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Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study

Identifieur interne : 006414 ( Main/Exploration ); précédent : 006413; suivant : 006415

Clinical progression and viral load in a community outbreak of coronavirus-associated SARS pneumonia: a prospective study

Auteurs : J. S. M. Peiris [Hong Kong] ; C. M. Chu [Hong Kong] ; V. C. C. Cheng [Hong Kong] ; K. S. Chan [Hong Kong] ; I. F. N. Hung [Hong Kong] ; L. L. M. Poon [Hong Kong] ; K. I. Law [Hong Kong] ; B. S. F. Tang [Hong Kong] ; T. Y. W. Hon [Hong Kong] ; C. S. Chan [Hong Kong] ; K. H. Chan [Hong Kong] ; J. S. C. Ng [Hong Kong] ; B. J. Zheng [Hong Kong] ; W. L. Ng [Hong Kong] ; R. W. M. Lai [Hong Kong] ; Y. Guan [Hong Kong] ; K. Y. Yuen [Hong Kong]

Source :

RBID : Pascal:03-0368163

Descripteurs français

English descriptors

Abstract

Background We investigated the temporal progression of the clinical, radiological, and virological changes in a community outbreak of severe acute respiratory syndrome (SARS). Methods We followed up 75 patients for 3 weeks managed with a standard treatment protocol of ribavirin and corticosteroids, and assessed the pattern of clinical disease, viral load, risk factors for poor clinical outcome, and the usefulness of virological diagnostic methods. Findings Fever and pneumonia initially improved but 64 (85%) patients developed recurrent fever after a mean of 8.9 (SD 3.1) days, 55 (73%) had watery diarrhoea after 7.5 (2.3) days, 60 (80%) had radiological worsening after 7.4 (2.2) days, and respiratory symptoms worsened in 34 (45%) after 8-6 (3.0) days. In 34 (45%) patients, improvement of initial pulmonary lesions was associated with appearance of new radiological lesions at other sites. Nine (12%) patients developed spontaneous pneumomediastinum and 15 (20%) developed acute respiratory distress syndrome (ARDS) in week 3. Quantitative reverse-transcdptase (RT) PCR of nasopharyngeal aspirates in 14 patients (four with ARDS) showed peak viral load at day 10, and at day 15 a load lower than at admission. Age and chronic hepatitis B virus infection treated with lamivudine were independent significant risk factors for progression to ARDS (p=0.001). SARS associated coronavirus in faeces was seen on RT-PCR in 65 (97%) of 67 patients at day 14. The mean time to seroconversion was 20 days. Interpretation The consistent clinical progression, shifting radiological infiltrates, and an inverted V viral-load profile suggest that worsening in week 2 is unrelated to uncontrolled viral replication but may be related to immunopathological damage.


