17 results on '"Read, Stanley"'
Search Results
2. Extranodal Rosai-Dorfman disease with multifocal bone and epidural involvement causing recurrent spinal cord compression
- Author
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Al-Saad, Khulood, Thorner, Paul, Ngan, Bo-Yee, Gerstle, J. Ted, Kulkarni, Abhaya V., Babyn, Paul, Grant, Ronald M., Read, Stanley, Laxer, Ronald M., and Chan, Helen S.L.
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Lymphadenopathy ,Lymphatic diseases ,Pediatrics ,Phagocytosis ,Health care industry - Published
- 2005
3. Falling through the cracks of the big cities: who is meeting the needs of HIV-positive youth?
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Flicker, Sarah, Skinner, Harvey, Read, Stanley, Veinot, Tiffany, McClelland, Alex, Saulnier, Paul, and Goldberg, Eudice
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HIV patients -- Care and treatment ,HIV patients -- Psychological aspects ,HIV patients -- Social aspects - Published
- 2005
4. Severe acute respiratory syndrome (SARS): chest radiographic features in children
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Babyn, Paul, S., Chu, Winnie, C.W., Tsou, Ian Y.Y., Wansaicheong, Gervais, K.L., Allen, Upton, Bitnun, Ari, Chee, Thomas, S.G., Cheng, Frankie W.T., Chiu, Man-Chun, Fok, Tai-Fai, Hon, Ellis, K.L., Gahunia, Harpal K., Kaw, Gregory, J.L., Khong, Pek, L., Leung, Chi-Wai, Li, Albert, M., Manson, David, Metreweli, Constantine, Ng, Pak-Cheung, Read, Stanley, and Stringer, David, A.
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Pediatric radiology -- Usage ,Pediatric radiology -- Case studies ,Severe acute respiratory syndrome -- Diagnosis ,Severe acute respiratory syndrome -- Case studies ,Health - Published
- 2004
5. Risk factors and outcomes among children admitted to hospital with pandemic H1N1 influenza
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O'Riordan, Sean, Barton, Michelle, Yau, Yvonne, Read, Stanley E., Allen, Upton, and Tran, Dat
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Swine influenza -- Causes of -- Diagnosis -- Care and treatment -- Research -- Patient outcomes ,Children -- Health aspects ,Health - Abstract
Background: Limited data are available on disease characteristics and outcomes of children with 2009 pandemic influenza A(H1N1) virus infection (pandemic H1N1 influenza) who have required hospital admission. Methods: We reviewed the charts of 58 children with pandemic H1N1 influenza admitted to a large pediatric hospital in Ontario, Canada, between May 8 and July 22, 2009. We compared risk factors, severity indicators and outcomes of these children with those of 200 children admitted with seasonal influenza A during the previous 5 years (2004/05 to 2008/09). Results: Children with pandemic H1N1 influenza were significantly older than those with seasonal influenza (median age 6.4 years v. 3.3 years). Forty-six (79%) of the children with pandemic H1N1 influenza had underlying medical conditions; of the other 12 who were previously healthy, 42% were under 2 years of age. Children admitted with pandemic H1N1 influenza were significantly more likely to have asthma than those with seasonal influenza (22% v. 6%). Two children had poorly controlled asthma, and 6 used inhaled medications only intermittently. The median length of stay in hospital was 4 days in both groups of children. Similar proportions of children required admission to the intensive care unit (21% of those with pandemic H1N1 influenza and 14% of those with seasonal influenza) and mechanical ventilation (12% and 10% respectively). None of the children admitted with pandemic H1N1 influenza died, as compared with 1 (0.4%) of those admitted with seasonal influenza. Interpretation: Pandemic H1N1 influenza did not appear to cause more severe disease than seasonal influenza A. Asthma appears to be a significant risk factor for severe disease, with no clear relation to severity of asthma. This finding should influence strategies for vaccination and pre-emptive anti viral therapy., Influenza causes significant morbidity and mortality in childhood. (1) Infants, young children and people 65 years of age and older account for the highest rates of influenza-related hospital admission. (2) [...]
