D Baroncini

Multiple Sclerosis Center, Hospital of Gallarate, ASST della Valle Olona, Gallarate, Italy.

44 publications 1992 – 2022 ORCID

What does D Baroncini research?

D Baroncini studies improved ways to diagnose celiac disease, a condition where the body reacts poorly to gluten, leading to damage in the intestines. By using a method called Narrow Band Imaging with magnification endoscopy, Baroncini's research aims to help doctors find intestinal damage that standard methods often miss. This is important because better diagnosis can lead to more effective treatment and less need for unnecessary tests like biopsies.

Key findings

  • In a study of 44 patients, Narrow Band Imaging with magnification endoscopy identified 12 cases of partial villous atrophy that standard endoscopy missed, achieving an overall accuracy of 95%.
  • The use of NBI-ME may significantly reduce the number of unnecessary biopsies for patients suspected of having celiac disease.
  • Improved diagnostic accuracy helps in timely treatment and better management of patients with celiac disease.

Frequently asked questions

Does Dr. Baroncini study celiac disease?
Yes, Dr. Baroncini focuses on diagnosing celiac disease to improve accuracy and treatment.
What imaging techniques has Dr. Baroncini researched?
Dr. Baroncini has researched Narrow Band Imaging with magnification endoscopy to detect intestinal damage related to celiac disease.
Is Dr. Baroncini's work relevant to patients with suspected celiac disease?
Absolutely, their work helps improve the diagnosis for those with suspected celiac disease, potentially leading to better outcomes.

Publications in plain English

Switch from sequestering to anti-CD20 depleting treatment: disease activity outcomes during wash-out and in the first 6 months of ocrelizumab therapy.

2022

Multiple sclerosis (Houndmills, Basingstoke, England)

Signoriello E, Lus G, Bonavita S, Lanzillo R, Saccà F +15 more

Plain English
This study looked at how switching treatments affects disease activity in patients with multiple sclerosis (MS). Researchers found that during the period when patients stopped their previous treatment (wash-out), there were 35 relapses among 165 patients, particularly in those who switched from fingolimod. After starting ocrelizumab therapy, 12 patients showed signs of disease activity within the first six months, suggesting that shifting from certain treatments may increase relapse risk temporarily. Who this helps: This information is valuable for patients with MS and their doctors in making treatment decisions.

PubMed

A real-world study of alemtuzumab in a cohort of Italian patients.

2022

European journal of neurology

Russo CV, Saccà F, Frau J, Annovazzi P, Signoriello E +27 more

Plain English
This study looked at how effective alemtuzumab, a treatment for multiple sclerosis, is in real-world settings for Italian patients who had previously tried other therapies. Researchers tracked 322 patients from January 2015 to December 2018 and found that the average number of relapses dropped significantly from 0.99 before starting alemtuzumab to 0.13 during treatment. Moreover, after two years of treatment, 90% of patients had no disease progression, and about 20% showed improvement in their condition. Who this helps: Patients with multiple sclerosis, especially those who have not responded well to other therapies.

PubMed

Long-term follow-up (up to 11 years) of an Italian pediatric MS cohort treated with Natalizumab: a multicenter, observational study.

2022

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Baroncini D, Ghezzi A, Guaschino C, Moiola L, Filippi M +17 more

Plain English
This study looked at how well the drug Natalizumab works for children with aggressive multiple sclerosis (MS) over a period of up to 11 years. Researchers followed 92 children who were treated with Natalizumab, finding that the number of relapses decreased significantly from an average of 2.2 relapses per year before treatment to just 0.08 relapses per year during treatment. This is important because it shows that Natalizumab is effective in managing MS symptoms in children without introducing new safety concerns. Who this helps: This benefits pediatric MS patients and their doctors by providing evidence for effective long-term treatment options.

PubMed

Towards a validated definition of the clinical transition to secondary progressive multiple sclerosis: A study from the Italian MS Register.

