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1.
Frontiers of Medicine ; (4): 378-388, 2022.
Article in English | WPRIM | ID: wpr-939871

ABSTRACT

Macrolide and corticosteroid resistance has been reported in patients with Mycoplasma pneumoniae (MP) pneumonia (MPP). MP clearance is difficult to achieve through antibiotic treatment in sensitive patients with severe MPP (SMPP). SMPP in children might progress to airway remodeling and even bronchiolitis/bronchitis obliterans. Therefore, identifying serum biomarkers that indicate MPP progression and exploring new targeted drugs for SMPP treatment require urgency. In this study, serum samples were collected from patients with general MPP (GMPP) and SMPP to conduct proteomics profiling. The Fc fragment of the IgG-binding protein (FCGBP) was identified as the most promising indicator of SMPP. Biological enrichment analysis indicated uncontrolled inflammation in SMPP. ELISA results proved that the FCGBP level in patients with SMPP was substantially higher than that in patients with GMPP. Furthermore, the FCGBP levels showed a decreasing trend in patients with GMPP but the opposite trend in patients with SMPP during disease progression. Connectivity map analyses identified 25 possible targeted drugs for SMPP treatment. Among them, a mechanistic target of rapamycin kinase (mTOR) inhibitor, which is a macrolide compound and a cell proliferation inhibitor, was the most promising candidate for targeting SMPP. To our knowledge, this study was the first proteomics-based characterization of patients with SMPP and GMPP.


Subject(s)
Child , Humans , Biomarkers , Carrier Proteins , Immunoglobulin Fc Fragments , Immunoglobulin G , Macrolides , Mycoplasma pneumoniae , Pneumonia, Mycoplasma/drug therapy , Proteomics
2.
Chinese Journal of Contemporary Pediatrics ; (12): 707-712, 2021.
Article in Chinese | WPRIM | ID: wpr-888470

ABSTRACT

OBJECTIVE@#To study the drug resistance of @*METHODS@#BALF specimens were collected from 245 children with RMPP who were admitted to the Children's Hospital Affiliated to Zhengzhou University from March 2016 to December 2020. A rapid cultured drug sensitivity assay was used to detect the resistance of MP isolates to nine commonly used antimicrobial drugs. The real-time PCR was used to measure MP DNA. The direct sequencing was used to detect gene mutations in MP 23SrRNA V region central ring.@*RESULTS@#Among the 245 BALF specimens, 207 tested positive for MP DNA, with a positive rate of 84.5%. The results of drug susceptibility test showed that the children with RMPP had a resistance rate of > 70% to macrolide antimicrobial drugs, with the highest resistance rate to clarithromycin, followed by roxithromycin, clindamycin, acetylspiramycin, erythromycin, and azithromycin, and these children had a resistance rate of < 5% to quinolone antimicrobial drugs. Among the 207 MP DNA-positive specimens, 41 (19.8%) had no drug-resistance gene mutations and 166 (80.2%) had drug-resistance gene mutations, among which 154 (74.4%) had an A→G mutation at 2063 locus of 23SrRNA V region central ring, 7 (3.4%) had an A→G mutation at 2064 locus, and 5 (2.4%) had mutations in both 2063 and 2064 loci. Among the 166 specimens with point mutations of the MP 23SrRNA gene, 159 (95.8%) had point mutations at 2063 locus. The A→G point mutation at 2063 locus of 23SrRNA V region central ring had a great impact on resistance to macrolide antimicrobial drugs. There was a significant difference in the distribution of alleles at 2063 locus between the children with resistance to clarithromycin, roxithromycin, clindamycin, acetylspiramycin, erythromycin, and azithromycin (@*CONCLUSIONS@#MP in the BALF of children with RMPP has a relatively high resistance rate to macrolide antimicrobial drugs. Resistance to macrolide antimicrobial drugs is closely associated with the A→G point mutation in the 23SrRNA gene, and the point mutation at 2063 locus of 23SrRNA V region central ring may affect the drug-resistance mechanism of MP.


