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2.
Int J Tuberc Lung Dis ; 20(6): 786-92, 2016 06.
Article in English | MEDLINE | ID: mdl-27155182

ABSTRACT

SETTING: The management of multidrug-resistant tuberculosis (MDR-TB) is strictly regulated in Norway. However, nationwide studies of the epidemic are lacking. OBJECTIVE: To describe the MDR-TB epidemic in Norway over two decades. DESIGN: Retrospective analysis of data on MDR-TB cases in Norway, 1995-2014, obtained from the national registry, patient records and the reference laboratory, with genotyping and cluster analysis data. Data for non-MDR-TB cases were collected from the national registry. RESULTS: Of 4427 TB cases, 89 (2.0%) had MDR-TB, 7% of whom had extensively drug-resistant TB (XDR-TB) and 24% pre-XDR-TB. Of the 89 MDR-TB cases, 96% were immigrants, mainly from the Horn of Africa or the former Soviet Union (FSU); 37% had smear-positive TB; and 4% were human immunodeficiency virus co-infected. Of the 19% infected in Norway, the majority belonged to a Delhi/Central Asian lineage cluster in a local Somali community. Among the MDR-TB cases, smear-positive TB and FSU origin were independent risk factors for XDR/pre-XDR-TB. Treatment was successful in 66%; 17% were lost to follow-up, with illicit drug use and adolescence being independent risk factors. Forty-four per cent of patients treated with linezolid discontinued treatment due to adverse effects. CONCLUSION: MDR-TB is rare in Norway and is predominantly seen in immigrants from the Horn of Africa and FSU. Domestic transmission outside immigrant populations is minimal.


Subject(s)
Epidemics , Extensively Drug-Resistant Tuberculosis/epidemiology , HIV Infections/epidemiology , Tuberculosis, Multidrug-Resistant/epidemiology , Adolescent , Adult , Africa/ethnology , Antitubercular Agents/therapeutic use , Child , Child, Preschool , Cluster Analysis , Emigrants and Immigrants , Extensively Drug-Resistant Tuberculosis/drug therapy , Female , Follow-Up Studies , Genotyping Techniques , HIV Infections/drug therapy , Humans , Linezolid/therapeutic use , Lost to Follow-Up , Male , Middle Aged , Norway/epidemiology , Retrospective Studies , Risk Factors , Tuberculosis, Multidrug-Resistant/drug therapy , USSR/ethnology , Young Adult
3.
J Clin Endocrinol Metab ; 95(1): 167-77, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19906787

ABSTRACT

BACKGROUND: Between 1985 and 2006, the National Cooperative Growth Study (NCGS) monitored the safety and efficacy of recombinant human growth hormone (rhGH) in 54,996 children. METHODS: Enrolled patients were followed until rhGH discontinuation. Investigators submitted adverse event reports for targeted events or those potentially rhGH-related. RESULTS: Early concerns about de novo leukemia in patients without risk factors have not been substantiated--three observed vs. 5.6 expected in age-matched general population based on years at risk [standard incidence ratio (SIR), 0.54; 95% confidence interval (CI), 0.11-1.58]. De novo malignancies (intracranial and extracranial) were not significantly increased in patients without risk factors (29 confirmed vs. 26 expected; SIR, 1.12; 95% CI, 0.75-1.61). Second neoplasms occurred in 49 patients, of whom 37 had irradiation for their initial tumors (including five of 16 retinoblastoma patients, three of whom had bilateral retinoblastoma) consistent with an increased risk with rhGH. Thirty-three patients developed type 1 diabetes mellitus (DM) (37 expected; SIR, 0.90; 95% CI, 0.62-1.26). Type 2 DM and nonspecified DM were reported in 20 and eight patients, respectively. Two deaths were reported in patients with Prader-Willi syndrome and five deaths from aortic dissection in patients with Turner syndrome. In patients with organic GH deficiency and idiopathic panhypopituitarism, 11 events of acute adrenal insufficiency occurred, including four deaths, consistent with a reported increased risk for adrenal insufficiency in hypopituitary patients with or without rhGH treatment. CONCLUSION: After more than 20 yr, leukemia, a major safety issue initially believed associated with GH, has not been confirmed, but other signals, including risk of second malignancies in patients previously treated with irradiation, have been detected or confirmed through the NCGS. These data further clarify the events associated with rhGH and, although confirming a favorable overall safety profile, they also highlight specific populations at potential risk.