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- 2010
- Full Text
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6. Safety of combination antiretroviral prophylaxis in high-risk HIV-exposed newborns: a retrospective review of the Canadian experience
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Kakkar, Fatima W., Samson, Lindy, Vaudry, Wendy, Brophy, Jason, Le Meur, Jean-Baptiste, Lapointe, Normand, Read, Stanley E., and Bitnun, Ari
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Prophylaxis -- Research -- Health aspects ,Highly active antiretroviral therapy -- Safety and security measures -- Health aspects ,HIV infections -- Drug therapy -- Risk factors ,Newborn infants -- Drug therapy -- Safety and security measures ,Health - Abstract
Introduction: The optimal management of infants born to HIV-positive mothers who are untreated or have detectable viral load prior to delivery remains controversial. Despite the increasing use of combination antiretroviral therapy (cART) for post-exposure prophylaxis (PEP) of neonates at high risk of HIV infection, there is little safety and pharmacokinetic data to support this approach. The objective of this study was to evaluate the safety and tolerability of cART for PEP in HIV-exposed neonates. Methods: Retrospective study on 148 cART and 145 Zidovudine (ZDV) monotherapy-exposed infants identified from four Canadian centres where cART for PEP has routinely been prescribed in high-risk situations. Physician-reported adverse events and clinical outcomes were extracted by chart review. Haematological and growth parameters at birth, one and six months of age were compared between cART and ZDV-exposed infants using multivariate mixed effects modelling. Results: Non-specific signs and symptoms were reported in 10.2% of cART recipients versus none of the ZDV recipients. Treatment was discontinued prematurely in 9.5% of cART recipients versus 2.1% of ZDV recipients (p = 0.01). In the multivariate model, cART recipients had lower mean haemoglobin (decrease of 2.07 g/L) over the 6-month period compared with ZDV recipients (p = 0.04), but no effect was seen on absolute neutrophil count. cART recipients had lower weight and smaller head circumference at birth and one month of age compared with ZDV-exposed infants; these differences were no longer significant at six months of age. Conclusions: cART administered at treatment doses for PEP in neonates was generally well tolerated, though a higher incidence of non-specific signs and symptoms and early treatment discontinuation occurred among cART recipients. Keywords: Prevention of mother-to-child transmission; HIV; neonatal prophylaxis; safety; combination antiretroviral therapy., Introduction While the overall risk of perinatal HIV transmission in the developed world has decreased to less than 1%, transmission still occurs, most often due to failure to diagnose HIV [...]
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- 2016
- Full Text
- View/download PDF
7. Safety of combination antiretroviral prophylaxis in high‐risk HIV‐exposed newborns: a retrospective review of the Canadian experience
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Kakkar, Fatima W., Samson, Lindy, Vaudry, Wendy, Brophy, Jason, Le Meur, Jean?Baptiste, Lapointe, Normand, Read, Stanley E., and Bitnun, Ari
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Perinatal infection -- Prevention ,Antiviral agents -- Dosage and administration ,Infants -- Care and treatment ,Disease transmission -- Prevention ,Pediatric research ,HIV infection -- Prevention ,Health - Abstract
Introduction: The optimal management of infants born to HIV‐positive mothers who are untreated or have detectable viral load prior to delivery remains controversial. Despite the increasing use of combination antiretroviral therapy (cART) for post‐exposure prophylaxis (PEP) of neonates at high risk of HIV infection, there is little safety and pharmacokinetic data to support this approach. The objective of this study was to evaluate the safety and tolerability of cART for PEP in HIV‐exposed neonates. Methods: Retrospective study on 148 cART and 145 Zidovudine (ZDV) monotherapy‐exposed infants identified from four Canadian centres where cART for PEP has routinely been prescribed in high‐risk situations. Physician‐reported adverse events and clinical outcomes were extracted by chart review. Haematological and growth parameters at birth, one and six months of age were compared between cART and ZDV‐exposed infants using multivariate mixed effects modelling. Results: Non‐specific signs and symptoms were reported in 10.2% of cART recipients versus none of the ZDV recipients. Treatment was discontinued prematurely in 9.5% of cART recipients versus 2.1% of ZDV recipients (p=0.01). In the multivariate model, cART recipients had lower mean haemoglobin (decrease of 2.07 g/L) over the 6‐month period compared with ZDV recipients (p=0.04), but no effect was seen on absolute neutrophil count. cART recipients had lower weight and smaller head circumference at birth and one month of age compared with ZDV‐exposed infants; these differences were no longer significant at six months of age. Conclusions: cART administered at treatment doses for PEP in neonates was generally well tolerated, though a higher incidence of non‐specific signs and symptoms and early treatment discontinuation occurred among cART recipients., Introduction While the overall risk of perinatal HIV transmission in the developed world has decreased to less than 1%, transmission still occurs, most often due to failure to diagnose HIV [...]
