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Article: Gender disparities in symptomology of COVID-19 among adults in Arkansas.

Patel, Jenil R / Amick, Benjamin C / Vyas, Keyur S / Bircan, Emine / Boothe, Danielle / Nembhard, Wendy N

2023 Volume 35, Page(s) 102290

Abstract: Only a few studies and reports assessing the natural history and symptomatology for COVID-19 by gender have been reported in literature to date. Thus, the objective of this study was to examine patterns in symptomology of COVID-19 by gender among a ... ...

Abstract	Only a few studies and reports assessing the natural history and symptomatology for COVID-19 by gender have been reported in literature to date. Thus, the objective of this study was to examine patterns in symptomology of COVID-19 by gender among a diverse adult population in Arkansas. Data on COVID-19 symptoms was collected at day of testing, 7th day and 14th day among participants at UAMS mobile testing units throughout the state of Arkansas. Diagnosis for SARS-CoV-2 infection was confirmed via nasopharyngeal swab and RT-PCR methods. Data analysis was conducted using Chi-square test and Poisson regression to assess the differences in characteristics by gender. A total of 60,648 community members and patients of Arkansas received RT-PCR testing. Among adults testing positive, we observed a statistically significant difference for fever (p < 0.001) and chills (p = 0.04). Males were more likely to report having a fever (22.6% vs. 17.1%; p < 0.001) and chills (14.9% vs. 12.6%; p = 0.04) compared to females. Among adults testing negative, females were more likely to report each symptom than males. To conclude, we observed a greater prevalence of certain symptoms such as fever and chills among men testing positive for COVID-19, compared to women during the time of testing. These differences elucidate the important issue of rapidly emerging health disparities during the COVID-19 pandemic.
Language	English
Publishing date	2023-06-23
Publishing country	United States
Document type	Journal Article
ZDB-ID	2785569-7
ISSN	2211-3355
ISSN	2211-3355
DOI	10.1016/j.pmedr.2023.102290
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Article ; Online: Social determinants of health and COVID-19: An evaluation of racial and ethnic disparities in attitudes, practices, and mental health.

Patel, Jenil R / Brown, Clare C / Prewitt, T Elaine / Alfanek, Zain / Stewart, M Kathryn

PLOS global public health

2023 Volume 3, Issue 1, Page(s) e0000558

Abstract: Previous evaluations have reported racial minorities feel they are at greater risk of contracting COVID-19, but that on average, they have better preventative practices, such as wearing face masks and avoiding large gatherings. In this study, we explored ...

Abstract	Previous evaluations have reported racial minorities feel they are at greater risk of contracting COVID-19, but that on average, they have better preventative practices, such as wearing face masks and avoiding large gatherings. In this study, we explored associations between social determinants of health (SDOH), race and ethnicity, COVID-19 practices and attitudes, and mental health outcomes during the pandemic. We examined associations between SDOHs and practices, attitudes, and mental health symptoms by race and ethnicity using multivariable linear and logistic regressions in 8582 Arkansan pulse poll respondents (September-December, 2020). Compared to White respondents, mean attitude and practice scores were greater (indicating safer) among Black (4.90 vs. 3.45 for attitudes; 2.63 vs. 2.41 for practices) and Hispanic respondents (4.26 vs. 3.45 for attitudes; 2.50 vs. 2.41 for practices). Respondents' SDOH scores by race/ethnicity were: White (3.65), Black (3.33), and Hispanic (3.22). Overall, attitude and practice scores decreased by 0.35 and 0.09, respectively, for every one-point increase in SDOH. Overall, a one-point increase in SDOH was associated with 76% and 85% increased odds of screening negative for anxiety and depression, respectively. To conclude, underlying social inequities are likely driving safer attitudes, practices, and worse anxiety and depression symptoms in Black and Hispanic Arkansans. In terms of policy implications, our study supports the urgency of addressing SDOHs for rural states similar to Arkansas.
Language	English
Publishing date	2023-01-23
Publishing country	United States
Document type	Journal Article
ISSN	2767-3375
ISSN (online)	2767-3375
DOI	10.1371/journal.pgph.0000558
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Article: Racial disparities in symptomatology and outcomes of COVID-19 among adults of Arkansas.

