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Proceedings of the Waikato Clinical School Research
Seminar, Wednesday 12 September 2007
Brief interventions in primary health care: referral
and intake assessment processes, Julia Davis. University of
Waikato
The Brief Interventions Project was a large study evaluating
brief mental health interventions (4-6 sessions) as provided by the Waikato
Primary Health Organisation in 2006-2007. GPs referred nearly 1500 people in the
Waikato region to Brief Interventions therapists in the space of a year.
Analyses of GP referral rates found broad differences in referral rates between
GPs, from no referrals to more than 40 patients referred. These differences
could not be accounted for by practice locality (e.g. rural compared with urban
GPs). Alternative explanations might include different strategies for managing
patients’ mental health concerns, different utilization of mental health
professionals by GPs, or varying levels of GP’s ‘psychological
mindedness’ in the conceptualization and treatment of psychological
distress. Intake assessment results suggest that those people referred by GPs
were appropriate for referral to the Brief Interventions service. Finally, some
demographic groups were under-represented in the group who were referred (such
as males, and people identifying as Maori), although referral rates are
reflective of the demographic profile of GP patients. Based on these results,
issues for the continued provision of brief interventions and its evaluation
were discussed.
Mental health outcomes for primary care patients
enrolled in the Waikato PHO Brief Interventions Project. John Fitzgerald, Karma
Galyer, Juanita Ryan, Lauren Gaffaney. The Psychology Centre, Hamilton
Accessing mental health care is challenging, particularly
when difficulties are not severe enough for secondary care services. The Waikato
PHO Brief Interventions Project aimed to increase access to care by funding up
to six sessions of counselling for GP patients with mild to moderate
psychological distress. This type of brief intervention in primary care has had
positive outcomes internationally, but had not been investigated in New Zealand.
Evaluation participants completed the Brief Symptom Inventory-18 (BSI-18
n=107, matched pairs = 85) and The General Health
Questionniare-12 (GHQ-12 n=100, matched pairs = 81) at their
first and last session. Patients’ scores were significantly
improved at outcome, with 68% of the group showing reliable change on the BSI-18
and 64% on the GHQ-12. Therapists’ (n = 254) and patients’
(n=152) feedback concurred that the interventions improved
psychological wellbeing. Qualitative examples of the benefits obtained included
symptom reduction, skill development, and insight into the problem experienced.
These results provide support for the value of a brief intervention service for
mental health care in a New Zealand setting. Ongoing evaluation is required to
check that benefits continue to be maintained, and to identify relevant areas
for service development.
Factors affecting clinical decision-making in
bronchiolitis. D Graham, K-C Hsiao, M Ferry-Parker, N Manikkam, Child Health,
Waikato Hospital, Hamilton
Aim: To evaluate clinicians decision-making
process in acute bronchiolitis, including relative impact of clinical status and
pulse oximetry.
Methods: Multi-centre randomised controlled
study on clinicians’ management preferences using hypothetical vignettes
of an infant with acute bronchiolitis. Four possible vignettes were generated
using two different clinical presentations combined with two different pulse
oximetry readings, and randomly distributed, one per clinician. Clinicians
indicated investigation and management preferences. Eligible clinicians included
paediatric medicine nurses and doctors and emergency medicine nurses and doctors
working in New Zealand public hospitals.
Results: From 299 vignettes, 63.6% of
clinicians decided to either perform no investigation or only perform nasal
virology. Investigations chosen included chest x-rays (33.4%), full blood counts
(12.4%), electrolytes (12.0%) and blood cultures (8.4%). Therapy chosen included
inhaled bronchodilators (15.4%), systemic corticosteroids (7.0%), and
antibiotics (7.0%), and supplemental oxygen (53.9%).
Well infants were less likely than unwell infants to have
un-necessary investigations (OR 2.47, CI 1.51-4.04), more likely to have
ineffective therapies (OR 0.61, CI 0.38-0.98) and as likely to have necessary
therapies (OR 1.41, CI 0.84-2.38). Infants with lower pulse oximetry values were
more likely to have un-necessary investigations (OR 2.69, CI 01.65-4.40), more
likely to have ineffective therapies (OR 7.98, CI 4.62-13.79) and as likely to
have necessary therapies (OR 0.62, CI 0.36-1.04) as children with higher pulse
oximetry values. Well children with lower pulse oximetry were more likely to
have un-necessary investigations (OR 5.50, CI 2.29-13.21), more likely to have
ineffective therapies (OR 24.38, CI 9.98-59.55) and less likely to have
necessary therapies (OR 0.03, CI 0.00-0.09) than well children with higher pulse
oximetry values. Unwell children with higher pulse oximetry were as likely to
have un-necessary investigations (OR 1.83, CI .97-3.48), less likely to have
ineffective therapies (OR 3.36, CI 1.64-6.91) and less likely to have necessary
therapies (OR 9.32, CI 3.38-25.73) than unwell children with lower pulse
oximetry values.
