Popa University of Medicine and Pharmacy Iasi, Romania Pulmonology Lung transplantation is a medical and surgical intervention widely used but still not performed in Romania. Although it is a new chance for life, transplanted patients are vulnerable and therapy dependent. Objective: highlighting pre-transplant management particularities in patients with chronic respiratory diseases and future perspectives. There are scientific guidelines in patient management for lung transplantation.
However, out of the guidelines we are confronting with severe restrictions from the health system, economical and psychological acceptance from patients. Those limitations are less measurable and unpredictable, so they could generate mistrust and confusion.
Conclusion: lung transplantation is a complex technique with a low rate of success in our country.
Pre-transplant management is under great pressure from mass media which could generate big misunderstanding from the people.
Discovering all the negative influences in the health system can raise the trust in doctors. Interveniile medicale i chirurgicale n transplantul pulmonar au evoluat de- a lungul timpului, astfel nct astzi se poate vorbi de transplant i n cazul persoanelor n vrst sau a celor cu multiple comorbiditi i limitri funcionale.
Datorit faptului c mecanismele de limitare funcional pre-transplant sunt multifactoriale, evaluarea acestor pacieni utilizeaz o baterie larg de teste ale capacitii de efort, ale funciei musculare, ale gradului de mobilitate i ale nivelului de activitate fizic.
Dup o evaluare preliminar complex, realizat de ctre o echip interdisciplinar, se stabilete un PRP individualizat care cuprinde obligatoriu tehnici de conservare a energiei, exerciii de for ct i de anduran i exerciii de cretere a amplianei toraco-pulmonare.
Baza de date rezultate cercetare GT – articole | Excel-fin
Toate acestea sunt premizele unui prognostic mai bun i implicit a unor costuri mai reduse pentru sistemul de sntate. Although fiberoptic bronchoscopy facilitates early detection of acute pulmonary allograft rejection or infection after lung transplantation, definitive evidence for a positive impact on survival is yet to be demonstrated. Benefits of transbronchial lung biopsies include the possibility of an early detection of specific histological features especially acute cellular rejection or lymphocytic bronchiolitiswhich have been associated with higher risk of chronic lung allograft rejection, and, also, the possibility of a longitudinal insight into immunological events in the allograft, recurrent respiratory papillomatosis and bevacizumab treatment can assist long-term management.
Bronchoalveolar lavage is an important method for the assessment of infection in immunosuppressed hosts. It helps to detect bacterial, viral, fungal, recurrent respiratory papillomatosis and bevacizumab treatment protozoal infections with high sensitivity and specificity.
In addition, the visualization of the anastomosis, performed at every fiberoptic bronchoscopy after lung transplant, is of utmost importance for an early detection of anastomotic defects or possible dehiscence.
The large airway monitoring recurrent respiratory papillomatosis and bevacizumab treatment prompt attention to developing strictures and thereby prevents downstream post-obstructive bronchiectasis. This lecture reviews the evidence for and against the utility of performing surveillance bronchoscopy postlung transplantation, discuss the pro and con arguments and how the application of this procedure can be customized in the individual patient.
Rezultate: Pe parcursul a 10 ani de derulare a PN de tratament a PAH - au fost tratati in total 74 de pacienti. Au avut indicatie de evaluare pentru transplant pulmonar 52 de pacienti 70,27dar au ajuns sa fie evaluati intr-un centru de referinta doar 7 pacienti reprezentand 13,46 din cei 52 care aveau indicatie.
Dintre acestia doar 3 pacienti au fost inclusi pe lista de transplant restul nu cancer mamar incidenta completat investigatiile sau au renuntat.
O singura pacienta a ajuns recurrent respiratory papillomatosis and bevacizumab treatment fie transplantata la 8 luni de la punerea pe lista, dar evolutia a fost nefavorabila, cu multiple complicatii postranspalnt si deces dupa un an.
Al 2-lea pacient a asteptat disperat 16 luni donatorul, dupa care a survenit decesul. Cea de-a 3-a pacienta a prezentat o complicatie severa in un abces cerebral, vindecat actualmente si dupa 2 ani a fost scoasa de pe lista de asteptare a renuntat.
Concluziii: Indicatia teoretica de transplant o are un procent foarte mare de pacienti cu PAH, dar conditiile practice posibilitatile de adresare, costurile, suportul psihosocial, donatorii sunt dezastruoase iar rezultatele sunt modeste, discutabile. Method: year retrospective analysis of the evolution of patients with PAH in the local national treatment program, following the indication and results of lung transplantation. Results: Recurrent respiratory papillomatosis and bevacizumab treatment the 10 years of PAH treatment registrya total of 74 patients were under treatment.
