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1.
Int J Cardiol ; 241: 326-329, 2017 Aug 15.
Article in English | MEDLINE | ID: mdl-28499667

ABSTRACT

BACKGROUND: Stanford acute type A aortic dissection (ATAAD) is a potentially lethal condition. Epidemiology studies show a statistical incidence in Europe of approximately 2-16 cases/100,000 inhabitants/year. In Germany, the estimated incidence (here subsumed under "thoracic aortic dissection" with 4.63 cases/100,000 inhabitants/year) is mainly extracted from medical death certificates by the German Federal Statistical Office. The prehospital incidence of ATAAD deaths is largely unknown. Since patients often die in the pre-hospital setting, the incidence of ATAAD is therefore likely to be higher than current estimates. MATERIAL AND METHODS: For the period from 2010 to 2014, we retrospectively analyzed all in-hospital ATAAD data from two of the largest cardiac surgical centers that treat ATAAD in the Berlin-Brandenburg region. In addition, autopsy reports of all forensic medicine institutes and of one large pathological provider in the region were analyzed to identify additional non-hospitalized ATAAD patients. Based on these findings, the regional incidence of ATAAD was calculated. RESULTS: In addition to in-hospital ATAAD patients (n=405), we identified additional 145 lethal ATAAD cases among 14,201 autopsy reports. The total of 550 ATAAD cases led to an estimated incidence of 11.9 cases/100,000 inhabitants/year for the whole Berlin-Brandenburg region. Arterial hypertension, pre-existing aortic dilatation, and hereditary connective tissue disorder were found in, respectively, 62.7%, 10%, and 1.8% of patients. CONCLUSION: ATAAD is more frequent than previously reported. Our results show that when patients who die outside of cardiac surgery centers are included, the incidence of ATAAD significantly exceeds the rate reported by the Federal Statistical Office.


Subject(s)
Aorta/pathology , Aortic Aneurysm/epidemiology , Aortic Aneurysm/pathology , Aortic Dissection/epidemiology , Aortic Dissection/pathology , Adult , Aged , Aged, 80 and over , Aortic Dissection/mortality , Aortic Aneurysm/mortality , Berlin/epidemiology , Female , Germany/epidemiology , Hospitalization/trends , Humans , Incidence , Male , Middle Aged , Retrospective Studies
2.
Curr Cardiol Rev ; 9(4): 274-80, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24313644

ABSTRACT

During the past years transcatheter aortic valve implantation (TAVI) has evolved to a standard technique for the treatment of high risk patients suffering from severe aortic stenosis. Worldwide the number of TAVI procedures is increasing exponentially. In this context both the transapical antegrade (TA) and the transfemoral retrograde (TF) approach are predominantly used and can be considered as safe and reproducible access sites for TAVI interventions. As a new technology TAVI is in a constant progress regarding the development of new devices. While in the first years only the Edwards SAPIEN(TM) and the Medtronic CoreValve(TM) prostheses were commercial available, recently additional devices obtained CE-mark approval and others have entered initial clinical trials. In addition to enhance the treatment options in general, the main driving factor to further develop new device iterations is to solve the drawbacks of the current TAVI systems: paravalvular leaks, occurrence of AV-blocks and the lack of full repositionability.


Subject(s)
Aortic Valve/surgery , Cardiac Catheterization/methods , Heart Valve Prosthesis Implantation/methods , Heart Valve Prosthesis , Prosthesis Design , Aortic Valve Stenosis/etiology , Aortic Valve Stenosis/surgery , Aortic Valve Stenosis/therapy , Heart Valve Prosthesis Implantation/adverse effects , Heart Valve Prosthesis Implantation/instrumentation , Heart Valve Prosthesis Implantation/trends , Humans , Treatment Outcome
3.
Curr Cardiol Rev ; 2013 Dec 02.
Article in English | MEDLINE | ID: mdl-24313646