Subject(s)
Growth Disorders/drug therapy , Human Growth Hormone/adverse effects , Human Growth Hormone/therapeutic use , Case-Control Studies , Cause of Death , Child , Child, Preschool , Comorbidity , Diabetes Complications/epidemiology , Female , Follow-Up Studies , Growth Disorders/complications , Growth Disorders/mortality , Human Growth Hormone/deficiency , Humans , Incidence , Male , Neoplasms/complications , Neoplasms/epidemiology , Neoplasms/mortality , Pancreatitis/chemically induced , Pancreatitis/epidemiology , Product Surveillance, Postmarketing , Recombinant Proteins/adverse effects , Recombinant Proteins/therapeutic use , Retrospective Studies , Scoliosis/chemically induced , Scoliosis/epidemiology , Time Factors
4.
Scand J Urol Nephrol ; 35(4): 330-3, 2001 Sep.
Article in English | MEDLINE | ID: mdl-11676362

ABSTRACT

A 36-year-old renal transplant patient developed 9 years after a successful transplantation a fatal secondary varicella infection. The disseminated varicella infection was associated with hepatitis with liver necrosis, disseminated intravascular coagulation and fibrinolysis and glomerulonephritis. To our knowledge this is the first description of glomerulonephritis associated with varicella infection in a renal transplanted patient. The autopsy showed morphologically a mesangial glomerulonephritis with minor proliferative activity and extensive deposits by electronmicroscopy, mainly in the mesangium. The ongoing immunosuppression may have modified the mesangial cell response to the deposition of immune complexes.


Subject(s)
Abdominal Pain/etiology , Chickenpox/complications , Glomerulonephritis/complications , Hepatitis, Viral, Human/complications , Kidney Transplantation , Adult , Chickenpox/pathology , Glomerulonephritis/pathology , Hepatitis, Viral, Human/diagnosis , Hepatitis, Viral, Human/pathology , Humans , Kidney/pathology , Liver/pathology , Male
5.
J Clin Endocrinol Metab ; 86(7): 3061-9, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11443168

ABSTRACT

Comprehensive recommendations on the diagnosis of Turner syndrome (TS) and the care of affected individuals were published in 1994. In the light of recent advances in diagnosis and treatment of TS, an international multidisciplinary workshop was convened in March 2000, in Naples, Italy, in conjunction with the Fifth International Symposium on Turner Syndrome to update these recommendations. The present paper details the outcome from this workshop. The genetics and diagnosis of the syndrome are described, and practical treatment guidelines are presented.


Subject(s)
Turner Syndrome/diagnosis , Turner Syndrome/therapy , Adolescent , Adult , Child , Female , Fertility , Humans , Learning , Pregnancy , Prenatal Diagnosis , Puberty , Turner Syndrome/genetics , Turner Syndrome/psychology
6.
Scand J Gastroenterol ; 34(2): 194-8, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10192200

ABSTRACT

BACKGROUND: Preliminary results from combination therapy with interferon-alpha and ribavirin (IFN/Rib) in patients with chronic hepatitis C have been promising, with up to 50% sustained hepatitis C virus (HCV) RNA response. The aim of this study was to investigate whether a sustained HCV RNA response could be obtained with combination therapy in patients who were non-responders or relapsers after IFN treatment. METHODS: In a multicenter study we randomized 53 HCV RNA-positive patients into 2 treatment groups. They all had biopsy-confirmed chronic hepatitis C, and all were recruited from a previous IFN study: 26 were previous non-responders and 27 responders with relapse. Group A received interferon-alpha2a, 4.5 MIU thrice weekly for 6 months, and group B received ribavirin, 1000-1200 mg/day, in combination with the same dose of interferon-alpha2a for 6 months. Median Knodell index was 5.0 in both groups. Genotype 1 was found in 24 (45%), type 2 in 3 (6%), and type 3 in 26 (49%). RESULTS: Sustained clearance of HCV viremia 6 months after interferon-alpha2a treatment stop was obtained in 12 of 53 patients (23%): 6 of 27 in the IFN group (22%) and 6 of 26 (23%) in the IFN/Rib group (NS). Nine of 27 (33%) former responders with relapse, compared with 3 of 26 (12%) non-responders, obtained a sustained HCV RNA response (P = 0.054). In previous relapse patients sustained loss of viremia was more frequent in genotype 3 (50%) than in genotype 1 (11%) patients (P = 0.022). CONCLUSIONS: In a group of previous IFN-alpha2a-treated chronic HCV patients we obtained a similar sustained clearance of viremia when retreated either with IFN-alpha2a alone or with a combination of IFN-alpha2a and ribavirin for 6 months. Previous relapse patients with HCV genotype 3 obtained sustained loss of viremia significantly more often (50%) than type-patients (11%). Previous IFN responders with relapse responded better than previous non-responders.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C, Chronic/drug therapy , Interferon-alpha/therapeutic use , Ribavirin/therapeutic use , Adult , Biopsy , Drug Administration Schedule , Drug Therapy, Combination , Female , Hepacivirus/isolation & purification , Hepatitis C, Chronic/blood , Hepatitis C, Chronic/pathology , Humans , Interferon alpha-2 , Interferon-alpha/administration & dosage , Male , Middle Aged , RNA, Viral/blood , Recombinant Proteins , Ribavirin/administration & dosage , Viremia
7.
Pediatrics ; 102(1): e12, 1998 Jul.
Article in English | MEDLINE | ID: mdl-9651464