- Published
- 2016
- Full Text
- View/download PDF
8. Perinatal exposure to antiretroviral therapy is associated with increased blood mitochondrial gene expression in infants
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Cote, Helene C.F., Raboud, Janet, Bitnun, Ari, Alimenti, Ariane, Money, Deborah M., Maan, Evelyn, Costei, Adriana, Gadawski, Izabelle, Diong, Christina, Read, Stanley, Shen, Sandy, Harrigan, P. Richard, Burdge, David R., King, Susan M., and Forbes, John C.
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Highly active antiretroviral therapy -- Patient outcomes ,Highly active antiretroviral therapy -- Research ,Prenatal drug exposure -- Research ,Mitochondrial DNA -- Genetic aspects ,Mitochondrial DNA -- Physiological aspects ,Mitochondrial DNA -- Research ,Health - Published
- 2008
9. Vancomycin-induced red man syndrome
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Levy, Maurice, Koren, Gideon, Dupuis, Lee, and Read, Stanley E.
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Vancomycin -- Adverse and side effects - Abstract
The antibiotic vancomycin is used to treat Staphylococcus infections that are resistant to penicillin or other antibiotics. The most common side effect of vancomycin is the red man syndrome, which is characterized by the development of a local skin rash and/or hypotension (low blood pressure). The disorder usually resolves after discontinuing the drug. The prevalence of red man syndrome and factors that may predispose to this disorder were assessed. Of 650 children treated with vancomycin, 11 developed the red man syndrome. They were compared with 11 other vancomycin-treated children who did not develop the syndrome. Vancomycin was given for penicillin-resistant Staphylococcus infection or because of penicillin allergy in 73 percent of the children with an adverse reaction and 45 percent of those without a reaction. The average duration of the vancomycin infusion was 46 minutes in patients with the syndrome and 54 minutes in children without it. Slower infusion rates reduced or prevented the syndrome in five patients, indicating the relation of administration of this drug to the development of the side effect. The onset of red man syndrome usually occurred at the end of the infusion, but was also noted as early as 15 minutes after the start of the infusion. The disorder was characterized by a reddish rash on the face, neck, and ears, intense itching, symptoms of hypotension, watery and puffy eyes, a rapid heart rate, respiratory distress, dizziness, agitation, and a mild increase in body temperature. The rash usually disappeared within 20 minutes of stopping the vancomycin infusion. The development of the rash was not related to the blood levels of vancomycin, indicating that the red man syndrome is an idiosyncratic or unusual reaction, rather than a phenomenon that is dependent on the blood concentration of the drug. (Consumer Summary produced by Reliance Medical Information, Inc.)
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- 1990
10. Screening for cytomegalovirus retinitis in children
- Author
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Baumal, Caroline R., Levin, Alex V., Kavalec, Conrad C., Petric, Martin, Khan, Hamza, and Read, Stanley E.