Patel, Jenil R / Amick, Benjamin C / Vyas, Keyur S / Bircan, Emine / Boothe, Danielle / Nembhard, Wendy N

Preventive medicine reports

2022 Volume 28, Page(s) 101840

Abstract: Few reports have suggested that non-Hispanic (NH) blacks may present with different symptoms for COVID-19 than NH-whites. The objective of this study was to investigate patterns in symptomatology and COVID-19 outcomes by race/ethnicity among adults in ... ...

Abstract	Few reports have suggested that non-Hispanic (NH) blacks may present with different symptoms for COVID-19 than NH-whites. The objective of this study was to investigate patterns in symptomatology and COVID-19 outcomes by race/ethnicity among adults in Arkansas. Data on COVID-19 symptoms were collected on day of testing, 7th and 14th day among participants at UAMS mobile testing units throughout the state of Arkansas. Diagnosis for SARS-CoV-2 infection was confirmed via nasopharyngeal swab and RT-PCR methods. Data analysis was conducted using Chi-square test and Poisson regression to assess the differences in characteristics by race/ethnicity. A total of 60,648 individuals were RT-PCR tested from March 29, 2020 through October 7, 2020. Among adults testing positive, except shortness of breath, Hispanics were more likely to report all symptoms than NH-whites or NH-blacks. NH-whites were more likely to report fever (19.6% vs. 16.6%), cough (27.5% vs. 26.1%), shortness of breath (13.6% vs. 9.6%), sore throat (16.7% vs. 10.7%), chills (12.5% vs. 11.8%), muscle pain (15.6% vs. 12.4%), and headache (20.3% vs. 17.8%). NH-blacks were more likely to report loss of taste/smell (10.9% vs. 10.6%). To conclude, we found differences in COVID-19 symptoms by race/ethnicity, with NH-blacks and Hispanics more often affected with specific or all symptoms, compared to NH-whites. Due to the cross-sectional study design, these findings do not necessarily reflect biological differences by race/ethnicity; however, they suggest that certain race/ethnicities may have underlying differences in health status that impact COVID-19 outcomes.
Language	English
Publishing date	2022-05-24
Publishing country	United States
Document type	Journal Article
ZDB-ID	2785569-7
ISSN	2211-3355
ISSN	2211-3355
DOI	10.1016/j.pmedr.2022.101840
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Article ; Online: The effectiveness of removal from exposure and reduction of exposure for managing occupational asthma: Summary of an updated Cochrane systematic review.

Henneberger, Paul K / Patel, Jenil R / de Groene, Gerda J / Beach, Jeremy / Tarlo, Susan M / Pal, Teake M / Curti, Stefania

American journal of industrial medicine

2020 Volume 64, Issue 3, Page(s) 165–169

Abstract: Background: The objective was to update the 2011 Cochrane systematic review on the effectiveness of workplace interventions for the treatment of occupational asthma.: Methods: A systematic review was conducted with the selection of articles and ... ...

Abstract	Background: The objective was to update the 2011 Cochrane systematic review on the effectiveness of workplace interventions for the treatment of occupational asthma. Methods: A systematic review was conducted with the selection of articles and reports through 2019. The quality of extracted data was evaluated, and meta-analyses were conducted using techniques recommended by the Cochrane Handbook for Systematic Reviews of Interventions. Results: Data were extracted from 26 nonrandomized controlled before-and-after studies. The mean number of participants per study was 62 and the mean follow-up time was 4.5 years. Compared with continued exposure, removal from exposure had an increased likelihood of improved symptoms and change in spirometry. Reduction of exposure also had more favorable results for symptom improvement than continued exposure, but no difference for change in spirometry. Comparing exposure removal to reduction revealed an advantage for removal with both symptom improvement and change in spirometry for the larger group of patients exposed to low-molecular-weight agents. Also, the risk of unemployment was greater for exposure removal versus reduction. Conclusions: Exposure removal and reduction had better outcomes than continued exposure. Removal from exposure was more likely to improve symptoms and spirometry than reduction among patients exposed to low-molecular-weight agents. The potential benefits associated with exposure removal versus reduction need to be weighed against the potential for unemployment that is more likely with removal from exposure. The findings are based on data graded as very low quality, and additional studies are needed to generate higher quality data.
MeSH term(s)	Adult ; Air Pollutants, Occupational/adverse effects ; Asthma, Occupational/etiology ; Asthma, Occupational/therapy ; Environmental Restoration and Remediation ; Female ; Harm Reduction ; Humans ; Male ; Middle Aged ; Observational Studies as Topic ; Occupational Exposure/adverse effects ; Occupational Exposure/prevention & control ; Occupational Health Services/methods ; Spirometry ; Workplace
Chemical Substances	Air Pollutants, Occupational
Language	English
Publishing date	2020-12-29
Publishing country	United States
Document type	Journal Article ; Meta-Analysis ; Systematic Review
ZDB-ID	604538-8
ISSN	1097-0274 ; 0271-3586
ISSN (online)	1097-0274
ISSN	0271-3586
DOI	10.1002/ajim.23208
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Article ; Online: Workplace interventions for treatment of occupational asthma.