2022

Multiple sclerosis (Houndmills, Basingstoke, England)

Iaffaldano P, Lucisano G, Guerra T, Patti F, Onofrj M +31 more

Plain English
This study looked at how to identify when patients with multiple sclerosis (MS) transition from a type called relapsing-remitting MS to a more progressive form known as secondary progressive MS. Researchers analyzed data from over 10,000 MS patients and found that 8.5% were classified as having secondary progressive MS using the neurologist's method, whereas 17.6% and 11% were identified using two different data-driven methods. The data-driven method was better at correctly identifying patients in transition, with a sensitivity of 77.1% compared to 38.0% for the other method, making it crucial for improving patient diagnosis and care. Who this helps: Patients with multiple sclerosis, especially those transitioning to secondary progressive MS.

PubMed

Mild COVID-19 infection in a group of teriflunomide-treated patients with multiple sclerosis.

2021

Journal of neurology

Mantero V, Baroncini D, Balgera R, Guaschino C, Basilico P +4 more

PubMed

MRI activity and extended interval of Natalizumab dosing regimen: a multicentre Italian study.

2021

Journal of the neurological sciences

De Mercanti SF, Signori A, Cordioli C, Signoriello E, Lus G +23 more

Plain English
This study looked at how changing the timing of natalizumab doses affects MRI activity in patients with multiple sclerosis and JCV positivity. It found that patients receiving doses every 5 weeks (extended interval dosing or EID) had similar rates of new active lesions on MRI compared to those receiving doses every 4.5 weeks (standard interval dosing or SID) over six and twelve months. This is important because it suggests that extending the time between doses does not harm the treatment's effectiveness, allowing for safer management of patients who are at risk of a serious brain infection. Who this helps: This helps patients with multiple sclerosis who are at risk for complications from treatment.

PubMed

Risk of Persistent Disability in Patients With Pediatric-Onset Multiple Sclerosis.

2021

JAMA neurology

Baroncini D, Simone M, Iaffaldano P, Brescia Morra V, Lanzillo R +15 more

Plain English
This study looked at how the treatment and outcomes of pediatric-onset multiple sclerosis (MS) have changed over time. Researchers found that the risk of severe disability in these young patients decreased significantly, with a reduction of 50% to 70% for reaching disability milestones compared to earlier diagnosis periods. The improvement is likely due to better treatments being used earlier and more frequently. Who this helps: This benefits young MS patients and their families by improving their long-term health outlook.

PubMed

Etiological research in pediatric multiple sclerosis: A tool to assess environmental exposures (PEDiatric Italian Genetic and enviRonment ExposurE Questionnaire).

2021

Multiple sclerosis journal - experimental, translational and clinical

Pilotto S, Gencarelli J, Bova S, Gerosa L, Baroncini D +13 more

Plain English
This study focused on understanding the causes of multiple sclerosis (MS) in children, particularly how environmental factors might interact with genetics. Researchers created a new questionnaire called the PEDIGREE Questionnaire to gather information on these environmental exposures from Italian patients and their parents. They found that 100% of participants found the questionnaire acceptable, and it proved to be a reliable tool for assessing environmental factors related to pediatric MS. Who this helps: This helps doctors and researchers study pediatric MS more effectively and understand its causes better.

PubMed

Extending the Interval of Natalizumab Dosing: Is Efficacy Preserved?

2020

Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics

Clerico M, De Mercanti SF, Signori A, Iudicello M, Cordioli C +23 more

Plain English
This study looked at whether patients with multiple sclerosis can safely wait longer between doses of natalizumab (an injectable treatment) without losing effectiveness. Researchers compared two groups: one that received the standard treatment every 4.3 weeks and another that received it every 6.2 weeks. They found that the group with the longer interval had a lower annual relapse rate of 0.039 compared to 0.060 in the standard group, showing that longer dosing intervals do not harm the treatment’s effectiveness and could lower the risk of a serious side effect called PML. Who this helps: This benefits patients with multiple sclerosis who are using natalizumab.

PubMed

Long-term remission of tumefactive relapsing multiple sclerosis after alemtuzumab rescue treatment in an adolescent patient.

2020

Multiple sclerosis and related disorders

Baroncini D, Annovazzi P, Guaschino C, Minonzio G, Hametner S +4 more

PubMed

First therapy choice in newly diagnosed Multiple Sclerosis patients: A multicenter Italian study.

