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UnknownScoping review to identify strategies and interventions improving interprofessional collaboration and integration in primary care.

Objective

To identify strategies and interventions used to improve interprofessional collaboration and integration (IPCI) in primary care.

Design

Scoping review DATA SOURCES: Specific Medical Subject Headings terms were used, and a search strategy was developed for PubMed and afterwar...
S-EPMC9621161 | biostudies-literature
UnknownInactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia.
Mutations in TDP2, encoding tyrosyl-DNA phosphodiesterase 2, have been associated with a syndromal form of autosomal recessive spinocerebellar ataxia, type 23 (SCAR23). This is a very rare and progressive neurodegenerative disorder described in only nine patients to date, and caused by splice site o...
S-EPMC10449949 | biostudies-literature
UnknownFrailty screening in older patients undergoing elective colorectal surgery: Comparative study of seven screening instruments.

Background

Frailty screening instruments are increasingly studied as risk predictors for adverse postoperative outcomes. However, because of the lack of comparative research, it is unclear which screening instrument performs best. This study therefore compared the diagnostic accuracy of seve...
S-EPMC11970229 | biostudies-literature
UnknownChromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease.
Congenital structural heart disease (CHD) is the leading cause of infant death from birth defects. Postnatal survival primarily depends on the type and severity of the defect. In addition, worse cardiac prognosis is observed when extra-cardiac anomalies (ECA) are associated. This retrospective chart...
S-EPMC11785992 | biostudies-literature
UnknownImpact of NSAIDs and endurance exercise on myocardial fibrosis and arrhythmogenesis in murine coxsackieviral myocarditis
Not available
S-EPMC12343846 | biostudies-literature
UnknownDevelopment of a toolkit to improve interprofessional collaboration and integration in primary care using qualitative interviews and co-design workshops.

Background

Despite numerous attempts to improve interprofessional collaboration and integration (IPCI) in primary care, patients, care providers, researchers, and governments are still looking for tools and guidance to do this more efficiently. To address these issues, we decided to develop ...
S-EPMC10149845 | biostudies-literature
UnknownFetal sex determination in twin pregnancies using non-invasive prenatal testing.
Non-invasive prenatal testing (NIPT) is accurate for fetal sex determination in singleton pregnancies, but its accuracy is not well established in twin pregnancies. Here, we present an accurate sex prediction model to discriminate fetal sex in both dichorionic diamniotic (DCDA) and monochorionic dia...
S-EPMC6609680 | biostudies-literature
UnknownSuperiority of trans-oral over trans-nasal sampling in detecting Streptococcus pneumoniae colonization in adults.
The human nasopharynx is the main reservoir for Streptococcus pneumoniae. We applied conventional and molecular methods to determine the prevalence of S. pneumoniae nasopharyngeal colonization in adults. Paired trans-orally and trans-nasally obtained nasopharyngeal samples from 268 parents of 24-mon...
S-EPMC3610877 | biostudies-literature
UnknownProtocol for postmortem bedside endoscopic procedure to sample human respiratory and olfactory cleft mucosa, olfactory bulbs, and frontal lobe.
We present a protocol for the rapid postmortem bedside procurement of selected tissue samples using an endoscopic endonasal surgical technique that we adapted from skull base surgery. We describe steps for the postmortem collection of blood, cerebrospinal fluid, a nasopharyngeal swab, and tissue sam...
S-EPMC10837096 | biostudies-literature
UnknownRare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge.
Non-invasive prenatal testing has been introduced for the detection of Trisomy 13, 18, and 21. Using genome-wide screening also other "rare" autosomal trisomies (RATs) can be detected with a frequency about half the frequency of the common trisomies in the large population-based studies. Large prosp...
S-EPMC9712527 | biostudies-literature
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