Subject(s)
Child , Humans , Anti-Bacterial Agents/pharmacology , Bronchoalveolar Lavage Fluid , Drug Resistance, Bacterial/genetics , Mycoplasma pneumoniae/genetics , Pneumonia, Mycoplasma/drug therapy
3.
China Journal of Chinese Materia Medica ; (24): 5958-5976, 2021.
Article in Chinese | WPRIM | ID: wpr-921719

ABSTRACT

To systematically evaluate the clinical efficacy of 14 oral Chinese patent medicines combined with Azithromycin in the treatment of mycoplasma pneumonia in children with network Meta-analysis. Computer retrieval was performed for such databases as CNKI, VIP, Wanfang, CBM, PubMed, EMbase and Cochrane Library to screen out randomized controlled trials of oral Chinese patent medicines combined with Azithromycin in the treatment of mycoplasma pneumonia in children from the time of database establishment to September 2020. The included studies were evaluated by the Cochrane Risk Assessment tool. Stata 14.0 and Review Manager 5.3 software were used for data statistical analysis. A total of 60 RCTs were included in this study, involving 14 oral Chinese patent medicines. The efficacy ranking based on network Meta-analysis was as follows:(1)in terms of total effective rate, top five Chinese patent medicines in surface under the cumulative ranking curve(SUCRA) were Xiao'er Xiaoji Zhike Oral Liquid, Xiao'er Chiqiao Qingre Granules, Xiao'er Feike Granules, Pudilan Xiaoyan Oral Liquid and Lanqin Oral Liquid;(2)in terms of antifebrile time, top five Chinese patent medicines in SUCRA were Huaiqihuang Granules, Xiao'er Magan Granules, Xiao'er Kechuanling Granules/Oral Liquid, Shuanghuang-lian Oral Liquid for children and Xiao'er Xiaoji Zhike Oral Liquid;(3)in terms of cough disappearance time, top five Chinese patent medicines in SUCRA were Xiao'er Magan Granules, Huaiqihuang Granules, Xiao'er Chiqiao Qingre Granules, Xiao'er Feire Kechuan Oral Liquid and Xiao'er Kechuanling Granules/Oral Liquid;(4)in terms of rale disappearance time, top five Chinese patent medicines in SUCRA were Xiao'er Magan Granules, Huaiqihuang Granules, Xiao'er Feire Kechuan Oral Liquid, Shuanghuanglian Oral Liquid for children and Yupingfeng Granules. The results showed that on the basis of the use of Azithromycin, combined administration with oral Chinese patent medicines could improve the overall clinical efficacy in the treatment of mycoplasma pneumonia in children. However, due to the large differences in the quality and the number of included studies among various therapeutic measures, the ranking results of SUCRA of Chinese patent medicines need to be verified by high-quality multi-center, large-sample, randomized double-blind trials in the future.


Subject(s)
Child , Humans , Azithromycin , China , Drugs, Chinese Herbal , Network Meta-Analysis , Nonprescription Drugs , Pneumonia, Mycoplasma/drug therapy , Randomized Controlled Trials as Topic
4.
Medwave ; 20(7): e8006, 2020.
Article in English, Spanish | LILACS | ID: biblio-1122649

ABSTRACT

Una de las principales causas de neumonía en niños entre 5 y 15 años es el Mycoplasma pneumoniae, una bacteria que causa manifestaciones clínicas atípicas como la miositis y encefalitis. Reportamos un caso de una niña de cinco años que presentó limitación funcional en extremidades inferiores precedida por una infección respiratoria superior. Posteriormente, se complicó con neumonía y encefalitis. Se administraron antibióticos y antivirales debido al deterioro clínico del paciente. La serología de inmunoglobulinas para Mycoplasma pneumoniae fue positiva; mientras que los demás estudios virales fueron negativos. El curso clínico fue favorable con disminución progresiva de la dificultad respiratoria, trastorno del sensorio y mejoría en la limitación funcional en las extremidades inferiores a los 15 días de tratamiento.


