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1. |
Adverse events associated with MMR vaccines in Japan |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 205-211
MIKIO KIMURA,
HARUMI KUNO‐SAKAI,
SHUDO YAMAZAKI,
AKIO YAMADA,
MICHIKO HISHIYAMA,
HITOSHI KAMIYA,
KOJI UEDA,
TOSHIRO MURASE,
MUNEHIRO HIRAYAMA,
AKIRA OYA,
SADAHIKO NOZAKI,
RYOSUKE MURATA,
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摘要:
AbstractThe largest nationwide active surveillance of four Measles‐Mumps‐Rubella (MMR) vaccines was conducted in Japan. A total of 1255 pediatricians actively participated in the study, which comprised 8.6% of all members of the Japanese Pediatric Society. The total number of registered recipients of MMR vaccines was 38 203. They were arbitrarily given one of the MMR vaccines produced by three makers (Takeda, Osaka city, Kitasato Minato‐ku, Tokyo and Biken Suita city, Japan) or the standard MMR vaccine made of designated strains (Kitasato's measles‐AIK‐C, Biken's mumps‐Urabe Am9 and Takeda's rubella‐To336) produced by Takeda, Kitasato and Biken and were observed for 35 days.The rates of virologically confirmed aseptic meningitis per 10 000 recipients were 16.6, 11.6, 3.2 and 0 for the standard MMR, Takeda MMR, Kitasato MMR and Biken MMR vaccines, respectively. The incidence of convulsions between 15 and 35 days was the highest with the standard MMR vaccine and the incidence of fever associated with vomiting occurring between 15 and 35 days (symptoms relevant to aseptic meningitis) were also the highest with the standard MMR vaccine. The incidence of parotid swelling was the lowest with Takeda MMR vaccine.This surveillance revealed that incidences of aseptic meningitis after administration of the standard MMR vaccine and of Biken MMR vaccine were different. This posed questions about the manufacturing consistency of the Urabe Am9 mumps virus vaccines. On the other hand, the National Institute of Health found that the biological characteristics of the Urabe Am9 mumps virus contained in the standard MMR vaccine and in the Biken MMR vaccine were different. The Biken Company reported that the mumps vaccine in the standard MMR vaccine was a mixture of two Urabe Am9 mumps vaccine bulks; one identical to that contained in the Biken MMR vaccine and the other produced by a different manufact
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03471.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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2. |
Clinical features of measles in immunocompromised children |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 212-217
TAKASHI NAKANO,
YOSHIKI SHIMONO,
KENJI SUGIYAMA,
HIDEHIRO NISHIHARA,
MASAMUNE HIGASHIGAWA,
YOSHIHIRO KOMADA,
MASAHIRO ITO,
MINORU SAKURAI,
AZUSA YOSHIDA,
KENJI KITAMURA,
TOSHIAKI IHARA,
HITOSHI KAMIYA,
MINORU HAMAZAKI,
TETSUTARO SATA,
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摘要:
AbstractMeasles is often fatal for immunocompromised hosts. Protective immunity against measles has been studied but is still not completely understood. Recently, five cases of measles were encountered in immunocompromised children. Two of these were allogeneic bone marrow transplanted cases (one common variable immunodeficiency and one severe aplastic anemia) in remission, one Wilms' tumor case in remission, one hepatoblastoma case after cytotoxic therapy at disease onset and one exaggerating hemophagocytic syndrome case with suppressed natural killer cell activity. Clinical symptoms, laboratory findings and the immunologic backgrounds of these five patients were investigated.One of the patients, an 8 year old boy with hemophagocytic syndrome, died of giant cell pneumonia which was confirmed in the section of necropsy lung specimen. Two other patients who received allogeneic bone marrow transplants were not immune to measles, despite their own and their donors' immunizations. Their clinical symptoms were rather severe but both patients recovered and have remained seropositive for as long as 13 months.This fatality from measles is the first reported in a patient with hemophagocytic syndrome. Suppressed natural killer cell activity may be a poor prognostic factor. Also, secondary immunization failure for measles can occur in bone marrow transplanted patients with rather severe clinical symptoms.
