The aim of this study was to investigate which situations Haemodialysis patients consider as the hardest for avoiding fluid intake. The data collection was performed with a questionnaire which was distributed to Haemodialysis patients who fulfilled the inclusioncriteria. Of 158 Haemodialysis patients 103 Haemodialysis patients chose to participate in the study. The participants were chosen from different dialysis centres (n=12) in north and south of sweden, excluding the middle of Sweden. The questionnaire that was given out consisted of 32 situations, the response format included nine alternatives, that included different kind of difficultes.

The purpose of this study was to describe how patients with hemodialysis experience their dialysis treatment. The study was conducted as a qualitative descriptive design. The study is based on six interviews. The interviews were transcribed in their entirety and analyzed according to content analysis inspired by Granheim and Lundman. The result is based on five categories; Stress and requirements, Life-supporting Haemodialysis treatment, physical impairments, social constraints and a positive view on Haemodialysis.

AbstractThe aim of the study was to examine the relation between estimated fluidintake and real fluidintake among dialysis patients. The data were collected through study specific questionnaire and data from the medical record. Patients attached to eleven Swedish dialysis units were asked to participate. The number of patients that fulfilled the inclusion criteria were 222 persons of whom145 (65%) chose to participate in the study. The dialysis patients estimated their fluid intake for a day in average 9,06 deciliter.

Bakgrund:Tidigare forskning visade att anhöriga till personer som undergår hemodialysbehandling går igenom en svår tid. Syfte:Syftet var att beskriva vuxna patienters upplevelser i samband med hemodialysbehndling Metod:En systematisk litteraturstudie genomfördes på tio kvalitativa studier. Dessa analyserades enligt Evans (2002) beskrivande modell. Resultat:Analysen av materialet resulterade i att fem teman med tolv tillhörande subteman, där patienternas upplevelser i samband med hemodilalysbehandlingen framkom. Slutsats:Resultatet beskriver patienternas upplevelser och problem på olika sätt.

Syftet med studien var att beskriva hälsorelaterad livskvalitet, ångest/depression och vårdtillfredsställelse hos kvinnor med bröstcancer tidigt i sjukdomsförloppet samt att undersöka om det fanns ett samband mellan dessa aspekter. Vidare studerades förklarande bakgrundsfaktorer; demografiska, socioekonomiska och medicinska faktorer samt psykosocialt stöd. Denna tvärsnittsstudie genomfördes som en enkätstudie kompletterat med medicinska data från Regionalt register för bröstcancer i Uppsala/Örebroregionen. Totalt 1574 förfrågningar om deltagande gick ut, varav 69 % valde att delta i studien. Niohundratrettiotvå kvinnor ingick i de slutliga analyserna (59 %).