<p>The aim of the study was to measure patient waiting and service times, describe the causes of high waiting time as well as to determine staff and patient derived norms on waiting times at the Manzini Regional Hospital HIV Clinic. Literature reviewed show that complaints regarding long waiting time have been effectively dealt with through patient flow analysis studies, which measure patient waiting and service times as well as other characteristics. A descriptive cross sectional quantitative survey methodology was undertaken using a time-delimited sample of all patients attending the HIV clinic over one week and all the staff who were in contact with the patients. Waiting time tracking instruments and short questionnaires were used to collect data from both patients and staff. Data were analysed quantitatively.</p>

Magister Public Health - MPH / The aim of the study was to measure patient waiting and service times, describe the causes of high waiting time as well as to determine staff and patient derived norms on waiting times at the Manzini Regional Hospital HIV Clinic. Literature reviewed show that complaints regarding long waiting time have been effectively dealt with through patient flow analysis studies, which measure patient waiting and service times as well as other characteristics. A descriptive cross sectional quantitative survey methodology was undertaken using a time-delimited sample of all patients attending the HIV clinic over one week and all the staff who were in contact with the patients. Waiting time tracking instruments and short questionnaires were used to collect data from both patients and staff. Data were analysed quantitatively. / South Africa

Consider a sequence (Formula presented.) of i.i.d. uniform random variables taking values in the alphabet set {1, 2,…, d}. A k-superpattern is a realization of (Formula presented.) that contains, as an embedded subsequence, each of the non-order-isomorphic subpatterns of length k. We focus on the (non-trivial) case of d = k = 3 and study the waiting time distribution of (Formula presented.). Our restricted set-up leads to proofs that are very combinatorial in nature, since we are essentially conducting a string analysis.

Background: Organ transplantation is seen as a treatment to save lives. There are great differences in the transplantation process between different countries. Patients have previously described the process of organ transplantation as restrictive and emotionally draining with an overhanging fear of death before transplant. Aim: The aim of this study was to describe patients’ experiences of waiting for organ transplantation.  Method: This literature-based study was conducted with analysis of qualitative research to gain knowledge about the patients’ experiences. Analysis of the eleven articles was performed by using Friberg’s five-step method. Results: Two main themes and six subthemes emerged from the analysis. The main themes The need for support and information highlighted the patients need for support and adequate information from both family and health care professionals. This was seen as a way to handle the uncertainty that the waiting time could bring. The other main theme The time on the waiting list described that waiting for an organ transplantation could bring restrictions to their daily life. Patients described the time on the waiting list as uncertain and many thoughts about the donor arose. Also, hope about their future was prominent throughout the time on the waiting list. At times this hope could turn to despair. Conclusion: Waiting for an organ transplantation is a multifaceted experience. Support from family was considered crucial and therefore should be included when possible. Nurses are responsible for giving enough and appropriate information and support to the patients during their wait.

Background: The history of transplantation goes back a long time and has been the last resort as a treatment to save a person's life. The availability of organs does not correspond to the need, there are also limited studies on how the patient's health processes are affected during the waiting time for a new organ. Aim: The aim of this study was to describe patientexperiences of waiting for an organ transplant. Method: This literature-based study was based on qualitative research to describe patient experiences of managing the waiting time for an organ transplant. 11 articles were analyzed according to Friberg's (2017) five step model. Results: The article analysis resulted in two main themes and six sub-themes. The main theme New Challenges highlighted that the patients are in need for both support and information during the time that they are waiting for an organ transplant. The second main theme, Emotional stress highlighted what feelings the patient can endure during the waiting time for a transplantation. The feelings of both hope and uncertainty are described by the patients. Conclusion: When nurses take responsibility for the caring and the six areas of competence, which means that patients who are on the waiting list for an organ transplant have their nursing needs met.

This dissertation is a collection of papers on anomalous phenomena in physics, biology, and sociology. These phenomena are primarily analyzed in terms of their temporal and spatiotemporal statistical properties. The analysis is based on both numerical simulations and, in some cases, real-world physiological and sociological data. The primary methods of analysis are diffusion entropy analysis, power spectral analysis, multifractal analysis, and survival (or waiting-time) analysis.

