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Marked improvements in glycaemic outcomes following insulin pump therapy initiation in people with type 1 diabetes: a nationwide observational study in Scotland.
Jeyam, Anita; Gibb, Fraser W; McKnight, John A; Kennon, Brian; O'Reilly, Joseph E; Caparrotta, Thomas M; Höhn, Andreas; McGurnaghan, Stuart J; Blackbourn, Luke A K; Hatam, Sara; McCrimmon, Rory J; Leese, Graham; Lindsay, Robert S; Petrie, John; Chalmers, John; Philip, Sam; Wild, Sarah H; Sattar, Naveed; McKeigue, Paul M; Colhoun, Helen M.
Afiliação
  • Jeyam A; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK. anita.jeyam@igmm.ed.ac.uk.
  • Gibb FW; Royal Infirmary of Edinburgh, Edinburgh Centre for Endocrinology and Diabetes, Edinburgh, UK.
  • McKnight JA; Western General Hospital, NHS Lothian, Edinburgh, UK.
  • Kennon B; Queen Elizabeth University Hospital, Glasgow, UK.
  • O'Reilly JE; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Caparrotta TM; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Höhn A; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • McGurnaghan SJ; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Blackbourn LAK; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • Hatam S; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
  • McCrimmon RJ; Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.
  • Leese G; Ninewells Hospital, Dundee, UK.
  • Lindsay RS; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Petrie J; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • Chalmers J; Diabetes Centre, Victoria Hospital, Kirkcaldy, UK.
  • Philip S; Grampian Diabetes Research Unit, Diabetes Centre, Aberdeen Royal Infirmary, Aberdeen, UK.
  • Wild SH; Usher Institute of Population Health Sciences and Informatics, Centre for Population Health Sciences, School of Molecular, Genetic and Population Health Sciences, University of Edinburgh, Edinburgh, UK.
  • Sattar N; Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
  • McKeigue PM; Usher Institute of Population Health Sciences and Informatics, Centre for Population Health Sciences, School of Molecular, Genetic and Population Health Sciences, University of Edinburgh, Edinburgh, UK.
  • Colhoun HM; MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Diabetologia ; 64(6): 1320-1331, 2021 06.
Article em En | MEDLINE | ID: mdl-33686483
ABSTRACT
AIMS/

HYPOTHESIS:

Our aim was to assess the use of continuous subcutaneous insulin infusion (CSII) in people with type 1 diabetes in Scotland and its association with glycaemic control, as measured by HbA1c levels, frequency of diabetic ketoacidosis (DKA) and severe hospitalised hypoglycaemia (SHH), overall and stratified by baseline HbA1c.

METHODS:

We included 4684 individuals with type 1 diabetes from the national Scottish register, who commenced CSII between 2004 and 2019. We presented crude within-person differences from baseline HbA1c over time since initiation, crude DKA and SHH event-rates pre-/post-CSII exposure. We then used mixed models to assess the significance of CSII exposure, taking into account (1) the diffuse nature of the intervention (i.e. structured education often precedes initiation); (2) repeated within-person measurements; and (3) background time-trends occurring pre-intervention.

RESULTS:

HbA1c decreased after CSII initiation, with a median within-person change of -5.5 mmol/mol (IQR -12.0, 0.0) (-0.5% [IQR -1.1, 0.0]). Within-person changes were most substantial in those with the highest baseline HbA1c, with median -21.0 mmol/mol (-30.0, -11.0) (-1.9% [-2.7, -1.0]) change in those with a baseline >84 mmol/mol (9.8%) within a year of exposure, that was sustained -19.0 mmol/mol (-27.6, -6.5) (-1.7% [-2.5, -0.6]) at ≥5 years. Statistical significance and magnitude of change were supported by the mixed models results. The crude DKA event-rate was significantly lower in post-CSII person-time compared with pre-CSII person-time 49.6 events (95% CI 46.3, 53.1) per 1000 person-years vs 67.9 (64.1, 71.9); rate ratio from Bayesian mixed models adjusting for pre-exposure trend 0.61 (95% credible interval [CrI] 0.47, 0.77; posterior probability of reduction pp = 1.00). The crude overall SHH event-rate in post-CSII vs pre-CSII person-time was also lower 17.8 events (95% CI 15.8, 19.9) per 1000 person-years post-exposure vs 25.8 (23.5, 28.3) pre-exposure; rate ratio from Bayesian mixed models adjusting for pre-exposure trend 0.67 (95% CrI 0.45, 1.01; pp = 0.97). CONCLUSIONS/

INTERPRETATION:

CSII therapy was associated with marked falls in HbA1c especially in those with high baseline HbA1c. CSII was independently associated with reduced DKA and SHH rates. CSII appears to be an effective option for intensive insulin therapy in people with diabetes for improving suboptimal glycaemic control.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Diabetes Mellitus Tipo 1 / Controle Glicêmico / Hipoglicemiantes / Insulina Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Diabetes Mellitus Tipo 1 / Controle Glicêmico / Hipoglicemiantes / Insulina Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article