Mustafa M. Haddad
Mayo Clinic
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Featured researches published by Mustafa M. Haddad.
BJUI | 2017
Bimal Bhindi; Robert Houston Thompson; Ross J. Mason; Mustafa M. Haddad; Jennifer R. Geske; Anil N. Kurup; James D. Hannon; Stephen A. Boorjian; Bradley C. Leibovich; Thomas D. Atwell; Grant D. Schmit
To evaluate the association between renal tumour complexity and outcomes in a large cohort of patients undergoing percutaneous cryoablation (PCA).
Abdominal Radiology | 2016
Mustafa M. Haddad; K.W. Merrell; Christopher L. Hallemeier; Geoffrey B. Johnson; Taofic Mounajjed; Kenneth R. Olivier; Jeff L. Fidler; Sudhakar K. Venkatesh
Stereotactic body radiation therapy (SBRT) is a noninvasive treatment technique for selected patients with primary liver tumors and liver-confined oligometastatic disease. Recently, SBRT has emerged as an alternative treatment option in non-surgical candidates and in whom percutaneous treatment methods are not possible or contraindicated. The experience with SBRT continues to grow. There are currently no imaging guidelines for assessment of tumor response and follow-up schedule following SBRT. SBRT produces characteristic radiation-induced changes in the treated tumor and surrounding liver parenchyma. Knowledge of these changes is essential in the interpretation of follow-up imaging and assessment of treatment response. In this review, we will describe the CT, MRI, and PET imaging findings following SBRT of both the targeted liver tumor and surrounding hepatic parenchyma.
European Urology | 2018
Bimal Bhindi; Ross J. Mason; Mustafa M. Haddad; Stephen A. Boorjian; Bradley C. Leibovich; Thomas D. Atwell; Adam J. Weisbrod; Grant D. Schmit; R. Houston Thompson
BACKGROUNDnWhile partial nephrectomy (PN) is considered the standard approach for a tumor in a solitary kidney, percutaneous cryoablation (PCA) is emerging as an alternative nephron-sparing option.nnnOBJECTIVEnTo compare outcomes between PCA and PN for tumors in a solitary kidney.nnnDESIGN, SETTING, AND PARTICIPANTSnPatients who underwent PCA or PN between 2005 and 2015 for a single primary renal tumor in a solitary kidney were identified using Mayo Clinic Registries. Exclusion criteria were inherited tumor syndromes and salvage procedures.nnnINTERVENTIONnPCA and PN.nnnOUTCOME MEASUREMENTS AND STATISTICAL ANALYSISnTo achieve balance in baseline characteristics, we used inverse probability of treatment weighting (IPTW) based on propensity to receive treatment. The risk of having a post-treatment complication and percent drop in estimated glomerular filtration rate (eGFR), as well as the risks of local/ipsilateral recurrence, distant metastasis, and cancer-specific mortality, were compared between groups using logistic, linear, and Fine-and-Gray competing risk regression models.nnnRESULTS AND LIMITATIONSnThe cohort included 118 patients (PCA: 54; PN: 64) with a median follow-up of 47 mo (interquartile range 18, 74). In unadjusted analyses, PCA was associated with a lower risk of complications (15% vs 31%; odds ratio [OR]=0.38; 95% confidence interval [CI] 0.15, 0.96; p=0.04). However, upon accounting for baseline differences with IPTW adjustment, there was no longer a significant difference in the risk of complications (28% vs 29%; OR=0.95; 95% CI 0.53, 1.69; p=0.9). There were no significant differences between PCA and PN in percentage drop in eGFR at discharge (mean: 11% vs 16%; β=-5%; 95% CI -13, 3; p=0.2) or at 3 mo (12% vs 9%; β=3%; 95% CI -3, 10; p=0.3). Likewise, no significant differences were noted in local recurrence (HR=0.87; 95% CI 0.38, 1.98; p=0.7), distant metastases (HR=0.60; 95% CI 0.30, 1.20; p=0.2), or cancer-specific mortality (HR=1.13; 95% CI 0.32, 3.98; p=0.8). Limitations include the sample size, given the relative rarity of renal masses in solitary kidneys.nnnCONCLUSIONSnOur study found no significant difference in complications, renal function outcomes, and oncologic outcomes between PN and PCA for patients with a tumor in a solitary kidney. Validation in a larger multi-institutional analysis may be warranted.nnnPATIENT SUMMARYnPartial nephrectomy (surgery) and percutaneous cryoablation are both options for treating a kidney tumor while preserving the normal portion of the kidney. In patients with a tumor in their only kidney, we found no difference in the risk of complications, kidney function outcomes, or cancer control outcomes between these two approaches.
