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1.
Public Health ; 215: 31-38, 2023 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-36634404

RESUMEN

OBJECTIVES: This article describes the prevalence and epidemiological trends of COVID-19 mortality in the largest registry in the Kingdom of Saudi Arabia (KSA). STUDY DESIGN: A prospective epidemiological cohort study using data from all healthcare facilities in KSA collected between March 23, 2020, and April 30, 2022. Data on the number of daily deaths directly related to COVID-19 were gathered, analyzed, and reported. METHOD: Data analysis was carried out using national and regional crude case fatality rate and death per 100,000 population. Descriptive statistics using numbers and proportions were used to describe age, gender, nationality, and comorbidities. The mortality trend was plotted and compared with international figures. In addition, the most common comorbidities associated with mortality and the proportion of patients who received COVID-19 vaccine were reported. RESULTS: The total reported number of deaths between March 23, 2020, and April 30, 2022, was 9085. Crude case fatality rate was 1.21%, and death per 100,000 population was 25.38, which compared favorably to figures reported by several developed countries. The highest percentages of deaths were among individuals aged between 60 and 69 years, males (71%), and individuals with diabetes (60%). Only 2.8% of mortalities occur in patients who received COVID-19 vaccine. Diabetes, hypertension, and heart failure had the highest attributable risk of mortality among patients who died due to COVID-19. CONCLUSION: Case fatality rate and death per 100,000 population in KSA are among the lowest in the world due to multiple factors. Several comorbidities have been identified, namely, diabetes, hypertension, obesity, and cardiac arrhythmias.


Asunto(s)
COVID-19 , Diabetes Mellitus , Hipertensión , Masculino , Humanos , Persona de Mediana Edad , Anciano , Arabia Saudita/epidemiología , Estudios de Cohortes , Vacunas contra la COVID-19 , Prevalencia , Estudios Prospectivos , Diabetes Mellitus/epidemiología
2.
Clin Microbiol Infect ; 20(5): 469-74, 2014 May.
Artículo en Inglés | MEDLINE | ID: mdl-24460984

RESUMEN

The Saudi Arabian Ministry of Health implemented a pro-active surveillance programme for Middle East respiratory syndrome (MERS) coronavirus (MERS-CoV). We report MERS-CoV data from 5065 Kingdom of Saudi Arabia individuals who were screened for MERS-CoV over a 12-month period. From 1 October 2012 to 30 September 2013, demographic and clinical data were prospectively collected from all laboratory forms received at the Saudi Arabian Virology reference laboratory. Data were analysed by referral type, age, gender, and MERS-CoV real-time PCR test results. Five thousand and 65 individuals were screened for MER-CoV: hospitalized patients with suspected MERS-CoV infection (n = 2908, 57.4%), healthcare worker (HCW) contacts (n = 1695; 33.5%), and family contacts of laboratory-confirmed MERS cases (n = 462; 9.1%). Eleven per cent of persons tested were children (<17 years of age). There were 108 cases (99 adults and nine children) of MERS-CoV infection detected during the 12-month period (108/5065, 2% case detection rate). Of 108 cases, 45 were females (six children and 39 adults) and 63 were males (three children and 60 adults). Of the 99 adults with MERS-CoV infection, 70 were hospitalized patients, 19 were HCW contacts, and ten were family contacts. There were no significant increases in MERS-CoV detection rates over the 12-month period: 2.6% (19/731) in July 2013, 1.7% (19/1100) in August 2013, and 1.69% (21/1238) in September 2013. Male patients had a significantly higher MERS-CoV infection rate (63/2318, 2.7%) than females (45/2747, 1.6%) (p 0.013). MERS-CoV rates remain at low levels, with no significant increase over time. Pro-active surveillance for MERS-CoV in newly diagnosed patients and their contacts will continue.


Asunto(s)
Infecciones por Coronavirus/diagnóstico , Infección Hospitalaria/diagnóstico , Coronavirus del Síndrome Respiratorio de Oriente Medio/aislamiento & purificación , Vigilancia de la Población , Adolescente , Adulto , Infecciones por Coronavirus/epidemiología , Infección Hospitalaria/epidemiología , Familia , Femenino , Personal de Salud/estadística & datos numéricos , Humanos , Masculino , Tamizaje Masivo , Coronavirus del Síndrome Respiratorio de Oriente Medio/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Arabia Saudita/epidemiología , Factores Sexuales , Adulto Joven
3.
Lancet ; 374(9703): 1786-91, 2009 Nov 21.
Artículo en Inglés | MEDLINE | ID: mdl-19914707

RESUMEN

Mass gatherings of people challenge public health capacities at host locations and the visitors' places of origin. Hajj--the yearly pilgrimage by Muslims to Saudi Arabia--is one of the largest, most culturally and geographically diverse mass gatherings in the world. With the 2009 pandemic influenza A H1N1 and upcoming Hajj, the Saudi Arabian Ministry of Health (MoH) convened a preparedness consultation in June, 2009. Consultants from global public health agencies met in their official capacities with their Saudi Arabian counterparts. The MoH aimed to pool and share public health knowledge about mass gatherings, and review the country's preparedness plans, focusing on the prevention and control of pandemic influenza. This process resulted in several practical recommendations, many to be put into practice before the start of Hajj and the rest during Hajj. These preparedness plans should ensure the optimum provision of health services for pilgrims to Saudi Arabia, and minimum disease transmission on their return home. Review of the implementation of these recommendations and their effect will not only inform future mass gatherings in Saudi Arabia, but will also strengthen preparedness efforts in other settings.


