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Institution

Lahore General Hospital

HealthcareLahore, Pakistan
About: Lahore General Hospital is a healthcare organization based out in Lahore, Pakistan. It is known for research contribution in the topics: Medicine & Population. The organization has 422 authors who have published 311 publications receiving 1929 citations.


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Journal ArticleDOI
A. Sibley, Kwang Hyub Han1, A. Abourached, Laurentius A. Lesmana2, Mihály Makara, Wasim Jafri3, Riina Salupere4, Abdullah M. Assiri, Adrian Goldis, Faisal Abaalkhail5, Zaigham Abbas6, A. Abdou7, F. Al Braiki, F. Al Hosani, K. Al Jaberi, M. Al Khatry, M. A. Al Mulla, H. Al Quraishi7, A. Al Rifai, Y. Al Serkal, Altaf Alam8, Seyed Moayed Alavian9, Hamad I. Al-Ashgar5, S. Alawadhi7, L. Al-Dabal7, P. Aldins, Faleh Z. Al-Faleh10, Abdullah S. Alghamdi, R. Al-Hakeem, Abdulrahman Aljumah11, A. Almessabi, Adel Alqutub, Khalid Alswat10, Ibrahim Altraif11, M. Alzaabi, N. Andrea, Mohamed A. Babatin, A. Baqir, M. T. Barakat, Ottar M. Bergmann, Abdul Rahman Bizri12, Sarah Blach, Asad Chaudhry, M. S. Choi13, T. Diab, Samsuridjal Djauzi2, E. S. El Hassan7, S. El Khoury14, Chris Estes, S. Fakhry, J. I. Farooqi15, J. I. Farooqi16, H. Fridjonsdottir17, Rino Alvani Gani2, A. Ghafoor Khan16, Liana Gheorghe, Magnus Gottfredsson18, S. Gregorcic19, Jessie Gunter, Behzad Hajarizadeh20, Behzad Hajarizadeh21, Saeed Hamid3, Irsan Hasan2, Almoutaz Hashim5, Gabor Horvath, Béla Hunyady22, R. Husni23, Agita Jeruma, Jon G. Jonasson24, Jon G. Jonasson17, B. Karlsdottir, Do Young Kim1, Young Seok Kim25, Z. Koutoubi26, Valentina Liakina27, Valentina Liakina28, Young-Suk Lim29, A. Löve24, A. Löve18, Matti Maimets4, Reza Malekzadeh30, Mojca Maticic19, Muhammad S. Memon31, Shahin Merat30, Jacques E Mokhbat23, Fadi H. Mourad12, David H. Muljono32, David H. Muljono33, Arif Nawaz34, N. Nugrahini, S. Olafsson, S. Priohutomo, H. Qureshi35, P. Rassam14, Homie Razavi, Devin Razavi-Shearer, Kathryn Razavi-Shearer, Baiba Rozentale, M. Sadik31, K. Saeed, A. Salamat36, Faisal M. Sanai10, A. Sanityoso Sulaiman2, R. A. Sayegh37, Ala I. Sharara12, M. Siddiq34, A. M. Siddiqui38, G. Sigmundsdottir, B. Sigurdardottir, Danute Speiciene27, Andri Sanityoso Sulaiman2, Marwa Sultan, M. Taha, Junko Tanaka39, H. Tarifi, G. Tayyab40, Ieva Tolmane, M. Ud Din, M. Umar2, M. Umar41, M. Umar42, Jonas Valantinas27, J. Videčnik-Zorman19, Cesar Yaghi37, Evy Yunihastuti2, M. A. Yusuf34, Bader Faiyaz Zuberi43, Jonathan Schmelzer 
TL;DR: The current treatment rate and efficacy are not sufficient to manage the disease burden of hepatitis C virus and alternative strategies are required to keep the number of HCV individuals with advanced liver disease and liver‐related deaths from increasing.
Abstract: The disease burden of hepatitis C virus (HCV) is expected to increase as the infected population ages. A modelling approach was used to estimate the total number of viremic infections, diagnosed, treated and new infections in 2013. In addition, the model was used to estimate the change in the total number of HCV infections, the disease progression and mortality in 2013-2030. Finally, expert panel consensus was used to capture current treatment practices in each country. Using today's treatment paradigm, the total number of HCV infections is projected to decline or remain flat in all countries studied. However, in the same time period, the number of individuals with late-stage liver disease is projected to increase. This study concluded that the current treatment rate and efficacy are not sufficient to manage the disease burden of HCV. Thus, alternative strategies are required to keep the number of HCV individuals with advanced liver disease and liver-related deaths from increasing.