One of the leading causes of pneumonia in children between 5 to 15 years is Mycoplasma pneumoniae, a bacterium that causes atypical clinical manifestations such as myositis and encephalitis. We report a 5-year-old girl who presented functional limitations of the lower extremities preceded by an upper respiratory infection. Later on, she developed pneumonia and encephalitis. Antibiotics and antivirals were administered due to the clinical deterioration of the patient. IgM serology for Mycoplasma pneumoniae was positive, while the other viral studies were negative. The clinical course was favorable with a progressive decrease in respiratory distress, sensorial disorder, and improvement in the functional limitations of the lower limbs after 15 days of treatment.


Subject(s)
Humans , Female , Child, Preschool , Pneumonia, Mycoplasma/diagnosis , Encephalitis/diagnosis , Mycoplasma pneumoniae/isolation & purification , Myositis/diagnosis , Pneumonia, Mycoplasma/microbiology , Pneumonia, Mycoplasma/drug therapy , Acute Disease , Encephalitis/microbiology , Encephalitis/drug therapy , Anti-Bacterial Agents/administration & dosage , Myositis/microbiology , Myositis/drug therapy
5.
Colomb. med ; 49(2): 160-163, Apr.-June 2018. tab
Article in English | LILACS | ID: biblio-952909

ABSTRACT

Abstract Introduction: Community-acquired pneumonia (CAP) is a global disease responsible for a large number of deaths, with significant economic impact. As diagnostic tools have increased in sensitivity, understanding of the etiology of CAP has begun to change. Mycoplasma pneumoniae is one of the major pathogens causing CAP. Macrolides and related antibiotics are first-line treatments for M. pneumoniae. Macrolide resistance has been spreading for 15 years and now occurs in worldwide. We undertook the first study on macrolide resistance of M. pneumoniae in Yantai. This may be helpful to determine the appropriate therapy for CAP in this population. Objective: To investigate the rate and mechanism of macrolide resistance in Yantai. Methods: Pharyngeal swab samples were collected from adult CAP patients. Samples were assayed by polymerase chain reaction (PCR) and cultivated to test for M. pneumoniae. Nested PCR was used to specifically amplify M. pneumoniae 23S rRNA gene fragments containing mutations, and amplicons were analyzed by CE-SSCP for macrolide resistance mutations. Results were confirmed by sequencing. Twenty-seven strains of M. pneumoniae were isolated and the activities of nine antibiotics against M. pneumoniae were tested in vitro. Results: Out of 128 samples tested, 27 were positive for M. pneumoniae. Mycoplasma 100% macrolides resistance to Mycoplasma pneumoniae. The mechanism of macrolides resistance was A2063G point mutation in the sequence directly binding to macrolides in the 23S rRNA V domain in vitro. The mean pyretolytic time for the fluoroquinolone group was 4.7 ±2.9 d, which was significantly shorter than 8.2 ±4.1 d for the azithromycin group. Conclusions: Macrolides are not the first-line treatment for M. pneumoniae respiratory tract infections in Yantai.


Resumen Introducción: Neumonía adquirida por en la comunidad (NAC) es una enfermedad responsable por un gran número de muertes y un impacto económico importante. Debido a que el diagnostico incrementó la sensibilidad, se cambió la etiología de la NAC. Adicionalmente, Mycoplasma pneumoniae es uno de los patógenos que causan la NAC. Los macrólidos y antibióticos relacionados son la primera línea de tratamiento para M. pneumoniae. La resistencia a macrólidos se aumentó en los últimos 15 años y ahora se encuentra distribuido en todo el mundo. Nosotros realizamos el primer estudio de resitencia a M. pneumoniae a los macrólidos en Yantai. Esto podría ser útil para determinar una terapia apropiada para NAC en esta población. Objetivo: Investigar la tasa y el mecanismo para la resitencia a los macrólidos en Yantai. Métodos: Se colectaron muestras faringeas usando un hisopo. Las muestras se analizaron mediante la reacción en cadena de la polimerasa (PCR) y por cultivo para M. pneumoniae. Se uso una PCR anidad para amplificar fragmentos del gen 23S rRNA especifico con las mutaciones para M. pneumoniae. Se analizaron amplicomes por CE-SSCP para determinar la resitencia a los macrólidos. Estos resultados se confirmaron por secuenciación. Se aislaron 27 cepas de M. pneumoniae y se probaron nueve antibióticos in vitro. Resultados: De 128 muestras, 27 fueron positivas para M. pneumoniae. Se determinó una resistencia a macrólidos por Mycoplasma del 100%. Los mecanismos de esta resitencia fue una mutacion punctual A2063G en la secuencia que se une directamente a los macrólidos en el dominio 23S rRNA V in vitro. El tiempo piotolítico medio para el grupo de fluoroquinolonas fue 4.7 ±2.9 d, que fue significativamente más corto que para el grupo de azitromicina: 8.2 ±4.1 d. Conclusiones: Los macrólidos no son la primera linea de tratamiento para las infecciones del tracto respiratorio contra M. pneumoniae respiratory tract infections en Yantai.


Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Pneumonia, Mycoplasma/epidemiology , Community-Acquired Infections/epidemiology , Anti-Bacterial Agents/pharmacology , Mycoplasma pneumoniae/isolation & purification , Pneumonia, Mycoplasma/microbiology , Pneumonia, Mycoplasma/drug therapy , China/epidemiology , Polymerase Chain Reaction , Point Mutation , Community-Acquired Infections/microbiology , Community-Acquired Infections/drug therapy , Macrolides/pharmacology , Drug Resistance, Bacterial/genetics
6.
Braz. j. infect. dis ; 18(3): 294-299, May-June/2014. tab
Article in English | LILACS | ID: lil-712954

ABSTRACT

BACKGROUND: The aim of this study was to clarify retrospectively the characteristics of children hospitalized for respiratory tract infection caused by macrolide-resistant Mycoplasma pneumoniae (M. pneumoniae). METHODS: Children who were hospitalized for respiratory tract infection due to M. pneumoniae were enrolled in this study. The diagnosis of M. pneumoniae infection was made on the grounds of polymerase chain reaction results. RESULTS: Thirty-three children were hospitalized due to lower respiratory tract infection with M. pneumoniae. Of the 33 children, 31 (median age five years) were identified as being infected with macrolide-resistant M. pneumoniae (A2063G:30, A2064G:1) by sequence analysis. Of the 31 children infected with macrolide-resistant M. pneumoniae, 21 (68%) had received 14- or 15-membered macrolide antibiotics and four (13%) had received minocycline before hospitalization. During hospitalization, minocycline was administered to 16 (52%) of the 31 children infected with macrolide-resistant M. pneumoniae. Of the 20 children infected with macrolide-resistant M. pneumoniae under eight years of age, six (30%) were treated with minocycline during hospitalization. The difference in total febrile days between children receiving minocycline treatment before hospitalization and children not receiving minocycline treatment was three days. CONCLUSIONS: The majority of hospitalized children with respiratory tract infection due to macrolide-resistant M. pneumoniae infection was of preschool age and had received 14- or 15-membered macrolide antibiotics before hospitalization. Because macrolide-resistant M. pneumoniae is widespread in Japan, the administration of minocycline as a second-line antibiotic in children under eight years of age cannot be withheld when clinical symptoms do not improve with macrolide antibiotics. .


Subject(s)
Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male , Anti-Bacterial Agents/therapeutic use , Drug Resistance, Bacterial , Macrolides , Mycoplasma pneumoniae/genetics , Pneumonia, Mycoplasma/drug therapy , Hospitalization , Polymerase Chain Reaction , Pneumonia, Mycoplasma/diagnosis , Retrospective Studies
7.
Neumol. pediátr ; 8(2): 74-78, 2013. ilus, tab
Article in Spanish | LILACS | ID: lil-701692

ABSTRACT

Atypical pneumonias are a significant percentage of causal agents of pneumonia in children. Dominate over 5years of age, although in the last three years there is an increase in cases in children three years of age, especially secondary to Mycoplasma. In this review, we will refer to Mycoplasma pneumoniae, as the atypical germ most common and important in the epidemiology of children with pulmonary involvement. Mycoplasma pneumonia, can explain 20-25 percent of pneumonia in children, especially in preschool and school age.