Conclusions:
Infants with acute bronchiolitis are over investigated and often inappropriately
treated. The decision making process is strongly and inappropriately influenced
by pulse oximetry readings. Clinical practice should focus on the patient and
clinical findings, rather than on pulse oximetry. It may be appropriate to
review the risks, as well as the benefits, of pulse oximetry in routine
paediatric practice.
The use of the
general health questionnaire 12 in detecting mental health difficulties in
primary care. TJ Halliday. Hamilton Psychological Service
The focus of this presentation is on the use of the GHQ-12
within two primary care practices in order to explore case selection, and
referral decisions made by general practitioners. Results from the current study
found that a number of clients presenting with mental health difficulties were
identified by the GHQ-12, but not referred on by general practitioners. Of those
that were recognized, few were referred on to specialist mental health
providers. The discussion and recommendations focus on outlining a role for
psychologists in enhancing screening and referral accuracy, enhancing
appropriate access to specialist services where necessary, and identifying those
individuals whose needs may be better met within the primary care
environment.
A Phase I pharmacokinetic study of PR-104, a
hypoxia-targeting agent, in patients with solid tumors. MB
Jameson1, D
Rischin2, M
Pegram3, J
Gutheil4, A
Patterson5, W
Denny5, W
Wilson5;
1Waikato Hospital, Hamilton, New Zealand;
2Peter MacCallum Cancer Centre, Melbourne,
Australia; 3University of California, Los
Angeles, CA, USA; 4Proacta, Inc., San Diego,
CA, USA; 5Auckland Cancer Society Research
Centre, Auckland, New Zealand
Background: PR-104 is a novel pre-prodrug
(precursor of a prodrug) designed to form a cytotoxic nitrogen mustard
(alkylating agent) in hypoxic regions of tumors. Following IV administration,
PR-104 is converted by systemic phosphatases to the alcohol intermediate
PR-104A, which, under hypoxic conditions, is reduced to form the active
DNA-crosslinking mustard species PR-104H. This phase I trial defines a Maximally
Tolerated Dose (MTD) and pharmacokinetics (PK) for this schedule.
Methods: Patients (pts) with
relapsed/recurrent solid tumors received PR-104 as a 1-hour IV infusion every 3
weeks with PK sampling on days 1-2 of cycle 1. Cohorts of ≥3 pts were
treated starting at 135 mg/m2.
Results: 23 pts have been enrolled: median
age 51 years (range 29-72); 13 (57%) male. Most pts had received prior radiation
or chemotherapy and had metastatic disease. Six dose levels (135, 216, 354, 550,
770, and 1100 mg/m2) have been evaluated.
Dose-limiting toxicity (DLT) was observed in one patient at 1100
mg/m2 (grade 3 fatigue) and this dose level was
expanded to 6 pts. In the first 4 cohorts, 54 adverse events (AEs) were
considered drug-related by the investigator including nausea (26% of all AEs),
fatigue (19%), vomiting (11%) and anorexia (6%); remaining AEs each constituted
< 3% of the total. Of 16 grade 3 AEs, 3 were considered drug-related by the
investigator (anemia, dehydration and vomiting). Prophylactic anti-emetics
largely prevented nausea and vomiting at higher doses, at which dose-related
decreases in neutrophils and platelets were seen.
Conclusions: PR-104 has shown manageable
toxicities similar to other cytotoxic agents, with no serious mucositis,
diarrhea or alopecia. DLT is likely to be myelosuppression based on preclinical
and current clinical data, with the MTD close to 1100
mg/m2. The preclinical PK target for the
alcohol intermediate has been exceeded at higher doses and, while no objective
responses have been documented, reductions in tumor volume have been seen at
these doses.
Cmax and AUC for PR-104 and PR-104A:
Value (SD)
Retention of patients in the "Get Checked" free
annual diabetes review program in Waikato, New Zealand. G Joshy
1, RA
Lawrenson1, D
Simmons2.
1Waikato Clinical School, University of Auckland, Hamilton, Waikato, New
Zealand; 2Addenbrooke’s Hospital,
Cambridge University Hospitals NHS Foundation Trust, Cambridge, United
Kingdom
Aim: To characterise the retention of
patients in the "Get Checked" free annual diabetes review program in New
Zealand.
Methods: Retrospective review of Waikato
Primary Health registered patients who had at least one "Get Checked" review
between 1st July 2000 and 30th Jun 2006. The time reviews were analysed using
Kaplan-Meier survival curves. Predictors for the likelihood of a second review
were identified using Cox's regression analysis.