Only 3 patients were included on the transplant list the rest did not complete their investigations or gave up. Only one patient was transplanted 10 months after listing, but the evolution was unfavorable, with multiple post- transplant complications and death after one year.
The second patient desperately waited for the donor, however after 16 months death occurred. The third patient presented a severe complication in a brain abscess, currently cancer de colon bolsa heces and papillomavirus hpv cin 1 2 years was removed from the waiting list. Unfortunately 35 recurrent respiratory papillomatosis and bevacizumab treatment patients Conclusions: The theoretical indication for lung transplantation has a very high percentage of patients with PAH, but the practical conditions addressing possibilities, costs, psychosocial support, donors are disastrous and the results are modest.
After recovering from the procedure, the patients usually are at risk for developing graft rejection or various infectious complications due to complex and life-long immune-suppression.
- Oxiuros medicacion
- Rzumate Conferinta Oradea Oct | Biopsy | Tuberculosis
- Neurochirurgie Otorinolaringologie (ORL) Iunie - jurnale medicale - malaimare.ro
Звонок из Соединенных Штатов.
- Otorinolaringologie (ORL) Pneumologie Iunie - jurnale medicale - malaimare.ro
- На этот раз это прозвучало как приказ.
- Cancerul de san se vindeca
We present the case of a male patient, transplanted in for idiopathic pulmonary fibrosis that developed severe bilateral lung edema. The complex medical workup revealed a very rare complication of lung transplantation that benefited from a curable treatment. Granulocyte-macrophage colony stimulating factor GM-CSF has an important role in the differentiation of alveolar macrophages, causing impaired surfactant clearance in the most frequent forms as autoimmune PAP.
The conventional treatments are represented by whole-lung lavage and administering of inhale GM-CSF therapy.
We present the case of female, 45 years old, non smoker; diagnosed with PAP in May who received bilateral sequential lung transplant three years later, due to a progressive dyspnea and deterioration of lung function despite the traditional treatment.
After 4 years and 5 months, the patient is stable, in a good clinical condition and with a high quality of life. The evolution complicated with pulmonary fibrosis and respiratory recurrent respiratory papillomatosis and bevacizumab treatment could be a bad prognosis factor and an indication for the lung transplant in patients with PAP.
Also, the cases reported in the literature underline that PAP is both indication and a rare, possible complication of the lung transplant.
We present our experience with patients with rare diseases which were transplanted in Vienna and monitored both in Vienna and Bucharest.
Robert Hillman to develop a portable voice monitoring system for assessing voice disorders. The system uses a small non-invasive sensor placed on the neck that plugs into a smartphone. We are recruiting patients with muscle tension dysphonia no lesions or vocal fold nodules must be bilateral lesions to participate in this study.
Victor Babes, Timisoara, Romania Lung transplantation has become an accepted treatment for end-stage pulmonary parenchymal and vascular diseases. Bacterial infections comprise approximately half of all infectious complications. Infection with M. Lung transplant recipients are at increased risk for infectious complications compared to other solid organ transplant SOT recipients due to the direct contact between the pathogens and the graft in an immunosuppressed patient.
Other factors include: the loss of effective lymphatic drainage, and the decrease of mechanical defense due to reduced mucociliary clearance and decreased cough. Tuberculosis TB is a serious opportunistic infection reported in lung transplant recipients.
Its incidence ranges between 6.
Jurnale medicale Neurochirurgie, Otorinolaringologie (ORL), 2010, Iunie
Rates also vary depending on the type of organ transplant performed as well as on local screening practices and immunosuppression protocols. The rates and risk of TB in transplant recipients are highly dependent upon the key features, such as the frequency of TB in the recipient and donor population, the organ transplanted highest in lung transplant recipientsthe type and intensity of recipient screening for TB, and the use of prior or current anti-TB drug intake, preventively or curatively.
The clinical manifestations of TB are subtle and the diagnosis is difficult, which might lead to treatment delays, multiple repetition of tests might be needed. The risk of TB is highest in the first year post-transplant, during the time of maximal immunosuppression.
Meticulous postoperative surveillance, however, is still crucial for the management of lung transplant patients with recurrent respiratory papillomatosis and bevacizumab treatment to early detection and treatment of rejection and infection.
Rzumate Conferinta Oradea Oct 2017
However, improved methods for screening organ donors and recipients need to be identified, and alternative therapies that have lower toxicity profiles are needed for transplant recipients. Though the disease course may vary among patients and many patients experience periods of relative stability, disease progression and worsening of symptoms are inevitable for the majority of patients.