Henneberger, Paul K / Patel, Jenil R / de Groene, Gerda J / Beach, Jeremy / Tarlo, Susan M / Pal, Teake M / Curti, Stefania

The Cochrane database of systematic reviews

2019 Volume 10, Page(s) CD006308

Abstract: Background: The impact of workplace interventions on the outcome of occupational asthma is not well understood.: Objectives: To evaluate the effectiveness of workplace interventions on occupational asthma.: Search methods: We searched the Cochrane ...

Abstract	Background: The impact of workplace interventions on the outcome of occupational asthma is not well understood. Objectives: To evaluate the effectiveness of workplace interventions on occupational asthma. Search methods: We searched the Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE (PubMed); EMBASE(Ovid); NIOSHTIC-2; and CISILO (CCOHS) up to July 31, 2019. Selection criteria: We included all eligible randomized controlled trials, controlled before and after studies and interrupted time-series of workplace interventions for occupational asthma. Data collection and analysis: Two authors independently assessed study eligibility and risk of bias, and extracted data. Main results: We included 26 non-randomized controlled before and after studies with 1,695 participants that reported on three comparisons: complete removal from exposure and reduced exposure compared to continued exposure, and complete removal from exposure compared to reduced exposure. Reduction of exposure was achieved by limiting use of the agent, improving ventilation, or using protective equipment in the same job; by changing to another job with intermittent exposure; or by implementing education programs. For continued exposure, 56 per 1000 workers reported absence of symptoms at follow-up, the decrease in forced expiratory volume in one second as a percentage of a reference value (FEV1 %) was 5.4% during follow-up, and the standardized change in non-specific bronchial hyperreactivity (NSBH) was -0.18.In 18 studies, authors compared removal from exposure to continued exposure. Removal may increase the likelihood of reporting absence of asthma symptoms, with risk ratio (RR) 4.80 (95% confidence interval (CI) 1.67 to 13.86), and it may improve asthma symptoms, with RR 2.47 (95% CI 1.26 to 4.84), compared to continued exposure. Change in FEV1 % may be better with removal from exposure, with a mean difference (MD) of 4.23 % (95% CI 1.14 to 7.31) compared to continued exposure. NSBH may improve with removal from exposure, with standardized mean difference (SMD) 0.43 (95% CI 0.03 to 0.82).In seven studies, authors compared reduction of exposure to continued exposure. Reduction of exposure may increase the likelihood of reporting absence of symptoms, with RR 2.65 (95% CI 1.24 to 5.68). There may be no considerable difference in FEV1 % between reduction and continued exposure, with MD 2.76 % (95% CI -1.53 to 7.04) . No studies reported or enabled calculation of change in NSBH.In ten studies, authors compared removal from exposure to reduction of exposure. Following removal from exposure there may be no increase in the likelihood of reporting absence of symptoms, with RR 6.05 (95% CI 0.86 to 42.34), and improvement in symptoms, with RR 1.11 (95% CI 0.84 to 1.47), as well as no considerable change in FEV1 %, with MD 2.58 % (95% CI -3.02 to 8.17). However, with all three outcomes, there may be improved results for removal from exposure in the subset of patients exposed to low molecular weight agents. No studies reported or enabled calculation of change in NSBH.In two studies, authors reported that the risk of unemployment after removal from exposure may increase compared with reduction of exposure, with RR 14.28 (95% CI 2.06 to 99.16). Four studies reported a decrease in income of 20% to 50% after removal from exposure.The quality of the evidence is very low for all outcomes. Authors' conclusions: Both removal from exposure and reduction of exposure may improve asthma symptoms compared with continued exposure. Removal from exposure, but not reduction of exposure, may improve lung function compared to continued exposure. When we compared removal from exposure directly to reduction of exposure, the former may improve symptoms and lung function more among patients exposed to low molecular weight agents. Removal from exposure may also increase the risk of unemployment. Care providers should balance the potential clinical benefits of removal from exposure or reduction of exposure with potential detrimental effects of unemployment. Additional high-quality studies are needed to evaluate the effectiveness of workplace interventions for occupational asthma.
Language	English
Publishing date	2019-10-08
Publishing country	England
Document type	Journal Article ; Review
ISSN	1469-493X
ISSN (online)	1469-493X
DOI	10.1002/14651858.CD006308.pub4
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Article ; Online: Location of Receipt of Initial Treatment and Outcomes in Long-Term Breast Cancer Survivors.

