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1.
Injury ; 55(3): 111216, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38000939

ABSTRACT

BACKGROUND: Despite a focus of opioid-related research internationally, there is limited understanding of long-term opioid use in adults following injury. We analysed data from the 'Community Opioid Dispensing after Injury' data linkage study. AIMS: This paper aims to describe the baseline characteristics of the injured cohort and report opioid dispensing patterns following injury-related hospitalisations. METHODS: Retrospective cohort study of adults hospitalised after injury (ICD-10AM: S00-S99, T00-T75) in Queensland, Australia between 1 January 2014 and 31 December 2015, prior to implementation of opioid stewardship programs. Data were person-linked between hospitalisation, community opioid dispensing and mortality collections. Data were extracted for 90-days prior to the index hospital admission, to establish opiate naivety, to 720 days after discharge. Median daily oral morphine equivalents (i.e., dose) were averaged for each 30-day interval. Cumulative duration of dispensing and dose were compared by demographic and clinical characteristics, stratified by drug dependency status. RESULTS: Of the 129,684 injured adults, 61.3 % had no opioids dispensed in the 2-year follow-up period. Adults having any opioids dispensed in the community (38.7 %) were more likely older, female, to have fracture injuries and injuries with a higher severity, compared to those with no opioids dispensed. Longer durations and higher doses of opioids were seen for those with pre-injury opioid use, more hospital readmissions and repeat surgeries, as well as those who died in the 2-year follow-up period. Median dispensing duration was 24-days with a median daily end dose of 13 oral morphine equivalents. If dispensing occurred prior to the injury, duration increased 10-fold and oral morphine equivalents doubled. Adults with a documented dependency prior to, or after, the injury had significantly longer durations of use and higher doses than the rest of the cohort receiving opioids. Approximately 7 % of the total cohort continued to be dispensed opioids at 2-years post injury. CONCLUSION: This is a novel population-level profile of opioid dispensing patterns following injury-related hospitalisation, described for the time period prior to the implementation of opioid stewardship programs and regulatory changes in Queensland. Detailed understanding of this pre-implementation period is critical for evaluating the impact of these changes moving forward.


Subject(s)
Analgesics, Opioid , Opioid-Related Disorders , Adult , Humans , Female , Analgesics, Opioid/therapeutic use , Retrospective Studies , Drug Prescriptions , Opioid-Related Disorders/epidemiology , Morphine Derivatives , Practice Patterns, Physicians'
5.
Vet Rec ; 124(15): 410, 1989 Apr 15.
Article in English | MEDLINE | ID: mdl-2728289
7.
Vet Rec ; 123(22): 584, 1988 Nov 26.
Article in English | MEDLINE | ID: mdl-3212914
8.
Parasite Immunol ; 10(2): 193-207, 1988 Mar.
Article in English | MEDLINE | ID: mdl-2453831

ABSTRACT

Zygotes and ookinetes of the rodent malaria Plasmodium berghei can be enriched 50-fold, from whole blood cultures by ammonium chloride lysis. Three monoclonal antibodies (MoAbs) raised against such enriched preparations specifically bind to a determinant of Mr 21 kD as assessed by 125I-labelled goat anti-mouse IgG probed immunoblots of Western transfers of SDS-PAGE gels. Indirect immunofluorescence indicates that the 21 kD determinant bound by specific MoAbs, whilst not detectable on gametocytes or gametes, appears on the parasite surface within 2 h of exflagellation/fertilization and increases thereafter. The three MoAbs specifically binding the 21 kD determinant block oocyst development in mosquitoes by at least 90%, as assessed either by in-vitro membrane feeds or by live feeds on passively immunized mice. These MoAbs reduce ookinete formation in vitro by between 52 and 100%. Possible mechanisms of action of these MoAbs are discussed.