The most common symptoms are dry cough, dyspnoea and fatigue. IPF patients are susceptible to anxiety and depression. The combination recurrent respiratory papillomatosis and bevacizumab treatment poor prognosis, uncertainty of disease course and severe symptom burden heavily impacts quality of life QOL both for patients and family members.
Management of IPF requires regular evaluations and implementation of both pharmacological and nonpharmacological treatments. Antifibrotic therapies have a disease recurrent respiratory papillomatosis and bevacizumab treatment effect and slow down decline in lung function. Lung transplantation remains the only curative treatment for the small minority of patients who are eligible for this major intervention. Patients should be encouraged to attend a pulmonary rehabilitation maintenance programme, which has been shown to improve dyspnoea, QOL, physical activity and body composition.
Patients with IPF may have subclinical or overt comorbid conditions including pulmonary hypertension, gastroesophageal reflux, obstructive sleep apnea, obesity, and emphysema. Identification and treatment of comorbidities may improve QOL and potentially influences prognosis. A synchronized comprehensive management strategy is vital to match IPF patients needs recurrent respiratory papillomatosis and bevacizumab treatment the disease course. A model for continuous care in IPF includes assessing patients needs, backing patients by giving cinformation and support, delivering comfort care by focusing on treating symptoms and taking into account comorbidities, striving to prolong life by disease modification, helping and preparing patients and their caregivers for the eventual end-of-life events that are likely to occur.
Datorit faptului c multe din terapiile farmacologice non- specifice se dovedesc a fi insuficiente pentru ncetinirea ritmului de progresie al bolii, iar terapiile specifice sunt adesea controversate i costisitoare, reabilitarea pulmonar RP trebuie s fac parte obligatoriu din tratamentul integrativ al acestor complexe patologii. Dup o evaluare preliminar realizat de ctre o echip multidisciplinar, se stabilete un program de RP individualizat.
Aceste programe se desfoar n centre specializate, sub ndrumarea unor cadre medicale competente.
Living with Papilloma: Jacob's Story
Acestea vor prescrie tipul de exerciii necesare, ritmul i nivelul de efort, combinnd diferite tehnici tehnici de conservare a energiei, exerciii de rezisten i for a membrelor superioare i inferioare precum i exerciii de cretere a amplianei toraco-pulmonare. Puinele studii disponibile la ora actual, au demonstrat c programele de RP duc la creterea toleranei la efort, scderea gradului de dispnee i la mbuntirea calitii vieii pacienilor cu PID.
Pe lang diagnosticarea precoce, terapia farmacologic si RP, pacienii trebuie consiliai n vederea renunrii la fumat, dietei alimentare, vaccinrii antigripale i antipneumococice, oxigenoterapiei de recurrent respiratory papillomatosis and bevacizumab treatment durat i acolo unde este cazul, referire sintomi virus del papilloma umano transplant pulmonar.
Opacitati reticulare cu distributie subpleurala, cu predominanta bazala ce asociaza leziuni chistice aerice de tip honey-combing si bronsiectazii de tractiune, reprezinta modelul imagistic de pneumonie interstitiala usuala UIPce suprapune o fibroza pulmonara idiopatica FPI.
Ecografia este o metoda de diagnostic non-invaziva, non-iradianta, ce apreciaza orice modificare de densitate pulmonara. Multiple linii B coada de cometa si o ingrosare a liniei pleurale sunt elementele de morfologie ecografica caracteristice unui sindrom interstitial fibros. Au fost evaluati 23 de pacienti cu diagnostic de FPI realizat prin consens multidisciplinar.
Modificarile HRCT opacitati in sticla mata, reticulatia, honey-combing, bronsiectazii recurrent respiratory papillomatosis and bevacizumab treatment comparat cu cele ecografice numarul de linii B si grosimea liniei pleurale.
Rezultate: toti pacientii au prezentat multiple linii B distribuite bilateral, cu o distanta medie intre ele de 6,7mm, caracteristica unui sindrom interstitial. Concluzie: ecografia pulmonara este o metoda utila in screeningul si monitorizarea fibrozei pulmonare.
Lung sonography is a non-invasive, non-radiation technique, very sensitive to detect any alterations in the lung parenchymal density. Diffuse sub-pleural abnormalities as those occur in IPF are characterized by the presence of multiple B-lines and thickening of pleura line.
Twenty three patients with a multidisciplinary consensus IPF diagnosis underwent lung ultrasound LUS to assess the fibrotic index based on the evidence of B-lines and the characterization of the pleura line. Results: All patients recurrent respiratory papillomatosis and bevacizumab treatment diffuse bilateral B-lines.
The main distance between two adjacent B lines was 6. A fragmented, irregular, blurred pleura line are the features of severe fibrosis.