105 results on '"Jaffer F"'
Search Results
2. Moderate alcohol intake associates with a decreased risk of venous thrombosis: mediation through decreased stress-associated brain activity
- Author
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Mezue, K, primary, Osborne, M T, additional, Abbasi, T, additional, Zureigat, H, additional, Abohashem, S, additional, Gharios, C, additional, Akuffo, E, additional, Cardeiro, A, additional, Pitman, R, additional, Shin, L, additional, Jaffer, F, additional, Rosovsky, R, additional, and Tawakol, A, additional
- Published
- 2021
- Full Text
- View/download PDF
3. Faulty repolarisation reserve in alternating hemiplegia of childhood: broadened phenotype from a cohort ECG study
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JAFFER, F, AVBERSEK, A, ENRAH, ???, AYLETT, S, HANNA, M G, HOULDEN, H, NEVILLE, B, KURIAN, M A, LAMBIASE, P, BEHR, E, CROSS, J H, KASKI, J P, and SISODIYA, S M
- Published
- 2015
4. Supplement to: Case 28–2010: A 32-year-old woman, 3 weeks post partum, with substernal chest pain.
- Author
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Sabatine, M S, Jaffer, F A, Staats, P N, and Stone, J R
- Published
- 2010
5. Clinical and genetic spectrum of hemiplegic migraine in a paediatric patient cohort
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JAFFER, F, ILLINGWORTH, M, KURIAN, M A, HANNA, M G, HOULDEN, H, and PRABHAKAR, P
- Published
- 2014
6. High Risk Findings on Low Dose CT in a Coccidioidomycosis Endemic Area
- Author
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Jaffer, F., primary, Chan, Y.-M., additional, Kumar, S., additional, Rao, S., additional, Parbtani, R., additional, Vedantham, S., additional, and Malo, J., additional
- Published
- 2020
- Full Text
- View/download PDF
7. Retrospective Analysis of Immune Checkpoint Modulator Related Pneumonitis
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Hothi, S.S., primary, Rao, S., additional, Parbtani, R., additional, Bardwell, J., additional, Witt, K., additional, and Jaffer, F., additional
- Published
- 2020
- Full Text
- View/download PDF
8. Mutual influence of cholesterol esterase and pseudocholinesterase on the biodegradation of dental composites
- Author
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Finer, Y, Jaffer, F, and Santerre, J.P
- Published
- 2004
- Full Text
- View/download PDF
9. Abstract No. 439 The favorable impacts of resolvin D1 in arteriovenous fistula maturation in mice disappears in a uremic environment
- Author
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Cui, J., primary, Grau, M., additional, and Jaffer, F., additional
- Published
- 2020
- Full Text
- View/download PDF
10. 280The impact of epicardial collateral use on the outcomes of retrograde chronic total occlusion percutaneous coronary intervention
- Author
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Karacsonyi, J, primary, Karmpaliotis, D, additional, Alaswad, K, additional, Jaffer, F A, additional, Yeh, R W, additional, Martinez-Parachini, J R, additional, Tajti, P, additional, Kandzari, D E, additional, Krestyaninov, O, additional, Jaber, W, additional, Choi, J, additional, Rangan, B V, additional, Ungi, I, additional, Banerjee, S, additional, and Brilakis, E S, additional
- Published
- 2019
- Full Text
- View/download PDF
11. Interactions between resin monomers and commercial composite resins with human saliva derived esterases
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Jaffer, F., Finer, Y., and Santerre, J.P.
- Published
- 2002
- Full Text
- View/download PDF
12. Atypical periodic paralysis and myalgia: A novel RYR1 phenotype
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Matthews, E, Neuwirth, C, Jaffer, F, Scalco, RS, Fialho, D, Parton, M, Rayan, D, Suetterlin, K, Sud, R, Spiegel, R, Mein, R, Houlden, H, Schaefer, A, Healy, E, Palace, J, Quinlivan, R, Treves, S, Holton, JL, Jungbluth, H, and Hanna, MG
- Subjects
RYR ,Periodic paralysis ,mutations ,musculoskeletal system ,tissues ,NO ,Periodic paralysis, RYR, mutations - Abstract
OBJECTIVE: To characterize the phenotype of patients with symptoms of periodic paralysis (PP) and ryanodine receptor (RYR1) gene mutations.METHODS: Cases with a possible diagnosis of PP but additional clinicopathologic findings previously associated with RYR1-related disorders were referred for a tertiary neuromuscular clinical assessment in which they underwent detailed clinical evaluation, including neurophysiologic assessment, muscle biopsy, and muscle MRI. Genetic analysis with next-generation sequencing and/or targeted Sanger sequencing was performed.RESULTS: Three cases with episodic muscle paralysis or weakness and additional findings compatible with a RYR1-related myopathy were identified. The McManis test, used in the diagnosis of PP, was positive in 2 of 3 cases. Genetic analysis of known PP genes was negative. RYR1 analysis confirmed likely pathogenic variants in all 3 cases.CONCLUSIONS: RYR1 mutations can cause late-onset atypical PP both with and without associated myopathy. Myalgia and cramps are prominent features. The McManis test may be a useful diagnostic tool to indicate RYR1-associated PP. We propose that clinicopathologic features suggestive of RYR1-related disorders should be sought in genetically undefined PP cases and that RYR1 gene testing be considered in those in whom mutations in SCN4A, CACNA1S, and KCNJ2 have already been excluded.
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- 2018
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- View/download PDF
13. Medical image of the week: Chylothorax
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Dicken J, Chopra M, Jaffer F, and Snyder L
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CT scan ,adenocarcinoma ,lcsh:R5-130.5 ,lcsh:Medical emergencies. Critical care. Intensive care. First aid ,milky ,lcsh:RC86-88.9 ,dyspnea ,mediastinal lymphadenopathy ,lung cancer ,pleural effusion ,chylothorax ,lymphadenopathy ,triglycerides ,lcsh:General works - Abstract
No abstract available. Article truncated after 150 words. A 73-year-old man with untreated stage IV adenocarcinoma of the lung was admitted to the hospital with several days of progressively worsening dyspnea on exertion. The chest CT showed a large left pleural effusion with enlarging bilateral hilar and mediastinal lymphadenopathy, compression of the superior vena cava and right main pulmonary artery consistent with progressive lung cancer (Figure 1). Therapeutic and diagnostic left sided thoracentesis was performed, removing approximately 450 ml of milky, pink fluid suggestive of hemochylothorax (Figure 2). Analysis of the fluid was significant for 27,720 red blood cells, 476 total nucleated cells with lymphocyte predominance (87%), glucose 158 mg/dl, cholesterol 63 mg/dl, and amylase 28 U/L. The pleural fluid was exudative (protein 4.4 g/dl) with a significantly elevated triglyceride level of 532 mg/dl. No malignant cells were identified in the fluid. This case illustrates a nontraumatic chylothorax secondary to metastatic adenocarcinoma of the lung. The leading cause …
- Published
- 2018
14. P5090Sortilin is a key driver of fibrocalcific aortic valve disease
- Author
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Schlotter, F, primary, Goettsch, C, additional, Rogers, M A, additional, Hutcheson, J D, additional, Blaser, M C, additional, Goto, S, additional, Lee, L H, additional, Delaughter, D M, additional, Merryman, W D, additional, Seidman, J G, additional, Jaffer, F A, additional, Body, S C, additional, Aikawa, M, additional, Singh, S A, additional, and Aikawa, E, additional
- Published
- 2018
- Full Text
- View/download PDF
15. Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation
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Jaffer, F, Fawcett, K, Sims, D, Heger, A, Houlden, H, Hanna, MG, Kingston, H, and Sisodiya, SM
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Clinical/Scientific Notes - Abstract
The allelic disorders rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood (AHC), and CAPOS/CAOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural deafness) are caused by ATP1A3 mutations.1,–,3 Intermediate RDP-AHC phenotypes are emerging. Positional mutations 274, 583, 867, and 923 lead to both RDP and AHC, suggesting different pathomechanisms.4,5 The E818K mutation underlies all reported cases of CAPOS/CAOS, including an AHC-CAPOS overlap syndrome.6 We report a family with features of all 3 ATP1A3-spectrum disorders.