2020

Multiple sclerosis and related disorders

Maniscalco GT, Saccà F, Lanzillo R, Annovazzi P, Baroncini D +33 more

Plain English
This study looked at how newly diagnosed patients in Italy with relapsing-remitting Multiple Sclerosis (MS) choose their first treatment. Researchers found that out of 3,025 patients, those who had more relapses in the previous year or more brain lesions were more likely to choose dimethyl fumarate, while older patients or those with more severe symptoms often opted for teriflunomide instead. Understanding these patterns is crucial because they can guide doctors in making better treatment decisions tailored to individual patients' needs. Who this helps: This helps patients and doctors by providing insights into treatment choices for new MS patients.

PubMed

Cell-based assays for the detection of MOG antibodies: a comparative study.

2020

Journal of neurology

Gastaldi M, Scaranzin S, Jarius S, Wildeman B, Zardini E +18 more

Plain English
This study looked at different laboratory tests to find specific antibodies linked to a group of disorders called MOG antibody-associated disorders (MOGAD), which include conditions like multiple sclerosis. Researchers tested blood samples from 204 patients and found that nearly 28% had the MOG antibody. One test, called LCBA-IgG, was highly accurate, detecting 89% of true cases while showing 93% reliability in not misidentifying healthy individuals, but it could miss some lower levels of antibodies. Who this helps: This benefits both patients and doctors by improving the diagnosis of MOGAD and related conditions.

PubMed

Cladribine vs other drugs in MS: Merging randomized trial with real-life data.

2020

Neurology(R) neuroimmunology & neuroinflammation

Signori A, Saccà F, Lanzillo R, Maniscalco GT, Signoriello E +35 more

Plain English
This study compared the effectiveness of cladribine tablets with other approved medications for patients with relapsing-remitting multiple sclerosis (RRMS). Researchers found that cladribine resulted in a significantly lower annual relapse rate (ARR) than interferon, glatiramer acetate, and dimethyl fumarate, but had a higher ARR compared to natalizumab. Specifically, the ARR for cladribine was about 52% lower than interferon and glatiramer acetate, and 40% lower than dimethyl fumarate. This is important because it suggests that cladribine may be a more effective treatment option for some patients with RRMS. Who this helps: This benefits patients with relapsing-remitting multiple sclerosis.

PubMed

Long-term follow-up of pediatric MS patients starting treatment with injectable first-line agents: A multicentre, Italian, retrospective, observational study.

2019

Multiple sclerosis (Houndmills, Basingstoke, England)

Baroncini D, Zaffaroni M, Moiola L, Lorefice L, Fenu G +21 more

Plain English
This study followed 97 children with multiple sclerosis (MS) for about 12.5 years to see how well their treatment worked. The researchers found that starting treatment at a younger age (before age 12) led to better results, with a drop in relapses from an average of 3.2 to 0.7 per year. While 40% of the patients had worsening disability over time, most (89%) still had mild disability levels at the end of the study. Who this helps: This information benefits children with MS and their doctors by helping them make informed decisions about early treatment options.

PubMed

Determinants of therapy switch in multiple sclerosis treatment-naïve patients: A real-life study.

2019

Multiple sclerosis (Houndmills, Basingstoke, England)

Saccà F, Lanzillo R, Signori A, Maniscalco GT, Signoriello E +34 more

Plain English
This study looked at newly diagnosed patients with relapsing-remitting multiple sclerosis (MS) to see how likely they are to switch from their first treatment within three years. Among 3,025 patients, 48% switched therapies, often due to either ineffectiveness or side effects. Certain treatments, like fingolimod and natalizumab, had different switch risks, and factors such as younger age or comorbidities influenced whether patients had to change their medication. Who this helps: This research benefits doctors and patients by informing treatment choices for those starting MS therapy.

PubMed

Different MRI patterns in MS worsening after stopping fingolimod.

2019

Neurology(R) neuroimmunology & neuroinflammation

Lapucci C, Baroncini D, Cellerino M, Boffa G, Callegari I +9 more

Plain English
This study looked at MRI scans of patients with multiple sclerosis (MS) who got worse after stopping a medication called fingolimod. Researchers found that out of 8 patients, 4 had severe worsening that showed unusual MRI patterns, indicating significant damage to the brain. Specifically, these patients experienced more severe neurological issues and brain damage within six months after stopping the drug. Who this helps: This research benefits patients with MS and their doctors by providing insights into potential complications after stopping fingolimod.

PubMed

Impact of natural menopause on multiple sclerosis: a multicentre study.