ABSTRACT

OBJECTIVE: Although cardiovascular malformations (CVMs) are well-recognized congenital anomalies in Turner syndrome, aortic dilation and dissection are less common and less familiar. Most of the relevant literature is limited to single cases reports or small series. We sought to increase the information available about the frequency and characteristics of aortic dilation in patients with Turner syndrome. DESIGN: A 1-page survey of cardiac abnormalities, including aortic dilation, was mailed to approximately 1000 (1040 verified) members of the Turner Syndrome Society as an enclosure in the June 1997 newsletter. We also conducted a literature review. PARTICIPANTS: A total of 245 patients or families of patient members of the Turner Syndrome Society responded to the survey ( approximately 24% response rate). RESULTS: A CVM was reported in 120 of 232 (52%) respondents to this questionnaire. Obstructive lesions of the left side of the heart predominated and included bicuspid aortic valve (38%) and coarctation (41%). Aortic dilation was reported in at least 15 of 237 respondents (6.3%; 95% confidence interval: 3.6%-10.3%); 2 of 15 (13%) had dissection. Twelve of 15 (80%) patients had an associated risk factor for aortic dilation such as a CVM or hypertension. The 3 (20%) patients who did not have a CVM or hypertension were all younger than 21 years. In the entire group with aortic dilation, 10 of 15 (67%) patients were younger than 21 years. All patients with aortic dilation had involvement of the ascending aorta, and 2 had additional involvement of the descending aorta distal to a repaired coarctation. An update of the literature revealed 68 patients with aortic dilation, dissection, or rupture. An associated CVM or hypertension was reported in 53 of 59 (90%) informative patients. At least 6 (10%) had no predisposing risk factor (information was inadequate for 9 of 68 patients). The following patterns of aortic involvement were identified: ascending +/- descending aorta with coarctation (14); ascending +/- descending aorta without coarctation (39); descending aorta with coarctation (3); descending thoracic or abdominal aorta without coarctation (4); and unspecified (8). Dissection or rupture was reported in 42/68 (62%). Two reported patients died suddenly from aortic dissection in the third trimester of assisted pregnancy. At least 20 (29%) patients were younger than 21 years. One of the 6 (17%) patients with isolated aortic dilation was in this younger group. CONCLUSIONS: More information is needed about the frequency and natural history of aortic dilation in Turner syndrome. This work contributes new patient data and increases the literature review. Despite the well-recognized limitations of self-reporting, this survey detected aortic dilation with or without dissection in approximately 6% of patients with Turner syndrome. Although rare, this is a potentially catastrophic occurrence, warranting greater awareness among health professionals. In this study and the literature, the vast majority of patients with aortic dilation have an associated risk factor such as a CVM, typically bicuspid aortic valve or coarctation, or systemic hypertension. These patients represent a higher risk group that should be followed appropriately, usually under the direction of a cardiologist. Patients undergoing assisted pregnancy also should be evaluated closely. It is generally accepted that at the time of diagnosis of Turner syndrome, all patients should have a complete cardiology evaluation including echocardiography. The small number of patients with aortic dilation without a CVM, who would not be under the long-term care of a cardiologist, makes it prudent to screen all patients with Turner syndrome for this potentially lethal abnormality. The specific timing for this screening is controversial. Our recommendations for prospective imaging do not represent a rigid standard of care.