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<term>Acute</term>
<term>Administration, Oral</term>
<term>Adult</term>
<term>Aged</term>
<term>Amoxicillin-Potassium Clavulanate Combination (administration & dosage)</term>
<term>China</term>
<term>Diagnosis</term>
<term>Disease Outbreaks (statistics & numerical data)</term>
<term>Disease Progression</term>
<term>Epidemiology</term>
<term>Evolution</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Human</term>
<term>Humans</term>
<term>Infusions, Intravenous</term>
<term>Length of Stay</term>
<term>Lung (diagnostic imaging)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Ofloxacin</term>
<term>Pneumopathy</term>
<term>Pregnancy</term>
<term>Pregnancy Complications, Infectious (diagnosis)</term>
<term>Pregnancy Complications, Infectious (therapy)</term>
<term>Prognosis</term>
<term>Pulse Therapy, Drug</term>
<term>Radiography</term>
<term>Risk factor</term>
<term>SARS Virus (isolation & purification)</term>
<term>Severe Acute Respiratory Syndrome (diagnosis)</term>
<term>Severe Acute Respiratory Syndrome (drug therapy)</term>
<term>Severe Acute Respiratory Syndrome (epidemiology)</term>
<term>Severe Acute Respiratory Syndrome (virology)</term>
<term>Survival Rate</term>
<term>Syndrome</term>
<term>Viral Load (statistics & numerical data)</term>
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<term>Administration par voie orale</term>
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Association amoxicilline-clavulanate de potassium (administration et posologie)</term>
<term>Charge virale ()</term>
<term>Complications de la grossesse et maladies infectieuses ()</term>
<term>Complications de la grossesse et maladies infectieuses (diagnostic)</term>
<term>Durée du séjour</term>
<term>Femelle</term>
<term>Flambées de maladies ()</term>
<term>Grossesse</term>
<term>Humains</term>
<term>Mâle</term>
<term>Ofloxacine</term>
<term>Perfusions veineuses</term>
<term>Pharmacothérapie administrée en bolus</term>
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<term>Évolution de la maladie</term>
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<term>Amoxicillin-Potassium Clavulanate Combination</term>
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<term>Pregnancy Complications, Infectious</term>
<term>Severe Acute Respiratory Syndrome</term>
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<term>Syndrome respiratoire aigu sévère</term>
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<term>Lung</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Severe Acute Respiratory Syndrome</term>
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<term>Severe Acute Respiratory Syndrome</term>
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<term>Virus du SRAS</term>
</keywords>
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<term>Disease Outbreaks</term>
<term>Viral Load</term>
</keywords>
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<term>Pregnancy Complications, Infectious</term>
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<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Syndrome respiratoire aigu sévère</term>
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<term>Syndrome respiratoire aigu sévère</term>
</keywords>
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<term>Severe Acute Respiratory Syndrome</term>
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<term>Syndrome respiratoire aigu sévère</term>
</keywords>
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<term>Administration, Oral</term>
<term>Adult</term>
<term>Aged</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Infusions, Intravenous</term>
<term>Length of Stay</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Ofloxacin</term>
<term>Pregnancy</term>
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<term>Radiography</term>
<term>Survival Rate</term>
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<term>Complications de la grossesse et maladies infectieuses</term>
<term>Durée du séjour</term>
<term>Femelle</term>
<term>Flambées de maladies</term>
<term>Grossesse</term>
<term>Humains</term>
<term>Mâle</term>
<term>Ofloxacine</term>
<term>Perfusions veineuses</term>
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<term>Evolution</term>
<term>Facteur risque</term>
<term>Pronostic</term>
<term>Diagnostic</term>
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<term>Études de suivi</term>
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<front>
<div type="abstract" xml:lang="en">Background We investigated the temporal progression of the clinical, radiological, and virological changes in a community outbreak of severe acute respiratory syndrome (SARS). Methods We followed up 75 patients for 3 weeks managed with a standard treatment protocol of ribavirin and corticosteroids, and assessed the pattern of clinical disease, viral load, risk factors for poor clinical outcome, and the usefulness of virological diagnostic methods. Findings Fever and pneumonia initially improved but 64 (85%) patients developed recurrent fever after a mean of 8.9 (SD 3.1) days, 55 (73%) had watery diarrhoea after 7.5 (2.3) days, 60 (80%) had radiological worsening after 7.4 (2.2) days, and respiratory symptoms worsened in 34 (45%) after 8-6 (3.0) days. In 34 (45%) patients, improvement of initial pulmonary lesions was associated with appearance of new radiological lesions at other sites. Nine (12%) patients developed spontaneous pneumomediastinum and 15 (20%) developed acute respiratory distress syndrome (ARDS) in week 3. Quantitative reverse-transcdptase (RT) PCR of nasopharyngeal aspirates in 14 patients (four with ARDS) showed peak viral load at day 10, and at day 15 a load lower than at admission. Age and chronic hepatitis B virus infection treated with lamivudine were independent significant risk factors for progression to ARDS (p=0.001). SARS associated coronavirus in faeces was seen on RT-PCR in 65 (97%) of 67 patients at day 14. The mean time to seroconversion was 20 days. Interpretation The consistent clinical progression, shifting radiological infiltrates, and an inverted V viral-load profile suggest that worsening in week 2 is unrelated to uncontrolled viral replication but may be related to immunopathological damage.</div>
</front>
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<li>Hong Kong</li>
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<name sortKey="Chan, C S" sort="Chan, C S" uniqKey="Chan C" first="C. S." last="Chan">C. S. Chan</name>
<name sortKey="Chan, K H" sort="Chan, K H" uniqKey="Chan K" first="K. H." last="Chan">K. H. Chan</name>
<name sortKey="Chan, K S" sort="Chan, K S" uniqKey="Chan K" first="K. S." last="Chan">K. S. Chan</name>
<name sortKey="Cheng, V C C" sort="Cheng, V C C" uniqKey="Cheng V" first="V. C. C." last="Cheng">V. C. C. Cheng</name>
<name sortKey="Chu, C M" sort="Chu, C M" uniqKey="Chu C" first="C. M." last="Chu">C. M. Chu</name>
<name sortKey="Guan, Y" sort="Guan, Y" uniqKey="Guan Y" first="Y." last="Guan">Y. Guan</name>
<name sortKey="Hon, T Y W" sort="Hon, T Y W" uniqKey="Hon T" first="T. Y. W." last="Hon">T. Y. W. Hon</name>
<name sortKey="Hung, I F N" sort="Hung, I F N" uniqKey="Hung I" first="I. F. N." last="Hung">I. F. N. Hung</name>
<name sortKey="Lai, R W M" sort="Lai, R W M" uniqKey="Lai R" first="R. W. M." last="Lai">R. W. M. Lai</name>
<name sortKey="Law, K I" sort="Law, K I" uniqKey="Law K" first="K. I." last="Law">K. I. Law</name>
<name sortKey="Ng, J S C" sort="Ng, J S C" uniqKey="Ng J" first="J. S. C." last="Ng">J. S. C. Ng</name>
<name sortKey="Ng, W L" sort="Ng, W L" uniqKey="Ng W" first="W. L." last="Ng">W. L. Ng</name>
<name sortKey="Poon, L L M" sort="Poon, L L M" uniqKey="Poon L" first="L. L. M." last="Poon">L. L. M. Poon</name>
<name sortKey="Tang, B S F" sort="Tang, B S F" uniqKey="Tang B" first="B. S. F." last="Tang">B. S. F. Tang</name>
<name sortKey="Yuen, K Y" sort="Yuen, K Y" uniqKey="Yuen K" first="K. Y." last="Yuen">K. Y. Yuen</name>
<name sortKey="Zheng, B J" sort="Zheng, B J" uniqKey="Zheng B" first="B. J." last="Zheng">B. J. Zheng</name>
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