463 citations

Journal ArticleDOI
TL;DR: Eltrombopag reduced the need for platelet transfusions in patients with chronic liver disease who were undergoing elective invasive procedures, but it was associated with an increased incidence of portal-vein thrombosis, as compared with placebo.
Abstract: Background Eltrombopag is an oral thrombopoietin-receptor agonist. This study evaluated the efficacy of eltrombopag for increasing platelet counts and reducing the need for platelet transfusions in patients with thrombocytopenia and chronic liver disease who are undergoing an elective invasive procedure. Methods We randomly assigned 292 patients with chronic liver disease of diverse causes and platelet counts of less than 50,000 per cubic millimeter to receive eltrombopag, at a dose of 75 mg daily, or placebo for 14 days before a planned elective invasive procedure that was performed within 5 days after the last dose. The primary end point was the avoidance of a platelet transfusion before, during, and up to 7 days after the procedure. A key secondary end point was the occurrence of bleeding (World Health Organization [WHO] grade 2 or higher) during this period. Results A platelet transfusion was avoided in 104 of 145 patients who received eltrombopag (72%) and in 28 of 147 who received placebo (19%) (P<0...

265 citations

Journal ArticleDOI
Wei Zhao1, Asif Rasheed, Emmi Tikkanen2, Jung-Jin Lee1, Adam S. Butterworth3, Joanna M. M. Howson3, Themistocles L. Assimes4, Rajiv Chowdhury3, Marju Orho-Melander5, Scott M. Damrauer1, Aeron Small1, Senay Asma6, Minako Imamura, Toshimasa Yamauch7, John C. Chambers8, Peng Chen9, Bishwa Raj Sapkota10, Nabi Shah, Sehrish Jabeen, Praveen Surendran3, Yingchang Lu11, Weihua Zhang8, Atif Imran, Shahid Abbas, Faisal Majeed, Kevin Trindade1, Nadeem Qamar, Nadeem Hayyat Mallick12, Zia Yaqoob, Tahir Saghir, Syed Nadeem Hasan Rizvi, Anis Memon, Syed Zahed Rasheed13, Fazal-ur-Rehman Memon, Khalid Mehmood14, Naveeduddin Ahmed15, Irshad Hussain Qureshi16, Tanveer-us-Salam17, Wasim Iqbal17, Uzma Malik16, Narinder K. Mehra18, Jane Z. Kuo, Wayne H-H Sheu, Xiuqing Guo19, Chao A. Hsiung20, Jyh-Ming Jimmy Juang21, Kent D. Taylor19, Yi-Jen Hung22, Wen-Jane Lee, Thomas Quertermous4, I-Te Lee, Chih-Cheng Hsu20, Erwin P. Bottinger11, Sarju Ralhan, Yik Ying Teo9, Tzung-Dau Wang21, Dewan S. Alam23, Emanuele Di Angelantonio3, Steve Epstein24, Sune F. Nielsen25, Børge G. Nordestgaard26, Anne Tybjærg-Hansen26, Robin Young3, M. Benn27, Ruth Frikke-Schmidt26, Pia R. Kamstrup26, Michigan Biobank20, J. Wouter Jukema27, Naveed Sattar28, Roelof A.J. Smit27, Ren-Hua Chung20, Kae-Woei Liang, Sonia S. Anand6, Dharambir K. Sanghera10, Samuli Ripatti2, Ruth J. F. Loos11, Jaspal S. Kooner8, E. Shyong Tai9, Jerome I. Rotter19, Yii-Der Ida Chen19, Philippe M. Frossard, Shiro Maeda, Takashi Kadowaki7, Muredach P. Reilly29, Guillaume Paré6, Olle Melander5, Veikko Salomaa30, Daniel J. Rader1, John Danesh3, Benjamin F. Voight1, Danish Saleheen1 
TL;DR: A genome-wide, multi-ancestry study of genetic variation for type 2 diabetes and coronary heart disease finds variants associated with both outcomes implicate new pathways as well as targets of existing drugs, including icosapent ethyl and adipocyte fatty-acid-binding protein.
Abstract: Danish Saleheen, Benjamin Voight and colleagues perform genome-wide analysis of multi-ancestry cohorts to identify genetic associations with type 2 diabetes (T2D) and coronary heart disease (CHD). They find novel loci and show that 24% of T2D loci are also associated with CHD and that greater genetic risk of T2D increases risk of CHD. To evaluate the shared genetic etiology of type 2 diabetes (T2D) and coronary heart disease (CHD), we conducted a genome-wide, multi-ancestry study of genetic variation for both diseases in up to 265,678 subjects for T2D and 260,365 subjects for CHD. We identify 16 previously unreported loci for T2D and 1 locus for CHD, including a new T2D association at a missense variant in HLA-DRB5 (odds ratio (OR) = 1.29). We show that genetically mediated increase in T2D risk also confers higher CHD risk. Joint T2D–CHD analysis identified eight variants—two of which are coding—where T2D and CHD associations appear to colocalize, including a new joint T2D–CHD association at the CCDC92 locus that also replicated for T2D. The variants associated with both outcomes implicate new pathways as well as targets of existing drugs, including icosapent ethyl and adipocyte fatty-acid-binding protein.

