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Featured researches published by Assaad Soweid.


Endoscopy | 2010

A randomized single-blind trial of standard diet versus fiber-free diet with polyethylene glycol electrolyte solution for colonoscopy preparation

Assaad Soweid; A. A. Kobeissy; F. R. Jamali; M. El-Tarchichi; A. Skoury; H. Abdul-Baki; L. El-Zahabi; A. El-Sayyed; Kassem Barada; Ala I. Sharara; Fadi H. Mourad; A. Arabi

BACKGROUND AND STUDY AIMS Colonoscopy preparation usually involves the intake of large volumes of polyethylene glycol electrolyte solution (PEG-ES) in combination with a clear-liquid diet (CLD). Liberalization of the diet might enhance the tolerance to PEG-ES without compromising the quality of the preparation. The primary aims of this study were to evaluate the efficacy and tolerability of PEG-ES given with a CLD compared with a fiber-free diet (FFD) for colonoscopy preparation. The incidence of adverse events among patients in the two diet groups was also assessed as a secondary outcome. METHODS This was a single-center randomized, prospective, single-blind study. A total of 200 patients undergoing colonoscopy were randomized to either CLD or FFD in addition to PEG-ES. RESULTS Patients in the FFD group were able to drink more PEG-ES (mean +/- SD, 3.9 +/- 0.3 L) compared with those in the CLD group (3.3 +/- 0.7 L) ( P < 0.01). The quality of the preparation was significantly better in the FFD group, with more patients having satisfactory preparations than those in the CLD group (81.4 % vs. 52.0 %; P < 0.001). Tolerance to the preparation was higher in the FFD group compared with the CLD group, with significantly more patients adhering to the FFD regimen ( P < 0.001). There were more adverse events experienced in the CLD group, with odds ratios of 1.9 for nausea (95 % confidence interval [CI] 1.0 - 3.6), 3.8 for vomiting (95 % CI 1.3 - 11.3), and 3.0 for headache (95 % CI 1.5 - 5.9). CONCLUSION FFD given with PEG-ES on the day before colonoscopy is a more effective regimen than the standard CLD regimen, and is better tolerated by patients.


Inflammatory Bowel Diseases | 2007

Clinical epidemiology of inflammatory bowel disease in Lebanon

Heitham Abdul-Baki; Ihab I. El-Hajj; Lara M. El-Zahabi; Cecilio Azar; Elie Aoun; Hala Zantout; Walid A. Nasreddine; Bassem Ayyach; Fadi H. Mourad; Assaad Soweid; Kassem Barada; Ala I. Sharara

Background: The objectives of this study were to determine the prevalence and incidence of inflammatory bowel disease (IBD) in a representative Lebanese cohort and to describe practice prevalence trends, disease characteristics, and impact on quality of life (QoL) of IBD patients in Lebanon. Methods: All of a university‐based health programs 2000–2004 computerized records that listed a diagnosis of Crohns disease (CD) or ulcerative colitis (UC) were reviewed. In addition, data on patients seen in the gastroenterology clinics and data from the IBD registry at the American University of Beirut Medical Center (AUBMC) from the same period were analyzed. Results: Of 15,073 insured individuals, 8 had a diagnosis of CD and 16 of UC, giving an age‐adjusted prevalence of 53.1 per 100,000 people for CD and 106.2 per 100,000 people for UC. The mean age at diagnosis for patients with CD and UC was 28.8 ± 11.1 and 32.0 ± 13.4 years, respectively, and there was a slight female predominance. The mean annual incidence was 4.1 per 100,000 people for UC and 1.4 per 100,000 people for CD (range, 0–6.9/100,000 for both). Of the 10,383 patients seen in the gastroenterology clinic from 2000 to 2004, 251 (2.4%) had IBD (142 UC, 100 CD, and 9 indeterminate), a ratio that trended upward over time (range, 1.8%–2.7%). The median IBD Quality‐of‐Life (IBDQ) questionnaire score was 124.9 ± 30.5, indicating that the disease had a moderately severe impact on QoL. Conclusions: The prevalence of IBD in this representative Lebanese cohort falls in the intermediate range of that reported for white populations in Europe and North America. Future studies are needed to examine local risk factors, disease genotypes and phenotypes, and epidemiologic time trends. The psychosocial burden of IBD in Lebanon appears significant.