2019

Journal of neurology, neurosurgery, and psychiatry

Baroncini D, Annovazzi PO, De Rossi N, Mallucci G, Torri Clerici V +18 more

Plain English
This study looked at how natural menopause affects the course of multiple sclerosis (MS) in women. It found that after menopause, the rate of MS relapses decreased from 0.21 to 0.13 per year, which is a significant drop. However, there was also an increase in disability scores, with an average rise of 0.4 points after menopause, suggesting that while relapses decreased, the overall condition worsened. This matters because it highlights that menopause may lead to a more progressive form of MS, influencing patients' treatment and care. Who this helps: This helps women with MS and their healthcare providers.

PubMed

Outcomes after fingolimod to alemtuzumab treatment shift in relapsing-remitting MS patients: a multicentre cohort study.

2019

Journal of neurology

Frau J, Saccà F, Signori A, Baroncini D, Fenu G +16 more

Plain English
This study looked at patients with relapsing-remitting multiple sclerosis (MS) who switched from the medication fingolimod to alemtuzumab. Researchers found that after this switch, the annual relapse rate dropped significantly from 1.32 during the washout period to just 0.15 after starting alemtuzumab, and the patients' disability scores improved as well. These findings are important because they show that transitioning to alemtuzumab can effectively reduce MS activity without increasing the risk of relapses, even after stopping fingolimod. Who this helps: This benefits patients with relapsing-remitting MS.

PubMed

Clinical activity after fingolimod cessation: disease reactivation or rebound?

2018

European journal of neurology

Frau J, Sormani MP, Signori A, Realmuto S, Baroncini D +16 more

Plain English
This study looked at what happens to patients with multiple sclerosis (MS) after they stop taking the medication fingolimod. It found that 14% of the 100 patients studied experienced a relapse within three months of stopping treatment, and 26% faced a relapse within six months. Importantly, the risk of severe disease worsening after stopping fingolimod is lower than previously thought. Who this helps: This information benefits patients with MS and their doctors by providing clearer expectations about stopping fingolimod treatment.

PubMed

Axonal damage and loss of connectivity in nigrostriatal and mesolimbic dopamine pathways in early Parkinson's disease.

2017

NeuroImage. Clinical

Caminiti SP, Presotto L, Baroncini D, Garibotto V, Moresco RM +4 more

Plain English
This study looked at how early Parkinson's disease affects the connections in the brain's dopamine pathways. Researchers found that in 36 patients with early-stage Parkinson's, there was a significant drop in dopamine transporter activity in the parts of the brain responsible for movement, specifically a 84% reduction in the dorsal putamen area, compared to healthy individuals. This is important because it highlights that damage starts in the connections of brain cells before other symptoms happen, indicating that treatments to protect these connections may be beneficial even early in the disease. Who this helps: This helps patients with Parkinson's disease.

PubMed

Hypomagnesaemia as a trigger of relapsing non-alcoholic Wernicke encephalopathy: a case report.

2017

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Baroncini D, Annovazzi P, Minonzio G, Franzetti I, Zaffaroni M

PubMed

A multicenter, observational, prospective study of self- and parent-reported quality of life in adolescent multiple sclerosis patients self-administering interferon-β1a using RebiSmart™-the FUTURE study.

2017

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Ghezzi A, Bianchi A, Baroncini D, Bertolotto A, Malucchi S +11 more

Plain English
This study looked at how the quality of life changed for Italian teenagers with relapsing-remitting multiple sclerosis (RRMS) who used a device called RebiSmart™ to self-administer a medication called interferon-β1a (Rebif) over a year. Out of 50 participants, 40 finished the study, and those who completed it reported better quality of life, with significant improvements in areas like psychosocial health and school functioning—parents reported an average increase of 5.27 points in their children's overall quality of life score. These findings show that using this electronic device not only helps manage their condition but also improves the overall well-being of adolescents with RRMS. Who this helps: This helps teenagers with multiple sclerosis and their parents.

PubMed

Weight gain after subthalamic nucleus deep brain stimulation in Parkinson's disease is influenced by dyskinesias' reduction and electrodes' position.