193 citations

Journal ArticleDOI
TL;DR: This cross-sectional analysis reports the retinoblastoma stage at diagnosis across the world during a single year, investigates associations between clinical variables and national income level, and investigates risk factors for advanced disease at diagnosis.
Abstract: Importance: Early diagnosis of retinoblastoma, the most common intraocular cancer, can save both a child's life and vision. However, anecdotal evidence suggests that many children across the world are diagnosed late. To our knowledge, the clinical presentation of retinoblastoma has never been assessed on a global scale. Objectives: To report the retinoblastoma stage at diagnosis in patients across the world during a single year, to investigate associations between clinical variables and national income level, and to investigate risk factors for advanced disease at diagnosis. Design, Setting, and Participants: A total of 278 retinoblastoma treatment centers were recruited from June 2017 through December 2018 to participate in a cross-sectional analysis of treatment-naive patients with retinoblastoma who were diagnosed in 2017. Main Outcomes and Measures: Age at presentation, proportion of familial history of retinoblastoma, and tumor stage and metastasis. Results: The cohort included 4351 new patients from 153 countries; the median age at diagnosis was 30.5 (interquartile range, 18.3-45.9) months, and 1976 patients (45.4%) were female. Most patients (n = 3685 [84.7%]) were from low- and middle-income countries (LMICs). Globally, the most common indication for referral was leukocoria (n = 2638 [62.8%]), followed by strabismus (n = 429 [10.2%]) and proptosis (n = 309 [7.4%]). Patients from high-income countries (HICs) were diagnosed at a median age of 14.1 months, with 656 of 666 (98.5%) patients having intraocular retinoblastoma and 2 (0.3%) having metastasis. Patients from low-income countries were diagnosed at a median age of 30.5 months, with 256 of 521 (49.1%) having extraocular retinoblastoma and 94 of 498 (18.9%) having metastasis. Lower national income level was associated with older presentation age, higher proportion of locally advanced disease and distant metastasis, and smaller proportion of familial history of retinoblastoma. Advanced disease at diagnosis was more common in LMICs even after adjusting for age (odds ratio for low-income countries vs upper-middle-income countries and HICs, 17.92 [95% CI, 12.94-24.80], and for lower-middle-income countries vs upper-middle-income countries and HICs, 5.74 [95% CI, 4.30-7.68]). Conclusions and Relevance: This study is estimated to have included more than half of all new retinoblastoma cases worldwide in 2017. Children from LMICs, where the main global retinoblastoma burden lies, presented at an older age with more advanced disease and demonstrated a smaller proportion of familial history of retinoblastoma, likely because many do not reach a childbearing age. Given that retinoblastoma is curable, these data are concerning and mandate intervention at national and international levels. Further studies are needed to investigate factors, other than age at presentation, that may be associated with advanced disease in LMICs.

151 citations

Journal ArticleDOI
TL;DR: Evidence from this study does not support a causal role of circulating serum urate levels in T2DM, CHD, ischemic stroke, or HF, and decreasing serum Urate levels may not translate into risk reductions for cardiometabolic conditions.

136 citations


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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20226
202183
202056
201941
201838
201716