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1.
J Appl Oral Sci ; 31: e20220480, 2023.
Article in English | MEDLINE | ID: mdl-37194792

ABSTRACT

The use of cocaine and its main derivative, crack, can cause some systemic effects that may lead to the development of some oral disorders. To assess the oral health of people with a crack cocaine use disorder and identify salivary protein candidates for biomarkers of oral disorders. A total of 40 volunteers hospitalized for rehabilitation for crack cocaine addiction were enrolled; nine were randomly selected for proteomic analysis. Intraoral examination, report of DMFT, gingival and plaque index, xerostomia, and non-stimulated saliva collection were performed. A list of proteins identified was generated from the UniProt database and manually revised. The mean age (n=40) was 32 (±8.88; 18-51) years; the mean DMFT index was 16±7.70; the mean plaque and gingival index were 2.07±0.65 and 2.12±0.64, respectively; and 20 (50%) volunteers reported xerostomia. We identified 305 salivary proteins (n=9), of which 23 were classified as candidate for biomarkers associated with 14 oral disorders. The highest number of candidates for biomarkers was associated with carcinoma of head and neck (n=7) and nasopharyngeal carcinoma (n=7), followed by periodontitis (n=6). People with a crack cocaine use disorder had an increased risk of dental caries and gingival inflammation; less than half had oral mucosal alterations, and half experienced xerostomia. As possible biomarkers for 14 oral disorders, 23 salivary proteins were identified. Oral cancer and periodontal disease were the most often associated disorders with biomarkers.


Subject(s)
Crack Cocaine , Dental Caries , Xerostomia , Humans , Crack Cocaine/adverse effects , Crack Cocaine/metabolism , Proteomics , Xerostomia/chemically induced , Xerostomia/metabolism , Saliva/metabolism , Salivary Proteins and Peptides
2.
J. vasc. bras ; 15(2): 126-133, tab
Article in English, Portuguese | LILACS | ID: lil-787535

ABSTRACT

CONTEXTO: O consumo de crack é um dos grandes desafios em saúde pública, e o uso dessa droga tem efeitos diretos na saúde de seus usuários. OBJETIVOS: Avaliar o perfil das alterações vasculares em pacientes com dependência de crack em Centro de Atenção Psicossocial para Álcool e Drogas (CAPS-AD) e observar os possíveis efeitos vasculares periféricos. MÉTODOS: Trata-se de um estudo observacional, descritivo, de corte transversal. Os pacientes da amostra foram submetidos a um questionário objetivo para avaliar questões demográficas, padrão de uso da droga, coexistência de diabetes melito, hipertensão arterial ou tabagismo, exame físico e ecográfico. Os dados foram sumarizados e analisados estatisticamente com teste qui-quadrado ou teste exato de Fisher. RESULTADOS: A média de idade da amostra foi de 33,29 (±7,15) anos, e 74% eram do gênero masculino. A média de idade de início de uso da droga foi de 23,4 (±7,78) anos, com tempo médio de uso de 9,58 (±5,64) anos. O consumo médio diário de pedras de crack foi de 21,45 (±8,32) pedras. A alteração de pulsos em membros inferiores foi mais frequente em mulheres. A prevalência do espessamento da parede arterial nos membros inferiores foi de 94,8%. O tempo de uso da droga apresentou associação estatística (p = 0,0096) com alteração do padrão de curva espectral das artérias dos membros inferiores. CONCLUSÕES: Há alterações vasculares periféricas em usuários de crack. O tempo de uso da droga exerceu um maior impacto nesse sistema, o que sugere associação entre o uso do crack e a diminuição de fluxo arterial.