ABSTRACT

During the past years TAVI has evolved to a standard technique for the treatment of high risk patients suffering from severe aortic stenosis. Worldwide the number of TAVI procedures is increasing exponentially. In this context both the transapical antegrade (TA) and the transfemoral retrograde (TF) approach are predominantly used and can be considered as safe and reproducible access sites for TAVI interventions. As a new technology TAVI is in a constant progress regarding the development of new devices. While in the first years only the Edwards SAPIEN™ and the Medtronic CoreValve™ prostheses were commercial available, recently additional devices obtained CE-mark approval and others have entered initial clinical trials. In addition to enhance the treatment options in general, the main driving factor to further develop new device iterations is to solve the drawbacks of the current TAVI systems: paravalvular leaks, occurrence of AV-blocks and the lack of full repositionability.

4.
Herz ; 38(5): 513-26; quiz 527-8, 2013 Aug.
Article in German | MEDLINE | ID: mdl-23897600

ABSTRACT

Coronary artery disease (CAD) is a leading cause of morbidity and mortality in western countries and is of significant socio-economic importance due to its increasing prevalence. Until percutaneous coronary interventions (PCI) were established, CAD could only be treated by surgical revascularization or pharmacological therapy. In-stent restenosis remains a major problem after stent implantation. However, the use of new materials and stent coatings have led to a significant reduction in in-stent restenosis. Thus, surgical revascularization and PCI are currently of equal value for the treatment of CAD. The decision-making for PCI or surgical revascularization depends on various factors such as number of diseased vessels, complexity of the coronary stenoses, concomitant diseases, and the patient's general condition. The therapeutic regime of every patient should be adjusted to the recommendations of the European and German Society for Cardiology, while controversial and complex cases should be discussed in an interdisciplinary case conference ("heart team").


Subject(s)
Blood Vessel Prosthesis/adverse effects , Coronary Artery Disease/surgery , Graft Occlusion, Vascular/etiology , Graft Occlusion, Vascular/prevention & control , Percutaneous Coronary Intervention/adverse effects , Percutaneous Coronary Intervention/methods , Stents/adverse effects , Coronary Artery Disease/complications , Humans , Treatment Outcome
6.
Herz ; 38(2): 112-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23471357

ABSTRACT

Conventional aortic valve replacement is the standard approach for treating aortic stenosis, it is performed via a full or partial sternotomy, and is associated with low risks for patients and with excellent long-term outcomes. This also holds true for octogenarians, if they present without relevant comorbidities. After resection of the calcified native leaflets, biological prostheses with good functionality and durability are implanted. Elderly patients with an increasing risk profile, however, should be treated by a heart team using transcatheter approaches including cardiac surgery.


Subject(s)
Aortic Valve Stenosis/surgery , Forecasting , Heart Valve Prosthesis Implantation/methods , Heart Valve Prosthesis Implantation/trends , Heart Valve Prosthesis/trends , Aged , Aged, 80 and over , Heart Valve Prosthesis Implantation/instrumentation , Humans , Risk Assessment
7.
Internist (Berl) ; 54(1): 28-34, 36-8, 2013 Jan.
Article in German | MEDLINE | ID: mdl-23263747

ABSTRACT

Due to increasing life expectancy in the coming decades the number of elderly patients with aortic valve stenosis (AS) and various concomitant diseases will increase. Conventional surgical aortic valve replacement represents the treatment of choice in patients with severe and symptomatic AS. Transfemoral and transapical aortic valve implantation (T-AVI) has evolved as a standard procedure for patients with severe AS who are technically inoperable or at very high risk for surgical valve replacement. The T-AVI approach has been shown to be superior to the standard medical treatment in these high-risk patients. All patients to be considered for T-AVI should be discussed in a consensus conference consisting of cardiac surgeons and cardiologists (heart team).


