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| ID | Type | Description | Link |
|---|---|---|---|
| 2022-A02234-39 | Other Identifier | ANSM |
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Vitamin C is essential for numerous biological processes as it acts as a cofactor in various hydroxylation reactions, but also as a powerful antioxidant. As humans have lost the ability to synthetize Vitamin C, this micronutrient is found exclusively in the food, and more particularly in fresh fruits and vegetables.
The term 'hypovitaminosis C' refers to a plasmatic Vitamin C concentration < 28 µmol/L. It encompasses two distinct situations, according to the severity of the deprivation:
The epidemiology and risk factors of hypovitaminosis C in ageing populations are poorly documented. The few studies dealing with this question are mostly retrospective, including a low number of patients, and relying on an imperfect methodology. Despite these limitations, data suggest hypovitaminosis C could concern up to 50% of the hospitalized geriatric population.
Despite this probably high prevalence, hypovitaminosis C is barely diagnosed and thus rarely supplemented. This is particularly true for the elderlies who are at risk high of being Vitamin C depleted.
Moreover, several risk factors have been described to be associated with Vitamin C depletion or deficiency, sometimes both. But only a few of them have been validated for the geriatric population.
Thus, there is a real need for a better understanding of hypovitaminosis C epidemiology and risk factors in the geriatric population, in order to diagnose earlier, more frequently, and more precisely these cases. It is important to note that an easy and safe supplementation exists (1 g of Vitamin C for 2 weeks).
A better understanding of risk factors is also a key element to apply corrective measures on modifiable risk factors in order to prevent the recurrence of hypovitaminosis C.
In the present research protocol, the investigators hypothesized hypovitaminosis C could concern half of the hospitalized geriatric patients in acute care units.
The primary objective of this study is to evaluate the prevalence of hypovitaminosis C in a geriatric acute care unit, by using a prospective design and including a statistically sufficient number of patients.
The secondary objectives are :
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Elderly patients | Experimental | Only one group of patients will be constituted. It will be composed of 453 patients aged more than 75 years old and hospitalized in a geriatric acute care unit. If the patient consent to participate in the study, a 4-mL blood sample will be collected concomitantly with a general laboratory evaluation that will be performed when the patient enters the unit. No other sample will be taken., and tThe participation of the patient to the study will end after the result of the test or after the end of the vitamin C supplementation. A telephone call is organized to follow up on any adverse effectswith this blood sample collection. No further visit is organised. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Plasmatic Vitamin C concentrations (known as ascorbemia) on a single blood sample | Diagnostic Test | If the patient consents to participate in the study, a 4-mL blood sample will be collected and performed when the patient enters the unit. No other sample will be taken, and the participation of the patient to the study will end after the result of the test or after the end of the vitamin C supplementation. A telephone call is organized to follow up on any adverse effects. The blood sample will be collected up to 3 days after admission |
| Measure | Description | Time Frame |
|---|---|---|
| Plasmatic Vitamin C concentration (ascorbemia). It is expressed in µmol/L and determined using a laboratory assay. | Ascorbemia will be classified as follows:
| Day 1 : Ascorbemia will be measured only once for each patient, concomitantly with a general laboratory evaluation that will be performed when the patient enters the unit. |
| Measure | Description | Time Frame |
|---|---|---|
| Plasmatic Vitamin C concentration (ascorbemia). It is expressed in µmol/L and determined using a laboratory assay. | For this secondary outcome, hypovitaminosis C will be divided into two sub-groups:
| Day 1 : Ascorbemia will be measured only once for each patient, concomitantly with a general laboratory evaluation that will be performed when the patient enters the unit. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Service de Médecine Gériatrique of the Hôpital Edouard Herriot (Pavillon K) | Lyon | France |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 37612102 | Background | Quillon A, Guittard L, Goldet K, Etienne M, Blond E, Nourredine M, Martin-Gaujard G, Doh S. A cross-sectional study to evaluate hypovitaminosis C prevalence and risk factors in an acute geriatric unit in Lyon, France: the HYPO-VIT-C protocol. BMJ Open. 2023 Aug 23;13(8):e075924. doi: 10.1136/bmjopen-2023-075924. |
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| ID | Term |
|---|---|
| D001206 | Ascorbic Acid Deficiency |
| ID | Term |
|---|---|
| D001361 | Avitaminosis |
| D003677 | Deficiency Diseases |
| D044342 | Malnutrition |
| D009748 | Nutrition Disorders |
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| Risk factors for Hypovitaminosis C | Information will be collected about the risk factors of interest for Hypovitaminosis C:
| No later than Day 0 : Data are systematically collected during the initial questioning. These data are not specific to the research project. |
| Vitamin C depletion | No later than Day 0 : Data are systematically collected during the initial questioning. These data are not specific to the research project. |
| Vitamin C deficiency | No later than Day 0 : Data are systematically collected during the initial questioning. These data are not specific to the research project. |
| Follow-up of adverse events in case of vitamin C supplementation. | The collection of adverse events from patients supplemented with Vitamin C either by a telephone call from the patient or from the department in which he/she is being treated. | A call will be made no later than 45 days after the sample is taken for patients supplemented with vitamin C. |
| D009750 |
| Nutritional and Metabolic Diseases |