BACKGROUND: Consumption of crack is one of the major challenges in public health and taking this drug has direct effects on the health of those who use it. OBJECTIVES: To evaluate the profile of vascular abnormalities in patients receiving treatment for crack dependency at a Psychosocial Care Center for Alcohol and Drugs and to observe possible peripheral vascular effects. METHODS: The study design is observational, descriptive and cross-sectional. An objective questionnaire was administered to the patients in the sample to collect data on demographic details; drug use profile; and concomitant diabetes mellitus, arterial hypertension and/or smoking; and physical and ultrasound examinations were conducted. Data were summarized and analyzed statistically with the chi-square test or Fisher’s exact test. RESULTS: The mean age of the sample was 33.29 (±7.15) years, and 74% were male. Mean age at onset of drug use was 23.4 (±7.78) years and mean time since onset was 9.58 (±5.64) years. Mean consumption of crack rocks was 21.45 (±8.32) per day. The rate of abnormal lower limb pulses was higher among women. The prevalence of artery wall thickening in lower limbs was 94.8%. Time since starting to use crack exhibited a statistically significant association (p = 0.0096) with abnormalities in the spectral curve profiles of lower limb arteries. CONCLUSIONS: Crack users exhibit peripheral vascular disorders. Length of time since starting to use the drug had the greatest impact on this system, suggesting an association between crack use and reduced arterial flow.


Subject(s)
Humans , Male , Female , Adult , Crack Cocaine/adverse effects , Crack Cocaine/history , Crack Cocaine/metabolism , Substance-Related Disorders , Substance-Related Disorders/complications , Time Factors , Comorbidity , Prevalence , Cross-Sectional Studies , Surveys and Questionnaires/classification , Venous Thrombosis/complications , Lower Extremity/physiopathology
3.
Drug Alcohol Depend ; 116(1-3): 64-71, 2011 Jul 01.
Article in English | MEDLINE | ID: mdl-21227602

ABSTRACT

BACKGROUND: With an estimated 1 million active injection drug users (IDUs), injection drug use continues to be a public health concern in the United States. Risky injection practices have been associated with the transmission of HIV, Hepatitis B and C, as well as other skin and soft tissue infections. METHODS: We used data from 463 respondents, aged 18 and older, who were past-year IDUs in the 2005-2008 National Survey of Drug Use and Health (NSDUH). We investigated correlates of risky injection behavior among these recent IDUs. RESULTS: Older age (≥ 35 versus 18-25) was associated with reusing one's own needle at last injection (aOR=1.80 [1.02-3.17], as were past year heroin (aOR=2.59 [1.18-5.66]) and cocaine injection (aOR=2.17 [1.13-4.15]). Past year crack cocaine use was positively associated with not cleaning needles with bleach (aOR=2.18 [1.10-4.33]). Past year cocaine injection was associated with obtaining needles in a risky manner (aOR=2.29 [1.23-4.25]). Methamphetamine injection was associated with obtaining needles in less risky ways (aOR=0.41 [0.20-0.84]). CONCLUSION: Our findings indicate that some IDUs are continuing to engage in high risk injection behaviors. The identification of potential at-risk populations of IDUs may have implications for harm reduction interventions and HIV prevention programs.


Subject(s)
Needle Sharing/statistics & numerical data , Risk-Taking , Substance Abuse, Intravenous/epidemiology , Adolescent , Adult , Central Nervous System Stimulants/metabolism , Crack Cocaine/metabolism , Databases, Factual , Drug Users , Female , Humans , Male , Needle Sharing/adverse effects , Needles , Time Factors , United States/epidemiology , United States/ethnology , Young Adult
4.
Anal Chim Acta ; 685(1): 15-20, 2011 Jan 24.
Article in English | MEDLINE | ID: mdl-21168546

ABSTRACT

A new electrochemical method has been described and characterized for the determination of cocaine using screen-printed biosensors. The enzyme cytochrome P450 was covalently attached to screen-printed carbon electrodes. Experimental design methodology has been performed to optimize the pH and the applied potential, both variables that have an influence on the chronoamperometric determination of the drug. This method showed a reproducibility of 3.56% (n=4) related to the slopes of the calibration curves performed in the range from 19 up to 166nM. It has been probed the used of this kind of biosensors in the determination of cocaine in street samples, with an average capability of detection of 23.05±3.53nM (n=3, α=ß=0.05).