Las neumonías atípicas constituyen un porcentaje importante de agentes causales de neumonía en niños. Predominan en mayores de 5 años de edad, aunque en los últimos años, existe un incremento de casos en niños de 3años de edad, sobre todo secundario al Mycoplasma. En esta revisión, nos referiremos al Mycoplasma pneumoniae, como el germen de los atípicos más frecuente e importante en la epidemiología del niño con afectación pulmonar. Las neumonías por mycoplasma, pueden explicar del 20 al 25 por ciento de las neumonías en niños, sobre todo en edades preescolares y escolares.


Subject(s)
Humans , Child , Pneumonia, Mycoplasma/diagnosis , Pneumonia, Mycoplasma/drug therapy , Anti-Bacterial Agents/therapeutic use , Clinical Laboratory Techniques , Pneumonia, Mycoplasma/complications , Pneumonia, Mycoplasma/transmission , Radiography, Thoracic
8.
Biomédica (Bogotá) ; 32(2): 174-178, abr.-jun. 2012. tab
Article in Spanish | LILACS | ID: lil-656824

ABSTRACT

El metaneumovirus humano es un nuevo patógeno asociado a infecciones respiratorias, principalmente en niños, que produce cuadros clínicos que van desde leves hasta graves, los cuales pueden incluso requerir tratamiento en unidades de cuidados intensivos. Hasta el momento, la reacción en cadena de la polimerasa con transcripción inversa y el cultivo celular son los métodos más usados para su diagnóstico. Se presentan los seis primeros casos de metapneumovirus humano en niños de Medellín, Colombia.


Human metapneumovirus is a newly discovered pathogen associated with respiratory disease and occurring mainly in children. It produces an acute viral respiratory disease picture that varies from mild disease to severe, and which can require strict surveillance in intensive care units. Currently, reverse transcriptase polymerase chain reaction and cell culture are the most common methods for its diagnosis. The first six cases of human metapneumovirus in Colombia are presented from Medellín.


Subject(s)
Child , Child, Preschool , Female , Humans , Infant , Male , Metapneumovirus/isolation & purification , Paramyxoviridae Infections/virology , Pneumonia, Viral/virology , /therapeutic use , Hypoxia/etiology , Anti-Bacterial Agents/therapeutic use , Clarithromycin/therapeutic use , Colombia/epidemiology , Fever/etiology , Immunologic Tests , Paramyxoviridae Infections/complications , Paramyxoviridae Infections/diagnosis , Paramyxoviridae Infections/epidemiology , Paramyxoviridae Infections , Pneumonia, Mycoplasma/complications , Pneumonia, Mycoplasma/drug therapy , Pneumonia, Viral/complications , Pneumonia, Viral/epidemiology , Pneumonia, Viral , Reverse Transcriptase Polymerase Chain Reaction , Superinfection , Virus Cultivation
9.
Rev. chil. neuro-psiquiatr ; 49(1): 56-61, mar. 2011. ilus
Article in Spanish | LILACS | ID: lil-592065

ABSTRACT

Mycoplasma pneumoniae produce 10 to 20 percent of atypical pneumonia, and secondarily affects by autoimmune mechanisms the central and peripheral nervous system. This presentation prospects to understand others pathologies than pneumonia, originated by mycoplasma pneumonia, like hemorrhagic cerebral microvasculitis, Bickerstaff syndrome and autoimmune hemolytic anemia expressed by an adolescent. They were an immunomimetic manifestation of this bacteria, same days after pulmonary box. The microvasculitis shows blood in the CSF, retinal hemorrhages and special MR imaging s. Protuberancia! syndrome was identified by a multidirectional nystagmus, facial diplegia, involvement of the sixth cranial nerve and quadriplegia with pyramidal signs. The autoimmune hemolytic anemia was the last complication. Generally all these syndromes have been isolated described in relation to this bacterial infection. In this case they occurred simultaneously. The cerebral vasculitis took a special way, apparently not described before with these characteristics. Our conclusions are that mycoplasma pneumoniae can affect simultaneously different parenchyma expressing immunomimetic responses.