- Published
- 2017
16. Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype
- Author
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Jaffer F, Avbersek A, Vavassori R, Fons-Estupina C, Campistol-Plana J, Stagnaro M, De Grandis E, Veneselli E, Rosewich H, Gianotta M, Zucca C, Ragona F, Granata T, Nardocci N, Mikati M, Helseth AR, Boelman C, Minassian BA, Johns S, Garry SI, Scheffer IE, Gourfinkel-An I, Carrilho I, Aylett SE, Parton M, Hanna MG, Houlden H, Neville B, Kurian MA, Novy J, Sander JW, Lambiase PD, Behr ER, Schyns T, Arzimanoglou A, Cross JH, Kaski JP, and Sisodiya SM
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Adult ,Male ,SUDEP ,Adolescent ,Heart Diseases ,Heart Ventricles ,International Cooperation ,Hemiplegia ,alternating hemiplegia of childhood ,ATP1A3 ,Na+ /K + -ATPase ,electrocardiogram ,Na+/K+-ATPase ,Age Factors ,Autonomic Nervous System Diseases ,Child ,Child, Preschool ,Cohort Studies ,Electrocardiography ,Female ,Heart Rate ,Humans ,Infant ,Infant, Newborn ,Mutation ,Sodium-Potassium-Exchanging ATPase ,Young Adult ,Medicine (all) ,Arts and Humanities (miscellaneous) ,Neurology (clinical) ,Preschool ,Original Articles ,Newborn ,cardiovascular system - Abstract
Alternating hemiplegia of childhood is rare and usually results from mutations in cardiac- and brain-expressed ATP1A3. In an ECG study of 52 cases, Jaffer et al. reveal dynamic cardiac repolarisation or conduction abnormalities in over 50%. Abnormalities are more common in those ≥16 years, and suggest impaired cardiac repolarisation reserve., Alternating hemiplegia of childhood is a rare disorder caused by de novo mutations in the ATP1A3 gene, expressed in neurons and cardiomyocytes. As affected individuals may survive into adulthood, we use the term ‘alternating hemiplegia’. The disorder is characterized by early-onset, recurrent, often alternating, hemiplegic episodes; seizures and non-paroxysmal neurological features also occur. Dysautonomia may occur during hemiplegia or in isolation. Premature mortality can occur in this patient group and is not fully explained. Preventable cardiorespiratory arrest from underlying cardiac dysrhythmia may be a cause. We analysed ECG recordings of 52 patients with alternating hemiplegia from nine countries: all had whole-exome, whole-genome, or direct Sanger sequencing of ATP1A3. Data on autonomic dysfunction, cardiac symptoms, medication, and family history of cardiac disease or sudden death were collected. All had 12-lead electrocardiogram recordings available for cardiac axis, cardiac interval, repolarization pattern, and J-point analysis. Where available, historical and prolonged single-lead electrocardiogram recordings during electrocardiogram-videotelemetry were analysed. Half the cohort (26/52) had resting 12-lead electrocardiogram abnormalities: 25/26 had repolarization (T wave) abnormalities. These abnormalities were significantly more common in people with alternating hemiplegia than in an age-matched disease control group of 52 people with epilepsy. The average corrected QT interval was significantly shorter in people with alternating hemiplegia than in the disease control group. J wave or J-point changes were seen in six people with alternating hemiplegia. Over half the affected cohort (28/52) had intraventricular conduction delay, or incomplete right bundle branch block, a much higher proportion than in the normal population or disease control cohort (P = 0.0164). Abnormalities in alternating hemiplegia were more common in those ≥16 years old, compared with those
- Published
- 2015
17. The clinical and genetic heterogeneity of paroxysmal dyskinesias
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Gardiner, A.R. Jaffer, F. Dale, R.C. Labrum, R. Erro, R. Meyer, E. Xiromerisiou, G. Stamelou, M. Walker, M. Kullmann, D. Warner, T. Jarman, P. Hanna, M. Kurian, M.A. Bhatia, K.P. Houlden, H.
- Abstract
Paroxysmal dyskinesia can be subdivided into three clinical syndromes: paroxysmal kinesigenic dyskinesia or choreoathetosis, paroxysmal exercise-induced dyskinesia, and paroxysmal non-kinesigenic dyskinesia. Each subtype is associated with the known causative genes PRRT2, SLC2A1 and PNKD, respectively. Although separate screening studies have been carried out on each of the paroxysmal dyskinesia genes, to date there has been no large study across all genes in these disorders and little is known about the pathogenic mechanisms. We analysed all three genes (the whole coding regions of SLC2A1 and PRRT2 and exons one and two of PNKD) in a series of 145 families with paroxysmal dyskinesias as well as in a series of 53 patients with familial episodic ataxia and hemiplegic migraine to investigate the mutation frequency and type and the genetic and phenotypic spectrum. We examined the mRNA expression in brain regions to investigate how selective vulnerability could help explain the phenotypes and analysed the effect of mutations on patient-derived mRNA. Mutations in the PRRT2, SLC2A1 and PNKD genes were identified in 72 families in the entire study. In patients with paroxysmal movement disorders 68 families had mutations (47%) out of 145 patients. PRRT2 mutations were identified in 35% of patients, SLC2A1 mutations in 10%, PNKD in 2%. Two PRRT2 mutations were in familial hemiplegic migraine or episodic ataxia, one SLC2A1 family had episodic ataxia and one PNKD family had familial hemiplegic migraine alone. Several previously unreported mutations were identified. The phenotypes associated with PRRT2 mutations included a high frequency of migraine and hemiplegic migraine. SLC2A1 mutations were associated with variable phenotypes including paroxysmal kinesigenic dyskinesia, paroxysmal non-kinesigenic dyskinesia, episodic ataxia and myotonia and we identified a novel PNKD gene deletion in familial hemiplegic migraine. We found that some PRRT2 loss-of-function mutations cause nonsense mediated decay, except when in the last exon, whereas missense mutations do not affect mRNA. In the PNKD family with a novel deletion, mRNA was truncated losing the C-terminus of PNKD-L and still likely loss-of-function, leading to a reduction of the inhibition of exocytosis, and similar to PRRT2, an increase in vesicle release. This study highlights the frequency, novel mutations and clinical and molecular spectrum of PRRT2, SLC2A1 and PNKD mutations as well as the phenotype-genotype overlap among these paroxysmal movement disorders. The investigation of paroxysmal movement disorders should always include the analysis of all three genes, but around half of our paroxysmal series remain genetically undefined implying that additional genes are yet to be identified.
- Published
- 2015
18. Atorvastatin decreases venous outflow inflammation and prolonged AVF patency in a murine arteriovenous fistula model
- Author
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Cui, J, primary, Jhajj, H, additional, Kessinger, C, additional, and Jaffer, F, additional
- Published
- 2017
- Full Text
- View/download PDF
19. Impact of diabetes mellitus on acute outcomes of percutaneous coronary intervention in chronic total occlusions: insights from a US multicentre registry
- Author
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Martinez‐Parachini, J. R., primary, Karatasakis, A., additional, Karmpaliotis, D., additional, Alaswad, K., additional, Jaffer, F. A., additional, Yeh, R. W., additional, Patel, M., additional, Bahadorani, J., additional, Doing, A., additional, Nguyen‐Trong, P.‐K., additional, Danek, B. A., additional, Karacsonyi, J., additional, Alame, A., additional, Rangan, B. V., additional, Thompson, C. A., additional, Banerjee, S., additional, and Brilakis, E. S., additional
- Published
- 2016
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- View/download PDF
20. Medical image of the week: athersclerotic aneurysm of great vessels
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Jaffer F and Pepito DL
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CT scan ,treatment ,lcsh:R5-130.5 ,lcsh:Medical emergencies. Critical care. Intensive care. First aid ,great vessels ,lcsh:RC86-88.9 ,tobacco ,smoking ,aneurysm ,atherosclerotic aneurysm ,magnetic resonance imaging ,atherosclerosis ,lcsh:General works ,MRI - Abstract
No abstract available. Article truncated at 150 words. A 60 year-old man with a 33 pack-year history of tobacco abuse, presented with difficulty speaking and voice change for several weeks. His review of systems was positive for fatigue, night sweats and weight loss. Physical exam of the oropharynx with flexible laryngoscopy demonstrated immobile bilateral true and false vocal cords fixed in the para-median position without laryngeal lesions. Concern for intra-thoracic process with recurrent laryngeal nerve involvement, a computed tomography (CT) of the chest and thoracic vessels demonstrated unusual appearing arteries with multiple penetrating atherosclerotic ulcers versus saccular aneurysms scattered throughout the aorta and its major branches (Figures 1 and 2). A magnetic resonance imaging (MRI) with contrast, demonstrated multiple foci of saccular outpouchings involving the arch vessels distal to their origins with the largest dilatation measuring 26 x 25 mm in the case of proximal innominate (Figure 3). Although imaging lacked resolution, it was specialist opinion that the ...