Sinha, Arup K / Patel, Jenil R / Shen, Yu / Ueno, Naoto T / Giordano, Sharon H / Tripathy, Debu / Lopez, David S / Barcenas, Carlos H

PloS one

2017 Volume 12, Issue 1, Page(s) e0170081

Abstract: Purpose: Cancer outcomes differ depending on where treatment is received. We assessed differences in outcomes in long-term breast cancer survivors at a specialty care hospital by location of their initial treatment.: Methods: We retrospectively ... ...

Abstract	Purpose: Cancer outcomes differ depending on where treatment is received. We assessed differences in outcomes in long-term breast cancer survivors at a specialty care hospital by location of their initial treatment. Methods: We retrospectively examined a cohort of women diagnosed with invasive early-stage breast cancer who did not experience recurrence for at least 5 years after the date of diagnosis and were evaluated at The University of Texas MD Anderson Cancer Center between January 1997 and August 2008. The location of initial treatment was categorized as MD Anderson (MDA-treated) or other (OTH-treated). Outcomes analyzed included recurrence-free survival (RFS), distant relapse-free survival (DRFS), and overall survival (OS). The Kaplan-Meier product-limit method was used to compare outcomes between the two groups. Cox proportional hazards models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI). Results: We identified 5,091 breast cancer survivors (median follow-up 8.6 years), of whom 89.1% were MDA-treated. The 10-year OS, RFS, and DRFS rates were 90.9%, 88.4%, and 89.0% in the MDA-treated group and 74.3%, 49.8%, and 52.7% in the OTH-treated group, respectively. We observed worse outcomes in the OTH-group in both the univariate analysis and the multivariable analysis (OS: HR = 4.8, 95% CI = 3.9-6.0; RFS: HR = 5.8, 95% CI = 4.8-7.0; DRFS: HR = 5.4, 95% CI = 4.5-6.6). Conclusion: Long-term breast cancer survivors who initiated their treatment at MD Anderson had better outcomes. Location of initial treatment could be an independent risk factor for survival outcomes at specialty care hospitals. This analysis has limitations inherent to retrospective observational studies such as other unmeasured variables may be associated with worse prognosis.
MeSH term(s)	Adult ; Biomarkers, Tumor/metabolism ; Breast Neoplasms/mortality ; Breast Neoplasms/pathology ; Breast Neoplasms/therapy ; Carcinoma, Ductal, Breast/mortality ; Carcinoma, Ductal, Breast/pathology ; Carcinoma, Ductal, Breast/therapy ; Carcinoma, Lobular/mortality ; Carcinoma, Lobular/pathology ; Carcinoma, Lobular/therapy ; Combined Modality Therapy ; Female ; Health Services/utilization ; Humans ; Middle Aged ; Neoplasm Grading ; Neoplasm Invasiveness ; Neoplasm Recurrence, Local/mortality ; Neoplasm Recurrence, Local/pathology ; Neoplasm Recurrence, Local/therapy ; Neoplasm Staging ; Prognosis ; Quality of Health Care/organization & administration ; Receptor, ErbB-2/metabolism ; Receptors, Estrogen/metabolism ; Receptors, Progesterone/metabolism ; Retrospective Studies ; Survival Rate
Chemical Substances	Biomarkers, Tumor ; Receptors, Estrogen ; Receptors, Progesterone ; ERBB2 protein, human (EC 2.7.10.1) ; Receptor, ErbB-2 (EC 2.7.10.1)
Language	English
Publishing date	2017
Publishing country	United States
Document type	Journal Article
ISSN	1932-6203
ISSN (online)	1932-6203
DOI	10.1371/journal.pone.0170081
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Article ; Online: Cancer Incidence, Mortality, Years of Life Lost, Years Lived With Disability, and Disability-Adjusted Life Years for 29 Cancer Groups From 2010 to 2019: A Systematic Analysis for the Global Burden of Disease Study 2019.