JAMA Surgery | 2013

Smoking and the Risk of Mortality and Vascular and Respiratory Events in Patients Undergoing Major Surgery

Khaled M. Musallam; Frits R. Rosendaal; Ghazi Zaatari; Assaad Soweid; Jamal J. Hoballah; Pierre Sfeir; Salah Zeineldine; Hani Tamim; Toby Richards; Donat R. Spahn; Luca A. Lotta; Flora Peyvandi; Faek R. Jamali

IMPORTANCE The effects of smoking on postoperative outcomes in patients undergoing major surgery are not fully established. The association between smoking and adverse postoperative outcomes has been confirmed. Whether the associations are dose dependent or restricted to patients with smoking-related disease remains to be determined. OBJECTIVE To evaluate the association between current and past smoking on the risk of postoperative mortality and vascular and respiratory events in patients undergoing major surgery. DESIGN Cohort study using the American College of Surgeons National Surgical Quality Improvement Program database. We obtained data on smoking history, perioperative risk factors, and 30-day postoperative outcomes. We assessed the effects of current and past smoking (>1 year prior) on postoperative outcomes after adjustment for potential confounders and effect mediators (eg, cardiovascular disease, chronic obstructive pulmonary disease, and cancer). We also determined whether the effects are dose dependent through analysis of pack-year quintiles. SETTING AND PARTICIPANTS A total of 607,558 adult patients undergoing major surgery in non-Veterans Affairs hospitals across the United States, Canada, Lebanon, and the United Arab Emirates during 2008 and 2009. MAIN OUTCOMES AND MEASURES The primary outcome measure was 30-day postoperative mortality; secondary outcome measures included arterial events (myocardial infarction or cerebrovascular accident), venous events (deep vein thrombosis or pulmonary embolism), and respiratory events (pneumonia, unplanned intubation, or ventilator requirement >48 hours). RESULTS The sample included 125,192 current (20.6%) and 78,763 past (13.0%) smokers. Increased odds of postoperative mortality were noted in current smokers only (odds ratio, 1.17 [95% CI, 1.10-1.24]). When we compared current and past smokers, the adjusted odds ratios were higher in the former for arterial events (1.65 [95% CI, 1.51-1.81] vs 1.20 [1.09-1.31], respectively) and respiratory events (1.45 [1.40-1.51] vs 1.13 [1.08-1.18], respectively). No effects on venous events were observed. The effects of smoking mediated through smoking-related disease were minimal. The increased adjusted odds of mortality in current smokers were evident from a smoking history of less than 10 pack-years, whereas the effects of smoking on arterial and respiratory events were incremental with increased pack-years. CONCLUSIONS AND RELEVANCE Smoking cessation at least 1 year before major surgery abolishes the increased risk of postoperative mortality and decreases the risk of arterial and respiratory events evident in current smokers. These findings should be carried forward to evaluate the value and cost-effectiveness of intervention in this setting. Our study should increase awareness of the detrimental effects of smoking-and the benefits of its cessation-on morbidity and mortality in the surgical setting.


Journal of Clinical Gastroenterology | 2007

Prevalence of endoscopically identified heterotopic gastric mucosa in the proximal esophagus : Endoscopist dependent?

Cecilio Azar; Faek R. Jamali; Hala Tamim; Heitham Abdul-Baki; Assaad Soweid

Goals The aim of this study is to determine the prevalence of heterotopic gastric mucosa in the proximal esophagus (HGMPE) and whether thorough endoscopic search may influence such prevalence. Background Heterotopic gastric mucosa in the esophagus (sometimes known as inlet patch) refers to a discrete area of gastric mucosa, with a spherical or ellipsoid configuration, that is typically located in the proximal esophagus. The prevalence of endoscopically diagnosed HGMPE varies from 0.1% to 10%. Endoscopic detection may be difficult as HGMPE is often located at or just below the upper esophageal sphincter. It might be associated with severe complications such as bleeding, perforation, fistula, and stricture formation, in addition to the development of adenocarcinoma. Study During a 2-year period, 455 consecutive patients with various gastrointestinal complaints underwent esophagogastroduodenoscopy by a single endoscopist (group 1). This endoscopist paid special attention to detecting HGMPE by thoroughly examining the proximal esophagus upon withdrawal of the endoscope. During the same period of time, endoscopy reports of 472 patients who underwent esophagogastroduodenoscopy in the same hospital by 3 other endoscopists were retrospectively reviewed (group 2). These endoscopists were aware of the existence of the HGMPE and reported that the presence of HGMPE would be included as an endoscopic finding in their reports. Results In the first group, HGMPE was identified in 12 out of 455 patients (2.6%). Whereas in the second group, only 2 out of 472 patients (0.4%) had reports identifying HGMPE (P<0.01). Conclusions Endoscopic detection of HGMPE is influenced by the endoscopists thorough search of this entity, and thus, more time devoted to such a search may lead to higher detection rates.