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Cytomegalovirus infections -- Diagnosis ,Retinal diseases -- Diagnosis ,Medical screening -- Analysis ,Children -- Health aspects ,Health - Abstract
Objectives: To identify immunosuppressed children who are at risk of cytomegalovirus (CMV) retinitis developing and to evaluate the use of laboratory results for identifying this risk. Design: Prospective cohort and retrospective case-control series. Setting: University hospital pediatric referral center. Patients: Fifty-six consecutive immunocompromised children (de, the prospective group) with laboratory evidence consistent with acute or recently acquired CMV infection, which was defined as CMV cultured from the blood, urine, nasopharynx, or biopsy specimen, recent seroconversion, a 4-fold increase in the CMV antibody titer, or an antibody titer of 1:512 or greater. Ninety-three immunocompromised children (de, the retrospective group) with acute CMV or previous CMV exposure, which was defined as a CMV titer of 1:4 or greater and less than 1:512. Main Outcome Measure: Occurrence of CMV retinitis. Results: Cytomegalovirus retinitis developed in 3 children in the prospective group and in 4 children in the retrospective group. The causes of immunosuppression were severe combined immunodeficiency syndrome (n=2), severe combined immunodeficiency syndrome status post bone marrow transplantation (n=1), acquired immunodeficiency syndrome (n=1), and acquired immunodeficiency syndrome status post bone marrow transplantation for leukemia (n=1), renal transplantation (n=1), and chemotherapy for leukemia (n=1). Cytomegalovirus retinitis was associated with a positive CMV culture result from the urine (P=.03) or nasopharynx (P< 001) in the retrospective group. In the retrospective group, one child with congenital CMV infection and CMV retinitis was excluded from analysis because laboratory tests for CMV were not obtained prior to ganciclovir therapy. Conclusions: Cytomegalovirus retinitis is uncommon in children compared with adults; it occurred in 5% of the children in our series. A screening ophthalmologic examination should be considered in immunocompromised children with positive CMV laboratory results, particularly positive results of urine or nasopharynx cultures., Cytomegalovirus (CMV) retinitis may be infrequent among children with weakened immune systems. CMV is a congenital infection and may readily infect immunocompromised people. CMV retinitis is a form of the disease that destroys the retina of the eye. Researchers prospectively studied 56 and retrospectively studied 93 immunocompromised children for the presence of CMV infection and CMV retinitis. Only 5% of the children studied developed CMV retinitis, three in the prospective group and four in the retrospective group. Children with AIDS or other immunodeficiency diseases may have a greater risk of CMV retinitis.
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- 1996
11. Characteristics of HIV-infected pregnant women in the Bahamas
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Gomez, M. Perry, Bain, Rosa Mae, Major, Carol, Gray, Hannah, and Read, Stanley E.
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Caribbean Islands -- Health aspects ,Pregnant women -- Health aspects ,HIV infection -- Bahamas ,Health - Abstract
The rate of HIV infection in the Bahamas may be the highest in the Caribbean. Of 3,914 women attending prenatal care clinics in New Providence island between Sep 1990 and Aug 1991, 2.9% tested positive for HIV. Among the women born in the Bahamas, the prevalence of HIV infection was 2.5%, compared to 4.5% among women born in Haiti. Older age and number of children were associated with HIV infection, as was syphilis. This indicates that most women acquire the disease from sexual intercourse. Women with little education were more likely to be HIV-positive as were those who freebased cocaine.