Kocarnik, Jonathan M / Compton, Kelly / Dean, Frances E / Fu, Weijia / Gaw, Brian L / Harvey, James D / Henrikson, Hannah Jacqueline / Lu, Dan / Pennini, Alyssa / Xu, Rixing / Ababneh, Emad / Abbasi-Kangevari, Mohsen / Abbastabar, Hedayat / Abd-Elsalam, Sherief M / Abdoli, Amir / Abedi, Aidin / Abidi, Hassan / Abolhassani, Hassan / Adedeji, Isaac Akinkunmi /

Adnani, Qorinah Estiningtyas Sakilah / Advani, Shailesh M / Afzal, Muhammad Sohail / Aghaali, Mohammad / Ahinkorah, Bright Opoku / Ahmad, Sajjad / Ahmad, Tauseef / Ahmadi, Ali / Ahmadi, Sepideh / Ahmed Rashid, Tarik / Ahmed Salih, Yusra / Akalu, Gizachew Taddesse / Aklilu, Addis / Akram, Tayyaba / Akunna, Chisom Joyqueenet / Al Hamad, Hanadi / Alahdab, Fares / Al-Aly, Ziyad / Ali, Saqib / Alimohamadi, Yousef / Alipour, Vahid / Aljunid, Syed Mohamed / Alkhayyat, Motasem / Almasi-Hashiani, Amir / Almasri, Nihad A / Al-Maweri, Sadeq Ali Ali / Almustanyir, Sami / Alonso, Nivaldo / Alvis-Guzman, Nelson / Amu, Hubert / Anbesu, Etsay Woldu / Ancuceanu, Robert / Ansari, Fereshteh / Ansari-Moghaddam, Alireza / Antwi, Maxwell Hubert / Anvari, Davood / Anyasodor, Anayochukwu Edward / Aqeel, Muhammad / Arabloo, Jalal / Arab-Zozani, Morteza / Aremu, Olatunde / Ariffin, Hany / Aripov, Timur / Arshad, Muhammad / Artaman, Al / Arulappan, Judie / Asemi, Zatollah / Asghari Jafarabadi, Mohammad / Ashraf, Tahira / Atorkey, Prince / Aujayeb, Avinash / Ausloos, Marcel / Awedew, Atalel Fentahun / Ayala Quintanilla, Beatriz Paulina / Ayenew, Temesgen / Azab, Mohammed A / Azadnajafabad, Sina / Azari Jafari, Amirhossein / Azarian, Ghasem / Azzam, Ahmed Y / Badiye, Ashish D / Bahadory, Saeed / Baig, Atif Amin / Baker, Jennifer L / Balakrishnan, Senthilkumar / Banach, Maciej / Bärnighausen, Till Winfried / Barone-Adesi, Francesco / Barra, Fabio / Barrow, Amadou / Behzadifar, Masoud / Belgaumi, Uzma Iqbal / Bezabhe, Woldesellassie M Mequanint / Bezabih, Yihienew Mequanint / Bhagat, Devidas S / Bhagavathula, Akshaya Srikanth / Bhardwaj, Nikha / Bhardwaj, Pankaj / Bhaskar, Sonu / Bhattacharyya, Krittika / Bhojaraja, Vijayalakshmi S / Bibi, Sadia / Bijani, Ali / Biondi, Antonio / Bisignano, Catherine / Bjørge, Tone / Bleyer, Archie / Blyuss, Oleg / Bolarinwa, Obasanjo Afolabi / Bolla, Srinivasa Rao / Braithwaite, Dejana / Brar, Amanpreet / Brenner, Hermann / Bustamante-Teixeira, Maria Teresa / Butt, Nadeem Shafique / Butt, Zahid A / Caetano Dos Santos, Florentino Luciano / Cao, Yin / Carreras, Giulia / Catalá-López, Ferrán / Cembranel, Francieli / Cerin, Ester / Cernigliaro, Achille / Chakinala, Raja Chandra / Chattu, Soosanna Kumary / Chattu, Vijay Kumar / Chaturvedi, Pankaj / Chimed-Ochir, Odgerel / Cho, Daniel Youngwhan / Christopher, Devasahayam J / Chu, Dinh-Toi / Chung, Michael T / Conde, Joao / Cortés, Sanda / Cortesi, Paolo