13 research outputs found
Is Concept of ‘Style’ Used or Abused in Psychology?
The concept of style is very common in Psychology. Tracking that stylistic approach, we were interested, is this approach just on the level of use, or probably, it is overused, or even its abused. In order to obtain basic information that can lead us further, we conduct analysis of the Encyclopedia Dictionary (content, text and discourse analysis), following strict methodological procedure. We figured out that there is a stylistic intention, and that although the style is not explained as a key concept in the dictionary, it was used for explanation of different concepts, both alone or as a part of complex concept. Although, its most prominent usage was as cognitive style, as a word "style" it was mentioned 691 times, or one word "style” on every sixth page. We suppose that stylistic approach in psychology is offering possibility for generalization (scientific aspect) as well appreciation of individuality. Probably the "Style "concept is overused, and still it is not abused. We can support the thesis that style is still in style.Keywords: style, content, text, discourse analysis, cognitive style, scientific generalization, individuality
Proactive Coping Inventory – Test-Retest Data on Macedonian Population
The presented analysis concerning the Proactive Coping Inventory test-retest data on Macedonian population was conducted in two time frames, first in 2003/2004 and consequently in 2013 in order to determine whether there are differences in the use of proactive coping as a healthy way of coping with stressful experiences having on mind the constant changes in everyday life and environment. The analysis was done for the purpose of initiating further research in the field of coping styles and promoting proactive coping.Keywords: Coping, Proactive Coping, Proactive Coping Inventory
Poli(laktid-ko-glikolid) mikročestice kao sustav za kontrolirano oslobađanje proteina: priprava i karakterizacija
Poly(DL-lactide-co-glycolide) (PDLLGA) and poly(L-lactide-co-glycolide) (PLLGA) copolymers were prepared by bulk ring opening polymerization of lactide and glycolide and characterized by GPC, FTIR, 1H NMR and DSC. Copolymers with different molar masses at a constant lactide/glycolide ratio were used for preparation of bovine serum albumin (BSA)-loaded microparticles by the double emulsion w/o/w method. The influence of the copolymer molar mass and composition on the microparticle morphology, size, yield, degradation rate, BSA-loading efficiency and BSA release profile were studied. For microparticles prepared from PDLLGA copolymers, a biphasic profile for BSA release was found and for those made from PLLGA copolymers the release profile was typically triphasic; both of them were characterized by high initial burst release. Possible reasons for such behavior are discussed.Poli(DL-laktid-ko-glikolid) (PDLLGA) i poli(L-laktid-ko-glikolid) (PLLGA) kopolimeri priređeni su polimerizacijom laktida i glikolida uz otvaranje prstenova i karakterizirani pomoću GPC, FTIR, 1H NMR i DSC. Kopolimeri različitih molarnih masa i stalnog omjera laktida i glikolida upotrebljeni su za pripravu mikročestica s goveđim serumskim albuminom (BSA) metodom dvostruke emulzije tipa voda/ulje/voda. Proučavan je utjecaj molarne mase i sastava kopolimera na oblik, veličinu, iskorištenje i stupanj razgradnje mikročestica, uklapanje i oslobađanje BSA. Za mikročestice pripravljene s PDLLGA kopolimerom utvrđen je bifazični profil oslobađanja BSA, a za mikročestice s PLLGA kopolimerom trifazičan profil. Za obje vrste karakteristično je brzo početno oslobađanje. Razmatrani su mogući uzroci takvog ponašanja
Television Induced Fear Scale, Coping Strategies to Reduce Fear from TV and Television Mediation Scale – Adaptation Process on Macedonian Sample-Our Experience
The presented results were obtained from a pilot study concerning the children’s television watching habits (aged 9 to 12), their fright reactions and their way of coping with the fear. In the following text we present a detailed report of the adaptation process of the scales: “Television Induced Fear Scale”, “Coping Strategies to Reduce Fear from TV” and “Television Mediation Scale”.Keywords: Television, Fear, Media, Mediation, Coping
Model framework for off label use of medicines
Background
The drug licensing regulatory system ensures that marketed
drugs to be used, meet the high standards and requirements
for quality, efficacy and safety. Unfortunately,
in practice, prescribers are often obliged to deviate from
granted medicine marketing authorisation, due to the lack
of availability of appropriate medicines for patient’s therapeutic
needs and progress. This concept of medicines use
not mentioned in the approved labelling (FDA Modernization
Act) or outside of the terms of Summary of Product
Characteristics regarding indication, age, dosage, pharmaceutical
form and route of administration (British NHS
Guideline) is defined as off-label use of licensed medicines.
On the global level, many supportive evidence and
health care needs confirm that off-label medicines use
occurs in every country and each level or specialty area
of healthcare (Conroy, 2003). Moreover, it is an integral
part of Good Medical Practice and may provide the best
available option or even the standard of care in a particular
health condition (Dresser and Frader, 2009). In general,
this concept is legal and may be appropriate, but it can be
associated with safety, clinical and ethical concerns, emphasizing
the increased incidence of adverse events associated
with off-label medicines uses in particularly vulnerable
patient groups (Gazarian and Kelly, 2006).
A concerning issue is that the majority of all off-label
uses have limited to no scientific support (Radley et al.,
2006) and a considerable number of prescribers have no or
limited knowledge about off-label medicine use or do not
meet regulations regarding off-label use, if they exist. (Piñeiro
Pérez et al., 2014).
Experience shows that to ensure the quality of off-label
use of medicines, there should be a formal mechanism
to assess the feasibility, monitoring the safety and efficiency
of medication used based on this concept.Thus, in continuum,
the off-label use of medicines has been an essential
part of the ethical and legal considerations as well as,
many regulatory initiatives.