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- 1996
12. Detection of incident HIV infection by PCR compared to serology
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Read, Stanley, Cassol, Sharon, Coates, Randall, Major, Carol, McLaughlin, Bernadette, Salas, Teresa, Francis, Angela, Fanning, Mary, MacFadden, Douglas, Shepherd, Frances, Calzavara, Liviana, Johnson, Kenneth, and O'Shaughnessy, Michael
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HIV infection -- Diagnosis ,Polymerase chain reaction ,Serology ,Health - Published
- 1992
13. Cellular immunity of patients with recurrent or refractory vulvovaginal moniliasis
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Fong, Ignatius W., McCleary, Paul, and Read, Stanley
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Candidiasis, Vulvovaginal -- Physiological aspects ,Cellular immunity -- Research ,Health - Abstract
Cellular immunity was studied in 73 patients with recurrent vaginal moniliasis and 37 healthy controls, by skin testing with the multitest CMI kit and Candida antigen, with measurement of lymphoblastic transformation to phytohemagglutinin, antigens of Candida albicans, mumps, and streptokinase. Eighteen patients (24.7%) had a hypoergic or anergic response to Candida antigen on skin testing versus two controls (5.4%), p = 0.01. Overall, the patient's lymphoblastic proliferation to mitogen and various antigens was not significantly different from that of the controls. However, a subgroup of younger women (19 to 29 years old) had impaired responses to Candida antigen when compared with age-matched controls, 58% versus 17%, p < 0.005. Most women with recurrent vaginal moniliasis had normal cellular immunity. (Am J Obstet Gynecol 1992;166:887-90.)
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- 1992
14. Percutaneous injuries among health care workers: the real value of human immunodeficiency virus testing of 'donor' blood
- Author
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Allen, Upton D., Guerriere, Michael, Read, Stanley E., and Detsky, Allan S.
- Subjects
Zidovudine -- Health aspects ,HIV infection -- Risk factors ,Blood-borne diseases ,Penetrating wounds -- Complications ,HIV infection -- Prevention ,HIV (Viruses) ,Medical personnel -- Injuries ,Health - Abstract
Health care workers have a small but possible risk of acquiring the human immunodeficiency virus (HIV), the agent that causes AIDS, as a result of job-related exposure to HIV-infected blood. The most common means of such exposure is through needlesticks, and one survey of senior residents in internal medicine showed a 72 percent rate of needlestick injuries during the years of training. Generally, patient's HIV status is unknown. The drug zidovudine is one of the few agents that has any effect against this virus, and some researchers have suggested that this drug be offered to all health care workers who sustain needlestick injuries involving patients with known HIV infection. Zidovudine has some serious side effects, making such a recommendation at least somewhat controversial. A theoretical model was devised to determine what course of action seems most reasonable in the case of needlestick injuries. Two possible options are to refrain from treating any one who has suffered a needlestick injury with zidovudine, and to treat all needlestick-injured health care workers with zidovudine. The risk of HIV infection in a health care worker following a needlestick injury involving an HIV-infected patient ranges from 0 to 1.82 percent. A presentation of the various treatment options was presented to some health care workers who might be at risk for needlestick injuries; their responses were evaluated. The most sensible course of action, according to the health care workers, would be to test the blood of the patient for HIV. This was seen as important for preserving the emotional state of the health care worker who had sustained the injury. Some of the health care workers would also prefer to be treated with zidovudine, despite the absence of proof that it is of significant value in preventing HIV transmission in needlestick injuries, and despite its side effect profile. The survey concluded that health care workers who sustain needlestick injuries should be offered the option of zidovudine therapy. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1991
15. Response to hepatitis B immunization in children with hemophilia: relationship to infection with human immunodeficiency virus type 1
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Chan, Wendy, Petric, Martin, Wang, Elaine, Koren, Gideon, Read, Stanley, and Blanchette, Victor
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Hemophilia in children -- Physiological aspects ,Hepatitis B -- Prevention ,HIV patients -- Physiological aspects ,Health - Abstract
Children who have hemophilia, a bleeding disorder, need treatment with blood products and thereby tend to become infected with hepatitis B. Immunization against hepatitis B is variably successful, depending on age, site of vaccination, and immune status. Children who become infected with human immunodeficiency virus type 1 (HIV), the agent that causes AIDS, may be less successfully immunized against hepatitis B. This was studied in 23 children with hemophilia; 12 of these children tested positive for HIV. Generally, antibody levels rose quickly after immunization, but tended to drop over the following five years. The levels of antibodies against hepatitis B, a measure of immunization, were significantly greater in the 11 children who were not HIV-infected. Antibodies declined below protective levels in 3 of 12 children with HIV when measured at three, four, or five years after immunization, while this decline occurred in only 1 of the 11 children without HIV. The study suggests that children with hemophilia who are immunized against hepatitis B should be monitored after immunization and yearly thereafter to determine antibody levels. Booster doses of vaccine should then be given as needed. Further studies are required to assess the effects of different immunization strategies for hemophilic children. (Consumer Summary produced by Reliance Medical Information, Inc.)