Thesis (M. A. (Nursing)) -- University of Limpopo, 2020 / Background: Long patient waiting time for services is demonstrated by daily long queues of patients in Primary Health Care (PHC) and hospitals Outpatients departments. Aim: The aim of the study was to determine the factors contributing to long waiting time at Blouberg Health Centre (BHC), Capricorn District, Limpopo Province. Methods: A quantitative, descriptive and cross-sectional research design was used to describe factors contributing to long waiting time. The study population consisted 31356 patients in the financial year 2017/2018. Simple random probability sampling was used to select 395 respondents. Data were collected using self-developed questionnaire. All questionnaires were completed and returned. The 395 questionnaires were then analyzed using the Statistical Package for Social Sciences (SPSS, version 25). Descriptive statistics were used to analyze and describe and summarized data. Findings: The findings were presented in the form of distribution graphs and tables. Inferential statistics were used based on probability and allowed judgement to be made about variables. The study revealed factors considered most important were lack of commitment; full time study leaves at the same year; workshops; sick leaves; increased population; sitting in tearoom for hours; many foreign national without passports; staff shortages; laissez faire working style and transfers or escorting patients, while the nearby Hellen Franz Hospital (HFH) also transfer to the same hospitals, leading to mismanagement of budget reduced manpower and increased death rate. Recommendations: The study recommends that all Primary Health Care (PHC) settings should use numbers for patients when entering facilities to monitor the queuing and prevent dissatisfaction that can result from long waiting. Conclusion: It is of paramount importance to provide clearer, transparent information to the recipients of the Primary health care services that they might receive. The provincial coordinators are accountable to the waiting time management with the assistance of the PHC specialist nurse and Nursing Management.

Bakgrund: Vårdpersonalen på en akutmottagning har stora krav på sig, ansvar för många patienter och måste fatta många egna beslut, ibland med mycket kort betänketid. Vårdpersonalen möter många olika patienter med olika problem och personligheter, och måste bemöta varje patient så att denne känner sig bekräftad och sedd. Syfte: Syftet med litteraturöversikten är att undersöka patienters upplevelse av att vårdas på en akutmottagning. Metod: Artiklar till arbetet har söks i olika databaser. Aktuella artiklar har lästs och relevanta fynd har markerats, för att analyseras och sammanställa ett resultat. Resultat: Analysen resulterade i tre underrubriker: Information, Bemötande och Vårdmiljö, med uppdelning av positiva och negativa upplevelser. Många patienter var nöjda med vården, men hade låga förväntningar från början. Patienterna har förstående för personalens tuffa arbetsmiljö, men önskade att få bättre information om väntetid och undersökningar. De tyckte att väntetiden var för lång, och kände sig ofta ensamma och övergivna. Slutsats: Mycket behöver förändras för att patienterna ska få en mer positiv upplevelse av akuten. Detta arbeta kan hjälpa till att belysa vilka punkter som vården måste arbeta extra mycket med för att patienterna ska känna sig trygga, exempelvis bättre information om väntetider och ett bemötande där sjusköterskan ser hela patienten. / Background: The demands and expectations on a nurse in the emergency room are high. They are responsible for many patients and have to make many decisions on their own, sometimes with very short reflection time. They face a wide variety of patients with different problems and personalities, each requiring their own method of approach and interaction in order for him or her to feel acknowledged. Aim: The aim of the literature review is to examine patient's experiences of being cared for in an emergency room. Method: Articles for the work has been searched in different databases. Articles in-question has been read and the relevant finding has been highlighted, to analyze and compile the results. Results: The analysis resulted in three subheadings: Information, Treatment and Care environment, with sectioning of positive and negative experiences. Many patients were satisfied with the care, but had low expectations from the start. Conclusion: There is much that needs to be changed to allow patients to have a more positive experience of the emergency room. Care units must work harder with to ensure that patients will feel secure and safe, for example, better information on waiting times and a treatment where the nurse sees the whole patient.

本論文主要是在探討依序選擇四個字串之下，是否存在一策略使得第二或第四字串有較大的機會比第一或第三字串先出現，也就是所謂的後選優勢是否存在。 利用電腦計算，我們發現字串長度為4,5,6時後選優勢確實存在，而當字串長度大於等於或等於7時，我們則證明了若第一字串為(0,0,...,0),(0,0,...,0,1),(1,1,...,1)或(1,1,...,1,0)時，後選者優勢亦存在。 / In the thesis, we consider about the first occurrence of four strings decided sequentially with teams. Team 1 consists string 1 and string 3; team 2 consists string 2 and string 4. It is interested in whether or not team 2 whose strings are decided after first string and third string are given separately gets an advantage in appearing with larger probability.Namely, given any string 1, we want to find a string 2 such that any string 3 corresponds to at least one string (string 4) making a larger probability for team 2 in appearing earlier than team 1. Based on the result from computer calculation, team 2 advantage over team 1 when the string length is 4, 5, and 6. This thesis also shows that team 2 gets an advantage for cases where string 1 is (0,0,...,0), (0,0,...,0,1), (1,1,...,1), (1,1,...,1,0) ,when the string length is larger than 6.