Journal of Vascular and Interventional Radiology | 2018
Mustafa M. Haddad; Grant D. Schmit; A. Nicholas Kurup; John J. Schmitz; Stephen A. Boorjian; Jennifer R. Geske; R. Houston Thompson; Matthew R. Callstrom; Thomas D. Atwell
PURPOSEnTo evaluate treatment outcomes with percutaneous cryoablation (PCA) based on renal cell carcinoma (RCC) histology.nnnMETHODS AND MATERIALSnPatients treated with PCA for a solitary, sporadic stage T1a RCC from 2003 to 2016 were identified from a single institutions renal ablation registry. Patients with multiple tumors, history of RCC, or genetic syndromes associated with RCC (nxa0= 60); no specific RCC subtype determined from core biopsy (nxa0= 66); RCC subtype other than clear-cell or papillary (nxa0= 7); or less than 3 mo of follow-up imaging (nxa0= 5) were excluded. In total, 173 patients met study inclusion criteria. Oncologic outcomes, clinical outcomes, and complications were evaluated based on tumor subtype.nnnRESULTSnOf the 173 patients who underwent PCA for a stage T1a RCC, 130 (75%) had clear-cell RCC (ccRCC) and 43 (25%) had papillary RCC (pRCC). Median tumor size was 2.9 cm (range, 1.3-4.0 cm). Technically successful cryoablation was achieved in all 173 patients. Local tumor recurrence developed in 6 patients with ccRCC (4.6%), new renal tumors developed in 1 patient (0.8%), and metastatic RCC developed in 1 patient (0.8%) who also had local tumor recurrence. No patients with pRCC showed local tumor recurrence, new renal tumors, or metastatic disease. The 5-year disease-free survival rate in patients with ccRCC was 88%, compared with 100% in patients with pRCC (Pxa0= .48). Nine patients (5.2%), all with ccRCC, experienced major complications (Pxa0= .11).nnnCONCLUSIONSnPercutaneous ablation is a viable treatment option for patients with clinical stage T1a pRCC and ccRCC. Percutaneous ablation may be a very favorable treatment strategy particularly for pRCC.
Journal of Vascular and Interventional Radiology | 2018
Mustafa M. Haddad; Chad J. Fleming; Scott M. Thompson; Christopher J. Reisenauer; Ahmad Parvinian; G. Frey; Beau B. Toskich; James C. Andrews
PURPOSEnTo evaluate the incidence of bleeding complications between transplenic (TS) and transhepatic (TH) access in portal venous interventions.nnnMATERIALS AND METHODSnRetrospective review of patients who underwent TS or TH access for portal venous system interventions from January 2000 to August 2017. Only procedures with clinical and laboratory follow-up were included (nxa0= 148). Twenty-four TS procedures were performed in 22 patients, and 124 TH procedures were performed in 114 patients. The main indications were for angioplasty/stent, embolization of varices/shunt, or portal vein embolization, with no difference between the groups. Mean patient age and sex were not significantly different between the groups (P values .445 and .682, respectively). Mean follow up was 2.3 years (range 0.1-14.2). There was no significant difference between the international normalized ratio (Pxa0= .300) and platelets (Pxa0= .234) before the procedure between the 2 cohorts.nnnRESULTSnTechnical success of vascular access and procedural success was achieved in 22/24 (91.6%) TS procedures and 120/124 (96.8%) TH procedures (Pxa0= .238). There was no significant difference in bleeding complications between the 2 groups (3/24 [12.5%] TS vs 10/124 [8.1%] TH; Pxa0= .44). There was no significant difference in major bleeding complications (SIR classification ≥ C; 1/24 [4.2%] TS vs 4/124 [3.2%] TH; Pxa0= .789).There was no significant difference in the hemoglobin before or after the procedure (g/dL), with average changexa0-1.1 g/dL (rangexa0-3.4 toxa0+1.0) in the TS group and 1.0 g/dL (rangexa0-4.5 toxa0+1.9) in the TH group (Pxa0= .540). Finally, there was no significant difference in proportion of patients requiring blood transfusion after the procedure (Pxa0= .520), with 2 (8.3%) in the TS group requiring an average of 4 units (range 2-6) and 17 (13.7%) in the TH group requiring an average of 3.5 units (range 1-26).nnnCONCLUSIONSnThese data suggest no significant difference in bleeding complications between TS and TH access for portal venous interventions.