- Published
- 2015
21. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients
- Author
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Panagiotakaki, E, De Grandis, E, Stagnaro, M, Heinzen, EL, Fons, C, Sisodiya, S, de Vries, B, Goubau, C, Weckhuysen, S, Kemlink, D, Scheffer, I, Lesca, G, Rabilloud, M, Klich, A, Ramirez-Camacho, A, Ulate-Campos, A, Campistol, J, Giannotta, M, Moutard, M-L, Doummar, D, Hubsch-Bonneaud, C, Jaffer, F, Cross, H, Gurrieri, F, Tiziano, D, Nevsimalova, S, Nicole, S, Neville, B, van den Maagdenberg, AMJM, Mikati, M, Goldstein, DB, Vavassori, R, Arzimanoglou, A, Panagiotakaki, E, De Grandis, E, Stagnaro, M, Heinzen, EL, Fons, C, Sisodiya, S, de Vries, B, Goubau, C, Weckhuysen, S, Kemlink, D, Scheffer, I, Lesca, G, Rabilloud, M, Klich, A, Ramirez-Camacho, A, Ulate-Campos, A, Campistol, J, Giannotta, M, Moutard, M-L, Doummar, D, Hubsch-Bonneaud, C, Jaffer, F, Cross, H, Gurrieri, F, Tiziano, D, Nevsimalova, S, Nicole, S, Neville, B, van den Maagdenberg, AMJM, Mikati, M, Goldstein, DB, Vavassori, R, and Arzimanoglou, A
- Abstract
BACKGROUND: Mutations in the gene ATP1A3 have recently been identified to be prevalent in patients with alternating hemiplegia of childhood (AHC2). Based on a large series of patients with AHC, we set out to identify the spectrum of different mutations within the ATP1A3 gene and further establish any correlation with phenotype. METHODS: Clinical data from an international cohort of 155 AHC patients (84 females, 71 males; between 3 months and 52 years) were gathered using a specifically formulated questionnaire and analysed relative to the mutational ATP1A3 gene data for each patient. RESULTS: In total, 34 different ATP1A3 mutations were detected in 85 % (132/155) patients, seven of which were novel. In general, mutations were found to cluster into five different regions. The most frequent mutations included: p.Asp801Asn (43 %; 57/132), p.Glu815Lys (16 %; 22/132), and p.Gly947Arg (11 %; 15/132). Of these, p.Glu815Lys was associated with a severe phenotype, with more severe intellectual and motor disability. p.Asp801Asn appeared to confer a milder phenotypic expression, and p.Gly947Arg appeared to correlate with the most favourable prognosis, compared to the other two frequent mutations. Overall, the comparison of the clinical profiles suggested a gradient of severity between the three major mutations with differences in intellectual (p = 0.029) and motor (p = 0.039) disabilities being statistically significant. For patients with epilepsy, age at onset of seizures was earlier for patients with either p.Glu815Lys or p.Gly947Arg mutation, compared to those with p.Asp801Asn mutation (p < 0.001). With regards to the five mutation clusters, some clusters appeared to correlate with certain clinical phenotypes. No statistically significant clinical correlations were found between patients with and without ATP1A3 mutations. CONCLUSIONS: Our results, demonstrate a highly variable clinical phenotype in patients with AHC2 that correlates with certain mutations and possibly clust
- Published
- 2015
22. Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype
- Author
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Jaffer, F, Avbersek, A, Vavassori, R, Fons, C, Campistol, J, Stagnaro, M, De Grandis, E, Veneselli, E, Rosewich, H, Gianotta, M, Zucca, C, Ragona, F, Granata, T, Nardocci, N, Mikati, M, Helseth, AR, Boelman, C, Minassian, BA, Johns, S, Garry, SI, Scheffer, IE, Gourfinkel-An, I, Carrilho, I, Aylett, SE, Parton, M, Hanna, MG, Houlden, H, Neville, B, Kurian, MA, Novy, J, Sander, JW, Lambiase, PD, Behr, ER, Schyns, T, Arzimanoglou, A, Cross, JH, Kaski, JP, Sisodiya, SM, Jaffer, F, Avbersek, A, Vavassori, R, Fons, C, Campistol, J, Stagnaro, M, De Grandis, E, Veneselli, E, Rosewich, H, Gianotta, M, Zucca, C, Ragona, F, Granata, T, Nardocci, N, Mikati, M, Helseth, AR, Boelman, C, Minassian, BA, Johns, S, Garry, SI, Scheffer, IE, Gourfinkel-An, I, Carrilho, I, Aylett, SE, Parton, M, Hanna, MG, Houlden, H, Neville, B, Kurian, MA, Novy, J, Sander, JW, Lambiase, PD, Behr, ER, Schyns, T, Arzimanoglou, A, Cross, JH, Kaski, JP, and Sisodiya, SM
- Abstract
Alternating hemiplegia of childhood is a rare disorder caused by de novo mutations in the ATP1A3 gene, expressed in neurons and cardiomyocytes. As affected individuals may survive into adulthood, we use the term 'alternating hemiplegia'. The disorder is characterized by early-onset, recurrent, often alternating, hemiplegic episodes; seizures and non-paroxysmal neurological features also occur. Dysautonomia may occur during hemiplegia or in isolation. Premature mortality can occur in this patient group and is not fully explained. Preventable cardiorespiratory arrest from underlying cardiac dysrhythmia may be a cause. We analysed ECG recordings of 52 patients with alternating hemiplegia from nine countries: all had whole-exome, whole-genome, or direct Sanger sequencing of ATP1A3. Data on autonomic dysfunction, cardiac symptoms, medication, and family history of cardiac disease or sudden death were collected. All had 12-lead electrocardiogram recordings available for cardiac axis, cardiac interval, repolarization pattern, and J-point analysis. Where available, historical and prolonged single-lead electrocardiogram recordings during electrocardiogram-videotelemetry were analysed. Half the cohort (26/52) had resting 12-lead electrocardiogram abnormalities: 25/26 had repolarization (T wave) abnormalities. These abnormalities were significantly more common in people with alternating hemiplegia than in an age-matched disease control group of 52 people with epilepsy. The average corrected QT interval was significantly shorter in people with alternating hemiplegia than in the disease control group. J wave or J-point changes were seen in six people with alternating hemiplegia. Over half the affected cohort (28/52) had intraventricular conduction delay, or incomplete right bundle branch block, a much higher proportion than in the normal population or disease control cohort (P = 0.0164). Abnormalities in alternating hemiplegia were more common in those ≥16 years old, compared wi
- Published
- 2015
23. Impact of diabetes mellitus on acute outcomes of percutaneous coronary intervention in chronic total occlusions: insights from a US multicentre registry.
- Author
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Martinez‐Parachini, J. R., Karatasakis, A., Karmpaliotis, D., Alaswad, K., Jaffer, F. A., Yeh, R. W., Patel, M., Bahadorani, J., Doing, A., Nguyen‐Trong, P.‐K., Danek, B. A., Karacsonyi, J., Alame, A., Rangan, B. V., Thompson, C. A., Banerjee, S., and Brilakis, E. S.
- Subjects
CORONARY heart disease treatment ,DIABETES complications ,CHI-squared test ,CHRONIC diseases ,CORONARY artery bypass ,FISHER exact test ,LONGITUDINAL method ,MEDICAL cooperation ,MYOCARDIAL revascularization ,SCIENTIFIC observation ,RESEARCH ,RESEARCH funding ,T-test (Statistics) ,TRANSLUMINAL angioplasty ,TREATMENT effectiveness ,DISEASE incidence ,RETROSPECTIVE studies ,DATA analysis software ,CORONARY angiography ,MANN Whitney U Test - Abstract
Aim To examine the impact of diabetes mellitus on procedural outcomes of patients who underwent percutaneous coronary intervention for chronic total occlusion. Methods We assessed the impact of diabetes mellitus on the outcomes of percutaneous coronary intervention for chronic total occlusion among 1308 people who underwent such procedures at 11 US centres between 2012 and 2015. Results The participants' mean ± sd age was 66 ± 10 years, 84% of the participants were men and 44.6% had diabetes. As compared with participants without diabetes, participants with diabetes were more likely to have undergone coronary artery bypass graft surgery (38 vs 31%; P = 0.006), and to have had previous heart failure (35 vs 22%; P = 0.0001) and peripheral arterial disease (19 vs 13%; P = 0.002). They also had a higher BMI (31 ± 6 kg/m
2 vs 29 ± 6 kg/m2 ; P = 0.001), similar Japanese chronic total occlusion scores (2.6 ± 1.2 vs 2.5 ± 1.2; P = 0.82) and similar final successful crossing technique: antegrade wire escalation (46 vs 47%; P = 0.66), retrograde (30 vs 28%; P = 0.66) and antegrade dissection re-entry (24 vs 25%; P = 0.66). Technical (91 vs 90%; P = 0.80) and procedural (89 vs 89%; P = 0.93) success was similar in the two groups, as was the incidence of major adverse cardiac events (2.2 vs 2.5%; P = 0.61). Conclusions In a contemporary cohort of people undergoing percutaneous coronary intervention for chronic total occlusion, nearly one in two (45%) had diabetes mellitus. Procedural success and complication rates were similar in people with and without diabetes. [ABSTRACT FROM AUTHOR]- Published
- 2017
- Full Text
- View/download PDF
24. 4:03 PMAbstract No. 339 - Atorvastatin decreases venous outflow inflammation and prolonged AVF patency in a murine arteriovenous fistula model
- Author
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Cui, J, Jhajj, H, Kessinger, C, and Jaffer, F
- Published
- 2017
- Full Text
- View/download PDF
25. Optimizing Multidisciplinary Simulation in Medical School for Larger Groups: Role Assignment by Lottery and Guided Learning
- Author
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Borges LF, Robertson JM, Kappler SM, Venkatan SK, Jin DX, Barnes EL, Jaffer FA, Saldana FL, Dudzinski DM, Stefanescu Schmidt AC, Drachman DE, Young MN, Hayden EM, Pelletier SR, and Shields HM
- Subjects
medical student ,manikin ,large group simulation ,gastroenterology ,cardiology ,Special aspects of education ,LC8-6691 ,Medicine (General) ,R5-920 - Abstract