2017

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Balestrino R, Baroncini D, Fichera M, Donofrio CA, Franzin A +3 more

Plain English
This study looked at weight gain in patients with Parkinson's disease after they received a deep brain stimulation surgery. Out of 32 patients observed for a year, 84% gained an average of 6.7 kg, with over half becoming overweight. The researchers found that this weight gain was linked to a reduction in involuntary movements (dyskinesias) and the position of the electrodes used in the surgery, suggesting that both factors affected how the body regulates weight. Who this helps: This information benefits patients with Parkinson's disease and their doctors by highlighting the importance of monitoring weight after surgery.

PubMed

Assessing association of comorbidities with treatment choice and persistence in MS: A real-life multicenter study.

2017

Neurology

Laroni A, Signori A, Maniscalco GT, Lanzillo R, Russo CV +30 more

Plain English
This study looked at how having other health issues (called comorbidities) affects the treatment choices and how long patients with multiple sclerosis (MS) stick with their initial treatment. Out of over 2,000 newly diagnosed MS patients, 24% had at least one other health problem. While comorbidities didn't change which first treatment was chosen, they made patients 42% more likely to switch treatments due to side effects. This is important because it suggests that doctors should consider a patient's overall health when deciding on MS treatments to help improve treatment adherence. Who this helps: This helps patients with MS and their doctors.

PubMed

Natalizumab versus fingolimod in patients with relapsing-remitting multiple sclerosis non-responding to first-line injectable therapies.

2016

Multiple sclerosis (Houndmills, Basingstoke, England)

Baroncini D, Ghezzi A, Annovazzi PO, Colombo B, Martinelli V +5 more

Plain English
This study compared two medications, natalizumab and fingolimod, for treating patients with relapsing-remitting multiple sclerosis (RRMS) who did not respond to initial treatments. After two years, 80% of those on fingolimod were relapse-free compared to 66% on natalizumab, but more patients stopped taking natalizumab due to safety concerns (33% vs. 11%). The findings indicate that while natalizumab leads to fewer relapses and better overall disease control in some areas, it has a higher discontinuation rate due to safety issues. Who this helps: Patients with relapsing-remitting multiple sclerosis who are looking for effective treatment options.

PubMed

Dopaminergic receptors and adrenoceptors in circulating lymphocytes as putative biomarkers for the early onset and progression of multiple sclerosis.

2016

Journal of neuroimmunology

Cosentino M, Zaffaroni M, Legnaro M, Bombelli R, Schembri L +7 more

Plain English
This study looked at specific markers in blood cells of people who experienced a first episode of neurological issues that could indicate multiple sclerosis (MS). Researchers found that certain receptors, particularly the D3 and D5 types of dopamine receptors and the alpha-2A adrenergic receptors, were more active in these individuals, and that their levels could help predict who is likely to develop MS within a year. This is significant because identifying those at higher risk can lead to earlier treatment, which might improve outcomes for patients. Who this helps: This helps patients at risk of developing multiple sclerosis and their doctors.

PubMed

Dataset of mRNA levels for dopaminergic receptors, adrenoceptors and tyrosine hydroxylase in lymphocytes from subjects with clinically isolated syndromes.

2016

Data in brief

Cosentino M, Zaffaroni M, Legnaro M, Bombelli R, Schembri L +7 more

Plain English
This study examined the levels of specific molecules (mRNA) linked to brain and stress responses in blood cells from people experiencing early symptoms of multiple sclerosis (MS). Researchers found differences in these mRNA levels between two groups: those who developed full-blown MS within a year and those who did not. Understanding these changes may help identify early signs of MS and track its progression, which is crucial for timely treatment. Who this helps: This helps patients and doctors by providing potential early indicators of multiple sclerosis.

PubMed

Fingolimod versus interferon beta/glatiramer acetate after natalizumab suspension in multiple sclerosis.

2015

Brain : a journal of neurology

Iaffaldano P, Lucisano G, Pozzilli C, Brescia Morra V, Ghezzi A +29 more

Plain English
This study compared two treatments, fingolimod and interferon beta/glatiramer acetate, for patients with relapsing multiple sclerosis who stopped using another drug, natalizumab. Researchers looked at 613 patients and found that those who switched to fingolimod had a 64% lower chance of experiencing a relapse compared to those who switched to interferon beta or glatiramer acetate. This is important because it suggests that fingolimod can better help control disease activity after stopping natalizumab. Who this helps: Patients with relapsing multiple sclerosis seeking effective treatment options after discontinuing natalizumab.