El Mycoplasma neumoniae es una bacteria productora del 10 al 20 por ciento de las neumonías atípicas, que secundariamente y por patomecanismos inmunomiméticos afecta al sistema nervioso central y periférico. Con esta presentación se busca dar significado a las variadas alteraciones que originó una neumonía por mycoplasma en un adolescente, que además presentó una micro vasculitis cerebral hemorrágica, un síndrome de Bickerstaffy una anemia hemolítica autoimune, como expresión de una respuesta inmunomimética desencadenada por la bacteria, días después de cuadro pulmonar. La microvasculitis produjo presencia de sangre en el LCR, hemorragias retinianas y una RM con imágenes características. El síndrome rombencefálico se identificó por un nistagmus multidireccional, diplejia facial, compromiso del sexto par y cuadriparesia con signos piramidales, que secuencial mente se complicaron con una anemia hemolítica autoimune. Todos estos síndromes han sido descritos aisladamente en relación a esta infección bacteriana, sin embargo, en este caso se produjeron simultáneamente y la vasculitis cerebral tomó un modo especial, al parecer no descrito antes con esas características. Se concluye que el mycoplasma neumoniae puede afectar con respuestas inmunomiméticas diversos parénquimas simultáneamente.


Subject(s)
Humans , Male , Adolescent , Anemia, Hemolytic, Autoimmune/etiology , Encephalitis/etiology , Pneumonia, Mycoplasma/complications , Vasculitis, Central Nervous System/etiology , Anti-Bacterial Agents/therapeutic use , Mycoplasma pneumoniae , Pneumonia, Mycoplasma/drug therapy
12.
Article in English | IMSEAR | ID: sea-119143

ABSTRACT

BACKGROUND: Community-acquired pneumonia is an important cause of mortality and hospitalization in all age groups. In temperate climates, Mycoplasma pneumoniae is a common respiratory pathogen causing pneumonia. Information on human Mycoplasma infection in India is scarce. METHODS: We aimed to determine the frequency of Mycoplasma pneumoniae infection among patients with community-acquired pneumonia in a prospective cross-sectional study. The assessment included clinical and radiological evaluation followed by microbiological evaluation for the specific pathogen. Microbiological investigations included aerobic and anaerobic blood culture, anti-Mycoplasma IgM antibody detection by gelatin particle agglutination test and ELISA, culture of respiratory tract secretions for Mycoplasma pneumoniae and other organisms, and detection of specific Mycoplasma pneumoniae antigen by indirect immunofluorescence. RESULTS: Sixty-two patients (42 men and 20 women; mean age 41.7 years) with community-acquired pneumonia were investigated prospectively. They included 42 immunocompetent and 20 immunocompromised patients. Six patients had definitive evidence of Mycoplasma pneumoniae infection and an additional 16 patients had a probable diagnosis. In all, 22 (35.5%) patients with pneumonia had Mycoplasma pneumoniae infection. Of these, 12 patients belonged to the immunocompromised group and 10 to the immunocompetent group. Patients with Mycoplasma pneumoniae infection also had secondary bacterial infection as evidenced by organisms isolated from blood in 50% and from respiratory tract secretions in 68%. CONCLUSION: Community-acquired pneumonia has a polymicrobial aetiology, of which the prevalence of Mycoplasma pneumoniae is 35%. The study has two implications: (i) Mycoplasma pneumoniae infection is frequently associated with secondary bacterial infection; and (ii) initial empirical antibiotic therapy for community-acquired pneumonia in India must include antibiotics with activity against Mycoplasma pneumoniae.


Subject(s)
Adolescent , Adult , Aged , Case-Control Studies , Community-Acquired Infections/drug therapy , Cross-Sectional Studies , Female , Humans , Immunologic Techniques , India/epidemiology , Male , Middle Aged , Mycoplasma pneumoniae/isolation & purification , Pneumonia, Mycoplasma/drug therapy , Prospective Studies
14.
Rev. méd. Panamá ; 23(2): 27-33, sept. 1998.
Article in Spanish | LILACS | ID: lil-409815