Subject(s)
Antibodies, Monoclonal/immunology , Antibodies, Protozoan/immunology , Antigens, Protozoan/analysis , Plasmodium berghei/immunology , Animals , Anopheles , Antigens, Protozoan/immunology , Binding, Competitive , Electrophoresis, Polyacrylamide Gel , Epitopes/analysis , Epitopes/immunology , Female , Fluorescent Antibody Technique , Hybridomas , Immunization, Passive , Immunoassay , Kinetics , Mice , Zygote/immunology
9.
Tijdschr Diergeneeskd ; 111(20): 1026-7, 1986 Oct 15.
Article in English | MEDLINE | ID: mdl-3775750
12.
15.
Vet Rec ; 96(1): 19, 1975 Jan 04.
Article in English | MEDLINE | ID: mdl-1167716
16.
Vet Rec ; 89(15): 415-7, 1971 Oct.
Article in English | MEDLINE | ID: mdl-5098195
17.
Vet Rec ; 87(20): 625-6, 1970 Nov 14.
Article in English | MEDLINE | ID: mdl-4921747
18.
J Lipid Res ; 10(4): 356-62, 1969 Jul.
Article in English | MEDLINE | ID: mdl-4307829

ABSTRACT

The inositol lipids of plant seeds consist of phosphatidyl inositol, the phytoglycolipids, and a previously uncharacterized ceramide-phosphate-polysaccharide. These three species have been separated from each other and from the common glycerophosphatides by a series of simple countercurrent distributions, first as the naturally occurring Ca-Mg salts and subsequently in the Na salt form. The new ceramide-phosphate-polysaccharide is present in each of the four plant phosphatides examined (corn, soybean, flax, safflower). It is devoid of glucosamine but contains the other carbohydrate components commonly found in the phytoglycolipids. The basic structural unit of the new glycolipid consists of a ceramide-phosphate-inositol-hexuronic acid moiety to which the other sugars (galactose, mannose, arabinose) are attached. Flax ceramide-phosphate-polysaccharide has fucose in addition to the other sugars.


Subject(s)
Amino Alcohols/analysis , Fatty Acids/analysis , Glycolipids/analysis , Phosphatidylinositols/analysis , Plants/analysis , Polysaccharides/analysis , Chromatography, Gel , Chromatography, Paper , Countercurrent Distribution , Dextrans , Fucose/analysis , Glycolipids/isolation & purification , Phosphates/analysis , Phosphatidylcholines/analysis , Seeds/analysis , Glycine max/analysis , Species Specificity , Uronic Acids/analysis , Zea mays/analysis
19.
J Lipid Res ; 10(4): 363-9, 1969 Jul.
Article in English | MEDLINE | ID: mdl-5797522

ABSTRACT

Phytoglycolipid has been isolated for the first time from plant leaves (Phaseolus vulgaris). The purified product (almost identical with the phytoglycolipid isolated from flax seed) was a ceramide attached through phosphate diester linkage to an oligosaccharide, which consisted of the usual trisaccharide unit (inositol, hexuronic acid, hexosamine) to which were attached mannose, galactose, and arabinose. The major fatty acids were the saturated 2-hydroxy C(22), C(24), and C(26) acids; the major long-chain bases were dehydrophytosphingosine (d-ribo-1,3,4-trihydroxy-2-amino-8-trans-octadecene) (53%) and phytosphingosine (d-ribo-1,3,4-trihydroxy-2-amino-octadecane) (32%). A ceramide and a cerebroside were also isolated. In the ceramide the major fatty acids and the major long-chain bases were the same as in the phytoglycolipid. In the cerebroside, the fatty acid composition was similar to that in the ceramide and phytoglycolipid, but the long-chain bases consisted of dehydrophytosphingosine and phytosphingosine (7:1) with a substantial amount of unidentified long-chain base. The sugar component was glucose.


Subject(s)
Glycolipids/analysis , Lipids/analysis , Plants/analysis , Amino Alcohols/analysis , Arabinose/analysis , Cellulose , Cerebrosides/analysis , Chemical Phenomena , Chemistry , Chromatography, Gas , Chromatography, Ion Exchange , Chromatography, Paper , Fatty Acids/analysis , Glycolipids/isolation & purification , Hexoses/analysis , Inositol/analysis , Lipids/isolation & purification , Methods , Oligosaccharides/analysis , Seeds/analysis , Species Specificity , Uronic Acids/analysis
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