Lancet Oncology | 2006

Spontaneous complete regression of hepatic epithelioid haemangioendothelioma

Zaher K. Otrock; Aghiad Al-Kutoubi; Mireille M. Kattar; Ghazi Zaatari; Assaad Soweid

A 75-year-old woman presented with a 3-month history of upper abdominal pain associated with distention and change in bowel habits. She also reported fatigue and weight loss of 5 kg in the preceding 4 months. She had no history of hepatitis, blood transfusions, or alcohol intake. Her family history was negative for malignant disease, and she was not taking any prescribed drugs. On examination, the patient was pale, but not icteric; vital signs were within normal limits. She had mild tender ness in the right upper quadrant of the abdomen without hepatosplenomegaly. Laboratory results were as follows (reference values in parentheses): alanine amino transferase 13 U/L (<50 U/L); aspartate aminotransferase 9 U/L (<50 U/L); γ glutamyl transferase 10 U/L (<50 U/L); alkaline phosphatase 105 U/L (<120 U/L); α feto protein 1·7 μg/L (1·0–9·0 U/mL); cancer antigen (CA) 19-9 6·6 U/mL (0–37 U/mL); carcino embryonic antigen 1·8 μg/L (0–5 μg/L); and CA 125 16·5 U/mL (0–40 U/mL). Further investigation included helical CT of the chest, abdomen, and pelvis, which showed multiple suspicious lesions in the liver (fi gure 1A) and a few lesions in the lung bases. Fine-needle aspiration and core biopsy of the liver lesions were done, and the biopsy sample showed epithelioid tumour cells arranged in small nests and short cords in desmoplastic stroma. The tumour cells had abundant eosinophilic cytoplasm and moderate nuclear pleiomorphism; multinucleated cells and occasional mitoses were noted (fi gure 2A). Some cells had intracellular lumina that were thought at fi rst to be vacuoles or glandular lumina. On the basis of these fi ndings, the tumour was initially diagnosed as a poorly diff erentiated carcinoma. Work-up—including upper and lower gastrointestinal endoscopy, ultrasonography, and mammography—were within normal limits. The patient refused any type of treatment, and was discharged home. Nevertheless, the patient was followed up regularly by her primary physician. 20 months later, after an improvement in her clinical condition and a weight gain of more than 10 kg, a repeat CT showed resolution of all hepatic lesions (fi gure 1B). The patient was followed up for more than 3·5 years and continues to do well. In view of the clinical behaviour of this neoplasm, path ological material was reassessed and imm u nostaining was done. Tumour cells were positive for vascular markers CD34 (fi gure 2B) and CD31, and were negative for epithelial markers (including cytokeratin 7, cytokeratin 20, cyto keratins 8/18 (Cam 5·2), and cytokeratins AE1/AE3); α feto protein; oestrogen receptors and progesterone receptors; and thyroid transcription factor 1 (TTF1, which is usually expressed in lung carcinoma). The morphological and immunophenotypic features are diagnostic of epithelioid haemangioendothelioma. Epithelioid haemangioendothelioma is an indolent mesenchymal neoplasm that arises from endothelial cells. This rare vascular neoplasm occurs frequently in soft tissues, liver, lung, bone, and spleen. It is a solid tumour of low-grade malignancy, consisting of epithelioid-like endothelial cells, and can be misdiagnosed as carcinoma—primary or metastatic. The clinical features of epithelioid haemangioendothelioma of the liver have been reviewed by several researchers. Makhlouf and colleagues analysed 137 patients with epithelioid haemangioendothelioma Lancet Oncol 2006; 7: 439–41


Acta Oto-laryngologica | 2006

Does Helicobacter pylori colonize the nasopharynx of children and contribute to their middle ear disease

Mohamed A. Bitar; Rami Mahfouz; Assaad Soweid; Eddy Racoubian; Mona Ghasham; Ghazi Zaatari; Nabil Fuleihan

