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1.
Epidemiol Infect ; 139(5): 658-65, 2011 May.
Article in English | MEDLINE | ID: mdl-20727248

ABSTRACT

Rates of herpes zoster (HZ) hospitalizations, antiviral prescriptions, and New South Wales emergency-department presentations for age groups <20, 20-39, 40-59 and ⩾60 years were investigated. Trends were analysed using Poisson regression to determine if rates increased following funding of varicella immunization in Australia in November 2005. The regression analysis revealed significantly increasing trends of between 2% and 6% per year in both antiviral prescriptions and emergency-department presentations in all except the <20 years age group. When considered together, the differential changes in rates observed by age group provides preliminary evidence to indicate that HZ incidence is increasing in adults aged >20 years. However, it is not possible to attribute the increasing trends in HZ observed directly to the varicella immunization programme, and continued monitoring and analyses of data for a longer duration, both pre- and post-vaccine introduction, is required.


Subject(s)
Chickenpox Vaccine/administration & dosage , Chickenpox Vaccine/immunology , Herpes Zoster/epidemiology , Immunization/statistics & numerical data , Adult , Aged , Aged, 80 and over , Antiviral Agents/therapeutic use , Australia/epidemiology , Drug Utilization/statistics & numerical data , Hospitalization/statistics & numerical data , Humans , Incidence , Middle Aged , Young Adult
2.
J Infect ; 50(3): 187-92, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15780411

ABSTRACT

OBJECTIVES: To describe changes in treatment decisions after receipt of nucleic acid amplification (NAA) test for the diagnosis of M. tuberculosis. METHODS: Retrospective notes review of treatment decisions in patients receiving a NAA test for suspected pulmonary or non-pulmonary tuberculosis at the Royal Free Hospital in London between March 2001 and February 2002. Notes were sought on a 50% random sample of patients with both smear and NAA negative specimens and all patients with other specimen results. RESULTS: Two hundred and fifty patients were tested with NAA; clinical details were obtained on 138; 61 were ever treated. Seventeen (17/18) smear-negative patients were started on treatment after a positive NAA; none of six smear-negative patients treated prior to a negative NAA result had treatment stopped. Seventeen (17/21) smear-positive patients were treated prior to NAA result and all were NAA positive; treatment was delayed in four smear-positive patients until receipt of an NAA and one NAA-negative patient was not treated. CONCLUSIONS: In routine practice a positive test in an untreated smear-negative patient leads to decision to treat in almost all, but the proportion testing positive is low (8% or 17/219). In patients already on treatment negative tests did not lead to decisions to stop.


Subject(s)
Antitubercular Agents/therapeutic use , Nucleic Acid Amplification Techniques , Practice Patterns, Physicians' , Tuberculosis, Pulmonary/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Child , Female , Humans , Male , Middle Aged , Predictive Value of Tests , Retrospective Studies , Sputum/microbiology , Tuberculosis, Pulmonary/drug therapy
3.
J Public Health (Oxf) ; 27(1): 114-7, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15637109

ABSTRACT

Universal screening for HIV in early pregnancy is strongly promoted policy in the United Kingdom with a target of 90 per cent uptake. We identified characteristics of women declining screening by conducting an audit at three hospitals in inner north London. In early 2002 midwives were asked to complete an audit form following first antenatal appointment. Of 2,710 women attending 401 (15 per cent) declined an HIV test. Of women who declined 38 per cent reported they had been tested for HIV in the past; 65 per cent accepted every other antenatal test. In multivariable analysis parity (OR: 1.19; 95 per cent CI 1.10-1.29 per additional child), declining other tests (OR: 3.10; 95 per cent CI 2.44-3.93 per test declined) and previous HIV testing (OR: 1.70; 95 per cent CI 1.30-2.23) were predictors of declining an HIV test. Women declining screening were not obviously from high-risk demographic groups: women from sub-Saharan Africa were not at greater risk of declining an HIV test than women from other regions.


Subject(s)
Diagnostic Tests, Routine/statistics & numerical data , HIV Infections/diagnosis , Patient Acceptance of Health Care/statistics & numerical data , Pregnancy Complications, Infectious/diagnosis , Prenatal Diagnosis/statistics & numerical data , Adult , Female , Health Care Surveys , Humans , Logistic Models , London , Middle Aged , Minority Groups/psychology , Minority Groups/statistics & numerical data , Patient Acceptance of Health Care/ethnology , Pregnancy , Religion , Risk Factors
4.
J Hosp Infect ; 57(3): 258-62, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15236857

ABSTRACT

Methicillin-resistant Staphylococcus aureus (MRSA) predominantly affects those over 65 years old. There may be a substantial pool of older people with MRSA in the community. We studied the prevalence in one London general practice, screening 258 older people living in their own home. MRSA (E-MRSA 15) was found in two participants (0.78%). Past history of MRSA was the only significant risk factor. The results of this and other studies suggest that national guidelines recommending early discharge for MRSA carriers have not resulted in widespread community acquisition amongst elderly people living in their own home. Community antibiotic policies for skin and soft-tissue infection do not require amendment. Patients with previous MRSA should be isolated and screened on admission especially to high-risk units.