Subject(s)
Aortic Dissection/epidemiology , Aortic Rupture/epidemiology , Turner Syndrome/complications , Adolescent , Adult , Aged , Aortic Dissection/etiology , Aortic Dissection/therapy , Aorta, Thoracic , Aortic Rupture/etiology , Aortic Rupture/therapy , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/etiology , Child , Confidence Intervals , Female , Heart Defects, Congenital/epidemiology , Humans , Incidence , Male , Middle Aged , Population Surveillance , Pregnancy , Pregnancy Complications, Cardiovascular/epidemiology , Pregnancy Complications, Cardiovascular/etiology , Surveys and Questionnaires , Treatment Outcome
8.
Scand J Gastroenterol ; 33(2): 195-200, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9517532

ABSTRACT

BACKGROUND: Hepatitis G virus (HGV) or GBV-C is frequently detected in patients co-infected with hepatitis C virus (HCV). This study investigated host and virologic factors influencing the response to HGV/GBV-C to alpha-interferon treatment. METHODS: HGV/GBV-C was detected and quantified by nested polymerase chain reaction. The influence of variables such as liver biopsy appearance, liver function abnormalities, and response of HCV to interferon treatment was monitored. RESULTS: Fourteen of the 25 HGV/GBV-C-infected patients treated with interferon (3-6 MIU three times a week for 6 months) became non-viraemic during treatment, although all relapsed after treatment withdrawal at 6 months, with no net change in virus load between 0 and 12 months. CONCLUSIONS: Predictive factors for clearance of HGV/GBV-C viraemia by interferon were pre-treatment severity of liver disease (median Knodell score of 4, compared with 7 for non-responders; P = 0.030) and alanine aminotransferase levels (median, 114, 182 for non-responders; P = 0.039). Clearance was associated with the treatment response of HCV. Nine of 13 who cleared HGV/GBV-C also cleared HCV, compared with 3 of 11 HGV/GBV-C non-responders; P = 0.05). The shared susceptibility of HGV/GBV-C and HCV to interferon treatment suggests a link between the mechanism of clearance of the two viruses.


Subject(s)
Flaviviridae/drug effects , Hepatitis, Viral, Human/therapy , Interferon-alpha/therapeutic use , Viremia/therapy , Adult , Aged , Alanine Transaminase/blood , Female , Flaviviridae/isolation & purification , Hepatitis C/blood , Hepatitis C/complications , Hepatitis C/pathology , Hepatitis, Viral, Human/blood , Hepatitis, Viral, Human/complications , Hepatitis, Viral, Human/pathology , Humans , Male , Middle Aged , Polymerase Chain Reaction , RNA, Viral/analysis , Treatment Outcome , Viral Load
9.
J Pediatr ; 132(2): 319-24, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9506648

ABSTRACT

OBJECTIVE: To carry out a multicenter, prospective, randomized trial of human growth hormone (GH), alone or in combination with oxandrolone (OX), in patients with Turner's syndrome (TS). METHODS: In an initial phase lasting 12 to 24 months, 70 girls with TS, verified by karyotype, were randomly assigned to one of four groups: (1) observation, (2) OX, (3) GH, or (4) GH plus OX. After completion of the first phase, group 3 subjects continued to receive GH only. All other subjects were treated with GH plus OX. Subjects were followed up until attainment of adult height and/or cessation of treatment. Data from this trial were compared with growth characteristics of 25 American historical subjects with TS (matched for age, height, parental target height, and karyotype) who never received either GH or androgens. RESULTS: Of the 70 subjects enrolled, 60 completed the clinical trial. The 17 subjects receiving GH alone all completed the trial and reached a height of 150.4+/-5.5 cm (mean +/- SD), 8.4+/-4.5 cm taller than their mean projected adult height at enrollment (95% confidence interval [CI]: 6.3 to 10.6 cm). The 43 subjects receiving GH plus OX attained a mean height of 152.1+/-5.9 cm, 10.3+/-4.7 cm taller than their mean projected adult height (95% CI: 8.9 to 11.7 cm). The historical control subjects had a mean adult height of 144.2+/-6.0 cm, precisely matching their original projected adult height of 144.2+/-6.1 cm. CONCLUSIONS: GH, either alone or in combination with OX, is capable of stimulating short-term growth and augmenting adult height in girls with TS. With early diagnosis and initiation of treatment, an adult height of more than 150 cm is a reasonable goal for most girls with TS.