ABSTRACT

OBJECTIVES: To determine the importance of Mycoplasma pneumoniae and Chlamydia pneumoniae in community-acquired pneumonia (CAP) of children from different latitudes and to compare clinical outcome using azithromycin (AZM) versus either amoxicillin-clavulanate (A-C) or erythromycin estolate (EE). METHODS: Ambulatory patients with CAP were identified at either the Children's Medical Center of Dallas, Texas or the Hospital del Niño of Panama City, Panama. Children 6 months to 15 years of age were enrolled and randomized to receive either AZM for 5 days or a 10 day course of either A-C or EE, for those younger or older than 5 years of age, respectively. Mycoplasma pneumoniae and C. pneumoniae were identified by measuring acute and convalescent serum antibody titers and by performing nasopharyngeal (NP) and oropharyngeal (OP) swabs for culture and polymerase chain reaction (PCR) testing. RESULTS: Overall 335 patients (168 in Dallas and 167 in Panama) were evaluated from February 1996 through December 1997. Acute M. pneumoniae infection was detected in 12 (7%) patients each in Dallas and Panama. Acute C. pneumoniae infection was observed in 10 (6%) children at each site. Infection caused by these [quot ]atypical[quot ] microorganisms occurred more frequently in children older than 5 years of age (23% vs 9%, P = 0.001, RR 2.5, 95% CI 1.4-4.3). No distinctive pattern of clinical or radiologic abnormalities was seen in relation to etiology. Clinical cure was achieved in 43 of 44 children infected by these bacteria regardless of treatment assignment. CONCLUSION: Mycoplasma pneumoniae and C. pneumoniae are common etiologic agents of CAP in older children from different latitudes. Children with CAP present with similar clinical and radiologic findings to those caused by other etiologic agents. Outcome was excellent for the three treatment regimens studied


Subject(s)
Humans , Male , Female , Infant , Child, Preschool , Child , Adolescent , Chlamydophila pneumoniae , Mycoplasma pneumoniae , Pneumonia, Bacterial/microbiology , Drug Therapy, Combination , Anti-Bacterial Agents/therapeutic use , Azithromycin/therapeutic use , Amoxicillin-Potassium Clavulanate Combination/therapeutic use , Erythromycin/therapeutic use , Community-Acquired Infections/drug therapy , Community-Acquired Infections/microbiology , Pneumonia, Bacterial/drug therapy , Pneumonia, Mycoplasma/drug therapy , Pneumonia, Mycoplasma/microbiology
15.
Actual. pediátr ; 8(1): 20-4, mar. 1998.
Article in Spanish | LILACS | ID: lil-292652

ABSTRACT

Se revisaron las historias de 107 niños con infección respiratoria aguda (IRA) baja que tenían una IgM positiva para Mycoplasma pneumoniae. La edad más afectada fue la de 2 a 6 años (58 por ciento). El tiempo de evolución antes de la consulta fue de 1 a 180 días, con un promedio de 10.7 días. El motivo de consulta más frecuente fue tos (95.3 por ciento), tos prolongada en el 22.45 por ciento, seguida de fiebre (73.5 por ciento), expectoración y rinitis (32.7 por ciento) respectivamente. Al examen se encontró: Sibilancias (67.3 por ciento), estertores crepitantes (30.8 por ciento) fiebre (37 por ciento), faringitis (15.9 por ciento), otitis (13.1 por ciento) y sinusitis (12 por ciento). El hallazgo radiológico más frecuente fue atrapamiento de aire (21.8 por ciento) derrame pleural abacteriano. La proteína C reactiva fue de < 4 mg por ciento en el 70.8 por ciento. El tratamiento fue a base de macrólidos, principalmente claritromicina (72-6 por ciento), broncodilatadores (40 por ciento) y estos asociados a esteroides en el 25.8 por ciento de los casos


Subject(s)
Humans , Child , Pneumonia, Mycoplasma/complications , Pneumonia, Mycoplasma/diagnosis , Pneumonia, Mycoplasma/epidemiology , Pneumonia, Mycoplasma/etiology , Pneumonia, Mycoplasma/physiopathology , Pneumonia, Mycoplasma/immunology , Pneumonia, Mycoplasma/microbiology , Pneumonia, Mycoplasma/drug therapy , Pneumonia, Mycoplasma , Pneumonia, Mycoplasma/therapy , Respiratory Tract Diseases/diagnosis , Respiratory Tract Diseases/drug therapy , Respiratory Tract Diseases/epidemiology , Respiratory Tract Diseases/etiology , Respiratory Tract Diseases/microbiology , Respiratory Tract Diseases/physiopathology
17.
Article in English | IMSEAR | ID: sea-43302