Subject(s)
Aortic Valve Stenosis/diagnosis , Aortic Valve Stenosis/surgery , Aortic Valve/surgery , Heart Valve Prosthesis Implantation/instrumentation , Heart Valve Prosthesis Implantation/methods , Heart Valve Prosthesis , Humans , Prosthesis Design
9.
Internist (Berl) ; 53(9): 1063-75; quiz 1076-8, 2012 Sep.
Article in German | MEDLINE | ID: mdl-22836917

ABSTRACT

Coronary artery disease (CAD) is a leading cause of morbidity and mortality in western countries and is of significant socio-economic importance due to its increasing prevalence. Until percutaneous coronary interventions (PCI) were established, CAD could only be treated by surgical revascularization or pharmacological therapy. In-stent restenosis remains a major problem after stent implantation. However, the use of new materials and stent coatings have led to a significant reduction in in-stent restenosis. Thus, surgical revascularization and PCI are currently of equal value for the treatment of CAD. The decision-making for PCI or surgical revascularization depends on various factors such as number of diseased vessels, complexity of the coronary stenoses, concomitant diseases, and the patient's general condition. The therapeutic regime of every patient should be adjusted to the recommendations of the European and German Society for Cardiology, while controversial and complex cases should be discussed in an interdisciplinary case conference ("heart team").


Subject(s)
Coronary Artery Disease/complications , Coronary Artery Disease/surgery , Myocardial Revascularization/adverse effects , Myocardial Revascularization/methods , Humans , Treatment Outcome
11.
Thorac Cardiovasc Surg ; 60(1): 70-7, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21789760

ABSTRACT

BACKGROUND: Epicardial left ventricular (LV) leads represent an alternative for CRT therapy if transvenous lead implantation fails. Data on endurance, performance, the impact of the surgical approach (lateral minithoracotomy vs. median sternotomy simultaneously with other cardiac surgery), and the optimal technical concept (screw-in vs. suture-on) is limited. METHODS: Over a period of 48 months we evaluated 130 consecutive patients with comparable characteristics. A total of 54 screw-in (MyoDex™ 1084T, SJM) and 76 suture-on (Capture Epi 4968, Medtronic) bipolar epicardial steroid-eluting LV leads were implanted either via a left lateral or a median thoracotomy. Sensing, pacing threshold, impedance and NYHA class were recorded at defined time points. RESULTS: No surgery-related death or major complication was observed. At the time of implantation, the pacing threshold, sensing and NYHA class did not differ significantly between the two groups. The impedances of screw-in leads were significantly lower compared to those of suture-on leads. Suture-on leads showed a moderate initial drop in their pacing threshold but afterwards remained stable. Screw-in leads were characterized by a moderate but significant increase in the pacing threshold in the first year followed by a continuous decrease thereafter. Twenty-four months post-implantation no differences between both lead types could be detected. Sensing and NYHA class improved in both groups. The surgical approach had no significant impact on lead functionality. CONCLUSION: Our study showed that the implantation of epicardial leads was safe with very low complication rates. There was no superior technical epicardial lead concept (screw-in vs. suture-on leads) and all epicardial leads demonstrated an excellent long-term performance and durability. Therefore, it seems that epicardial leads represent a good alternative to transvenous leads and surgeons should be encouraged to implant epicardial leads during concomitant cardiac surgery when the indications for CRT are present.


Subject(s)
Cardiac Resynchronization Therapy Devices , Cardiac Resynchronization Therapy , Heart Failure/therapy , Ventricular Function, Left , Aged , Cardiac Resynchronization Therapy/adverse effects , Cardiac Resynchronization Therapy/mortality , Cardiac Surgical Procedures , Equipment Design , Female , Germany , Heart Failure/physiopathology , Humans , Male , Middle Aged , Recovery of Function , Retrospective Studies , Sternotomy , Suture Techniques , Thoracotomy , Time Factors , Treatment Outcome
12.
Pharmacology ; 88(3-4): 167-73, 2011.
Article in English | MEDLINE | ID: mdl-21952163