Subject(s)
Anabolic Agents/therapeutic use , Body Height , Growth Hormone/therapeutic use , Oxandrolone/therapeutic use , Turner Syndrome/drug therapy , Child , Child, Preschool , Drug Therapy, Combination , Female , Humans , Prospective Studies , Treatment Outcome , Turner Syndrome/physiopathology
10.
Scand J Infect Dis ; 29(1): 17-22, 1997.
Article in English | MEDLINE | ID: mdl-9112292

ABSTRACT

Patients with chronic hepatitis C respond differently when treated with interferon. We randomized 116 patients with chronic hepatitis C in order to compare two dosage regimens of recombinant interferon alpha 2a:3 MIU x 3 per week for 6 months (arm A) or 6 MIU x 3 per week for 3 months and then 3 MIU x 3 per week for 3 months (arm B). There were no significant differences concerning outcome between the two dose regimens: sustained clearance of HCV viremia 6 months after the end of treatment was obtained in 12/59 (20%) in group A compared with 18/57 (32%) in group B (p = 0.24). In patients with genotype 1a, 4/31 (13%), in genotype 1b, none of 9 (0%), 9/15 (60%) in genotype 2, and 17/58 (29%) in genotype 3, showed sustained clearance of HCV viremia 6 months after the end of treatment (p = 0.002). In a stepwise logistic regression analysis, only pretreatment viral load (p = 0.0001), genotype (p = 0.001) and age (p = 0.04) were identified as independent predictors of sustained clearance of HCV viremia. Liver histology as assessed by Knodell index was significantly improved in patients with sustained HCV RNA response 6 months after the end of treatment (5.2 +/- 2.2 vs 2.6 +/- 2.2, p < 0.001), but not in responders with relapse or in non-responders. In conclusion, stepwise logistic regression analysis showed that viral load, HCV genotype and age were the only independent predictors for sustained HCV RNA response.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C/therapy , Interferon-alpha/therapeutic use , Age Factors , Alanine Transaminase/blood , Antiviral Agents/administration & dosage , Chi-Square Distribution , Chronic Disease , Female , Genotype , Hepacivirus/genetics , Hepatitis C/virology , Humans , Interferon alpha-2 , Interferon-alpha/administration & dosage , Liver/pathology , Logistic Models , Male , Norway , Odds Ratio , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , RNA, Viral/blood , Recombinant Proteins , Treatment Outcome , Viral Load , Viremia/therapy
11.
Scand J Gastroenterol ; 32(12): 1256-60, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9438325

ABSTRACT

BACKGROUND: Many patients with chronic hepatitis C have long periods of normal or near-normal liver enzyme levels, even though histologic alterations have been confirmed. The recommendation today is not to treat this patient group. METHODS: In a pilot study 23 hepatitis C virus (HCV) RNA-positive patients with alanine aminotransferase (ALAT) levels less than 1.5 times upper normal limits for at least 6 months on more than three occasions and with histologic liver abnormalities compatible with chronic hepatitis C were treated with 3 MU of interferon-alpha 2b three times a week for 6 months. RESULTS: Nine patients (39%) became HCV RNA-negative in serum during treatment, but only two (8.7%) remained so after 6 months' follow-up. Significantly more patients with genotype other than type 1 became HCV RNA-negative than patients with genotype 1 during treatment (P = 0.005). CONCLUSIONS: Patients with low-activity chronic hepatitis C have a response to interferon-alpha treatment similar to that of patients with increased ALAT levels. Genotype seems to influence the rate of response.