Results: 10,919 patients were reviewed at
least once during this five year period. There were 69% Europeans, 18% Maori, 3%
Pacific Islanders, and 4% Asian. 87% had Type 2 diabetes and 8% had Type 1
diabetes. Only 57% of the estimated 10,604 diabetes patients utilised the free
check in 2005/06. One and a half years after initial review, 35% were yet
to return for a second review (Figure 1). But those who were retained attended
subsequent reviews more regularly. Those who attended a second review
returned much earlier for the third review, 75% within 1.5 years after second
review. Maori and Asians took a significantly longer time to return for a second
review (median 1.4 years) compared with Europeans (1.1 years, p<0.0001).
Younger patients aged <40 years returned for a second review much later (1.8
years) compared with 65+ year olds (1.1 years, p<0.0001). No significant
gender difference was found. Younger patients aged <40 years (vs age 65+),
those of Maori or Asian origin (vs Europeans) and those with Type 1
diabetes (vs Type 2) were less likely to return for a second review.
Conclusions: In spite of this program being
of benefit and free to patients, a significant proportion of patients did
not return for a second review within 1.5 years after initial review. The loss
of those with Type-1 diabetes and younger patients may reflect their greater
contact with specialist rather than GP services. Excess drop out among ethnic
minorities need further investigation and intervention.
Figure 1. Kaplan-Meier Survival Curves for the
Time to Reviews (from the Previous Review, Conditional that Patients Attended
the Previous Review).
![]() ![]() Table 1. Survival Analysis of Time to Second
Review (from Initial Review)
![]() Preschool development and cognitive ability at 8
years in very low birth weight infants. NA Keene, D Bourchier, S McGregor. Child
Development Centre, Waikato Hospital, Hamilton
Very Low Birth Weight (VLBW) infants are at increased risk
for development problems due to being born so early and so small. Infants born
weighing less than 1250g, and discharged from Waikato Hospital New Born Unit,
are routinely followed up at the Child Development Centre, at 1 & 2 years
(age corrected for prematurity) and at age 4. The aims of this study were to:
(1) assess the cognitive outcome of these children at 8 years of age, and (2)
determine the potential value of the preschool developmental assessments in
predicting school-age outcomes.
Thirty five infants born in 1998, weighing less than 1250g,
were identified for the study. Twenty three children participated, 52% were
male. The mean age was 100.65 months (8yr 4mths) and the mean birth weight was
878.04gms (range 580g – 1112g). The Wechsler Intelligence Scale for
children, Fourth Edition (WISC IV) was used to assess cognitive ability.
Full Scale Cognitive scores (WISC IV, mean 100, SD 15) were
1 Standard Deviation below the mean (mean FSIQ 84.30, SD 18.17, median 90, range
50-109). A Repeated Measures ANOVA found that scores at 4 years were not
significantly different than scores at 8 years.
Overall, our hypotheses were supported, with VLBW infants
achieving substantially lower cognitive scores compared to normative data on the
WISC IV. Results suggest that the 4 year assessment is more predictive of 8 year
cognitive outcome than earlier assessments. Further results and clinical
significance will be discussed.
Diagnosing mental illness in general practice.
Steven Lillis, Graham Mellsop. Waikato Clinical School, University of
Auckland
A qualitative study was undertaken in the Waikato to
understand the use of diagnostic schema by general practitioners when making a
diagnosis of mental illness. The results suggested that formal classifications
were seldom used and that disease management imperitives were strong drivers of
diagnostic process. A subsequent nationwide survey of general practitioners
found that the most common reasons for not using diagnostic schema was lack of
familiarity and experience with them, perceived ridgidity and high complexity.
The most important roles of the diagnostic process are assistance with
pharmacological choices and communication with other health workers. It is
imperitive for classification systems to successfully integrate with practice
management systems.
Mindfulness-Based Stress Reduction (MBSR) training:
challenges and achievements for people with chronic health problems. P
Thomas1, J
Shennan2, W
Tuck2, J Bell
3, H
Conaglen4.1The
Psychology Centre, 2Health Waikato,
3Private Practice,
4Research Consultant
The evidence indicates that mindfulness-based stress
reduction training, or MBSR, is effective in alleviating suffering and improving
coping related to many chronic illnesses. We believe this is the first New
Zealand/Aotearoa pilot study of MBSR training for people with chronic health
problems; for example, chronic pain, diabetes, a history of strokes,
hypertension, and cancer. Between October 2005 and December 2006, forty-two
participants (randomly allocated to treatment and waitlist conditions) attended
and completed one of four eight-week MBSR training groups. The impact of MBSR
training on their physical and psychological health was monitored, and followed
up six months later. Research challenges included recruitment and conservation
of a sample big enough to be statistically significant, and consequent problems
for the study design. The significant achievements reported by two group members
with considerable health difficulties will be discussed, and possibilities for
future research will be noted.
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