ABSTRACT

BACKGROUND/AIMS: Mitochondrial permeability transition pore (MPTP) opening appears to play a key role in myocardial cell survival after ischemia-reperfusion injury and can be inhibited by cyclosporin A (CsA). We investigated whether low-dose CsA added to histidine-tryptophan-ketoglutarate (HTK) cardioplegia solution could improve myocardial protection during longer periods of global myocardial ischemia as encountered during cardiac surgery. METHODS: Rabbit hearts perfused on a Langendorff apparatus were arrested with cold HTK solution containing 1 µmol/l CsA. After 90 min of ischemia, the hearts were reperfused and pmax, max dp/dt, min dp/dt, myocardial stiffness, pO(2), coronary flow and heart rate recorded. Tissue ATP and malondialdehyde (MDA) were measured to assess cell energy content and oxidative stress, respectively. RESULTS: CsA-treated hearts recovered pmax (p = 0.026), max dp/dt (p = 0.028) and min dp/dt (p = 0.025) more quickly and to a greater extent than non-treated hearts. They required markedly less oxygen (p = 0.041) in the first 10 min of reperfusion. Hearts treated with CsA produced 44% less MDA (1.09 vs. 1.93, p = 0.008), while ATP levels were unchanged. CONCLUSIONS: HTK cardioplegia solution containing CsA at a dose well below that expected to cause systemic immunosuppressive effects leads to a significant and timelier recovery of myocardial contractility, while consuming less oxygen.


Subject(s)
Cardioplegic Solutions/pharmacology , Cardiotonic Agents/pharmacology , Cyclosporine/pharmacology , Immunosuppressive Agents/pharmacology , Myocardial Reperfusion Injury/prevention & control , Adenosine Triphosphate/metabolism , Animals , Glucose/pharmacology , Heart/drug effects , Heart/physiopathology , Male , Malondialdehyde/metabolism , Mannitol/pharmacology , Oxygen/metabolism , Potassium Chloride/pharmacology , Procaine/pharmacology , Rabbits , Ventricular Pressure/drug effects
13.
Thorac Cardiovasc Surg ; 59(8): 503-6, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21509721

ABSTRACT

In recent years, catheter-based aortic valve interventions have become established procedures for the treatment of high-risk and advanced age patients with aortic valve pathologies. One of the limitations of the widespread applicability of this procedure is the annulus size. Until recently, no prosthesis was available to treat patients with a large annulus. We report on a patient with high-grade aortic stenosis (AS) and a 27-mm annulus, who underwent transapical implantation (TAP) of an Edwards SAPIEN® 29-mm prosthesis (Edwards LifeScience, Irvine, CA, USA). Due to insufficient dilation of his heavily calcified, functionally bicuspid aortic valve leaflets during balloon aortic valvuloplasty (BAV), the TAP prosthesis did not anchor adequately. This was determined during follow-up as he developed progressive aortic insufficiency and orthopnea, and an echocardiography revealed that the valve had been displaced into the LVOT. A conventional aortic valve replacement and ascending aorta replacement were performed, at which time the TAP prosthesis was removed. The patient recovered uneventfully, and was discharged with a well-functioning aortic bioprosthetic valve and in good general condition.


Subject(s)
Aorta/surgery , Aortic Aneurysm/surgery , Aortic Valve Insufficiency/surgery , Aortic Valve Stenosis/surgery , Aortic Valve/surgery , Heart Valve Prosthesis Implantation/adverse effects , Aged, 80 and over , Aortic Valve Insufficiency/etiology , Dyspnea/etiology , Follow-Up Studies , Humans , Male , Prosthesis Design , Prosthesis Failure , Reoperation , Treatment Outcome
14.
Anaesth Intensive Care ; 38(2): 376-80, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20369777