Lawrence F Borges,1 Jamie M Robertson,2 Steven M Kappler,3 Suresh K Venkatan,4 David X Jin,5 Edward L Barnes,6 Farouc A Jaffer,7 Fidencio L Saldana,8 David M Dudzinski,4,7 Ada C Stefanescu Schmidt,7 Douglas E Drachman,7 Michael N Young,9 Emily M Hayden,10 Stephen R Pelletier,11 Helen M Shields5 1Division of Gastroenterology, Mount Auburn Hospital and Harvard Medical School, Cambridge, MA, USA; 2Department of Surgery, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA; 3Cleveland Clinic Digestive Diseases Center, Port St. Lucie, FL, USA; 4Learning Laboratory, Massachusetts General Hospital, Boston, MA, USA; 5Division of Gastroenterology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA; 6Division of Gastroenterology, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC, USA; 7Division of Cardiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; 8Division of Cardiovascular Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA; 9Cardiology Division, Dartmouth-Hitchcock Medical Center and Geisel School of Medicine, Lebanon, NH, USA; 10Department of Emergency Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA; 11Office of Educational Quality Improvement, Harvard Medical School, Boston, MA, USACorrespondence: Lawrence F BorgesDivision of Gastroenterology, Mount Auburn Hospital and Harvard Medical School, 330 Mt. Auburn Street, Suite # 405, Cambridge, MA 02138, USATel +1 (617) 498-9550Fax +1 (617) 498-9561Email Lawrence.Borges@mah.orgPurpose: Medical school simulations are often designed for a limited number of students to maximize engagement and learning. To ensure that all first-year medical students who wished to join had an opportunity to participate, we designed a novel method for larger groups.Patients and Methods: We devised a low technology “Orchestra Leader’s” chart approach to prominently display students’ roles, chosen by lottery. During simulation, the chart was mounted on an intravenous pole and served as a group organizational tool. A course instructor prompted students using the chart to accomplish the course objectives in a logical order. Real-life cardiologists and gastroenterologists provided the students with expert subspecialty consultation. We analyzed 125 anonymous student evaluation ratings for 3 years (2017– 2019) with a range of 8 to 19 students per laboratory session.Results: Our 2017– 2019 larger group sessions were all rated as excellent (1.26, Mean, SD ± .510) on the Likert scale where 1.0 is excellent and 5.0 is poor. There were no statistically significant differences in overall ratings among the 2017, 2018 and 2019 sessions. The subspecialists were uniformly rated as excellent. Verbatim free-text responses demonstrated resounding student appreciation for the role assignment by lottery method.Conclusion: We designed a novel, “Orchestra Leader’s” chart approach for accommodating larger groups in a multidisciplinary simulation laboratory using role assignment by lottery, roles depicted on an organizational chart, and expert instructor prompting. Our consistently excellent ratings suggest that our methods are useful for achieving well-rated larger group simulation laboratories.Keywords: medical student, manikin, large group simulation, gastroenterology, cardiology
- Published
- 2020
26. AVOIDING UNPLANNED HOSPITAL ADMISSIONS IN PATIENTS WITH NEUROMUSCULAR DISEASES: A REGIONAL COLLABORATIVE AUDIT OF HOSPITAL ADMISSIONS
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Jaffer, F, primary, Reilly, MM, additional, Quinlivan, RR, additional, Muntoni, F, additional, Orrell, R, additional, Wraige, E, additional, Saha, R, additional, Radunovic, A, additional, Mummery, C, additional, Parton, M, additional, and Hanna, M, additional
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- 2012
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27. Subject-Specific Estimation of Central Aortic Blood Pressure Using an Individualized Transfer Function: A Preliminary Feasibility Study
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Hahn, J., primary, Reisner, A. T., additional, Jaffer, F. A., additional, and Asada, H. H., additional
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- 2012
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28. P40 Episodic ataxia: screening candidate genes and genetic analysis of families
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Jaffer, F., primary, Graves, T., additional, Gibbons, V., additional, Gardiner, A., additional, Hersheson, J., additional, Hanna, M., additional, and Houlden, H., additional
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- 2012
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29. Abstract: P640 PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-Γ ACTIVATION REDUCES INFLAMMATION IN ATHEROSCLEROSIS AS ASSESSED BY SERIAL IN VIVO FLUORESCENCE MOLECULAR IMAGING
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Chang, K, primary, Francis, S, additional, Aikawa, E, additional, Figueiredo, J, additional, Patel, P, additional, Weissleder, R, additional, Plutzky, J, additional, and Jaffer, F, additional
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- 2009
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30. Advances in fluorescence imaging of the cardiovascular system
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CHANG, K, primary and JAFFER, F, additional
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- 2008
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31. Molecular imaging of myocardial infarction
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JAFFER, F, primary, SOSNOVIK, D, additional, NAHRENDORF, M, additional, and WEISSLEDER, R, additional
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- 2006
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32. Biological characterization of a novel biodegradable antimicrobial polymer synthesized with fluoroquinolones
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Woo, G. L. Y., primary, Yang, M. L., additional, Yin, H. Q., additional, Jaffer, F., additional, Mittelman, M. W., additional, and Santerre, J. P., additional
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- 2001
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33. Musculoskeletal MR imaging at 4 T and at 1.5 T: comparison of relaxation times and image contrast.
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Duewell, S H, primary, Ceckler, T L, additional, Ong, K, additional, Wen, H, additional, Jaffer, F A, additional, Chesnick, S A, additional, and Balaban, R S, additional
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- 1995
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34. Centric ordering is superior to gradient moment nulling for motion artifact reduction in EPI.
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Jaffer, Farouc A., Wen, Han, Jezzard, Peter, Balaban, Robert S., Wolff, Steven D., Jaffer, F A, Wen, H, Jezzard, P, Balaban, R S, and Wolff, S D
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- 1997
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35. Radiofrequency shielding of surface coils at 4.0 T.
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Ong, Kenneth C., Wen, Han, Chesnick, A. Scott, Duewell, Stefan, Jaffer, Farouc A., Balaban, Robert S., Ong, K C, Wen, H, Chesnick, A S, Duewell, S, Jaffer, F A, and Balaban, R S
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- 1995
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36. A Branched Fluorescent Peptide Probe for Imaging of Activated Platelets
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Tung, C.-H., Quinti, L., Jaffer, F. A., and Weissleder, R.
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Novel fluorescent probes for thrombi and activated-platelet detection were developed that were based on the glycoprotein IIb/IIIa (GP-IIb/IIIa) binding sequence, Pro-Ser-Pro-Gly-Asp-Trp. Linear, Pro-Ser-Pro-Gly-Asp-Trp-Aha-Gly-Cys(Cy5.5)-NH
2 (1PF), and branched, (Pro-Ser-Pro-Gly-Asp-Trp-Aha)2 -Lys-Gly-Cys(Cy5.5)-NH2 (2PF), fluorescent-labeled peptide probes were synthesized. A third probe, also branched, (Pro-Ser-Pro-Gly-Glu-Trp-Aha)2 -Lys-Gly-Cys(Cy5.5)-NH2 (2CF), was synthesized as control. The platelet-binding activity of the probes was tested in clots generated from human platelet-rich plasma. Fluorescence reflectance imaging results showed that 2PF has a 16-fold increase in fluorescence intensity compared to the autofluorescence of clots. The linear conjugate, 1PF, and free dye did not show appreciable fluorescence enhancement. 2PF fluorescence was also found 5.5-fold higher than that of the control probe, 2CF. Overall, our results suggest that 2PF binds tightly to GP-IIb/IIIa and potentially can be used for in vivo imaging of thrombosis. Keywords: Activated platelets; thrombi detection; fluorescence; IIb/IIIa; receptor imaging- Published
- 2005
37. Biological characterization of a novel biodegradable antimicrobial polymer synthesized with fluoroquinolones
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Woo, G. L. Y., Yang, M. L., Yin, H. Q., Jaffer, F., Mittelman, M. W., and Santerre, J. P.
- Abstract
Biomaterialrelated infections continue to represent a significant challenge to the medical community. Several approaches have been utilized to incorporate antimicrobial agents at the surface of implant devices in attempts to delay or eliminate the formation of biofilms. To date, most of these strategies have focused on drug conjugation or diffusionlimited systems for the delivery of such pharmaceutical agents. More recently, work has been presented on the feasibility of incorporating drugs into the backbone of polymers as a mainchain monomer. When sequenced into the backbone of the polymer with other monomers that are hydrolytically sensitive to enzymecatalyzed breakdown, it is thought that drugs may be able to be selectively released. Specifically, degradable polyurethanes have been synthesized with fluoroquinolone antibiotics and have shown an ability to kill bacteria when released following degradation of the polymer chains by the macrophagederived enzyme cholesterol esterase. However, specificity of the cleavage sites in the polymer was difficult to control. Since cholesterol esterase has specificity for hydrophobic moieties, it is desirable to alter the formulation of the polyurethanes to incorporate long hydrophobic monomers immediately adjacent to the ciprofloxacin molecule. Hence, the current study focuses on evaluating the enzymecatalyzed degradation of a degradable polyurethane synthesized with 1,12 diisocyanatododecane as a substitute for 1,6 diisocyanatohexane, which was used in previous work. Validation of specific ciprofloxacin release and the generation of antimicrobial are shown. A preliminary cell study to assess the cytotoxicity of this biodegradable antibiotic polymer shows that the material has no observable effects on cell proliferation or cell membrane structure. © 2001 Wiley Periodicals, Inc., J Biomed Mater Res 59: 35–45, 2002
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- 2002
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38. Platelet-derived growth factor synthesis in mesangial cells: induction by multiple peptide mitogens.
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Silver, B J, Jaffer, F E, and Abboud, H E
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Platelet-derived growth factor (PDGF) has been implicated in several nonmalignant pathophysiological processes, including proliferative diseases of the kidney. Glomerular mesangial cells secrete a PDGF-like factor and express the PDGF A-chain and c-sis (or B-chain) mRNAs. We report here that both mRNAs are induced by serum and this effect can be mimicked by recombinant PDGF, which also markedly stimulates DNA synthesis. Other growth factors, such as epidermal growth factor (EGF), transforming growth factor type alpha, basic fibroblast growth factor (bFGF), and tumor necrosis factor type alpha (TNF-alpha) also are mitogenic for human mesangial cells and induce expression of the PDGF mRNAs. EGF, TNF-alpha, and bFGF also stimulate these cells to secrete a PDGF-like factor. Furthermore, anti-PDGF antibody partially abrogates the mitogenic effect of EGF, suggesting that mitogen-stimulated PDGF synthesis in mesangial cells is at least partly responsible for cell growth induced by other growth factors. In contrast to these results, transforming growth factor type beta (TGF-beta), while inducing both mRNAs, is not mitogenic, indicating that its effect on message levels can be dissociated from DNA synthesis. These data suggest that several peptide growth factors regulate the growth of mesangial cells and that PDGF may be an effector molecule that plays a role in the mitogenic response to many of these growth stimuli.
