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1.
Clin Oncol (R Coll Radiol) ; 35(7): e421-e433, 2023 07.
Article in English | MEDLINE | ID: mdl-37019693

ABSTRACT

Vaccination has become an essential means of protection for solid tumour patients against coronavirus disease 2019 (COVID-19). In this systematic review, we sought to identify common safety profiles of the COVID-19 vaccine in patients with solid tumours. A search of Web of Science, PubMed, EMBASE and Cochrane was conducted for studies in English full-text that reported side-effect data experienced by patients with cancer who were at least 12 years old with solid tumours or a recent history of solid tumours after receiving either one or multiple doses of the COVID-19 vaccination. Study quality was assessed with the Newcastle Ottawa Scale criteria. Acceptable study types were retrospective and prospective cohorts, retrospective and prospective observational studies, observational analyses and case series; systematic reviews, meta-analyses and case reports were excluded. Among local/injection site symptoms, the most commonly reported were injection site pain and ipsilateral axillary/clavicular lymphadenopathy, whereas the most commonly reported systemic effects were fatigue/malaise, musculoskeletal symptoms and headache. Most side-effects reported were characterised as mild to moderate. A thorough evaluation of the randomised controlled trials for each featured vaccine led to the conclusion that in the USA and abroad, the safety profile seen in patients with solid tumours is comparable with that seen in the general public.


Subject(s)
COVID-19 Vaccines , COVID-19 , Neoplasms , Child , Humans , COVID-19/epidemiology , COVID-19/prevention & control , COVID-19 Vaccines/adverse effects , Observational Studies as Topic , Prospective Studies , Retrospective Studies , SARS-CoV-2 , Vaccination/adverse effects
2.
J Intellect Disabil Res ; 62(10): 854-863, 2018 10.
Article in English | MEDLINE | ID: mdl-30117608

ABSTRACT

BACKGROUND: Associations between childhood adversity and negative health outcomes are well documented within the general population; however, this relationship has yet to be confirmed in adults with intellectual and developmental disabilities (I/DD). Bridging the gap between public health and I/DD research is critical in order to better understand the ways in which the health of people with I/DD are compromised by adversity and social disadvantage and to develop preventative care frameworks and health-promoting practices specifically for adults with I/DD. The aim of this exploratory study was to examine the relationships among adversity, physical health and quality of life in a sample of adults with I/DD. METHOD: Participants were adults with I/DD currently residing within campus-based residences. Demographic data, psychiatric and medical diagnoses, adverse childhood experiences scores and quality of life scores were aggregated from participants' electronic medical records. A health history form was completed for each participant based on a review of participants' medical records. RESULTS: Results indicated childhood adversity was significantly associated with number of chronic medical conditions (r = .35, P < .001, 95% BCa CI [.13, .53]). Childhood adversity was not significantly related to quality of life. After controlling for demographic variables, childhood adversity remained a significant predictor of health history (B = .32, P < .005, 95% BCa CI [.10, .52]), with greater adversity predicting greater medical illness. CONCLUSION: Participants demonstrated higher rates of childhood adversity compared with the general population, suggesting that individuals with I/DD may be particularly vulnerable to experiencing adversity during development. Childhood adversity was a significant predictor of physical illness in adults with I/DD. These findings emphasise the importance of screening for childhood adversity histories in adults with I/DD. Additionally, results demonstrate the importance of offering preventative interventions geared at preventing physical illness and promoting health in adults with I/DD with adversity and trauma backgrounds.


Subject(s)
Adverse Childhood Experiences , Developmental Disabilities , Health Status , Intellectual Disability , Adult , Adverse Childhood Experiences/statistics & numerical data , Developmental Disabilities/epidemiology , Female , Humans , Intellectual Disability/epidemiology , Male , Middle Aged , Quality of Life , Residential Facilities
4.
Anal Quant Cytol Histol ; 15(5): 317-22, 1993 Oct.
Article in English | MEDLINE | ID: mdl-7505081

ABSTRACT

Previous studies have demonstrated quantitation of epidermal growth factor receptors (EGFR) to be of prognostic significance in breast, bladder, esophageal and other neoplasms. However, the relatively large quantity of unfixed tissue required for epidermal growth factor radioligand binding assays (RLBA) has precluded its application to cytologic specimens and small biopsy specimens. For this reason we evaluated reverse transcription intron differential polymerase chain reaction (RTIDPCR) as an assay of EGFR gene expression. Squamous cell carcinoma (A431 and SiHa), transitional cell carcinoma (HT1376, T24, RT4), mammary (MCF7) and endocervical (HeLa) adenocarcinoma, and leukemia (K562) cell lines were used to compare RTIDPCR and RLBA. RTIDPCR involved reverse transcription of RNA and amplification of cDNA using primers for beta-actin and EGFR. Good agreement was observed between the RLBA and RTIDPCR results. RNA extracted from fresh cells, Diff-Quik-stained smears and formalin-fixed, paraffin-embedded cell pellet sections yielded similar results. These data suggest that RTIDPCR may be useful in evaluating gene expression by cells processed as cytologic specimens.


Subject(s)
Epidermal Growth Factor/metabolism , ErbB Receptors/genetics , Genes, Neoplasm , Neoplasms/genetics , RNA, Neoplasm/genetics , Adenocarcinoma/genetics , Base Sequence , Carcinoma, Squamous Cell/genetics , Carcinoma, Transitional Cell/genetics , Gene Expression , Humans , Introns/genetics , Leukemia, Myeloid/genetics , Molecular Sequence Data , Polymerase Chain Reaction , Staining and Labeling , Tissue Embedding , Tissue Preservation , Tumor Cells, Cultured
5.
West J Med ; 159(1): 96, 1993 Jul.
Article in English | MEDLINE | ID: mdl-18750931
7.
Arthritis Rheum ; 22(5): 542-6, 1979 May.
Article in English | MEDLINE | ID: mdl-444317

ABSTRACT

A previously unreported case of congenital contractural arachnodactyly (CCA) is described. This hereditary connective tissue abnormality resembles Marfan's syndrome in certain respects, but is characterized by camptodactyly rather than joint laxity, as well as by congenital contractural deformities of the knees and elbows. In addition, there is a peculiar, fairly characteristic deformity of the external ear. Like Marfan's syndrome, it is transmitted in autosomal dominant fashion. Despite the superficial skeletal resemblance, however, the cardiovascular and ocular complications of Marfan's do not seem to occur and therefore differentiation of the two syndromes is important.


Subject(s)
Marfan Syndrome/genetics , Adult , Contracture/congenital , Contracture/genetics , Ear, External/abnormalities , Elbow/abnormalities , Female , Genes, Dominant , Humans , Knee/abnormalities , Marfan Syndrome/diagnostic imaging , Radiography
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