ABSTRACT

We describe the transcranial Doppler pattern during a period of cardiopulmonary resuscitation in a patient undergoing a transcatheter off-pump aortic valve implantation. Transcranial Doppler of the middle cerebral artery flow was measured as a part of a separate ongoing study. The patient developed a cardiac arrest during deployment of the valve prosthesis. The incidental presence of the transcranial Doppler allowed us to assess middle cerebral artery flow during cardiopulmonary resuscitation in real time. An initial lack of a diastolic flow pattern seen with transcranial Doppler at the beginning of cardiopulmonary resuscitation led to volume loading and optimisation of the resuscitation technique. After increasing the depth of external cardiac massage, the cerebral flow pattern improved to produce sufficient diastolic flow. The transcranial Doppler provided additional information during cardiopulmonary resuscitation, which was helpful in clinical management. The use of transcranial Doppler may be helpful for other cardiac procedures where cerebral malperfusion may occur.


Subject(s)
Cardiopulmonary Resuscitation , Cerebrovascular Circulation , Ultrasonography, Doppler, Transcranial , Aged , Aged, 80 and over , Aortic Valve/surgery , Female , Humans , Monitoring, Physiologic
16.
Eur J Clin Invest ; 39(9): 769-74, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19674078

ABSTRACT

BACKGROUND: Aspirin therapy is known to substantially reduce mortality and the rate of ischaemic complications after coronary artery bypass grafting (CABG). Rates of perioperative aspirin resistance cited in the literature are up to 50% and could be influenced by extracorporeal circulation. Thus, aspirin resistance after CABG may have a significant clinical relevance. MATERIALS AND METHODS: In 59 patients undergoing CABG (on-pump, off-pump and combined procedures) aspirin resistance was investigated by arachidonic acid induced platelet aggregometry. Clinical relevance was assessed with 12-month follow up. RESULTS: Two types of resistance were observed: A preoperative resistance (despite oral aspirin or in vitro addition) was present in 29% and a postoperative developing type was seen in 49% resulting in only 22% of patients with a 'normal' reaction to aspirin. If patients were already on oral aspirin at admission, the rate of resistance was significantly reduced. Off-pump surgery or pump-times exceeding 120 min had no significant impact on resistance. During the 12-month follow up (98.3%), there were three deaths (one stroke, one intestinal ischaemia, one mediastinitis after postoperative delirium) in patients with the perioperative resistance and none in other patients (P = 0.345). In none of those patients who presented with perioperative aspirin resistance, could this aspirin resistance be demonstrated when tested again after 12 months? CONCLUSIONS: Aspirin resistance is a transient phenomenon present in the majority of patients undergoing CABG. The three deaths in the resistant group may - although not statistically significant - indicate the possibility of a worse outcome for patients with aspirin resistance.


Subject(s)
Aspirin/pharmacology , Platelet Aggregation Inhibitors/pharmacology , Platelet Aggregation/drug effects , Aspirin/adverse effects , Coronary Artery Bypass/adverse effects , Coronary Artery Bypass/methods , Drug Administration Schedule , Drug Resistance/physiology , Female , Humans , In Vitro Techniques , Male , Platelet Aggregation/physiology , Platelet Aggregation Inhibitors/adverse effects , Platelet Function Tests , Postoperative Period , Preoperative Care/methods , Risk Assessment
17.
Comput Biol Med ; 37(10): 1384-93, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17240365

ABSTRACT

With the advent of off-pump coronary artery bypass grafting and minimally invasive coronary artery bypass grafting, significant efforts have been made to facilitate construction of the graft to coronary anastomosis. As a result, a number of anastomotic devices have been developed. While the ideal anastomotic device should be easy to use, to produce a geometrically optimal anastomosis with minimal endothelial damage and minimal blood-exposed non-intimal surface, a number of design constraints apply. This review collects the available pre-clinical and clinical data for some of the devices with special regard for surgical outcome, patency rate and the need for additional perioperative anticoagulation treatment.