Subject(s)
Carrier State/epidemiology , Community-Acquired Infections/epidemiology , Methicillin Resistance , Staphylococcal Infections , Staphylococcal Infections/epidemiology , Staphylococcus aureus , Age Distribution , Aged/statistics & numerical data , Anti-Bacterial Agents/therapeutic use , Carrier State/diagnosis , Carrier State/prevention & control , Community-Acquired Infections/diagnosis , Community-Acquired Infections/etiology , Community-Acquired Infections/prevention & control , Drug Utilization/standards , Family Practice/statistics & numerical data , Female , Humans , Infection Control/methods , Infection Control/standards , London/epidemiology , Male , Mass Screening/methods , Mass Screening/standards , Microbial Sensitivity Tests , Patient Discharge/standards , Population Surveillance/methods , Practice Guidelines as Topic , Prevalence , Recurrence , Residence Characteristics/statistics & numerical data , Risk Factors , Staphylococcal Infections/diagnosis , Staphylococcal Infections/etiology , Staphylococcal Infections/prevention & control
5.
Commun Dis Public Health ; 7(1): 73-6, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15137286

ABSTRACT

In January 2002 the Communicable Disease Surveillance Centre (CDSC) introduced outcome reporting for tuberculosis 12 months after start of treatment. To determine whether outcome could change with longer and more detailed follow up, we examined this at 12 months and two years for a cohort notified in 2000 at a central London hospital. At 12 months 61/94 (65%) notified patients had completed treatment, 10 (16%) had died, 11 (12%) were lost to follow up, six (6%) were transferred to another service in the UK, four (4%) were still on treatment, and treatment for one (1%) patient had been stopped. After a mean follow up of two years, 65 (69%) had completed treatment. In this London service with a high prevalence of HIV infection (at least 23%), low treatment success was due to deaths, transfers and losses to follow up. The last of these was often due to patients returning to their country of origin (7 of 11). Tuberculosis was the primary or contributing cause of death in at least 4/94 (4%) cases. Completion rates need to be interpreted with caution particularly in specialist units with highly mobile populations. This has implications for national targets as well as for models of care.


Subject(s)
Antitubercular Agents/therapeutic use , Disease Notification , Hospitals, Municipal , Treatment Outcome , Tuberculosis/drug therapy , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Cohort Studies , Continuity of Patient Care/statistics & numerical data , Follow-Up Studies , Hospitals, Municipal/statistics & numerical data , Humans , Infant , Infant, Newborn , London/epidemiology , Middle Aged , Patient Acceptance of Health Care/ethnology , Patient Acceptance of Health Care/statistics & numerical data , Population Dynamics , Registries , State Medicine , Survival Analysis , Tuberculosis/diagnosis , Tuberculosis/mortality , Tuberculosis/prevention & control
6.
Epidemiol Infect ; 132(6): 1099-108, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15635967

ABSTRACT

Drug-resistant tuberculosis can be transmitted (primary) or develop during the course of treatment (secondary). We investigated risk factors for each type of resistance. We compared all patients in England and Wales with isoniazid- and multidrug-resistant tuberculosis in two time-periods (1993-1994 and 1998-2000) with patients with fully sensitive tuberculosis, examining separately patients without and with previous tuberculosis (a proxy for primary and secondary drug-resistant tuberculosis). Patients with previous tuberculosis smear positivity and arrival in the United Kingdom <5 years were strongly associated with multidrug resistance and isoniazid resistance. In patients with no previous tuberculosis HIV infection, residence in London and foreign birth were risk factors for multidrug resistance, and non-white ethnicity, residence in London and HIV infection for isoniazid resistance. Risk factors for each type of resistance differ. Elevated risks associated with London residence, HIV positivity, and ethnicity were mainly seen in those without previous tuberculosis (presumed transmission).


Subject(s)
Antitubercular Agents/pharmacology , Drug Resistance, Bacterial , Drug Resistance, Multiple , Tuberculosis, Pulmonary/drug therapy , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Child , Child, Preschool , Emigration and Immigration , England/epidemiology , Female , Humans , Incidence , Infant , Infant, Newborn , Isoniazid/pharmacology , London/epidemiology , Male , Middle Aged , Population Surveillance , Risk Factors , Wales/epidemiology
7.
Aust N Z J Public Health ; 25(2): 138-40, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11357909

ABSTRACT

OBJECTIVES: To determine the true immunisation status of children identified by the Australian Childhood Immunisation Register (ACIR) as 90 days overdue, and determine why appropriately immunised children were flagged as overdue. METHODS: A telephone survey of immunisation providers and/or parents of a stratified random sample of 850 NSW children born on or after 1 January 1996 and identified by the ACIR as 90 days overdue for at least one scheduled immunisation at 17 June 1997. The survey was conducted in June to September 1997. RESULTS: Children in the sample ranged in age from 5 to 17 months. Only 526 (61.9%) could be traced. Of these, 452 (86.6%) were fully immunised, and 75% of immunisations were given on time (within 30 days of falling due). The overall proportion of NSW children identified by ACIR as 90 days overdue who were fully immunised was an estimated 85% (95% CI 82.6%-87.4%). For the 452 fully immunised children, a reason for the child's immunisation not appearing on the register could be attributed for only 248/452 (54.8%). There was evidence that the provider had failed to submit an encounter form for 141 of these children. CONCLUSIONS: In mid-1997, more than half the children identified by ACIR as 'overdue' were fully immunised. A significant reason for fully immunised continuing to be flagged as overdue was failure to return encounter forms. IMPLICATIONS: At the time of survey the ACIR could not accurately identify unimmunised children and was of limited use as a tool for public health services to follow up very overdue children.


Subject(s)
Immunization Programs/organization & administration , Immunization Schedule , Registries , Data Collection , Humans , Infant , New South Wales , Parents , Public Health Administration , Random Allocation
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