Objective. There is growing interest in studying the presence of HP in the upper aerodigestive tract. It was shown in several pilot studies that it colonizes the area, while other authors found no evidence of its presence there and a third group of authors believed that it had only a transient presence there. In this study we investigated a possible role for HP in middle ear disease in children. Material and methods. Consecutive patients undergoing myringotomy and adenoidectomy for chronic otitis media with effusion or recurrent otitis media were enrolled. Middle ear fluids were cultured on three types of agar plate (Brucella + laked horse blood; Brucella + sheep blood; and chocolate). A double polymerase chain reaction (PCR) was run to detect urease-C and adhesion subunit genes. Rapid urease enzyme testing and PCR were used on the adenoid specimens. Parents were interviewed regarding symptoms suggestive of gastroesophageal reflux in their children. Results. Eighteen patients were enrolled in the study (mean age 4.4 years; age range 3–8 years) with an equal gender distribution. All 28 middle ear fluid cultures were negative in all 3 media. Twenty-one of the 28 samples contained DNA, yet PCR revealed that none of them belonged to HP. Ten of the 13 adenoid specimens obtained were positive on rapid urease testing, but none on PCR. Seven of the 18 patients had at least 1 symptom suggestive of gastroesophageal reflux during the 6 months preceding the study but this did not have an impact on any of the results. Conclusion. There was no evidence from this study that Helicobacter pylori (HP) colonizes the nasopharynx of children with middle ear disease, whether dyspeptic or not. There is also no apparent role for this bacterium in middle ear pathology.


Endoscopy | 2014

Prediction of celiac disease at endoscopy

Kassem Barada; Robert H. Habib; Ahmad Malli; Jana G. Hashash; Houssam Halawi; Karim Maasri; Ayman Tawil; Fadi H. Mourad; Ala I. Sharara; Assaad Soweid; Ismail Sukkarieh; Zaher Chakhachiro; Mark Jabbour; Alessio Fasano; Debbie Santora; Carolina Arguelles; Joseph A. Murray; Peter H. Green

BACKGROUND AND STUDY AIMS Celiac disease is increasingly recognized worldwide, but guidelines on how to detect the condition and diagnose patients are unclear. In this study the prevalence and predictors of celiac disease were prospectively determined in a cross-sectional sample of Lebanese patients undergoing esophagogastroduodenoscopy (EGD). PATIENTS AND METHODS Consecutive consenting patients (n = 999) undergoing EGD answered a questionnaire and had blood taken for serologic testing. Endoscopic markers for celiac disease were documented and duodenal biopsies were obtained. The diagnosis of celiac disease was based on abnormal duodenal histology and positive serology. Risk factors were used to classify patients to either high or low risk for celiac disease. Independent predictors of celiac disease were derived via multivariate logistic regression. RESULTS Villous atrophy (Marsh 3) and celiac disease were present in 1.8 % and 1.5 % of patients, respectively. Most were missed on clinical and endoscopic grounds. The sensitivity of tissue transglutaminase (tTG) testing for the diagnosis of villous atrophy and celiac disease was 72.2 % and 86.7 %, respectively. The positive predictive value of the deamidated gliadin peptide (DGP) test was 34.2 % and that of a strongly positive tTG was 80 %. While the strongest predictor of celiac disease was a positive tTG (odds ratio [OR] 131.7, 95 % confidence interval [CI] 29.0 - 598.6), endoscopic features of villous atrophy (OR 64.8, 95 %CI 10.7 - 391.3), history of eczema (OR 4.6, 95 %CI 0.8 - 28.8), anemia (OR 6.7, 95 %CI 1.2 - 38.4), and being Shiite (OR 5.4, 95 %CI 1.1 - 26.6) significantly predicted celiac disease. A strategy of biopsying the duodenum based on independent predictors had a sensitivity of 93 % - 100 % for the diagnosis of celiac disease, with an acceptable (22 % - 26 %) rate of performing unnecessary biopsies. A strategy that excluded pre-EGD serology produced a sensitivity of 93 % - 94 % and an unnecessary biopsy rate of 52 %. CONCLUSION An approach based solely on standard clinical suspicion and endoscopic findings is associated with a significant miss rate for celiac disease. A strategy to biopsy based on the derived celiac disease prediction models using easily obtained information prior to or during endoscopy, maximized the diagnosis while minimizing unnecessary biopsies.