Subject(s)
Antiviral Agents/therapeutic use , Hepatitis C/therapy , Hepatitis, Chronic/therapy , Interferon-alpha/therapeutic use , Adult , Aged , Alanine Transaminase/blood , Antiviral Agents/adverse effects , Biopsy , Female , Hepatitis C/blood , Hepatitis C/pathology , Hepatitis, Chronic/blood , Hepatitis, Chronic/pathology , Humans , Interferon-alpha/adverse effects , Male , Middle Aged , Pilot Projects , Prospective Studies , RNA, Viral/analysis
12.
Scand J Infect Dis ; 28(4): 357-9, 1996.
Article in English | MEDLINE | ID: mdl-8893398

ABSTRACT

Among 116 patients with biopsy-confirmed chronic hepatitis C (Riba 2 or Riba 3 positive) in a multicenter study in southern Norway on interferon, we determined hepatitis C virus genotype by restriction fragment length polymorphism (RFLP) of the 5' NCR. The RFLP method was supplemented by and compared with a serological typing method based on the detection of type-specific antibody to peptide from the NS-4 region. A total of 102/106 (96%) patient sera showed detectable type-specific antibody to NS-4 peptides and corresponded in all cases, except two, to the genotype detected by polymerase chain reaction. Combining the results from RFLP genotyping and serotyping, genotype 1 was found in 40 (35%) (27 with 1a and 10 with 1b, 3 subtypes not determined), genotype 2 in 15 (13%) (subtype 2b in 14 and 1 subtype not determined), and genotype 3 in 58 (50%) of patients. The low mean age of the patients (34 years), the low prevalence of cirrhosis (3.5%), the short duration of the disease, and a high prevalence of intravenous-drug abusers may account for the low prevalence of infection with genotype 1b (9%). The epidemiological features of hepatitis C patients are markedly different from patient groups described in southern Europe in terms of risk factors, age, and genotype distribution.


Subject(s)
Hepacivirus/genetics , Hepatitis C/genetics , Adult , Aged , Chronic Disease , Female , Genotype , Hepacivirus/classification , Hepatitis C/epidemiology , Humans , Male , Middle Aged , Molecular Epidemiology , Multicenter Studies as Topic , Norway/epidemiology , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Prevalence , Risk Factors , Serotyping , Viral Proteins/analysis
13.
Pediatr Radiol ; 26(1): 37-9, 1996.
Article in English | MEDLINE | ID: mdl-8598992

ABSTRACT

Pelvic ultrasonographic (US) studies of four patients (ages 11-19 years) with Turner s syndrome, 45,X karyotype, and normal ovarian function were reviewed. All four had persistent menses, spontaneous breast development, and normal follicular stimulant hormone (FSH) serum concentrations. The US studies depicted normal postpubertal uterus and normal-sized ovaries with follicles. In three patients, ovaries were seen bilaterally, while in one only one gonad was identified. Radiologists should be aware that patients with Turner s syndrome, even with a single X chromosome, may occasionally have normal genital development.


Subject(s)
Ovary/diagnostic imaging , Turner Syndrome/diagnostic imaging , Uterus/diagnostic imaging , Adolescent , Adult , Child , Female , Humans , Karyotyping , Turner Syndrome/genetics , Ultrasonography
14.
Scand J Gastroenterol ; 30(11): 1119-24, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8578174

ABSTRACT

BACKGROUND: Recombinant interferon remains the cornerstone of treatment of chronic hepatitis C virus (HCV) infection. Still, evaluation of treatment on the basis of response indicators and long-term effect of the treatment raises several questions. METHODS: Seventy-four patients with chronic HCV infection were randomized to a high (3 MIU, 3/7 days) or low (1 MIU, 3/7 days) dose of recombinant interferon-alpha-2b for 48 weeks after a 4-week course of 3 MIU, 3/7 days. Response to treatment was assessed by means of liver enzymes (transaminases), HCV RNA, and liver histology. RESULTS: The higher maintenance dose was associated with a significantly higher rate of sustained alanine aminotransferase (ALAT) response (45% versus 19%) and with a significantly better chance of becoming HCV RNA-negative during therapy (47% versus 23%). In the high maintenance dose group 14 of the 29 (48%) patients with available HCV RNA data were negative at the 3-month follow-up, compared with 4 of 27 (15%) in the low maintenance dose group. Significantly more patients had improved liver biopsy findings after interferon in the high maintenance dose group (79%) than in the low maintenance dose group (36%). There was a close correlation between ALAT response and HCV RNA response. Of 17 patients who were HCV RNA-negative 3 months after the end of treatment, 10 remained HCV RNA-negative 2-4 years later. CONCLUSION: The study demonstrates a higher response rate as assessed by biochemistry, HCV RNA, and liver histology in the higher dose group.