Angelo / Costa, Vera Marisa / Cunha, Amanda Ramos / Dadras, Omid / Dagnew, Amare Belachew / Dahlawi, Saad M A / Dai, Xiaochen / Dandona, Lalit / Dandona, Rakhi / Darwesh, Aso Mohammad / das Neves, José / De la Hoz, Fernando Pio / Demis, Asmamaw Bizuneh / Denova-Gutiérrez, Edgar / Dhamnetiya, Deepak / Dhimal, Mandira Lamichhane / Dhimal, Meghnath / Dianatinasab, Mostafa / Diaz, Daniel / Djalalinia, Shirin / Do, Huyen Phuc / Doaei, Saeid / Dorostkar, Fariba / Dos Santos Figueiredo, Francisco Winter / Driscoll, Tim Robert / Ebrahimi, Hedyeh / Eftekharzadeh, Sahar / El Tantawi, Maha / El-Abid, Hassan / Elbarazi, Iffat / Elhabashy, Hala Rashad / Elhadi, Muhammed / El-Jaafary, Shaimaa I / Eshrati, Babak / Eskandarieh, Sharareh / Esmaeilzadeh, Firooz / Etemadi, Arash / Ezzikouri, Sayeh / Faisaluddin, Mohammed / Faraon, Emerito Jose A / Fares, Jawad / Farzadfar, Farshad / Feroze, Abdullah Hamid / Ferrero, Simone / Ferro Desideri, Lorenzo / Filip, Irina / Fischer, Florian / Fisher, James L / Foroutan, Masoud / Fukumoto, Takeshi / Gaal, Peter Andras / Gad, Mohamed M / Gadanya, Muktar A / Gallus, Silvano / Gaspar Fonseca, Mariana / Getachew Obsa, Abera / Ghafourifard, Mansour / Ghashghaee, Ahmad / Ghith, Nermin / Gholamalizadeh, Maryam / Gilani, Syed Amir / Ginindza, Themba G / Gizaw, Abraham Tamirat T / Glasbey, James C / Golechha, Mahaveer / Goleij, Pouya / Gomez, Ricardo Santiago / Gopalani, Sameer Vali / Gorini, Giuseppe / Goudarzi, Houman / Grosso, Giuseppe / Gubari, Mohammed Ibrahim Mohialdeen / Guerra, Maximiliano Ribeiro / Guha, Avirup / Gunasekera, D Sanjeeva / Gupta, Bhawna / Gupta, Veer Bala / Gupta, Vivek Kumar / Gutiérrez, Reyna Alma / Hafezi-Nejad, Nima / Haider, Mohammad Rifat / Haj-Mirzaian, Arvin / Halwani, Rabih / Hamadeh, Randah R / Hameed, Sajid / Hamidi, Samer / Hanif, Asif / Haque, Shafiul / Harlianto, Netanja I / Haro, Josep Maria / Hasaballah, Ahmed I / Hassanipour, Soheil / Hay, Roderick J / Hay, Simon I / Hayat, Khezar / Heidari, Golnaz / Heidari, Mohammad / Herrera-Serna, Brenda Yuliana / Herteliu, Claudiu / Hezam, Kamal / Holla, Ramesh / Hossain, Md Mahbub / Hossain, Mohammad Bellal Hossain / Hosseini, Mohammad-Salar / Hosseini, Mostafa / Hosseinzadeh, Mehdi / Hostiuc, Mihaela / Hostiuc, Sorin / Househ, Mowafa / Hsairi, Mohamed / Huang, Junjie / Hugo, Fernando N / Hussain, Rabia / Hussein, Nawfal R / Hwang, Bing-Fang / Iavicoli, Ivo / Ibitoye, Segun Emmanuel / Ida, Fidelia / Ikuta, Kevin S / Ilesanmi, Olayinka Stephen / Ilic, Irena M / Ilic, Milena D / Irham, Lalu Muhammad / Islam, Jessica Y / Islam, Rakibul M / Islam, Sheikh Mohammed Shariful / Ismail, Nahlah Elkudssiah / Isola, Gaetano / Iwagami, Masao / Jacob, Louis / Jain, Vardhmaan / Jakovljevic, Mihajlo B / Javaheri, Tahereh / Jayaram, Shubha / Jazayeri, Seyed Behzad / Jha, Ravi Prakash / Jonas, Jost B / Joo, Tamas / Joseph, Nitin / Joukar, Farahnaz / Jürisson, Mikk / Kabir, Ali / Kahrizi, Danial / Kalankesh, Leila R / Kalhor, Rohollah / Kaliyadan, Feroze / Kalkonde, Yogeshwar / Kamath, Ashwin / Kameran Al-Salihi, Nawzad / Kandel, Himal / Kapoor, Neeti / Karch, André / Kasa, Ayele Semachew / Katikireddi, Srinivasa Vittal / Kauppila, Joonas H / Kavetskyy, Taras / Kebede, Sewnet Adem / Keshavarz, Pedram / Keykhaei, Mohammad / Khader, Yousef Saleh / Khalilov, Rovshan / Khan, Gulfaraz / Khan, Maseer / Khan, Md Nuruzzaman / Khan, Moien A B / Khang, Young-Ho / Khater, Amir M / Khayamzadeh, Maryam / Kim, Gyu Ri / Kim, Yun Jin / Kisa, Adnan / Kisa, Sezer / Kissimova-Skarbek, Katarzyna / Kopec, Jacek A / Koteeswaran, Rajasekaran / Koul, Parvaiz A / Koulmane Laxminarayana, Sindhura Lakshmi / Koyanagi, Ai / Kucuk Bicer, Burcu / Kugbey, Nuworza / Kumar, G Anil / Kumar, Narinder / Kumar, Nithin / Kurmi, Om P / Kutluk, Tezer / La Vecchia, Carlo / Lami, Faris Hasan / Landires, Iván / Lauriola, Paolo / Lee, Sang-Woong / Lee, Shaun Wen Huey / Lee, Wei-Chen / Lee, Yo Han / Leigh, James / Leong, Elvynna / Li, Jiarui / Li, Ming-Chieh / Liu, Xuefeng / Loureiro, Joana A / Lunevicius, Raimundas / Magdy Abd El Razek, Muhammed / Majeed, Azeem / Makki, Alaa / Male, Shilpa / Malik, Ahmad Azam / Mansournia, Mohammad Ali / Martini, Santi / Masoumi, Seyedeh Zahra / Mathur, Prashant / McKee, Martin / Mehrotra, Ravi / Mendoza, Walter / Menezes, Ritesh G / Mengesha, Endalkachew Worku / Mesregah, Mohamed Kamal / Mestrovic, Tomislav / Miao Jonasson, Junmei / Miazgowski, Bartosz / Miazgowski, Tomasz / Michalek, Irmina Maria / Miller, Ted R / Mirzaei, Hamed / Mirzaei, Hamid Reza / Misra, Sanjeev / Mithra, Prasanna / Moghadaszadeh, Masoud / Mohammad, Karzan Abdulmuhsin / Mohammad, Yousef / Mohammadi, Mokhtar / Mohammadi, Seyyede Momeneh / Mohammadian-Hafshejani, Abdollah / Mohammed, Shafiu / Moka, Nagabhishek / Mokdad, Ali H / Molokhia, Mariam / Monasta, Lorenzo / Moni, Mohammad Ali / Moosavi, Mohammad Amin / Moradi, Yousef / Moraga, Paula / Morgado-da-Costa, Joana / Morrison, Shane Douglas / Mosapour, Abbas / Mubarik, Sumaira / Mwanri, Lillian / Nagarajan, Ahamarshan Jayaraman / Nagaraju, Shankar Prasad / Nagata, Chie / Naimzada, Mukhammad David / Nangia, Vinay / Naqvi, Atta Abbas / Narasimha Swamy, Sreenivas / Ndejjo, Rawlance / Nduaguba, Sabina O / Negoi, Ionut / Negru, Serban Mircea / Neupane Kandel, Sandhya / Nguyen, Cuong Tat / Nguyen, Huong Lan Thi / Niazi, Robina Khan / Nnaji, Chukwudi A / Noor, Nurulamin M / Nuñez-Samudio, Virginia / Nzoputam, Chimezie Igwegbe / Oancea, Bogdan / Ochir, Chimedsuren / Odukoya, Oluwakemi Ololade / Ogbo, Felix Akpojene / Olagunju, Andrew T / 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/ Murray, Christopher J L / Force, Lisa M