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03472.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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3. |
Detection of human immunodeficiency virus‐1 DNA, RNA and antibody, and occult blood in inactivated saliva: Availability of the filter paper disk method |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 218-223
JUNKO KAKIZAWA,
HIROSHI USHIJIMA,
SHINICHI OKA,
YUSEI IKEDA,
HEINZ C SCHRÖDER,
WERNER EG MÜLLER,
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摘要:
AbstractEighty three samples of saliva were collected from 60 subjects who were asymptomatic carriers of AIDS related complex (ARC) and AIDS. They included hemophiliacs, homosexuals and heterosexuals. Occult blood, human immunodeficiency virus‐1 (HIV‐1) antibody and DNA were assayed after heat treatment at 56°C by strip method, particle agglutination and polymerase chain reaction (PCR), respectively. HIV‐1 RNA was assayed by reverse transcription (RT)‐PCR after heat treatment at 56°C or 90°C, or after application to filter paper disks with drying and heat treatment at 90°C. Positive results were found in 53% (occult blood), 73% (HIV‐1 antibody), 23% (HIV‐1 DNA, 56°C), 34% (HIV‐1 RNA, 56°C), 33% (HIV‐1 RNA, 90°C) and 25% (HIV‐1 RNA, 90°C, filter paper disk), respectively.The results did not depend on the stage of the disease or the route of infection. Other studies have reported the use of the filter paper disk method to detect antibodies against HIV and HIV genomes in blood samples. The present study demonstrated that it could also be used for the detection of HIV
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03473.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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4. |
The outbreak of mumps in a small island in Japan |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 224-228
KEIKO ODA,
HIROHISA KATO,
AKIO KONISHI,
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摘要:
AbstractA major mumps outbreak occurred on a small island, Ikeshima, in Nagasaki Prefecture from August 1994 to February 1995. There were 236 patients with the mumps at Ikeshima Miners' Hospital during that period. The Measles‐Mumps‐Rubella (MMR, Toitsukabu) vaccination coverage in the 43 children at the nursery school was 65.1% and it was 61.9% in the 21 children aged 4–5 years not attending the nursery school. Coverage was 66.6% in the 63 kindergarten students and 53.7% in 56 first‐graders. The overall MMR vaccination coverage among these children was 61.7% (113/183) from 1989 to 1992. Children from the second grade to junior high school received monovalent mumps vaccine, Torii strain. None received Zishakabu MMR.The age of the patients ranged from 1 to 43 years, with a mean of 9.1 years. The majority (77.5%) were primary school children. The attack rates for vaccinated and unvaccinated children in grades one to six were: 6.7% (2/30) and 88.5% (23/26), 25% (3/12) and 44.1% (30/68), 11.1% (1/9) and 64.4% (29/45), 25% (2/8) and 60% (45/79), 22.2% (2/9) and 35.9% (28/78), 0% (0/5) and 24.7% (18/73), respectively. The overall frequency in the primary school was 41.4% (183/442 children). The frequency in the nursery school for children aged 4–5 years was 14.0% (6/43). It was 17.5% (11/63) in children aged 5–6 years in the kindergarten, 5.2% (11/213) in children not attending school with an age range of 1–5 years, and 4.2% (10/237) in junior high school students. Although the frequencies of MMR coverage for the nursery school children and kindergarteners were not high enough to eradicate mumps outbreaks, the MMR vaccination program was thought to have influenced the low frequency of mumps among the children. Close physical interactions among the first‐graders would have contributed to their high frequency of mumps.Some patients presented with suspected mumps parotitis several times, but no such serological confirmation of reinfecti
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03474.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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5. |
Definitions of severely mentally and physically disabled children in Japan: Do the differences affect the prevalence rates of these children? |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 229-232
YUKIKATSU NAKADA,
KYOKO KAMIYA,
ETSUKO TAKAESU,
SATOSHI OHSHIRO,
TOMIKO HOKAMA,
SATOSHI NAKASONE,
KIYOTAKE HIRAYAMA,
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摘要:
AbstractThe prevalence rate of severely mentally and physically disabled children (SDC) aged 6–15 years in Okinawa prefecture on 1 May 1989 was 0.74/1000 (143/192 038) according to Oshima's classification, compared with 0.89/1000 (170/192 038) according to the Ministry of Education's classification with minor modifications. The number of children in region classes 1, 2, 3 and 4 of Oshima's classification for SDC were 100, 34, 6 and 3, respectively. The difference (n= 27) between the total numbers of SDC according to the two classifications was mainly because of 21 children categorized as ‘walking with support’ who were included as SDC according to the Ministry of Education's classification but not as SDC according to Oshima's classification. Only region class 1 of Oshima's classification corresponded with region class 25 of the Ministry of Education's classification. The results of the present study indicate that the differences between the two definitions of SDC affect the reported prevalence rates of SDC. Therefore, changing patterns in the prevalence of SDC should be assessed by serial surveys using the same method in each dis
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03475.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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6. |
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1 |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 233-236
HIROYUKI IDA,
OWEN M RENNERT,
TAKERU ITO,
KIHEI MAEKAWA,
YOSHIKATSU ETO,
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摘要:
AbstractFive fatal cases of Japanese patients with type 1 Gaucher disease were studied. The causes of death included hemorrhage secondary to esophageal varices (two cases), respiratory distress (one case), hepatic failure (one case) and postoperative sepsis (one case). All of the patients had previous splenectomies, four patients had bone involvement and hepatic cirrhosis. The identified Gaucher genotypes were 1448C/1213G, 1603T/1603T, 1448C/1390G, ?/? and 1213G/1213G. The prognosis of type 1 Gaucher disease is generally good. We propose that patients with a similar clinical course and genotype to those presented in the present study should receive prompt comprehensive treatment. Patients with the 1213G mutation, pulmonary and liver involvement and a previous splenectomy should be considered as candidates for early vigorous treatment.
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03476.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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7. |
Serum and cerebrospinal fluid zinc levels in children with febrile convulsions |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 237-241
ZÜBEYDE GÜNDÜZ,
İSMET YAVUZ,
MEHMET KOPARAL,
SEFER KUMANDAŞ,
RECEP SARAYMEN,
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摘要:
AbstractThe mechanisms underlying febrile convulsions (FC), which have multiple etiological factors, are not yet clear. The aim of the present study was to determine whether there were any changes in serum and cerebrospinal fluid (CSF) zinc (Zn) levels in children with febrile convulsion during seizures. A total of 102 children were included in the study, with four groups formed as follows: group A, 40 children with FC (aged 9 months to 5 years); group B, 20 children having fever without convulsion (aged 6 months to 5 years); group C, 20 children with afebrile convulsion (aged 6 months to 6 years) and group D, 22 healthy children (aged 5 months to 6 years). Serum and CSF zinc levels for groups A, B and C and serum Zn levels only for group D were measured. The serum Zn levels of 17 children in group A were again measured during healthy periods. Serum Zn levels of groups A, B, C and D had a mean of 0.70 ± 0.10 mg/dL, 1.07 ± 0.08 mg/dL, 1.26 ± 0.32 mg/dL and 1.17 ± 0.21 mg/dL, respectively, and the values of group A were lower than those of the other three groups (P<0.001). In group B, serum Zn levels were also lower than those of groups C and D (P<0.05). The CSF Zn levels of groups A, B and C were found to have a mean of 0.07 ± 0.02 mg/L, 0.12 ± 0.02 mg/L and 0.14 ± 0.04 mg/L, respectively. In group A, the CSF Zn levels were lower than those of groups B and C (P<0.001), and in group B they were lower than those of group C (P<0.05). For the 17 patients in group A, serum Zn levels during healthy periods (0.87 ±0.10 mg/dL) were found to be higher than the values shortly after seizures, but lower than those of groups B, C and D (P<0.001). We could not observe any relationship between zinc levels of the serum and CSF and the degree and duration of the fever. These findings suggest that serum and CSF Zn levels decreased during infectious diseases, and that this decrease was more significant in patients
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03477.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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8. |
Relationships between clinical and histological profiles of non‐familial idiopathic neonatal hepatitis |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 242-247
FUJIHIKO NISHINOMIYA,
DAIKI ABUKAWA,
GORO TAKADA,
YUSAKU TAZAWA,
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摘要:
AbstractIdiopathic neonatal hepatitis (INH) is a syndrome characterized clinically and histologically but there is little information concerning the relationship between the clinical features and histological findings. In the present study, sixty‐two patients clinically diagnosed as non‐familial INH were histologically classified into four groups according to a provisional definition based on predominant lesions and examination of their clinical features. Patients of cholestasis (n= 23) and giant cell hepatitis (GCH,n= 21) were most frequent (37% and 33%, respectively), and patients of fatty liver (n= 10) and hepatitis (n= 8) were less common (16% and 13%). The GCH group showed a dominance of male, low birthweight, older and breast‐fed babies. The cholestasis group demonstrated a dominance of male, low birthweight, younger and bottle‐fed babies. The hepatitis group had the highest frequencies of high‐grade hepatomegaly and splenomegaly. Fifty six cases completely recovered. Two died of hepatic failure in early infancy and four had chronic liver diseases at the age of 12 months. The fatty liver group had the worst outcome. Histological features in non‐familial INH were variable and typical giant cell hepatitis was seen in only one‐third of patients. Characteristic clinical features in each histologically classified group may suggest heterogenous etiologies underlying non
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03478.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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9. |
Ultrasonography for the detection of ureteric reflux in infants with urinary infection |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 248-251
MASAHIRO HIRAOKA,
GOTARO HASHIMOTO,
SHUHEI HAYASHI,
CHIKAHIDE HORI,
SHINYA TSUCHIDA,
HIROKAZU TSUKAHARA,
YUKUO KONISHI,
MASAKATSU SUDO,
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摘要:
AbstractSeveral less harmful methods than voiding cysto‐urethrography for detecting significant ureteric reflux have been proposed. The present prospective study investigated whether ultrasonography was effective in identifying ureteric reflux in infants with their first febrile urinary infection. The subjects were 27 infants (24 boys and 3 girls) aged from 0 to 8 months. The urinary tract was scanned when the bladder was full, and before and during induced voiding. Infants with abnormal ultrasound findings underwent voiding cysto‐urethrography. The other infants were followed and those who had a recurrence of urinary infection underwent voiding cystography.Ten children underwent cysto‐urethrography, with eight refluxing ureters identified in six boys. Ultrasound revealed transient dilatation of the renal pelvis on voiding in five kidneys, transient dilatation of distal ureters in 12 and hydro‐ureteronephrosis in two. Each of the five kidneys with pelvic dilatation on voiding was associated with ureteric reflux grades III or IV. Of the 17 children who did not undergo cysto‐urethrography, only one had recurrence of urinary infection and was diagnosed with ureteric reflux. This girl was one of the three babies who were not scanned during voiding. More than half of the infants with febrile urinary infection were excluded from invasive examination without having recurrence of urinary infection. Thus, ultrasound scanning during voiding was effective for screening infants with their first urinary infection to detect significant ureter
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03479.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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10. |
Long‐term follow up of abdominal aortic aneurysm complicating Kawasaki disease: Comparison of the effectiveness of different imaging methods |
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Pediatrics International,
Volume 38,
Issue 3,
1996,
Page 252-255
YUUICHI FUYAMA,
ROUSEI HAMADA,
RITEI UEHARA,
ICHIRO YANO,
MASAKO FUJIWARA,
MASAKO MATOBA,
KENICHI KAWAMURA,
ZENJI NONAKA,
KIHEI MAEKAWA,
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摘要:
AbstractA 2 month old boy with Kawasaki disease developed the rare complication of abdominal aortic aneurysm (AAA). He was followed up over 7 years by ultrasonography (2D‐ECHO) with and without Doppler flow evaluation, angiography and computed tomography. Calcification was noted 33 months after the onset of the disease but the aneurysm did not decrease in size.2D‐ECHO was adequate for evaluating the size of an aneurysm, but did not show thrombus formation or calcification. Doppler flow studies did not show abnormally high blood flow velocities either at the inflow or outlet of aneurysms, which are indicative of stenosis. On the other hand an abdominal aortogram provided information regarding the luminal shape and abnormalities in flow pattern suggestive of thrombus formation. Fluoroscopy cannot demonstrate calcification in the early stages. Computed tomography (CT) was the imaging method of choice for the evaluation of obstructive or calcific changes; an organizing thrombus was clearly demonstrated and early detection of calcification was possi
ISSN:1328-8067
DOI:10.1111/j.1442-200X.1996.tb03480.x
出版商:Blackwell Publishing Ltd
年代:1996
数据来源: WILEY
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