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- 1989
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39. Anxiety and depression associate with heightened risk of deep venous thrombosis: mediation through neural pathways
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Mezue, K., Osborne, M. T., Shady Abohashem, Zureigat, H., Abbasi, T., Gharios, C., Cardeiro, A., Akuffo, E., Pitman, R., Shin, L., Jaffer, F., Rosovsky, R., and Tawakol, A.
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Cardiology and Cardiovascular Medicine - Abstract
Background Anxiety disorders and depression associate with an increased risk of deep venous thrombosis (DVT). However, it is unclear if this association persists after robust adjustment for confounders. Further, the mechanism mediating this potential link remains unknown. Prior studies show that anxiety and depression associate with heightened stress-associated neural activity (notably in the amygdala: AmygA), which in turn promotes chronic inflammation, a driver of thrombosis syndromes. Purpose To evaluate whether the association between anxiety/depression and DVT risk: A) persists after robustly accounting for potential confounders, and B) is mediated by upregulated stress-associated neural activity (namely AmygA). Methods Data were obtained from the Mass General Brigham Biobank, which included detailed health information on 118 871 adult participants. A subset of 1520 study subjects underwent clinical 18F-fluorodeoxyglucose positron emission tomography imaging during the follow up period, from which AmygA was measured as the ratio of amygdalar to regulatory (ventromedial pre-frontal cortex) activity. International Classification of Disease (ICD) codes in the medical record were used to define anxiety disorders, depression, and lower extremity DVT. Individuals on anticoagulant therapies for atrial fibrillation prior to enrolment and/or imaging were excluded. Cox analysis were performed wherein patients who developed DVT prior to Biobank enrolment (2599 subjects) were excluded. Mediation analysis was used to examine the role of AmygA in mediating the link between anxiety/depression and DVT. Results The median age of the study population was 57 years [interquartile range (IQR) 28] and 58.4% were female. DVT occurred in 1231 participants (1.2%) over a median follow up period of 3.3 years (IQR 3.0). Cox regression analysis showed that anxiety disorders and depression were independent predictors of incident DVT after controlling for confounders (Table 1; p Conclusion Anxiety disorders and depression associate with an increased risk of DVT via a mechanism that includes heightened stress-related neurobiological activity. Future studies should evaluate whether modulating this neural pathway could reduce the incidence of DVT. Funding Acknowledgement Type of funding sources: None.
40. Current Perspectives and Practices on Chronic Total Occlusion Percutaneous Coronary Interventions
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Patel, S. M., Menon, R. V., Burke, M. N., Jaffer, F. A., Yeh, R. W., Vo, M., Karmpaliotis, D., Lorenzo Azzalini, Carlino, M., Mashayekhi, K., Galassi, A. R., Rinfret, S., Ellis, S. G., Patel, M., Rangan, B. V., Karatasakis, A., Danek, B. A., Karacsonyi, J., Resendes, E., Banerjee, S., and Brilakis, E. S.
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Cardiologists ,Percutaneous Coronary Intervention ,Postoperative Complications ,Treatment Outcome ,Coronary Occlusion ,Attitude of Health Personnel ,Risk Factors ,Surveys and Questionnaires ,Chronic Disease ,Humans ,Risk Assessment - Abstract
We sought to examine contemporary perspectives and practices on chronic total occlusion (CTO) percutaneous coronary intervention (PCI).The frequency and success of CTO-PCI have been increasing in recent years.An online questionnaire was created and distributed to cardiologists within the United States and internationally.A total of 1149 responses were obtained. The United States (n = 845; 73.5%), Asia (n = 98; 8.5%), Europe (n = 88; 7.7%), South America (n = 42; 3.7%), and Canada (n = 33; 2.9%) accounted for most responses. Mean practice duration of the respondents was 16.4 ± 11.5 years and 66.9% were interventional cardiologists. Most respondents agreed that CTO-PCI results in an improvement of patient symptoms (90.7%), left ventricular function (79.3%), arrhythmia risk (69.2%), and overall survival (63.1%). Interventional cardiologists had a more favorable view of the benefits of CTO-PCI as compared with non-interventional cardiologists (P.001). Most respondents estimated the procedural success rates of contemporary CTO-PCI to be between 51%-75% (34.2%) and 76%-85% (30.2%), with interventional cardiologists estimating higher success rates than non-interventionalists (P.001). Perforation, mortality, and tamponade were the three most concerning complications. Time and procedure complexity were reported to be the most significant barriers to the development of a CTO-PCI program.Most cardiologists believe that CTO-PCI can provide significant clinical benefits and can be accomplished with moderate to high success rates. Interventional cardiologists have a more favorable view of CTO-PCI as compared with non-invasive cardiologists.
41. Clinical profile of patients with ATP1A3 mutations in alternating hemiplegia of childhood-a study of 155 patients
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Panagiotakaki, E., De Grandis, E., Stagnaro, M., Heinzen, E. L., Fons, C., Sisodiya, S., de Vries, B., Goubau, C., Weckhuysen, S., Kemlink, D., Scheffer, I., Lesca, G., Rabilloud, M., Klich, A., Ramirez-Camacho, A., Ulate-Campos, A., Campistol, J., Giannotta, M., Moutard, M. L., Doummar, D., Hubsch-Bonneaud, C., Jaffer, F., Cross, H., Gurrieri, F., Tiziano, D., Nevsimalova, S., Nicole, S., Neville, B., van den Maagdenberg, A. M., Mikati, M., Goldstein, D. B., Vavassori, R., Arzimanoglou, A., Italian IBAHC Consortium, French AHC Consortium, Collaborators: Bassi MT, International AHC Consortium., Borgatti, R, Cernetti, R, Di Rosa, G, Franchini, F, Gambardella, A, Giacanelli, M, Giannotta, M, Gobbi, G, Granata, T, De Grandis, E, Guerrini, R, Gurrieri, F, Incorpora, G, Nardocci, N, Neri, G, Ragona, F, Santucci, M, Sartori, S, Stagnaro, M, Tiziano, D, Vavassori, R, Veneselli, E, Vigevano, F, Zucca, C, Aicardi, J, An, I, Arbues, As, Arzimanoglou, A, Bahi- Buisson, N, Barthez, Ma, Billette de Villemeur, T, Bourgeois, M, Bru, M, Chabrol, B, Chaigne, D, Chaunu, Mp, Chiron, C, Cournelle, Am, Davoine, Cs, De St Martin, A, Deny, B, Desguerres, I, Des Portes, V, Doummar, D, Dulac, O, Dusser, A, Gerard, M, Gitiaux, C, Godet Kiesel, I, Gokben, S, Goutieres, F, Guerrin, Mh, Heron-Longe, B, Hubsch-Bonneaud, C, Hully, M, Husson, M, Ioos, Ch, Kaminska, A, Laroche, C, Lazaro, L, Lepine, A, Magy, L, Marchal, C, Michel, J, Milh, M, Motte, J, Moutard, Ml, Napuri, S, Nassogne, Mc, Neau, Jp, Nicole, S, Panagiotakaki, E, Passemard, S, Pedespan, Jm, Penniello- Valette MJ, Poncelin, D, Ponsot, G, Poulat, Al, Pouplard, F, Rabilloud, M, Riant, F, Rivier, F, Roelens, P, Roubergue, A, Sanlaville, D, Tardieu, M, Veyrieres, S, de Grandis, E, Fons, C, Sisodiya, S, de Jonghe, P, Goubeau, C, van den Maagdenberg AM, Mikati, M, Scheffer, I, Nevsimalova, S, Kemlink, D, Krepelova, A, Kolnikova, M, Sykora, P, Kaski, J, Hanna, M, Houlden, H, Ulate-Campos, A, Cancho, R, Eiris, J, López-Laso, E, Velázquez, R, Carilho, I, Ozelius, L, Suls, A, Ceulemans, B, Buyse, G, di Michele, M, Ferrari, M, Peeters-Scholte, Cm., Universitat de Barcelona, Biostatistiques santé, Département biostatistiques et modélisation pour la santé et l'environnement [LBBE], Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université de Lyon-Université de Lyon-Institut National de Recherche en Informatique et en Automatique (Inria)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS), Suls, Arvid, De Jonghe, Peter, Ceulemans, Berten, Italian IBAHC Consortium, French AHC Consortium, International AHC Consortium, UCL - (SLuc) Service de pédiatrie générale, and UCL - SSS/IREC/PEDI - Pôle de Pédiatrie
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Male ,[SDV]Life Sciences [q-bio] ,medicine.disease_cause ,Settore MED/03 - GENETICA MEDICA ,Epilepsy ,Genètica mèdica ,0302 clinical medicine ,ATP1A3 ,inglese ,Genetics(clinical) ,Pharmacology (medical) ,Young adult ,Child ,Genetics (clinical) ,Genetics ,Medicine(all) ,0303 health sciences ,Mutation ,Medical genetics ,General Medicine ,Middle Aged ,Prognosis ,3. Good health ,Child, Preschool ,Alternating hemiplegia of childhood ,Cohort ,Hemiplègia ,Female ,Sodium-Potassium-Exchanging ATPase ,Adult ,medicine.medical_specialty ,Adolescent ,Hemiplegia ,Biology ,Genotype-phenotype ,03 medical and health sciences ,Young Adult ,Internal medicine ,medicine ,Humans ,Preschool ,Genetic Association Studies ,030304 developmental biology ,Alternating hemiplegia of childhood, ATP1A3, Genotype-phenotype ,Health Surveys ,Infant ,Research ,Mutació (Biologia) ,Mutation (Biology) ,medicine.disease ,Clinical trial ,Human medicine ,030217 neurology & neurosurgery ,Alternating hemiplegia - Abstract
Background Mutations in the gene ATP1A3 have recently been identified to be prevalent in patients with alternating hemiplegia of childhood (AHC2). Based on a large series of patients with AHC, we set out to identify the spectrum of different mutations within the ATP1A3 gene and further establish any correlation with phenotype. Methods Clinical data from an international cohort of 155 AHC patients (84 females, 71 males; between 3 months and 52 years) were gathered using a specifically formulated questionnaire and analysed relative to the mutational ATP1A3 gene data for each patient. Results In total, 34 different ATP1A3 mutations were detected in 85 % (132/155) patients, seven of which were novel. In general, mutations were found to cluster into five different regions. The most frequent mutations included: p.Asp801Asn (43 %; 57/132), p.Glu815Lys (16 %; 22/132), and p.Gly947Arg (11 %; 15/132). Of these, p.Glu815Lys was associated with a severe phenotype, with more severe intellectual and motor disability. p.Asp801Asn appeared to confer a milder phenotypic expression, and p.Gly947Arg appeared to correlate with the most favourable prognosis, compared to the other two frequent mutations. Overall, the comparison of the clinical profiles suggested a gradient of severity between the three major mutations with differences in intellectual (p = 0.029) and motor (p = 0.039) disabilities being statistically significant. For patients with epilepsy, age at onset of seizures was earlier for patients with either p.Glu815Lys or p.Gly947Arg mutation, compared to those with p.Asp801Asn mutation (p
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42. Deconvolution without regularization in inverse electrocardiography.
