Nutrition and sickle cell disease

Reid, Marvin

doi:10.1016/j.crvi.2012.09.007

Cited by 29 publications

(29 citation statements)

References 109 publications

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“…Results from the study sample discussed in this article are consistent with characteristics of SS, SC, and SB+ thal and SB0 thal as documented in the literature (Mann‐Jiles & Morris, ; McGann et al., ; Reid, ; Tanabe et al., ). These associations are important in order to appropriately categorize several other findings in this study.…”

Section: Discussionsupporting

confidence: 89%

“…Persons with SCD often suffer from growth retardation and nutritional wasting. Increased metabolic demands with protein turnover and fluctuations of glucose and lipids are responsible for nutritional deficits (Reid, ). This significant negative energy balance can result in an increased rate of hospitalizations and poor clinical outcomes.…”

Section: Introductionmentioning

confidence: 99%

“…This significant negative energy balance can result in an increased rate of hospitalizations and poor clinical outcomes. Therefore, adequate nutrition and rest are essential to maximize outcomes for sickle cell patients, as complications related to the disease exacerbate metabolic demands (Reid, ). A low energy intake may be because of appetite suppression; elevated energy expenditures may be related to hemolysis, body composition, and inflammation (Reid, ).…”

Section: Introductionmentioning

confidence: 99%

“…SCD is a disease of autosomal recessive disorders with an inheritance of the hemoglobin S allele. SCD can occur in a homozygous state, such as sickle anemia, or can occur with another allele such as hemoglobin C or with a beta thalassemic allele (Mann‐Jiles & Morris, ; Reid, ). The most common genotypes seen in SCD are sickle cell anemia (HbSS), sickle C diseases (HbSC), sickle beta plus thalassemia (HbSB+ thal), and sickle beta null thalassemia (HbSB0thal).…”

Section: Introductionmentioning

confidence: 99%

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Sleep impairment and insomnia in sickle cell disease: A retrospective chart review of clinical and psychological indicators

Mann-Jiles

Thompson

Lester

2015

Journal of the American Association of Nurse Practitioners

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Purpose To examine clinical and psychological indicators associated with sleeplessness and insomnia in adult patients with sickle cell. Data sources PubMed, Scopus, Cochrane Library. Data were collected from adult sickle cell participants (N = 72) in outpatient clinics at a Midwest National Cancer Institute designated comprehensive cancer center. A retrospective chart review observed for clinical and psychological indicators associated with sleeplessness and insomnia. Conclusions Findings included that adults with sickle cell experienced insomnia (47%) and sleep impairment (15%). Significant associations existed between pain and sleep impairment (p = .00), insomnia and pain (p = .00), morning hours of sleep (p = .00), and evening hours (p = .00). Pain may contribute to insomnia or interrupt sleep; daytime sleeping was not conducive to nighttime sleep. Anxiolytics, antidepressants, and long‐acting opioids were not associated with insomnia (p = .00, p = .43, and p = .10), respectively; reduction in anxiety may reduce insomnia. Long‐acting opioids may provide for improved pain control sleep. Implications for practice Healthcare providers play a pivotal role in the assessment of sleep impairment or disorders. Effective management is necessary for improved quality of life. Further investigation is warranted to understand the meaning of sleep impairment in adult patients with sickle cell with prospective controlled studies to examine the efficacy of interventions.

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Section: Discussionsupporting

confidence: 89%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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Sleep impairment and insomnia in sickle cell disease: A retrospective chart review of clinical and psychological indicators

Mann-Jiles

Thompson

Lester

2015

Journal of the American Association of Nurse Practitioners

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“…However cerebral flow velocity was not correlated with BMI z ‐scores in their small sample. We have reported a high prevalence of malnutrition in children with SCA in Jamaica (Reid, ) and that iron deficiency anaemia is common (King et al , ). However, the relative contribution of nutritional status and haematology to TAMV and stroke risk in children with SCA in Jamaica has not been investigated.…”

mentioning

confidence: 99%

Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition

et al. 2018

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This study investigated the association of nutritional and haematological variables with maximum time-averaged mean velocity (TAMV) measured by transcranial Doppler (TCD) velocity and the agreement of classification between two protocols. TCD categories included: normal (<170 cm/s), conditional (170-199 cm/s) and abnormal (≥200 cm/s) based on TAMV in distal internal carotid artery (dICA), middle cerebral artery (MCA), internal carotid bifurcation, anterior and posterior cerebral arteries. Of 358 children with sickle cell anaemia (SCA) examined, the mean age (±standard deviation) was 7·4 ± 2·7 years; 13·1% and 6·7% had conditional and abnormal velocities, respectively. Children with abnormal TCD velocities had higher prevalence of prior stroke (P = 0·006). Increased TAMV was associated with younger age (P = 0·001), lower weight (P = 0·001), height (P = 0·007) and oxygen saturation (P = 0·005). There was no association of TAMV with height-age or body mass index (BMI) z-scores. Adjusting for gender, BMI z-score, age, previous stroke and oxygen saturation, mean corpuscular volume (P = 0·005) and reticulocyte count (P = 0·013) were positively associated with TAMV, while haemoglobin concentration (P = 0·009) was negatively associated. There was good agreement [99%; weighted Kappa 0·98 (95% confidence interval 0·89-1), P = 0·0001] in TCD classification using data from five vessels versus two vessels (dICA and MCA). Haematological variables, rather than nutritional status, may be useful markers that identify high-risk children with SCA.

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Functional foods: promising therapeutics for Nigerian Children with sickle cell diseases

Alabi

Adegboyega

Olawoyin

et al. 2022

Heliyon

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Nutrition and sickle cell disease

Cited by 29 publications

References 109 publications

Sleep impairment and insomnia in sickle cell disease: A retrospective chart review of clinical and psychological indicators

Sleep impairment and insomnia in sickle cell disease: A retrospective chart review of clinical and psychological indicators

Transcranial Doppler velocity among Jamaican children with sickle cell anaemia: determining the significance of haematological values and nutrition

Functional foods: promising therapeutics for Nigerian Children with sickle cell diseases

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