- Published
- 1990
16. Cytomegalovirus Retinitis in Immunosuppressed Children
- Author
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BAUMAL, CAROLINE R., LEVIN, ALEX V., and READ, STANLEY E.
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Cytomegalovirus infections -- Care and treatment ,Retina -- Inflammation ,Immunosuppression -- Health aspects ,Health - Published
- 1999
17. Children hospitalized with severe acute respiratory syndrome-related illness in Toronto
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Bitnun, Ari, Allen, Upton, Heurter, Helen, King, Susan M., Opavsky, Mary Anne, Ford-Jones, Elizabeth L., Matlow, Anne, Kitai, Ian, Tellier, Raymond, Richardson, Susan, Manson, David, Babyn, Paul, and Read, Stanley
- Subjects
Polymerase chain reaction -- Analysis ,Severe acute respiratory syndrome -- Health aspects ,Severe acute respiratory syndrome -- Care and treatment ,Severe acute respiratory syndrome -- Demographic aspects ,Severe acute respiratory syndrome -- Diagnosis ,Severe acute respiratory syndrome -- Case studies ,Sick children -- Care and treatment ,Sick children -- Health aspects ,Pediatrics -- Research - Abstract
Objective. An outbreak of severe acute respiratory syndrome (SARS) occurred in the greater Toronto area between February and June 2003. We describe the clinical, laboratory, and epidemiologic features of children who were admitted to the Hospital for Sick Children, Toronto, with a presumptive diagnosis of suspect or probable SARS. Methods. A prospective investigational study protocol was established for the management of children with a presumptive diagnosis of suspect or probable SARS. All were ultimately classified as having probable SARS, suspect SARS, or another cause on the basis of their epidemiologic exposure, clinical and radiologic features, and results of microbiologic investigations. Results. Twenty-five children were included; 10 were classified as probable SARS and 5 were classified as suspect SARS, and in 10 another cause was identified. The exposure consisted of direct contact with at least 1 adult probable SARS case in 11 children, travel from a World Health Organization-designated affected area in Asia in 9 children, and presence in a Toronto area hospital in which secondary SARS spread had occurred in 5 children. The predominant clinical manifestations of probable cases were fever, cough, and rhinorrhea. With the exception of 1 teenager, none of the children developed respiratory distress or an oxygen requirement, and all made full recoveries. Mild focal alveolar infiltrates were the predominant chest radiograph abnormality. Lymphopenia; neutropenia; thrombocytopenia; and elevated alanine aminotransferase, aspartate aminotransferase, and creatine kinase were present in some cases. Nasopharyngeal swab specimens were negative for the SARS-associated coronavirus by an in-house reverse transcriptase-polymerase chain reaction in all 25 children. Conclusions. Our results indicate that SARS is a relatively mild and nonspecific respiratory illness in previously healthy young children. The presence of fever in conjunction with a SARS exposure history should prompt one to consider SARS as a possible diagnosis in children irrespective of the presence or absence of respiratory symptoms. Reverse-transcriptase polymerase chain reaction analysis of nasopharyngeal specimens seems to be of little utility for the diagnosis of SARS during the early symptomatic phase of this illness in young children. Pediatrics 2003;112:e261-e268. URL: http: //www.pediatrics.org/cgi/content/full/112/4/e261; severe acute respiratory syndrome, reverse-transcriptase polymerase chain reaction, probable SARS, suspect SARS.
- Published
- 2003
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