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Greensite, F., Yao-Jin Qian, Alzarka, E., and Jaffer, F.
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- 1993
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43. Emergency coronary artery bypass surgery after chronic total occlusion percutaneous coronary intervention: Insights from the PROGRESS-CTO registry.
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Mutlu D, Rempakos A, Alexandrou M, Al-Ogaili A, Gorgulu S, Choi JW, Elbarouni B, Khatri JJ, Jaffer F, Riley R, Smith AJC, Davies R, Frizzel J, Patel M, Koutouzis M, Tsiafoutis I, Rangan BV, Mastrodemos OC, Sandoval Y, Burke MN, and Brilakis ES
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- Humans, Male, Aged, Female, Middle Aged, Chronic Disease, Postoperative Complications epidemiology, Postoperative Complications etiology, Incidence, Hospital Mortality trends, Treatment Outcome, Emergencies, Coronary Occlusion surgery, Coronary Occlusion epidemiology, Registries, Percutaneous Coronary Intervention adverse effects, Percutaneous Coronary Intervention methods, Percutaneous Coronary Intervention trends, Coronary Artery Bypass adverse effects, Coronary Artery Bypass trends
- Abstract
Background: Emergency coronary artery bypass surgery (eCABG) is a serious complication of chronic total occlusion (CTO) percutaneous coronary artery intervention (PCI)., Methods: We examined the incidence and outcomes eCABG among 14,512 CTO PCIs performed between 2012 and 2023 in a large multicenter registry., Results: The incidence of eCABG was 0.12% (n = 17). Mean age was 68 ± 6 years and 69% of the patients were men. The most common reason for eCABG was coronary perforation (70.6%). eCABG patients had larger target vessel diameter (3.36 ± 0.50 vs. 2.90 ± 0.52; p = 0.003), were more likely to have moderate/severe calcification (85.7% vs. 45.8%; p = 0.006), side branch at the proximal cap (91.7% vs. 55.4%; p = 0.025), and balloon undilatable lesions (50% vs. 7.4%; p = 0.001) and to have undergone retrograde crossing (64.7% vs. 30.8%, p = 0.006). eCABG cases had lower technical (35.3% vs. 86.7%; p < 0.001) and procedural (35.3% vs. 86.7%; p < 0.001) success and higher in-hospital mortality (35.3% vs. 0.4%; p < 0.001), coronary perforation (70.6% vs. 4.6%; p < 0.001), pericardiocentesis (47.1% vs. 0.8%; p < 0.001), and major bleeding (11.8% vs. 0.5%; p < 0.001)., Conclusions: The incidence of eCABG after CTO PCI was 0.12% and associated with high in-hospital mortality (35%). Coronary perforation was the most common reason for eCABG., Competing Interests: Declaration of competing interest Dr. Khatri: Personal Honoria for proctoring and speaking: Abbott Vascular, Medtronic, Terumo, Shockwave Medical. Dr. Jaffer has conducted sponsored research for Canon, Siemens, Shockwave, Teleflex, Mercator,Boston Scientific, HeartFlow, and Amarin; has served as a consul-tant for Boston Scientific, Siemens, Magenta Medical, International Medical Device Solutions, Asahi Intecc, Biotronik, Philips, Intravascular Imaging, and DurVena; owns equity interest in Intravascular Imaging Inc. and DurVena; and his employer, Massachusetts General Hospital, has licensing arrangements with Terumo, Canon, and Spectrawave for which he has the right to receive royalties. Dr. Davies: speaking honoraria from Abiomed, Asahi Intec, Boston Sci, Medtronic, Shockwave and Teleflex. She also serves on advisory boards for Abiomed, Avinger, Boston Sci, Medtronic and Rampart. Dr. Patel has received consulting honoraria from Abbott, Medtronic, Terumo, and Cardiovascular Systems. Dr. Sandoval: consulting/speaker honoraria from Abbott Diagnostics, Roche Diagnostics, Zoll, Philips. JACC Advances associate editor. Patent 20,210,401,347. Dr. Burke: consulting and received speaker honoraria from Abbott Vascular and Boston Scientific. Dr. Brilakis: consulting/speaker honoraria from Abbott Vascular, American Heart Association (associate editor Circulation), Biotronik, Boston Scientific, Cardiovascular Innovations Foundation (Board of Directors), CSI, Elsevier, GE Healthcare, IMDS, Medtronic, and Teleflex; research support: Boston Scientific, GE Healthcare; owner, Hippocrates LLC; shareholder: MHI Ventures, Cleerly Health, Stallion Medical., (Copyright © 2024. Published by Elsevier B.V.)
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- 2024
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44. Development of a Novel Score to Predict Urgent Mechanical Circulatory Support in Chronic Total Occlusion Percutaneous Coronary Intervention.
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Karacsonyi J, Stanberry L, Simsek B, Kostantinis S, Allana SS, Rempakos A, Okeson B, Alaswad K, Basir MB, Jaffer F, Poommipanit P, Khatri J, Patel M, Mahmud E, Sheikh A, Wollmuth JR, Yeh RW, Chandwaney RH, ElGuindy AM, Abi Rafeh N, Schimmel DR, Benzuly K, Burke MN, Rangan BV, Mastrodemos OC, Sandoval Y, Ungi I, and Brilakis ES
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- Humans, Risk Factors, Treatment Outcome, Prospective Studies, Stroke Volume, Chronic Disease, Ventricular Function, Left, Registries, Coronary Angiography methods, Percutaneous Coronary Intervention, Coronary Occlusion diagnosis, Coronary Occlusion surgery
- Abstract
Estimating the likelihood of urgent mechanical circulatory support (MCS) can facilitate procedural planning and clinical decision-making in chronic total occlusion (CTO) percutaneous coronary intervention (PCI). We analyzed 2,784 CTO PCIs performed between 2012 and 2021 at 12 centers. The variable importance was estimated by a bootstrap applying a random forest algorithm to a propensity-matched sample (a ratio of 1:5 matching cases with controls on center). The identified variables were used to predict the risk of urgent MCS. The performance of the risk model was assessed in-sample and on 2,411 out-of-sample procedures that did not require urgent MCS. Urgent MCS was used in 62 (2.2%) of cases. Patients who required urgent MCS were older (70 [63 to 77] vs 66 [58 to 73] years, p = 0.003) compared with those who did not require urgent MCS. Technical (68% vs 87%, p <0.001) and procedural success (40% vs 85%, p <0.001) was lower in the urgent MCS group compared with cases that did not require urgent MCS. The risk model for urgent MCS use included retrograde crossing strategy, left ventricular ejection fraction, and lesion length. The resulting model demonstrated good calibration and discriminatory capacity with the area under the curve (95% confidence interval) of 0.79 (0.73 to 0.86) and specificity and sensitivity of 86% and 52%, respectively. In the out-of-sample set, the specificity of the model was 87%. The Prospective Global Registry for the Study of Chronic Total Occlusion Intervention CTO MCS score can help estimate the risk of urgent MCS use during CTO PCI., Competing Interests: Declaration of Competing Interest Dr. Alaswad: consultant and speaker for Boston Scientific, Abbott Cardiovascular, Teleflex, and CSI Dr. Jaffer: sponsored research from Canon U.S.A., Siemens, Shockwave, Teleflex; Institutional grants: Abbott vascular, Boston Scientific, CSI, Philips, Asahi Intecc, and Biotronik; Consultant for Boston Scientific, Siemens, Biotronik, Magenta Medical, IMDS, and Asahi Intecc; Equity interest, Intravascular Imaging Inc.; DurVena; Massachusetts General Hospital has a patent licensing arrangement with Terumo, Canon U.S.A., and Spectrawave; FAJ has the right to receive royalties. Dr. Poommipanit: Asahi Intecc, Inc., Abbott, Vascular-Consultant. Dr. Khatri: received honoraria from Asahi Intecc; and is a speaker and proctor for Abbott Vascular. Dr. Patel: member of the Speakers Bureau for AstraZeneca. Dr. Yeh: grants and personal fees from Abbott Vascular, AstraZeneca, Medtronic, and Boston Scientific. Dr. ElGuindy: received consultancy and proctorship fees from Medtronic, Asahi Intecc, Boston Scientific, and Terumo. Dr. Abi-Rafeh: proctor and speaker honoraria from Boston Scientific and Abbott Vascular. Dr. Brilakis: consulting/speaker honoraria from Abbott Vascular, American Heart Association (associate editor Circulation), Amgen, Asahi Intecc, Biotronik, Boston Scientific, Cardiovascular Innovations Foundation (Board of Directors), CSI, Elsevier, GE Healthcare, IMDS, Medicure, Medtronic, Siemens, and Teleflex; research support: Boston Scientific, GE Healthcare; owner, Hippocrates LLC; shareholder: MHI Ventures, Cleerly Health, Stallion Medical. All other authors: Nothing to disclose., (Copyright © 2023 Elsevier Inc. All rights reserved.)
