Short Communication Volume 11 Issue 2
Professor of Nephrology, Portugal
Correspondence: Mateus Martins Prata, Professor of Nephrology, Av. Guerra Junqueiro 22,5º esq.1000-167 Lisboa, Portugal
Received: May 19, 2023 | Published: June 8, 2023
Citation: Prata MM. Some questions that occur to me and most likely to other nephrologists. Urol Nephrol Open Access J. 2023;11(2):47-49. DOI: 10.15406/unoaj.2023.11.00330
Through several questions, based on easily verifiable data, the author decided to contextualize the doubts currently existing in the field of nephrology in Portugal.
The graphs that accompany the questions show the existing data that support them. However, the questions remain unanswered, and at the moment, the only answer to all the questions asked would be "we don't know".
The lack of explanation that justifies the questions makes it impossible to introduce appropriate and effective clinical measures to change the current paradigm: extremely high levels of incidence and prevalence in dialysis, with an enormous impact on the national health budget.
Keywords: hemodialyse, peritoneal dialyses, incidence, prevalence, comprehensive price
Portugal is a country with a recognized high level of clinical activity in nephrology and with a number of public and private units for dialysis treatment and kidney transplantation, per million inhabitants, among the highest in Europe.1
There is a National Health Service open to the entire population and all expenses with dialysis treatments - hemo and peritoneal - and kidney transplantation, are fully supported by the national health budget.
Peritoneal dialysis and kidney transplantation are performed exclusively in the public sector. Chronic hemodialysis treatment is performed in both, predominantly in private units (90%), the most part belonging to large international companies (43% Nephrocare, 30% Diaverum, 10% Davita,4% B Braun and 13% others).
The national health budget (NHB) predominantly contemplates the treatment of the diseases and is very scarce with regard to prevention. The percentage of NHB for prevention is lower than the average found in other European countries.
All patients with stage 5 chronic kidney disease are observed in nephrology hospital departments in the state public sector and, when it is decided to place the patient on a renal replacement therapy and there is no capacity to do so, they are sent to private satellite units. Criteria for admission to renal replacement treatment are not uniform and are subject to personal views, moral and ethical issues.2
Since 2008, the Ministry of Health has created an online platform (MHOP)3 where, before starting the chronic dialysis program, the patient's demographic, clinical and laboratory data must be registered. This platform has always been under the responsibility and supervision of the National Health Board (NHB) and the Nacional Commission for Monitoring of Dialysis (NCMD) and any possibility has been allowed for the data to be known either by doctors, by the general population or by the patients themselves.
There is no explanation for this situation. Therefore, various hypotheses arise, such as the lack of much data, frequent errors, lack of transparency or something more complex that NHB considers not to be made public. For example, Edgar and collaborators refer in their article2 that in the MHOP, "the online registry designed to enable a detailed record of all movements of patients starting dialysis, such as hospital admissions, changing between modalities... " "only 5 patients were recorded as changing to peritoneal dialysis after hemodialysis (January 2010-December 2016).’’ In the Portuguese Society of Nephrology Society Dialysis Registry (PSNR),4 this transition is mentioned to have occurred in a much higher number: four hundred and fifty eight(458 pts) patients transitioned, during that period, from one modality to the other, value that in current practice is known to be certainly the correct.
This almost total lack of information means that, even for many of the physicians who have been working in nephrology for many years, they continue to have, in certain areas, such as dialysis, many unanswered questions.
Some of these questions are too important to be forgotten.
The health authorities - National Commission for Monitoring of Dialysis and the National Health Board – have the data that would very likely allow us to obtain concrete answers to most of these questions. Possibly they would also make it possible to establish appropriate and effective measures to change this paradigm.
Since 2008, 14 years ago, it has become mandatory to register all patients on the platform.3 Only one clinical article2 has been published taking those data into account: to study the crude survival of patients starting dialysis in Portugal. Nothing else was allowed. The problem of the extremely high incidence and prevalence of dialysis in the country does not seem to interest the responsible authorities. They have the data but are not at all concerned with these matters.
The normality with which national associations of doctors, of nurses and of chronic kidney and dialysis patients accept such a situation leaves me perplexed.
None.
Authors declare that there is no conflict of interest exists.
None.
©2023 Prata. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.