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Vpliv buloznega pemfigoida na kakovost življenja : diplomsko delo
ID Barbiš, Amanda (Author), ID Matić, Lucija (Mentor) More about this mentor... This link opens in a new window, ID Gogova, Tina (Reviewer)

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Abstract
Uvod: Bulozni pemfigoid je najpogostejša avtoimuna bulozna kronična bolezen. Ta prizadene kožo, včasih tudi sluznice. Pojavnost je največja pri starejši populaciji ljudi. Najpogostejša simptoma sta srbečica in nastanek mehurjev, ki so napolnjeni s prozorno tekočino in včasih vsebujejo tudi nekaj krvi. Ti najpogosteje prekrivajo predele rok in stopal. Prizadeta je lahko tudi ustna sluznica, najredkeje pa veznice, nos, žrelo, grlo, požiralnik, sapnik in anogenitalni predel. Zaradi vse daljše življenjske dobe se srečuje s to boleznijo vse več ljudi. Možni vzroki za pojavnost so lahko tudi uporaba nekaterih zdravil, posledica cepljenja, izpostavljenost UV-žarkom, poškodbam, okužbam in kirurškim posegom. Pomembno je hitro prepoznavanje stanja in obisk zdravnika, ki naprej odreja zdravljenje. Hitrejša kot je obravnava, boljša je prognoza bolezni. Namen: Namen diplomskega dela je bil raziskati vpliv buloznega pemfigoida na kakovost življenja pacientov. Cilji: Predstaviti bolezen bulozni pemfigoid in raziskati, kakšen vpliv ima na fizično, psihološko, socialno in duhovno zdravje pacientov ter njihovo vsakdanje življenje. Metode dela: Uporabili smo deskriptivno metodo raziskovanja s pregledom relevantne strokovne in znanstvene literature. Iskali smo v naslednjih podatkovnih bazah: PubMed, Medline in ScienceDirect ter izvedli dodatno raziskovanje prek iskalnika Google učenjak. Rezultati in razprava: Raziskave poudarjajo, da bulozni pemfigoid znatno vpliva na kakovost življenja predvsem zaradi srbenja, ki poslabšuje spanec, povzroča psihološke težave ter omejuje vsakodnevne dejavnosti. Standardno zdravljenje z lokalnimi steroidi in sistemskimi kortikosteroidi zmanjšuje intenzivnost bolezni in izboljšuje kakovost življenja, pri čemer psihološka podpora ostaja ključna za celostno obravnavo pacientov. Stres, utrujenost in suha koža poslabšujejo simptome, medtem ko jih hladna voda začasno lajša. Zaključek: Kakovost življenja pacientov z buloznim pemfigoidom je slabša v primerjavi z zdravimi posamezniki. Posega v vse vidike zdravja in ovira pacientovo vsakdanje življenje. Prizadete so aktivnosti, kot so spanje, koncentracija, učenje in opravljanje službenih dolžnosti. Vzbuja tudi občutke sramu in razdražljivosti. Najbolj moteč simptom je srbečica, ki je vzrok velike in pogoste želje po praskanju. Pomembna je zdravstvena vzgoja s strani zdravstvenih delavcev in spodbujanje k zdravljenju buloznega pemfigoida, kar občutno pripomore k boljšem počutju.

Language:Slovenian
Keywords:diplomska dela, zdravstvena nega, depresija, oskrba ran, avtoimunske bolezni
Work type:Bachelor thesis/paper
Typology:2.11 - Undergraduate Thesis
Organization:ZF - Faculty of Health Sciences
Place of publishing:Ljubljana
Publisher:[A. Barbiš]
Year:2025
Number of pages:25 str.
PID:20.500.12556/RUL-169743 This link opens in a new window
UDC:616-083
COBISS.SI-ID:238661123 This link opens in a new window
Publication date in RUL:07.06.2025
Views:451
Downloads:87
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Secondary language

Language:English
Title:The impact of bullous pemphigoid on quality of life : diploma work
Abstract:
Introduction: Bullous pemphigoid is the most common autoimmune bullous chronic disease affecting the skin and, in some cases, mucous membranes. It primarily occurs in the elderly population. The most frequent symptom is itching and the formation of blisters that are filled with clean fluid, or sometimes they may contain some blood. The most commonly affected areas are the hands and feet, though the oral mucosa may also be involved. Less commonly, the conjunctiva, nose, pharynx, larynx, esophagus, trachea, and anogenital region can be affected. The occurrence of this disease has been increasing over the past few decades, due to longer life expectancy. Possible triggers include the use of certain medications, vaccinations, exposure to UV rays, injuries, infections, and surgeries. Early identification of the condition and prompt medical attention are essential. The sooner the condition is addressed, the better the disease prognosis. Purpose: The aim of this thesis was to present the disease bullous pemphigoid, investigate how it affects the physical, psychological, social and spiritual well-being of patients and their daily lives. Methods: A descriptive research method was used, involving a review of relevant professional and scientific literature. Searches were conducted in the following databases: PubMed, Medline, ScienceDirect and additional research through the Google Scholar search engine. Results and discussion: Research highlights that bullous pemphigoid disease significantly affects quality of life, mainly due to itching, which impairs sleep, causes psychological problems and limits daily activities. Standard treatment, using local steroids and systemic corticosteroids, reduces the intensity of the disease and improves quality of life, with psychological support remaining key to the comprehensive treatment of patients. Stress, fatigue and dry skin worsen symptoms, while cold water temporarily relieves them. Conclusion: The quality of life of patients with bullous pemphigoid is worse compared to healthy individuals. It affects all aspects of health and interferes with patient’s daily lives. Activities such as sleeping, concentrating, learning, performing work duties, as well as feelings of shame and irritability, are impacted. The most bothersome symptom is itching, which causes a strong and frequent urge to scratch. Health education by healthcare professionals and encouragement to treat bullous pemphigoid are important, as they significantly contribute to improved well-being.

Keywords:diploma theses, nursing care, depression, wound care, autoimmune diseases

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