World Journal of Gastrointestinal Endoscopy | 2010

Endoscopic ultrasound-guided celiac plexus neurolysis

Assaad Soweid; Cecilio Azar

Endoscopic celiac plexus neurolysis (CPN) has become the procedure of choice for the management of patients with pancreatic cancer and abdominal pain unresponsive to medical treatment. It is necessary to differentiate between CPN and endoscopic celiac plexus block performed in patients with benign disease. In this review we describe the technique of this procedure with special emphasis on technical details.


Leukemia & Lymphoma | 2007

An overview of the pathogenesis and natural history of post-transplant T-cell lymphoma (corrected and republished article originally printed in Leukemia & Lymphoma, June 2007; 48(6): 1237 – 1241)

Faek R. Jamali; Zaher K. Otrock; Assaad Soweid; Ghassan Al-Awar; Rami Mahfouz; Ghassan R. Haidar; Ali Bazarbachi

Post-transplantation lymphoproliferative disorders (PTLDs) are well recognized complications of solid organ transplantation. The vast majority of early PTLDs are B-cell non-Hodgkin lymphomas. PTLDs of T-cell origin occur much less frequently and account for only a minority of cases. T-cell PTLDs have been reported to occur primarily at extranodal sites, commonly affecting bone marrow or splenic tissues. The small bowel is an uncommon site of origin of these tumors with only seven cases of primary intestinal post-transplant T-cell lymphomas reported in the literature. We hereby report a new case of primary intestinal post-transplant T-cell lymphoma, arising 18 years following renal transplantation, along with a literature review of all published cases.


World Journal of Gastroenterology | 2012

A randomized open-label trial of on-demand rabeprazole vs ranitidine for patients with non-erosive reflux disease

Abdallah A Kobeissy; Jana G. Hashash; Faek R. Jamali; Assaad Skoury; Reham Haddad; Sarah El-Samad; Rami Ladki; Rola Aswad; Assaad Soweid

AIM To compare the efficacy of the proton-pump inhibitor, rabeprazole, with that of the H₂-receptor antagonist, ranitidine, as on-demand therapy for relieving symptoms associated with non-erosive reflux disease (NERD). METHODS This is a single center, prospective, randomized, open-label trial of on-demand therapy with rabeprazole (group A) vs ranitidine (group B) for 4 wk. Eighty-three patients who presented to the American University of Beirut Medical Center with persistent gastroesophageal reflux disease (GERD) symptoms and a normal upper gastrointestinal endoscopy were eligible for the study. Patients in group A (n = 44) were allowed a maximum rabeprazole dose of 20 mg twice daily, while those in group B (n = 39) were allowed a maximum ranitidine dose of 300 mg twice daily. Efficacy was assessed by patient evaluation of global symptom relief, scores of the SF-36 quality of life (QoL) questionnaires, total number of pills used, and number of medication-free days. RESULTS Among the 83 patients who were enrolled in the study, 76 patients (40 in the rabeprazole group and 36 in the ranitidine group) completed the 4-wk trial. Baseline characteristics were comparable between both groups. After 4 wk, there was no significant difference in the subjective global symptom relief between the rabeprazole and the ranitidine groups (71.4% vs 65.4%, respectively; P = 0.9). There were no statistically significant differences between mean cumulative scores of the SF-36 QoL questionnaire for the two study groups (rabeprazole 22.40 ± 27.53 vs ranitidine 17.28 ± 37.06; P = 0.582). There was no significant difference in the mean number of pills used (rabeprazole 35.70 ± 29.75 vs ranitidine 32.86 ± 26.98; P = 0.66). There was also no statistically significant difference in the mean number of medication-free days between both groups. CONCLUSION Rabeprazole has a comparable efficacy compared to ranitidine when given on-demand for the treatment of NERD. Both medications were associated with improved quality of life.

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Faek R. Jamali

American University of Beirut

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Kassem Barada

American University of Beirut

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Ala I. Sharara

American University of Beirut

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Cecilio Azar

American University of Beirut

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Fadi H. Mourad

American University of Beirut

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Ghazi Zaatari

American University of Beirut

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Abdallah A Kobeissy

American University of Beirut

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Chakib M. Ayoub

American University of Beirut

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Hani Tamim

American University of Beirut

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Khaled M. Musallam

American University of Beirut

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