Hensikt: Hensikten med undersøkelsen var å beskrive, og å oppnå større forståelse for, hvordan ventelistepasienter ved Klinikk for ortopedi og revmatologi og pasientrepresentanter fra Brukerutvalget ved St. Olavs Hospital i Trondheim oppfattet ventetiden og kontakten med sykehuset i påvente av undersøkelse og behandling. Kunnskapen skal brukes til å forbedre informasjonen til og kommunikasjonen med ventelistepasientene. Metode: Datainnsamling ble gjort ved 24 individuelle intervju med pasienter fra ventelistene og et gruppeintervju med pasienter i en offisiell rolle som medlemmer av sykehusets Brukerutvalg. Analysen av intervjuene ble gjort med fenomenografisk tilnærming. Resultat: To sammenhengende hovedtema fremkom, der tema om Daglig liv som ventelistepasient dominerte over tema om Informasjon og kommunikasjon i ventetiden. De to tema ble belyst med seks hovedkategorier med til sammen 20 underkategorier som viste at ventelistepasientene opplevde en hverdag med mye smerter og hindringer i forhold til tidligere funksjonsnivå. De var lite opptatt av generell informasjon og hvordan den skriftlige informasjonen så ut. Den informasjon de hadde fått ble oppfattet som grei nok, men inneholdt ikke de opplysninger de hadde behov for. Det viktige var å få personlig, lett forståelig og forklarende informasjon av legen ved den polikliniske undersøkelsen der de eventuelt ble søkt til innleggelse og operasjon; på et tidlig tidspunkt i ventetiden få en konkret operasjonsdato å forholde seg til; få målrettet informasjon om hvordan de kunne forberede seg på operasjonen og tilrettlegge for seg selv etter operasjonen; at det var noen å komme i kontakt med hvis de ønsket det. I tillegg til samsvarende oppfatninger med ventelistepasientene var deltakerne fra Brukerutvalget mer opptatt av og kritisk til informasjonens innhold og form enn pasientene i de 24 individuelle intervjuene. Konklusjon: Pasientene ønsket kontroll over livet i ventetiden ved å få konkret og personlig informasjon om operasjonsdato, hensiktsmessige forberedelser, hva og hvordan i forhold til operasjon og rekonvalesens. Først når dette var oppfylt kunne de vise en begrenset interesse for informasjonens utforming / Aim: The aim of the study was to describe and achieve a greater understanding of how patients on the waiting list for surgery at the Department of Orthopaedic Surgery and Rheumatology and the group of patient representatives (Brukerutvalget) at St. Olav’s University Hospital in Trondheim experienced the waiting time and the contact with the hospital. The knowledge shall be used to improve the information to and the communication with patients on waiting list. Method: The data collection was done through 24 individual interviews with patients on waiting lists and one group interview with four of the patients having an official role as members of the hospital’s group of user representatives. The analysis of the interviews was done by a phenomenographic approach. Results: Two related main subjects appeared of which the subject of the daily life as a waiting list patient dominated over the subject of the information and communication received during the waiting time. These two subjects were illustrated by six main categories and 20 subcategories which showed that the waiting list patients experienced a daily life with much pain and hindrances compared to their earlier level of functionality. They were to a small degree interested in any general information and how the general information was presented. The information they had received was conceived as satisfactory, but did not contain the information they needed. The important thing was to get personal, easy to understand and well explained information from the doctor during the visit at the outpatient clinic, when they were eventually sought referred to the hospital for admission and operation, to get a fixed time for the operation early in the waiting time, to get systematic information about how to prepare for the operation and how to organize themselves after the operation, and finally that there should be a person to contact if they needed to. In addition to perceptions common with the waitinglist patients the participants from the group of user representatives were more concerned with and critical to the contents and presentation of the information than the patients from the 24 individual interviews. Conclutions: Personal and relevant information was needed to cope with the daily life. Not till the patients knew about a fixed time for the operation, appropriate preparations, the surgery and convalescence they could show a limited interest for the shaping of the information / <p>ISBN 978-91-85721-15-3</p>