ABSTRACT

A randomized control trial was designed to compare the efficacies of spiramycin given one gram twice daily and erythromycin given 500 mg thrice or four times daily in the treatment of acute exudative tonsillitis in adults whose ages were over 13 years old from January 1989 to January 1991 at a community clinic. A total of 120 cases were enrolled in the study. Fifty-three patients received spiramycin while 67 received erythromycin. Group A beta-hemolytic streptococci (GABHS), S. aureus, and positive titer of Mycoplasma pneumoniae were detected in 19, 47 and 8 per cent in spiramycin group and 21, 36 and 11 per cent in erythromycin group respectively. GABHS were totally eradicated on day 3 of treatment in both groups through eradication of S. aureus was slightly slower initially in the spiramycin group. Marked improvement was similarly achieved in both groups after 3 days of therapy. Dyspepsia was felt in 34.4 and 8.2 per cent of erythromycin and spiramycin groups respectively but was tolerable by most patients. We concluded that spiramycin given twice daily was as effectively as conventional erythromycin but spiramycin is more convenient to administer and causes much less gastro-intestinal side-effect.


Subject(s)
Acute Disease , Adult , Drug Administration Schedule , Erythromycin/administration & dosage , Exudates and Transudates , Female , Humans , Male , Mycoplasma pneumoniae/isolation & purification , Pneumonia, Mycoplasma/drug therapy , Prospective Studies , Spiramycin/administration & dosage , Streptococcal Infections/drug therapy , Streptococcus pyogenes/isolation & purification , Tonsillitis/drug therapy
18.
Ars cvrandi ; 21(10): 84, 86, 88, nov.-dez. 1988.
Article in Portuguese | LILACS, SES-SP | ID: lil-67591

ABSTRACT

O termo pneumonia indica uma inflamaçäo, em geral aguda, do parênquima pulmonar. O autor, no trabalho a seguir, näo tem a intençäo de tentar uma classificaçäo completa de todas as pneumonias, mas tem o propósito de fazer indicaçöes medicamenosas daquelas mais comuns, relacionando medidas de ordem geral e específicas junto com as formas de tratamento mais indicadas para cada casos


Subject(s)
Humans , Pneumonia/therapy , Pneumonia/drug therapy , Pneumonia, Mycoplasma/drug therapy , Pneumonia, Viral/drug therapy , Acquired Immunodeficiency Syndrome/drug therapy , Cross Infection , Pneumonia, Staphylococcal/drug therapy
20.
Rev. AMRIGS ; 30(3): 191-8, jul.-set. 1986. ilus
Article in Portuguese | LILACS | ID: lil-37136

ABSTRACT

Chama-se a atençäo sobre a infreqüência com que se diagnostica pneumonia por Mycoplasma pneumoniae, mencionando algumas explicaçöes para isto: grande número de pacientes näo procuram atendimento médico pela benignidade do processo, e os que o fazem geralmente näo säo hospitalizados; freqüentemente näo se considera esta possibilidade ou os critérios diagnósticos näo säo conhecidos; assitência laboratorial às vezes inadequada. Salienta-se que em casos de infecçäo respiratória aguda sempre deve ser considerada a possibilidade de micoplasmose. Säo descritos os principais dados clínicos e radiológicos da doença, enfatizando-se que o diagnóstico baseia-se na compatibilidade clínico-radiológico-laboratorial, particularmente pela presença de altos títulos de imunoglobulinas (anticorpos específicos e crioglutininas), pois a identificaçäo do Mycoplasma näo é possível em trabalho de rotina, restringindo-se aos estudos em nível de pesquisa. Abordam-se alguns aspectos imunológicos fundamentais à patogenia da doença. Finalmente säo mencionadas algumas recomendaçöes diagnósticas e terapêuticas


Subject(s)
Humans , Pneumonia, Mycoplasma/diagnosis , Pneumonia, Mycoplasma/drug therapy
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