CardioVascular and Interventional Radiology | 2018
Mustafa M. Haddad; Benjamin Simmons; Ian R. McPhail; Manju Kalra; Melissa J. Neisen; Matthew P. Johnson; Andrew H. Stockland; James C. Andrews; Sanjay Misra; Haraldur Bjarnason
ABSTRACTPurposeTo identify whether long-term symptom relief and stent patency vary with the use of covered versus uncovered stents for the treatment of benign SVC obstruction.Methods and MaterialsWe retrospectively identified all patients with benign SVC syndrome treated to stent placement between January 2003 and December 2015 (nxa0=xa059). Only cases with both clinical and imaging follow-up were included (nxa0=xa047). In 33 (70%) of the patients, the obstruction was due to a central line or pacemaker wires, and in 14 (30%), the cause was fibrosing mediastinitis. Covered stents were placed in 17 (36%) of the patients, and 30 (64%) patients had an uncovered stent. Clinical and treatment outcomes, complications, and the percent stenosis of each stent were evaluated.ResultsTechnical success was achieved in all cases at first attempt. Average clinical and imaging follow-up in years was 2.7 (range 0.1–11.1) (covered) and 1.7 (range 0.2–10.5) (uncovered), respectively. There was a significant difference (pxa0=xa00.044) in the number of patients who reported a return of symptoms between the covered (5/17 or 29.4%) and uncovered (18/30 or 60%) groups. There was also a significant difference (pxa0=xa0<xa00.001) in the mean percent stenosis after stent placement between the covered [17.9% (range 0–100)xa0±xa026.2] and uncovered [48.3% (range 6.8–100)xa0±xa033.5] groups. No significant difference (pxa0=xa00.227) was found in the time (days) between the date of the procedure and the date of clinical follow-up where a return of symptoms was reported [covered: 426.6 (range 28–1554)xa0±xa0633.9 and uncovered 778.1 (range 23–3851)xa0±xa01066.8]. One patient in the uncovered group had non-endovascular surgical intervention (innominate to right atrial bypass), while none in the covered group required surgical intervention. One major complication (SIR grade C) occurred that consisted of a pericardial hemorrhagic effusion after angioplasty that required covered stent placement. There were no procedure-related deaths.ConclusionBoth covered and uncovered stents can be used for treating benign SVC syndrome. Covered stents, however, may be a more effective option at providing symptom relief and maintaining stent patency if validated by further studies.
Journal of Vascular and Interventional Radiology | 2018
Ahmad Parvinian; C. Reisenauer; Emily C. Bendel; Mustafa M. Haddad; James C. Andrews; C. Fleming
Journal of Vascular and Interventional Radiology | 2018
Mustafa M. Haddad; Melissa J. Neisen; I. McPhail; Manju Kalra; Andrew H. Stockland; Emily C. Bendel; James C. Andrews; Newton B. Neidert; Sanjay Misra; Haraldur Bjarnason
Journal of Vascular and Interventional Radiology | 2018
Mustafa M. Haddad; Christopher J. Reisenauer; Ahmad Parvinian; Scott M. Thompson; Beau B. Toskich; James C. Andrews; Chad J. Fleming
Journal of Vascular and Interventional Radiology | 2018
Mustafa M. Haddad; Emily C. Bendel; A. Parvinian; W. Harmsen; I. McPhail; Andrew H. Stockland; V. Iyer; Sanjay Misra