Subject(s)
Antiviral Agents/administration & dosage , Hepatitis C/therapy , Interferon-alpha/administration & dosage , Adult , Aged , Base Sequence , Chronic Disease , Drug Administration Schedule , Female , Follow-Up Studies , Hepacivirus/genetics , Hepatitis C/enzymology , Hepatitis C/pathology , Hepatitis C/virology , Humans , Interferon alpha-2 , Liver/pathology , Male , Middle Aged , Molecular Sequence Data , RNA, Viral/analysis , Recombinant Proteins/administration & dosage , Transaminases/blood , Treatment Outcome
15.
Tidsskr Nor Laegeforen ; 115(27): 3382-6, 1995 Nov 10.
Article in Norwegian | MEDLINE | ID: mdl-7491582

ABSTRACT

During the last 20 years there has emerged a growing world-wide problem with regard to multidrug-resistant microbes. The most serious examples so far are vancomycin-resistant strains of Enterococcus faecium, totally resistant isolates of Mycobacterium tuberculosis and multiple-resistant Staphylococcus aureus and Streptococcus pneumoniae. With the exception of some few strains of methicillin-resistant S. aureus and vancomycin-resistant enterococci, such bacteria have not been found in Norway. In this article we discuss possible ways of preventing further selection and spread of multiple-resistant microbes. We stress the importance of infection control programmes and restrictive use of antibiotics.


Subject(s)
Drug Resistance, Multiple , Global Health , Communicable Disease Control , Drug Utilization , Humans , Norway
16.
Tidsskr Nor Laegeforen ; 115(28): 3504-7, 1995 Nov 20.
Article in Norwegian | MEDLINE | ID: mdl-7491604

ABSTRACT

Antibiotics are one of the cornerstones of modern medicine. During the last 20 years there has been an alarming world-wide spread of multiple-resistant bacteria. One of the main reasons is the overuse of all types of antibiotics, especially broad-spectrum drugs. This paper gives general advice on antibiotic therapy in Norway. We adovcate the use of drugs with little ecological impact, such as the penicillins. Whenever possible, empiric treatment with macrolides, tetracyclines cefalosporines, imipenem and fluoroquinolones should be avoided.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Drug Utilization , Anti-Bacterial Agents/adverse effects , Drug Resistance, Microbial , Humans , Norway
17.
Tidsskr Nor Laegeforen ; 115(28): 3508-10, 1995 Nov 20.
Article in Norwegian | MEDLINE | ID: mdl-7491605

ABSTRACT

There is an obvious need for teamwork between different specialists on the diagnosis and treatment of patients in an intensive care unit. The infectious disease specialist must contribute by establishing definite and quick diagnosis of infections and by employing an adequate and sensible antibiotic policy for successful treatment. The local microbiological flora should be kept at an acceptable level of resistance to antibiotics, and preventive measures should be chosen carefully. To achieve this goal, extensive knowledge on antibiotics and microbial epidemiology is essential.


Subject(s)
Bacterial Infections , Critical Care , Postoperative Complications , Bacterial Infections/drug therapy , Bacterial Infections/microbiology , Clinical Competence , Drug Resistance, Microbial , Humans , Postoperative Complications/drug therapy , Postoperative Complications/microbiology
20.
Scand J Infect Dis ; 26(2): 137-9, 1994.
Article in English | MEDLINE | ID: mdl-8036468

ABSTRACT

We report 3 cases of acute hepatitis E virus (HEV) infection imported from Asia. All 3 patients had fever and upper abdominal discomfort preceding jaundice which lasted 2-3 weeks with maximum bilirubin levels of 141-254 mmol/l. The ALT values peaked between 1,347 and 3,690 U/l. Both values normalized within 1-2 months. During the acute phase of the disease, all patients had high levels of IgG and IgM antibodies against HEV (anti-HEV) recombinant and synthetic peptides. The duration of the anti-HEV IgM was about 1-2 months.


Subject(s)
Hepatitis E/epidemiology , Acute Disease , Adult , Asia , Bilirubin/blood , Hepatitis Antibodies/blood , Hepatitis E virus/immunology , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Male , Myanmar/ethnology , Norway/epidemiology , Sri Lanka/ethnology , Travel
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