Subject(s)
Aryl Hydrocarbon Hydroxylases/metabolism , Biosensing Techniques/methods , Crack Cocaine/analysis , Carbon/chemistry , Crack Cocaine/metabolism , Cytochrome P450 Family 2 , Electrochemistry/methods , Enzymes, Immobilized/metabolism , Reproducibility of Results , Sensitivity and Specificity
5.
Int J Drug Policy ; 21(4): 321-9, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20116989

ABSTRACT

BACKGROUND: There is increasing public health evidence that women who use crack cocaine and are street-involved experience significant health problems and are more isolated with regards to accessing harm reduction and other health-related services. Simultaneously, there is growing acknowledgement that structural and 'everyday' violence are significant factors influencing the health of women who use illegal drugs. Little research has examined how these social processes play out for women who use crack cocaine. METHODS: A critical ethnography informed by the theoretical constructs of structural and everyday violence and intersectionality was undertaken to explore women's use of crack cocaine within an inner-city neighbourhood in Western Canada. Data collection included baseline survey (n=126), participant observation and field notes, informal interviews (n=53), and in-depth interviews (n=13). RESULTS: Based on thematic and theoretical analysis two interrelated themes were identified that reflected the interrelationships between women's use of crack, poverty, discrimination, racism, gendered relations of power, and legal policies and practices: (a) the context of health care; and (b) the smoking context. CONCLUSIONS: Structural inequities and 'everyday' violence are perilously damaging for women who use crack. Interventions to reduce these inequities are urgently needed if we are to reduce the significant suffering of women who are street-involved and use crack cocaine.


Subject(s)
Crack Cocaine/metabolism , Harm Reduction , Poverty , Violence/prevention & control , Women's Health , Adult , Cocaine-Related Disorders , Cross-Sectional Studies , Female , Ill-Housed Persons , Humans , Interview, Psychological , Middle Aged , Observation , Risk Factors , Risk-Taking , Sex Work/psychology , Sexual Behavior , Socioeconomic Factors , Substance Abuse, Intravenous/complications , Urban Population , Violence/psychology
6.
J Forensic Sci ; 42(5): 824-7, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9304829

ABSTRACT

Toxicological investigation of suspected cocaine-related deaths routinely involves the identification of cocaine (COC) and its metabolites including benzoylecgonine (BE) and ecgonine methyl ester (EME) in postmortem specimens. We utilized solid-phase extraction followed by gas chromatography/mass spectrometry for the qualitative and quantitative analysis of cocaine and eight cocaine-related analytes. These analytes included anhydroecgonine methyl ester (AEME), a unique product formed during cocaine smoking, and cocaethylene (CE), formed by transesterification of cocaine in the presence of ethanol. Thirteen pairs of postmortem heart blood and urine specimens were analyzed from cases of death due to acute cocaine intoxication, multiple drug intoxication, or other non-drug related causes. COC, EME, and BE were detected in all specimens. The range of concentrations in blood were: COC, 23-2088 ng/mL; BE, 215-9195 ng/mL; and EME, 220-7275 ng/ mL. AEME was identified in 2 blood and 10 urine specimens, and CE was identified in 1 blood specimen and 4 urine specimens. The identification of AEME in the specimens indicated that "crack" cocaine had been smoked, and the presence of CE indicated co-administration of cocaine and ethanol. The presence of these unique cocaine analysis in postmortem specimens provides valuable information regarding the cause and manner of death.


Subject(s)
Cocaine , Crack Cocaine , Postmortem Changes , Substance-Related Disorders/blood , Substance-Related Disorders/urine , Cocaine/analogs & derivatives , Cocaine/blood , Cocaine/metabolism , Cocaine/urine , Crack Cocaine/metabolism , Gas Chromatography-Mass Spectrometry , Humans , Narcotics/blood , Narcotics/urine , Smoking
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