Review
  18. A Review of Emerging Technologies for the Management of Diabetes Mellitus.IEEE transactions on bio-medical engineering · 2015
    Review
  19. Artificial Pancreas Project at Cambridge 2013.Diabetic medicine : a journal of the British Diabetic Association · 2015
    Review
  20. T1DM in 2014: Progress towards a bionic pancreas.Nature reviews. Endocrinology · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

P A BakhtianiHarold Schnitzer Diabetes Center, Oregon Health and Science University, Portland, OR, USA.
L M Zhao
J El Youssef
J R Castle
W K Ward
Oregon Health & Science University · USLegacy Health · US

Funding

OREGON CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTEUL1RR024140 · NCRR · OREGON HEALTH & SCIENCE UNIVERSITY · PI ORWOLL, ERIC S. · 2006 to 2011
$61.1M
Optimization of an Adaptive Dual-Hormone External Endocrine Pancreas.K23DK090133 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI EL YOUSSEF, JOSEPH · 2011 to 2015
$863k
NCRR NIH HHS UL1 RR024140NIDDK NIH HHS 5K23DK090133-03NIDDK NIH HHS K23 DK090133
6 · The paper itself

Abstract

Since the discovery of insulin, great progress has been made to improve the accuracy and safety of automated insulin delivery systems to help patients with type 1 diabetes achieve their treatment goals without causing hypoglycaemia. In recent years, bioengineering technology has greatly advanced diabetes management, with the development of blood glucose meters, continuous glucose monitors, insulin pumps and control systems for automatic delivery of one or more hormones. New insulin analogues have improved subcutaneous absorption characteristics, but do not completely eliminate the risk of hypoglycaemia. Insulin effect is counteracted by glucagon in non-diabetic individuals, while glucagon secretion in those with type 1 diabetes is impaired. The use of glucagon in the artificial pancreas is therefore a logical and feasible option for preventing and treating hypoglycaemia. However, commercially available glucagon is not stable in aqueous solution for long periods, forming potentially cytotoxic fibrils that aggregate quickly. Therefore, a more stable formulation of glucagon is needed for long-term use and storage in a bi-hormonal pump. In addition, a model of glucagon action in type 1 diabetes is lacking, further limiting the inclusion of glucagon into systems employing model-assisted control. As a result, although several investigators have been working to help develop bi-hormonal systems for patients with type 1 diabetes, most continue to utilize single hormone systems employing only insulin. This article seeks to focus on the attributes of glucagon and its use in bi-hormonal systems.

Indexed as

Pancreas, ArtificialBlood GlucoseDiabetes Mellitus, Type 1ForecastingGlucagonHumansHyperglycemiaHypoglycemiaHypoglycemic AgentsInsulinsBlood GlucoseGlucagonHypoglycemic AgentsInsulinsCSIIdiabetes complicationsglycaemic controlinsulin intensive managementinsulin pump therapytype 1 diabetes

Identifiers

PMID23602044
PMCPMC3766424
OpenAlexW2003594741

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.