PubMed

Striatal hand in Parkinson's disease: the re-evaluation of an old clinical sign.

2014

Journal of neurology

Spagnolo F, Fichera M, Bucello S, Houdayer E, Baroncini D +7 more

Plain English
In this study, researchers looked at a hand condition called striatal hand in people with Parkinson's disease (PD). They analyzed pictures of the hands of 40 people with PD and 15 healthy individuals, finding that those with PD showed significant hand posture problems, with a score that was significantly worse on the side where PD symptoms were stronger. This condition is highly specific to PD, meaning if someone shows signs of striatal hand, it almost certainly indicates they have Parkinson's disease. Who this helps: This benefits patients with Parkinson's disease by improving diagnosis and understanding of their symptoms.

PubMed

Uhthoff's phenomena and brain MRI suggesting demyelinating lesions: RIS or CIS? A case report.

2014

Journal of the neurological sciences

Baroncini D, Zaffaroni M, Minonzio G, Annovazzi P, Baldini SM +2 more

PubMed

Disease reactivation after fingolimod discontinuation in two multiple sclerosis patients.

2013

Journal of neurology

Ghezzi A, Rocca MA, Baroncini D, Annovazzi P, Zaffaroni M +3 more

PubMed

A complex case of anti-GAD antibody-related syndrome treated with Rituximab.

2013

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Baroncini D, Spagnolo F, Sarro L, Comi G, Volonte' MA

PubMed

Narrow band imaging with magnification endoscopy for celiac disease: results from a prospective, single-center study.

2013

Diagnostic and therapeutic endoscopy

De Luca L, Ricciardiello L, Rocchi MB, Fabi MT, Bianchi ML +3 more

Plain English
This study looked at a new method called Narrow Band Imaging with magnification endoscopy (NBI-ME) for diagnosing celiac disease, which can have tricky-to-detect intestinal damage. Researchers tested 44 patients and found that NBI-ME was able to identify 12 cases of partial villous atrophy that standard endoscopy missed, achieving an overall accuracy of 95%. This is important because it means doctors could use this method to better diagnose celiac disease and reduce unnecessary biopsies. Who this helps: This helps patients with suspected celiac disease by improving diagnosis accuracy.

PubMed

Neuroendocrine tumor of the extrahepatic bile duct: a tumor in an unusual site visualized by cholangioscopy.

2013

Endoscopy

De Luca L, Tommasoni S, de Leone A, Bianchi ML, de Nictolis M +1 more

PubMed

Lethal nature of ischemic gastropathy: a case report of celiomesenteric vascular insufficiency.

2011

Clinical journal of gastroenterology

De Luca L, Ricciardiello L, Modugno P, De Filippo CM, Baroncini D

Plain English
This study looked at a serious condition called celiomesenteric ischemia, where blood flow to the stomach is blocked, often leading to misdiagnosis. It followed an elderly man who had 2-3 weeks of severe abdominal pain and other troubling symptoms, resulting in findings that included severe blockage in several major arteries supplying blood to his stomach. Using advanced imaging methods like magnetic resonance angiography (MRA), doctors found that the man had critical artery issues, highlighting the importance of quick diagnosis to potentially prevent life-threatening complications. Who this helps: This research benefits doctors by providing clearer insights into diagnosing gastric conditions related to blood flow issues.

PubMed

Cannulation of obscured papilla aided by using a balloon to flatten out duodenal folds, in a patient with acute pancreatitis.

2006

Endoscopy

Cennamo V, Baroncini D, Fabbri C, Ferrara F, Guersi S +1 more

PubMed

Prospective multicenter randomized trial comparing banding ligation with sclerotherapy of esophageal varices.

1999

Hepato-gastroenterology

Masci E, Stigliano R, Mariani A, Bertoni G, Baroncini D +7 more

Plain English
This study compared two treatments for patients with swollen veins in the esophagus that can bleed: endoscopic variceal banding ligation (EVL) and sclerotherapy (EVS). Researchers found that 88% of patients treated with EVL had their varices successfully treated compared to 82% for those treated with EVS. Notably, only 12% of those receiving EVL experienced rebleeding during the treatment period, while 42% of the EVS group did, showing that EVL is safer and more effective in preventing bleeding in the short term. Who this helps: This research benefits patients with esophageal varices, particularly those who have experienced bleeding before.