JAMA oncology

2022 Volume 8, Issue 3, Page(s) 420–444

Abstract: Importance: The Global Burden of Diseases, Injuries, and Risk Factors Study 2019 (GBD 2019) provided systematic estimates of incidence, morbidity, and mortality to inform local and international efforts toward reducing cancer burden.: Objective: To ... ...

Abstract	Importance: The Global Burden of Diseases, Injuries, and Risk Factors Study 2019 (GBD 2019) provided systematic estimates of incidence, morbidity, and mortality to inform local and international efforts toward reducing cancer burden. Objective: To estimate cancer burden and trends globally for 204 countries and territories and by Sociodemographic Index (SDI) quintiles from 2010 to 2019. Evidence review: The GBD 2019 estimation methods were used to describe cancer incidence, mortality, years lived with disability, years of life lost, and disability-adjusted life years (DALYs) in 2019 and over the past decade. Estimates are also provided by quintiles of the SDI, a composite measure of educational attainment, income per capita, and total fertility rate for those younger than 25 years. Estimates include 95% uncertainty intervals (UIs). Findings: In 2019, there were an estimated 23.6 million (95% UI, 22.2-24.9 million) new cancer cases (17.2 million when excluding nonmelanoma skin cancer) and 10.0 million (95% UI, 9.36-10.6 million) cancer deaths globally, with an estimated 250 million (235-264 million) DALYs due to cancer. Since 2010, these represented a 26.3% (95% UI, 20.3%-32.3%) increase in new cases, a 20.9% (95% UI, 14.2%-27.6%) increase in deaths, and a 16.0% (95% UI, 9.3%-22.8%) increase in DALYs. Among 22 groups of diseases and injuries in the GBD 2019 study, cancer was second only to cardiovascular diseases for the number of deaths, years of life lost, and DALYs globally in 2019. Cancer burden differed across SDI quintiles. The proportion of years lived with disability that contributed to DALYs increased with SDI, ranging from 1.4% (1.1%-1.8%) in the low SDI quintile to 5.7% (4.2%-7.1%) in the high SDI quintile. While the high SDI quintile had the highest number of new cases in 2019, the middle SDI quintile had the highest number of cancer deaths and DALYs. From 2010 to 2019, the largest percentage increase in the numbers of cases and deaths occurred in the low and low-middle SDI quintiles. Conclusions and relevance: The results of this systematic analysis suggest that the global burden of cancer is substantial and growing, with burden differing by SDI. These results provide comprehensive and comparable estimates that can potentially inform efforts toward equitable cancer control around the world.
MeSH term(s)	Disability-Adjusted Life Years ; Global Burden of Disease ; Global Health ; Humans ; Incidence ; Neoplasms/epidemiology ; Prevalence ; Quality-Adjusted Life Years ; Risk Factors
Language	English
Publishing date	2022-01-31
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Systematic Review
ISSN	2374-2445
ISSN (online)	2374-2445
DOI	10.1001/jamaoncol.2021.6987
Database	MEDical Literature Analysis and Retrieval System OnLINE

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