The overall objective is to present a model regulatory
framework setting out guidelines and recommendations for
quality use of off-label medicines within the national profile
of health care policy.
A literature search was undertaken to identify the issues
and challenges related to off-label medicines use including
clinical, safety and ethical concerns.
Recommendations for model framework
Principles of good practice for off-label use of medicines
should include the following elements: identifying
the medical needs; compilation of a consensus list of accepted,
scientific based off-label uses; creating an official
expert group for the evaluation and approval of specific offlabel
uses; and, providing a safe and effective supply. The
main guiding principles and developed activities to support
a responsible decision-making with regard to off-label
medicines include: 1) the medical need- the best avail-
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Maced. pharm. bull., 62 (suppl) 607 - 608 (2016)
Oral presentations
Continuing professional development
able treatment in cases of specific characteristics when authorized
medicines cannot meet the patients’ need; 2) sufficient
scientific basis and/or clinical practice experience
to justify their action. Distinguish the routine off-label use,
which is the use of these medicines based on “high quality”
evidence and the use in specific exceptional circumstances;
3) information duty and a high degree of respect
for patient rights, involving the patient/carer in decisionmaking
process; 4) monitoring and reporting the outcomes,
efficiency and adverse reactions; 5) considering self-monitoring
of prescribing practices, liability and accountability.
An additional special responsibility which among others
falls on pharmacists should be to ensure that the prescriber
is conscious for off-label prescribing and the reasons for
that 6) production of compendia of certain medicines, enlisting
those off-label uses judged to be legitimate.7) financial
sustainability of an off-label use in medical practice.
Before deciding to compound a patient-specific preparation,
a step by step evaluation of alternatives should be
made. These alternatives include a therapeutic alternative,
dose rounding or manipulation of licensed dosage forms
(splitting tablets, crushing tablets/opening capsules, dispersing
their content in water or food, splitting suppositories,
the use of a preparation designed for another route of
administration).
Conclusion
Prescription, compounding, dispensing and administration
of off label use of medicines should be regulated
within the national profile of health care policy.
The regulation regarding the practice of off-label medicine
use differs between countries. Some countries have
this practice regulated by law, while in others it is covered
by good practice regulations or general professional
recommendations and ethical standards. Assuming that
there is no any general rule to regulate the “accurate” offlabel
use of medicines it is of paramount importance for
the countries to find a national solution to fulfil the ethical
and legal demand, especially in the areas of pharmaceutical
law and health insurance law. The common elements of
these regulatory frameworks are the physicians’ freedom to
prescribe off-label medicines if the scientific evidence exists
and the need to inform patients when making this decision.
Making policy efforts, by adopting appropriate guidelines
for off-label medicines use, based on scientific evidence,
with specifications of healthcare professionals’ responsibilities
and a registry of off-label drug use in every
day practice, would make possible a valuable approach towards
ensuring a quality use of these medicines. Recommended
solutions, as practiced in some countries, would
support prescribes in more direct and active approach to
handle the ethical and legal phenomenon associated with
the off-label use of medicines
Tuberculosis in the Prisons in the Republic of Macedonia, 2008-2017
BACKGROUND: Tuberculosis (TB) is a major health problem in penitentiary institutions (prisons), and its prevalence was reported to be multiple times higher compared to that of the general population. Conditions such as overcrowding, malnutrition and limited access to medical care which often exist in prisons increase the risk of reactivation, transmission and poor prognosis of tuberculosis disease among inmates.AIM: The main objective of this study was to present the epidemiological situation of TB in the prisons from 2008 till 2017 in the Republic of Macedonia (RM).PATIENTS AND METHODS: There are 13 different penitentiary institutions in the RM with a total capacity to house 2600 prisons inmates. Management of TB in the prisons is part of the National TB program in RM, and the Institute for Lung Diseases and Tuberculosis in Skopje is in charge of it. All prisoners with TB in the RM are registered in the Central Register for TB within this Institute. We use the data from the Central Register, and with the method of description, we present the epidemiological data and clinical characteristics of the prisoners about TB in prisons in RM for 10 years’ period.RESULTS: From 2008 till 2017 there were 58 TB cases registered in prisons in total. The absolute number of TB cases in the prisons is not big, but the incidence rate is higher than 100/100,000 population, or several times bigger than in the general population (except in 2012 and 2016). In 2017 there were 10 TB cases registered in the prisons with an incidence rate of 323.9/100,000 population which is many times higher than in the general population in RM. The majority of inmates with TB were young men with risk factors for TB infection or TB disease before incarceration such as drug abuse, alcohol, smoking, but there was no association with HIV infection. The most of the patients diagnosed in prison were new cases (54), secondary TB due to reactivation from the latent TB infection or secondary TB due to the environment. From 2008-2017 there were 82.75% successfully treated TB cases in the prisons, and there were no cases of multi-drug resistant tuberculosis (MDR-TB).CONCLUSION: The results from our study showed that the TB control in the prisons in RM is good with satisfactory treatment outcome. On the other hand, the high incidence rate showed that the prisons in RM provide conditions for TB transmission and with other additional risk factors present place for high TB prevalence. The study findings can be used for planning more effective TB control interventions for the prison population in RM
Land market development and small farms’ access to land in the pre-accession countries: final report
Maja Kikiritkova with participation of Queen's Day 2009
Fashion show – Inspired by the Netherlands (Macedonian designers and fashion students) (Jovan Petrovski, Nikola Buleski, Maja Kikiritkova, Daniela Simonovska, Hristina Despotovska