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Review
. 2020 Aug;26(4):379-385.
doi: 10.1097/MCC.0000000000000734.

Bone metabolism and fracture risk during and after critical illness

Affiliations
Free article
Review

Bone metabolism and fracture risk during and after critical illness

Anne-Françoise Rousseau et al. Curr Opin Crit Care. 2020 Aug.
Free article

Abstract

Purpose of review: There is growing evidence that bone health is impacted during and after critical illness in multiple ways. In this review, we provide a practical update on postcritical care bone loss with an insight on identification of persons at risk, prevention and treatment strategies.

Recent findings: Critical illness is associated with an increase in bone turnover and with an uncoupling between bone resorption and bone formation. This results in loss of bone mass, as highlighted by changes in bone marker serum levels and in bone mineral density. Data suggest that ICU survivors are at an increased risk of bone fractures, but this is not completely quantifiable. A key driving factor for ICU-related bone loss, beside inflammation, undernutrition and vitamin D deficiency, is immobilization. Bone health and muscle health are closely related, through myokines and osteokines. Even if not completely proven in the context of critical care, it is likely that preserving muscle mass and strength helps reducing bone loss.

Summary: A history of critical illness should be considered as a strong risk factor for osteopenia and osteoporosis. ICU-related bone loss should be part of the postintensive care syndrome, and should be targeted by prevention and treatment strategies. Optimized and individualized protein and micronutrient provision (with specific attention to calcium, vitamin D and selenium), associated with physiotherapy and muscle training, should be implemented early after ICU admission and continued after ICU discharge. Antiresorptive agents such as biphosphonates should be considered on an individualized basis.

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References

    1. Lee P, Nair P, Eisman JA, Center JR. Bone failure in critical illness. Crit Care Med 2016; 44:2270–2274.
    1. Orford N, Cattigan C, Brennan SL, et al. The association between critical illness and changes in bone turnover in adults: a systematic review. Osteoporos Int 2014; 25:2335–2346.
    1. Klein GL. Burn-induced bone loss: importance, mechanisms, and management. J Burns Wounds 2006; 5:e5.
    1. Gavala A, Makris K, Korompeli A, Myrianthefs P. Evaluation of bone metabolism in critically ill patients using CTx and PINP. BioMed Res Int 2016; 2016:1951707.
    1. Orford NR, Bailey M, Bellomo R, et al. The association of time and medications with changes in bone mineral density in the 2 years after critical illness. Crit Care 2017; 21:69.

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