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- 2023
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45. Intravascular Lithotripsy for the Treatment of Severely Calcified Coronary Artery Disease: A DISRUPT CAD III Intravascular Ultrasound Substudy.
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Bhogal S, Garcia-Garcia HM, Klein A, Benzuly K, Mangalmurti S, Moses J, Alaswad K, Jaffer F, Yong C, Nanjundappa A, Ben-Dor I, Mintz GS, Hashim H, and Waksman R
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- Humans, Constriction, Pathologic, Calcium, Treatment Outcome, Prospective Studies, Ultrasonography, Interventional, Coronary Artery Disease diagnostic imaging, Coronary Artery Disease therapy, Vascular Calcification diagnostic imaging, Vascular Calcification therapy, Lithotripsy adverse effects
- Abstract
Background: Coronary intravascular lithotripsy (IVL) has emerged as a novel technique for the treatment of severely calcified coronary lesions. We evaluated the mechanism and efficacy of IVL in facilitating optimal stent implantation in heavily calcified coronary lesions using intravascular ultrasound (IVUS)., Methods: Forty-six patients were initially enrolled as a part of the Disrupt CAD III study. Of these, 33 had pre-IVL, 24 had post-IVL, and 44 had post-stent IVUS evaluation. The final analysis was performed on 18 patients who had IVUS images interpretable at all three intervals. The primary endpoint was increase in minimum lumen area (MLA) from pre-IVL to post-IVL treatment to post-stenting., Results: Pre-IVL, MLA was 2.75 ± 0.84 mm
2 , percent area stenosis was 67.22 % ± 20.95 % with maximum calcium angle of 266.90° ± 78.30°, confirming severely calcified lesions. After IVL, MLA increased to 4.06 ± 1.41 mm2 (p = 0.0003), percent area stenosis decreased to 54.80 % ± 25.71 % (p = 0.0009), and maximum calcium angle decreased to 239.40° ± 76.73° (p = 0.003). There was a further increase in MLA to 6.84 ± 2.18 mm2 (p < 0.0001) and decrease in percent area stenosis to 30.33 % ± 35.08 % (p < 0.0001) post-stenting with minimum stent area of 6.99 ± 2.14 mm2 . The success rate of stent delivery, implantation, and post-stent dilation was 100 % post-IVL., Conclusion: In this first study evaluating the mechanism of IVL using IVUS, the primary endpoint of increase in MLA from pre-IVL to post-IVL treatment to post-stenting was successfully achieved. Our study showed that the use of IVL-assisted percutaneous coronary intervention is associated with improved vessel compliance, facilitating optimal stent implantation in de novo severely calcified lesions., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: All others have no conflicts of interest to declare., (Copyright © 2023 Elsevier Inc. All rights reserved.)- Published
- 2023
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46. Use of Mechanical Circulatory Support in Chronic Total Occlusion Percutaneous Coronary Intervention.
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Karacsonyi J, Deffenbacher K, Benzuly KH, Flaherty JD, Alaswad K, Basir M, Megaly MS, Jaffer F, Doshi D, Poommipanit P, Khatri J, Patel M, Riley R, Sheikh A, Wollmuth JR, Korngold E, Uretsky BF, Yeh RW, Chandwaney RH, Elguindy AM, Tammam K, AbiRafeh N, Schmidt CW, Okeson B, Kostantinis S, Simsek B, Rangan BV, Brilakis ES, and Schimmel DR
- Subjects
- Humans, Middle Aged, Aged, Treatment Outcome, Risk Factors, Stroke Volume, Ventricular Function, Left, Registries, Coronary Angiography, Chronic Disease, Percutaneous Coronary Intervention adverse effects, Coronary Occlusion diagnosis, Coronary Occlusion surgery, Coronary Occlusion etiology
- Abstract
The use of mechanical circulatory support (MCS) in chronic total occlusion (CTO) percutaneous coronary intervention (PCI) has received limited study. We analyzed the clinical and angiographic characteristics, and procedural outcomes of 7,171 CTO PCIs performed between 2012 and 2021 at 35 international centers. Mean age was 64.5 ± 10 years, mean left ventricular ejection fraction was 50 ± 13%. MCS was used in 4.5%, prophylactically in 78.7%, and urgently in 21.3%. The most common type of MCS overall was Impella CP (Abiomed) (55.5%), followed by intra-aortic balloon pump (14.8%) and TandemHeart (LivaNova Inc.) (10.0%). Prophylactic MCS patients were more likely to have diabetes mellitus (55% vs 42%, p <0.001) and had more complex lesions compared with cases without prophylactic MCS (Japan-CTO score: 2.80 ± 1.22 vs 2.39 ± 1.27, p <0.001). Cases with prophylactic MCS had similar technical (86% vs 87%, p = 0.643) but lower procedural (80% vs 86%, p = 0.028) success rates and higher rates of periprocedural major cardiac adverse events compared with no prophylactic MCS use (6.55% vs 1.68%, p <0.001). Urgent MCS use was associated with lower technical (68% vs 87%, p <0.001) and procedural (39% vs 86%, p <0.001) success rates and higher major cardiac adverse events compared with no-MCS use (32.26% vs 1.68%, p <0.001). The differences persisted in multivariable analyses. In summary, in this contemporary multicenter registry, MCS was used in 4.5% of CTO PCIs, mostly prophylactically (78.7%). Elective MCS cases had similar technical success but a higher risk of complications. Urgent MCS cases had lower technical and procedural success and higher periprocedural major complication rates., (Copyright © 2022 Elsevier Inc. All rights reserved.)
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- 2023
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47. Use of the Limited Antegrade Subintimal Tracking Technique in Chronic Total Occlusion Percutaneous Coronary Intervention.