Subject(s)
Anastomosis, Surgical/instrumentation , Coronary Artery Bypass/instrumentation , Animals , Coronary Artery Bypass, Off-Pump/instrumentation , Coronary Vessels/surgery , Equipment Design , Humans , Mammary Arteries/surgery , Minimally Invasive Surgical Procedures/instrumentation , Saphenous Vein/surgery , Surgical Instruments
18.
Thorac Cardiovasc Surg ; 54(1): 10-4, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16485182

ABSTRACT

OBJECTIVE: A chordally supported stentless mitral valve (SMV) may be a suitable prosthesis for patients with severe degenerative mitral valve disease. We analyzed the five-year results and compared them with results after conventional mitral valve repair or replacement. METHODS: 155 patients, operated on since August 1997, were evaluated. 53 patients (ages, 68 +/- 8 years, 37 female, valve repair not feasible) received a SMV (Quattro), 51 patients (69 +/- 9 years, 32 female) had mitral valve repair (MVR) and 51 patients (66 +/- 9 years, 32 female) had a conventional mitral valve replacement (MVP). There were no significant differences with respect to preoperative NYHA functional class, left ventricular ejection fraction, cardiac index and surgical risk, according to the EuroSCORE. Mean follow-up is 64 +/- 18 (21-89) months. RESULTS: Surgery was performed using a median sternotomy (32 [SMV]/20 [MVR]/34 [MVP]) or a lateral mini-thoracotomy 21/31/17 approach. The SMV was safely attached to the papillary muscles. In-hospital mortality was 1, 2 and 4 respectively; re-operation was required in 6, 2 and 3 patients. Five-year survival rate was 80.6 +/- 4.4 % (SMV), 80.2 +/- 5.6 % (CMV) and 82.6 +/- 5.6 % (MVP), p = n.s. After hospital discharge, there was no significant difference in mortality in comparison to an age-matched control population. Echocardiography revealed acceptable SMV hemodynamics with preservation of left ventricular function. CONCLUSION: Midterm results after SMV implantation are comparable to conventional approaches. Complete preservation of the annulo-ventricular continuity is advantageous and close to physiologic hemodynamics can be achieved. Long term follow-up is required.


Subject(s)
Heart Valve Prosthesis Implantation/methods , Mitral Valve Insufficiency/surgery , Mitral Valve Stenosis/surgery , Stents , Aged , Atrial Function, Left , Female , Follow-Up Studies , Hospital Mortality , Humans , Male , Middle Aged , Mitral Valve Insufficiency/physiopathology , Mitral Valve Stenosis/physiopathology , Prospective Studies , Reoperation , Stroke Volume , Survival Analysis , Treatment Outcome , Ventricular Function, Left
19.
Neuroreport ; 12(18): 3993-6, 2001 Dec 21.
Article in English | MEDLINE | ID: mdl-11742226

ABSTRACT

Nitric oxide (NO) is a key molecule in vascular headaches and the dura mater has been implicated as a tissue where vascular headache develops. Here we demonstrate expression, enzyme activity and cellular distribution of the intracellular receptor for NO, soluble guanylyl cyclase (sGC), in rat dura mater. Subcutaneous treatment of rats with the NO-donor glyceryl trinitrate (GTN) induced an increase of sGC expression and activity in dural blood vessels after 20-30 min. It has previously been shown that GTN induces headache in normal subjects after 20-30 min. Our findings suggest that an up-regulation of the NO target enzyme contributes to the pathogenesis of GTN-induced headache explaining the subacute rather than acute onset of symptoms.


Subject(s)
Dura Mater/drug effects , Dura Mater/enzymology , Guanylate Cyclase/metabolism , Nitroglycerin/pharmacology , Vasodilator Agents/pharmacology , Animals , Dura Mater/blood supply , Endothelium, Vascular/enzymology , