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SAMJ: South African Medical Journal

On-line version ISSN 2078-5135
Print version ISSN 0256-9574

SAMJ, S. Afr. med. j. vol.111 n.2 Pretoria Feb. 2021

http://dx.doi.org/10.7196/samj.2021.v111i2.15451 

CORRESPONDENCE

 

Artifactual hypoglycaemia in a patient with scleroderma and Raynaud s phenomenon

 

 

To the Editor: A 52-year-old woman was referred to our emergency centre with a 1-day history of diarrhoea. The referring clinician noted that the patient was hypoglycaemic and that finger-prick glucose levels remained low, despite numerous intravenous boluses of 50 mL 50% dextrose solution. On presentation to our centre, the patient was alert and co-operative, with a normal mental state. Her vital signs were within normal limits, but she was found to have concomitant persistent hypoglycaemia (-2.9 mmol/L) on a point-of-care glucometer, in the absence of hypoglycaemic symptoms.

On clinical evaluation, the patient had features of systemic sclerosis. She also had sclerodactyly (skin thickening of the fingers distal to the metacarpophalangeal joints) and bilateral Raynaud's phenomenon. The patient did not have the classic sympathetic and neuroglycopenic symptoms that accompany hypoglycaemia and, therefore, did not satisfy Whipple's triad. Whipple's triad confirms true hypoglycaemia and includes the following criteria: typical symptoms of hypoglycaemia, with low plasma glucose measured at the time of the symptoms, and relief of these symptoms when the glucose is raised to a normal level.[1] Clinically relevant hypoglycaemia is defined as a blood glucose <3.0 mmol/L, while levels <3.9 mmol/L should be regarded as a cautionary signal.[2] Plasma glucose levels measured at the same time as point-of-care glucose levels were normal.

The mechanism of artifactual hypoglycaemia can be explained by progressive obliteration of the capillary microcirculation; therefore, the blood flow in the utmost distal parts of the fingers becomes compromised, which leads to false low readings on glucometers.[3,4] Clinicians should be alert to other clinical states, such as cardiac diseases with peripheral cyanosis, peripheral vascular disease and hypoperfusion due to shock, which are commonly observed in emergency centres. These conditions are also associated with an impaired capillary flow and subsequent artifactual hypoglycaemia.[3]

This case highlights the importance of clinical examination and early identification of artifactual hypoglycaemia, which can prevent unnecessary treatment and possible iatrogenic complications.

Ridwaan Osman

Department of Emergency Medicine, Khayelitsha Hospital, Cape Town, South Africa

Elaine Erasmus

Department of Emergency Medicine, Khayelitsha Hospital, and Division of Emergency Medicine, Department of Family and Emergency Medicine, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa

Sa'ad Lahri

Department of Emergency Medicine, Khayelitsha Hospital, and Division of Emergency Medicine, Department of Family and Emergency Medicine, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa slahri7@gmail.com

Farzana Moosajee

Division of Rheumatology, Department of Medicine, Faculty of Medicine and Health Sciences, Tygerberg Hospital and Stellenbosch University, Cape Town, South Africa

 

References

1. Bishay RH, Suryawanshi A. Artifactual hypoglycaemia in systemic sclerosis and Raynaud's phenomenon: A clinical case report and short review. Case Rep Endocrinol 2016;2016:1. https://doi.org/10.1155/2016/7390927        [ Links ]

2. Kaplan H, Amod A, van Zyl FH, et al. Incidence of hypoglycaemia in the South African population with diabetes: Results from the IDMPS wave 7 study. J Endocrinol Metab Diabet S Afr 2019;24(2):58-64. https://doi.org/10.1080/16089677.2019.1608053        [ Links ]

3. Mertens J, Haddad M. Artifactual hypoglycemia in a patient with systemic sclerosis. Acta Clinica Belgica 2020:1-6. https://doi.org/10.1080/17843286.2020.1837575        [ Links ]

4. Fleischmajer R, Perlish JS. Capillary alterations in scleroderma. J Am Acad Dermatol 1980;2(2):161-170. https://doi.org/10.1016/S0190-9622(80)80396-3        [ Links ]

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