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Karacsonyi J, Kostantinis S, Simsek B, Alaswad K, Karmpaliotis D, Kirtane A, Jaffer F, Choi JW, Koutouzis M, Tsiafoutis I, Kandzari DE, Poommipanit P, Khatri JJ, Elbarouni B, Gorgulu S, ElGuindy A, Abi Rafeh N, Goktekin O, Ungi I, Rangan BV, Sandoval Y, Allana S, Burke MN, and Brilakis ES
- Subjects
- Male, Humans, Middle Aged, Aged, Female, Prospective Studies, Treatment Outcome, Registries, Percutaneous Coronary Intervention adverse effects, Percutaneous Coronary Intervention methods, Coronary Occlusion diagnostic imaging, Coronary Occlusion therapy, Coronary Occlusion etiology
- Abstract
Background: There are limited data on the limited antegrade subintimal tracking (LAST) technique for chronic total occlusion (CTO) percutaneous coronary intervention (PCI)., Objectives: The aim of this study was to analyze the frequency of use and outcomes of the LAST technique for CTO PCI., Methods: We analyzed 2,177 CTO PCIs performed using antegrade dissection and re-entry (ADR) in the PROGRESS-CTO (Prospective Global Registry for the Study of Chronic Total Occlusion Intervention) registry between 2012 and January 2022 at 39 centers. ADR was attempted in 1,465 cases (67.3%)., Results: Among antegrade re-entry cases, LAST was used in 163 (11.1%) (primary LAST in 127 [8.7%] and secondary LAST [LAST after other ADR approaches failed] in 36 [2.5%]), the Stingray system (Boston Scientific) in 980 (66.9%), subintimal tracking and re-entry in 387 (26.4%), and contrast-guided subintimal tracking and re-entry in 29 (2.0%). The mean patient age was 65.2 ± 10 years, and 85.8% were men. There was no significant difference in technical (71.8% vs 77.8%; P = 0.080) and procedural (69.9% vs 75.3%; P = 0.127) success and major cardiac adverse events (1.84% vs 3.53%; P = 0.254) between LAST and non-LAST cases. However, on multivariable analysis, the use of LAST was associated with lower procedural success (OR: 0.61; 95% CI: 0.41-0.91). Primary LAST was associated with higher technical (76.4% vs 55.6%; P = 0.014) and procedural (75.6% vs 50.0%; P = 0.003) success and similar major adverse cardiac event (1.57% vs 2.78%; P = 0.636) rates compared with secondary LAST., Conclusions: LAST was used in 11.1% of antegrade re-entry CTO PCI cases and was associated with lower procedural success on multivariable analysis, suggesting a limited role of LAST in contemporary CTO PCI., Competing Interests: Funding Support and Author Disclosures This work was supported by many philanthropy partners, including our anonymous donors, Drs Mary Ann and Donald A. Sens, Ms Dianne and Dr Cline Hickok, Ms Charlotte and Mr Jerry Golinvaux Family Fund, the Roehl Family Foundation, and the Joseph Durda Foundation, and Ms Wilma and Mr Dale Johnson. Dr Alaswad is a consultant and speaker for Boston Scientific, Abbott Cardiovascular, Teleflex, and Cardiovascular Systems, Inc. Dr Karmpaliotis has received honoraria from Abbott Vascular and Boston Scientific; and has equity in Saranas, Soundbite, and Traverse Vascular. Dr Kirtane is a consultant for Interventional Medical Device Solutions; and has received travel expenses/meals from Medtronic, Boston Scientific, Abbott Vascular, Abiomed, Cardiovascular Systems, Inc, Siemens, Philips, ReCor Medical, Chiesi, OpSens, Zoll, and Regeneron. Dr Jaffer has received sponsored research support from Canon, Siemens, Teleflex, Shockwave, Amarin, Mercator, Boston Scientific, and HeartFlow; is a consultant/speaker for Boston Scientific, Biotronik, Siemens, Magenta Medical, Interventional Medical Device Solutions, and Philips; and holds equity in Intravascular Imaging, Inc and DurVena, Inc. Massachusetts General Hospital has a patent licensing arrangement with Terumo, Canon, and Spectrawave. Dr Kandzari has received institutional research/grant support from Abbott Vascular, Biotronik, Boston Scientific, Cardiovascular Systems, Inc, Medtronic, Orbus Neich, and Teleflex; and has received personal consulting honoraria from Biotronik, Cardiovascular Systems, Inc, and Medtronic. Dr Poommipanit is a consultant for Asahi Intecc, Abbott, and Vascular-Consultant. Dr Khatri received honoraria from Asahi Intecc; and is a speaker and proctor for Abbott Vascular. Dr ElGuindy has received consultancy and proctorship fees from Medtronic, Asahi Intecc, Boston Scientific, and Terumo. Dr Abi Rafeh is a speaker for Boston scientific and Shockwave Medical. Dr Burke is a shareholder in Egg Medical and MHI Ventures. Dr Brilakis has received consulting/speaker honoraria from Abbott Vascular, American Heart Association (associate editor Circulation), Amgen, Asahi Intecc, Biotronik, Boston Scientific, Cardiovascular Innovations Foundation (Board of Directors), Cardiovascular Systems, Inc, Elsevier, GE Healthcare, Interventional Medical Device Solutions, Medicure, Medtronic, Siemens, and Teleflex; provides research support for Boston Scientific and GE Healthcare; is an owner of Hippocrates LLC; and is a shareholder in MHI Ventures, Cleerly Health, and Stallion Medical. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose., (Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)
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- 2022
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48. Primary vs Secondary Retrograde Approach in Chronic Total Occlusion Percutaneous Coronary Interventions.
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Kostantinis S, Alaswad K, Karmpaliotis D, Jaffer F, Jaber W, Nicholson W, Rinfret S, Khatri J, Poommipanit P, Karacsonyi J, Simsek B, Vemmou E, Nikolakopoulos I, Koutouzis M, Tsiafoutis I, Riley R, Sheikh A, Patel M, Gorgulu S, ElGuindy AM, Goktekin O, Abi Rafeh N, Rangan BV, Garcia S, Burke MN, and Brilakis ES
- Subjects
- Chronic Disease, Coronary Angiography methods, Humans, Registries, Risk Factors, Stroke Volume, Treatment Outcome, Ventricular Function, Left, Coronary Occlusion diagnosis, Coronary Occlusion etiology, Coronary Occlusion surgery, Percutaneous Coronary Intervention adverse effects, Percutaneous Coronary Intervention methods
- Abstract
Background: The retrograde approach to coronary chronic total occlusions (CTOs) can be used as the initial crossing strategy (primary retrograde) or after failure of antegrade crossing attempts (secondary retrograde)., Methods: We compared baseline clinical and angiographic characteristics and procedural outcomes of primary vs secondary retrograde crossing for CTO percutaneous coronary intervention (PCI) among 2789 procedures performed at 34 centers between 2012 and 2021., Results: Retrograde CTO-PCI was performed as the primary crossing strategy in 1086 cases (38.9%) and as a secondary approach in 1703 cases (61.1%). Patients in the primary group had slightly lower left ventricular ejection fraction (49.1% vs 50.4%; P=.02), were more likely to have had prior coronary artery bypass graft surgery (52.9% vs 38.4%; P<.001), and had higher J-CTO (3.31 ± 0.98 vs 2.99 ± 1.09; P<.001) and PROGRESS-CTO scores (1.47 ± 0.92 vs 1.29 ± 0.99; P<.001). Technical (81.4% vs 77.3%; P=.01) and procedural success rates (78.6% vs 74.1%; P<.01) were higher in the primary retrograde group, with no difference between in-hospital major adverse event rates (4.3% vs 4.0%; P=.66). Contrast volume (250 mL [interquartile range (IQR), 176-347] vs 270 mL [IQR, 190-367]; P<.001) and procedure time (175 minutes [IQR, 127-233] vs 180 minutes [IQR, 142-236]; P<.001) were lower in the primary group., Conclusions: Use of retrograde approach as the primary crossing strategy is associated with higher rates of technical and procedural success and similar rates of in-hospital major adverse cardiac events compared with secondary retrograde CTO-PCI.
- Published
- 2022
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49. The 2021 AHA/ACC Guideline for the Evaluation and Diagnosis of Chest Pain: An Interventionalist's Viewpoint.
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Riley RF, Batchelor WB, Goldstein JA, Al-Lamee R, Shah S, Tremmel JA, Jaffer F, and Henry TD
- Abstract
Competing Interests: Dr Robert F. Riley provides consultation for Boston Scientific, Abbott Vascular, Medtronic, and Shockwave Medical. Dr Farouc Jaffer is a speaker in Boston Scientific and provides consultation for Boston Scientific and Siemens Healthineers. Dr Jennifer Tremmel provides consultation for Boston Scientific and Abbott Vascular, is an advisory board member in Boston Scientific and Abbott Vascular, and reports research support from 10.13039/100008497Boston Scientific. The other authors have no conflicts to report.
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- 2022
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50. Outcomes of retrograde chronic total occlusion percutaneous coronary intervention: A report from the OPEN-CTO registry.
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Kalra S, Doshi D, Sapontis J, Kosmidou I, Kirtane AJ, Moses JW, Riley RF, Jones P, Nicholson WJ, Salisbury AC, Lombardi WL, McCabe JM, Pershad A, Hirai T, Hakemi E, Russo JJ, Prasad M, Ahmad Y, Hatem R, Gkargkoulas F, Spertus JA, Wyman RM, Jaffer F, Spaedy A, Cook S, Marso SP, Nugent K, Federici R, Yeh RW, Leon MB, Stone GW, Ali ZA, Parikh MA, Maehara A, Cohen DJ, Batres C, Grantham JA, and Karmpaliotis D
- Subjects
- Aftercare, Humans, Patient Discharge, Quality of Life, Registries, Treatment Outcome, Coronary Occlusion diagnostic imaging, Coronary Occlusion surgery, Percutaneous Coronary Intervention adverse effects
- Abstract
Objectives: We sought to assess in-hospital and long-term outcomes of retrograde compared with antegrade-only percutaneous coronary intervention for chronic total occlusion (CTO PCI)., Background: Procedural and clinical outcomes following retrograde compared with antegrade-only CTO PCI remain unknown., Methods: Using the core-lab adjudicated OPEN-CTO registry, we compared the outcomes of retrograde to antegrade-only CTO PCI. Primary endpoints included were in-hospital major adverse cardiac and cerebrovascular events (MACCE) (all-cause death, stroke, myocardial infarction [MI], emergency cardiac surgery, or clinically significant perforation) and MACCE at 1-year (all-cause death, MI, stroke, target lesion revascularization, or target vessel reocclusion)., Results: Among 885 single CTO procedures from the OPEN-CTO registry, 454 were retrograde and 431 were antegrade-only. Lesion complexity was higher (J-CTO score: 2.7 vs. 1.9; p < .001) and technical success lower (82.4 vs. 94.2%; p < .001) in retrograde compared with antegrade-only procedures. All-cause death was higher in the retrograde group in-hospital (2 vs. 0%; p = .003), but not at 1-year (4.9 vs. 3.3%; p = .29). Compared with antegrade-only procedures, in-hospital MACCE rates (composite of all-cause death, stroke, MI, emergency cardiac surgery, and clinically significant perforation) were higher in the retrograde group (10.8 vs. 3.3%; p < .001) and at 1-year (19.5 vs. 13.9%; p = .03). In sensitivity analyses landmarked at discharge, there was no difference in MACCE rates at 1 year following retrograde versus antegrade-only CTO PCI. Improvements in Seattle Angina Questionnaire Quality of Life scores at 1-year were similar between the retrograde and antegrade-only groups (29.9 vs 30.4; p = .58)., Conclusions: In the OPEN-CTO registry, retrograde CTO procedures were associated with higher rates of in-hospital MACCE compared with antegrade-only; however, post-discharge outcomes, including quality of life improvements, were similar between technical modalities., (© 2020 Wiley Periodicals LLC.)
- Published
- 2021
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