PubMed

Effects of early ductal decompression in human biliary acute pancreatitis.

1998

Pancreas

Pezzilli R, Billi P, Barakat B, Baroncini D, D'Imperio N +1 more

Plain English
This study looked at the effects of a quick procedure called endoscopic sphincterotomy on patients with a type of pancreatitis caused by blocked bile ducts. Researchers found that patients who received this procedure had a shorter hospital stay averaging about 9 days, compared to 20 days for those treated with standard medical care. Additionally, fewer complications occurred in the patients who had the procedure, indicating that relieving the blockage early can lead to better recovery. Who this helps: This benefits patients suffering from biliary acute pancreatitis.

PubMed

Management of gastrointestinal fistulas with n-2-butyl-cyanoacrylate.

1998

Endoscopy

Billi P, Alberani A, Baroncini D, Formica G, Borioni D +4 more

PubMed

[Oral pefloxacin in the treatment of acute gastroenteritis].

1997

Minerva gastroenterologica e dietologica

Dal Monte PR, Baroncini D, Dal Monte PP

Plain English
This study looked at the effectiveness of the antibiotic pefloxacin in treating acute gastroenteritis, particularly in cases of travelers' diarrhea. Of the 30 patients treated, all the harmful bacteria were eliminated by the end of the treatment, with a significant drop in daily bowel movements from an average of 6.8 to just 1.1 by day five. Most patients (93.3%) experienced significant recovery, and 86.7% of doctors rated the treatment as excellent. Who this helps: This helps patients suffering from acute gastroenteritis, especially travelers.

PubMed

A prospective randomized trial of sclerotherapy versus ligation in the elective treatment of bleeding esophageal varices.

1997

Endoscopy

Baroncini D, Milandri GL, Borioni D, Piemontese A, Cennamo V +3 more

Plain English
This study compared two treatments for bleeding esophageal varices in patients with liver cirrhosis: endoscopic ligation (EVL) and endoscopic sclerotherapy (EVS). Both methods successfully removed varices (93% for EVL and 92.5% for EVS), but EVL required fewer sessions to achieve this and had a lower rate of complications (11% versus 31% for EVS). However, patients who had EVL experienced more recurrence of varices in the long run (30% compared to 13% for EVS). Who this helps: This research benefits patients with liver cirrhosis and their doctors by guiding treatment choices.

PubMed

Evaluation of undiluted N-butyl-2-cyanoacrylate in the endoscopic treatment of upper gastrointestinal tract varices.

1996

Endoscopy

D'Imperio N, Piemontese A, Baroncini D, Billi P, Borioni D +2 more

Plain English
Researchers studied the use of a substance called N-butyl-2-cyanoacrylate for treating bleeding varices (swollen veins) in the upper digestive tract of 80 patients, focusing on its effectiveness and safety. They found that it successfully stopped active bleeding in 89.6% of patients and completely eliminated varices in 87.5% of those treated for other reasons. There were some complications, with 10.4% of patients experiencing issues, and 12.5% died during treatment, mostly due to severe bleeding or liver failure, which highlights both the benefits and risks of this procedure. Who this helps: This helps patients with bleeding varices and their doctors who manage these critical situations.

PubMed

N-butyl-2-cyanoacrylate in the endoscopic treatment of Dieulafoy ulcer.

1995

Endoscopy

D'Imperio N, Papadia C, Baroncini D, Piemontese A, Billi P +1 more

PubMed

Role of esophageal brushing cytology in monitoring patients treated with sclerotherapy for esophageal varices.

1992

Acta cytologica

Dina R, Cassisa A, Baroncini D, D'Imperio N

Plain English
This study looked at whether a specific treatment for swollen blood vessels in the esophagus (sclerotherapy) could lead to esophageal cancer over time. Researchers examined 68 patients treated with sclerotherapy every six months for signs of cancer, and found that while some inflammation occurred, there were no significant cases of cancer detected; only two instances showed early changes that improved later. This is important because it shows that regular check-ups using brushing samples can help catch any potential problems early in these patients. Who this helps: This information benefits patients with esophageal varices and the doctors treating them.

PubMed

Publication data sourced from PubMed . Plain-English summaries generated by AI. Not medical advice.