Asunto(s)
Control de Enfermedades Transmisibles/organización & administración , Brotes de Enfermedades/prevención & control , Subtipo H1N1 del Virus de la Influenza A , Gripe Humana/prevención & control , Islamismo , Viaje , Implementación de Plan de Salud/organización & administración , Humanos , Gripe Humana/epidemiología , Gripe Humana/transmisión , Guías de Práctica Clínica como Asunto , Arabia Saudita
4.
Clin Nephrol ; 50(2): 128-30, 1998 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-9725786

RESUMEN

Nocardia is a serious opportunistic infection in renal transplant recipients and nocardial brain abscess in these patients has a high mortality. In addition to antimicrobial therapy, treatment usually involves craniotomy and excision of the abscess. We describe a renal transplant recipient maintained on cyclosporine and prednisone developing Nocardia Asteroides brain abscess. After stereotactic aspiration of the abscess, successful treatment was achieved by triple therapy with trimethoprim sulfamethoxazole (TMP/SMX), ceftriaxone and amikacin. The allograft function remained stable. Long-term prophylaxis with TMP/SMX is necessary to prevent the relapse of nocardia.


Asunto(s)
Absceso Encefálico/tratamiento farmacológico , Absceso Encefálico/microbiología , Quimioterapia Combinada/uso terapéutico , Terapia de Inmunosupresión/efectos adversos , Trasplante de Riñón , Nocardiosis/tratamiento farmacológico , Nocardia asteroides , Infecciones Oportunistas/tratamiento farmacológico , Amicacina/uso terapéutico , Ceftriaxona/uso terapéutico , Humanos , Inmunosupresores/uso terapéutico , Masculino , Persona de Mediana Edad , Nocardiosis/etiología , Infecciones Oportunistas/etiología , Resultado del Tratamiento , Combinación Trimetoprim y Sulfametoxazol/uso terapéutico
5.
Clin Infect Dis ; 27(1): 52-6, 1998 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-9675450

RESUMEN

Corticosteroids are beneficial as treatment of certain tuberculosis syndromes. We reviewed all cases of peritoneal tuberculosis diagnosed at our institution over 10 years to evaluate the role of corticosteroid administration combined with antituberculous therapy. Nine patients were treated with steroids plus antituberculosis agents (cases), and 26 received antituberculosis treatment only (controls). The two groups were not significantly different in terms of their basic demographics or disease. Nineteen controls compared with one case had recurrent abdominal pain. Seven controls had 17 emergency department visits because of abdominal pain. Intestinal obstruction was diagnosed for five of these patients, four of whom underwent laparotomy revealing extensive adhesions. Three controls died, and no case died. No case required laparotomy, had a diagnosis of intestinal obstruction, or visited the emergency department because of abdominal pain. These findings suggest that corticosteroid administration combined with antituberculosis treatment reduces the frequency of morbidity and complications in patients with peritoneal tuberculosis.


Asunto(s)
Antituberculosos/uso terapéutico , Glucocorticoides/uso terapéutico , Peritonitis Tuberculosa/tratamiento farmacológico , Prednisona/uso terapéutico , Adulto , Quimioterapia Combinada , Femenino , Humanos , Masculino , Persona de Mediana Edad
6.
Drugs ; 52(1): 17-32, 1996 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-8799682

RESUMEN

Of the large number of agents under development for the treatment of herpes virus infections [herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), varicella zoster virus (VZV), cytomegalovirus (CMV), Epstein-Barr virus (EBV)], only ten have apparently reached clinical development. Aciclovir was approved for the treatment of HSV infections over 10 years ago, and it remains an important and reliable antiviral agent. Recent approvals in some countries of valaciclovir for VZV infection and famciclovir for both HSV and VZV infections demonstrate the rapidity of change in this field. Intravenous ganciclovir and foscarnet are approved for the treatment of CMV infection in the immunocompromised patient. Five of the antiherpetic drugs under current clinical development are nucleoside analogues or their prodrugs; another is a phosphorylated nucleoside (nucleotide). Four of the nucleoside agents-penciclovir, famciclovir, valaciclovir and lobucavir-are being developed for the management of HSV and VZV infections. Valaciclovir is also being developed for the prevention of CMV infections and famciclovir and lobucavir for the treatment of hepatitis B virus infection. Oral ganciclovir, lobucavir, ISIS 2922 and cidofovir are being developed for the suppression of CMV infections in immunocompromised patients. Sorivudine has been studied in VZV infections. n-Docosanol is under development for HSV infections, and cidofovir is being developed for both HSV and CMV infections, as well as for treatment of other viral diseases. Traditionally, the adverse effects associated with anti-CMV compounds have been more difficult to manage and are acceptable clinically only because of the severity of the underlying infection and lack of safer therapeutic alternatives. In general, toxicity issues continue to be problematic in the anti-CMV arena, although newer agents have improved the situation to some extent. In contrast, the safety of anti-HSV compounds has traditionally been excellent, establishing a safety standard that must be met by newer agents entering the field.


Asunto(s)
Antivirales/uso terapéutico , Infecciones por Herpesviridae/tratamiento farmacológico , Profármacos/uso terapéutico , Antivirales/farmacocinética , Antivirales/farmacología , Disponibilidad Biológica , Ensayos Clínicos como Asunto , Humanos , Profármacos/farmacocinética , Profármacos/farmacología
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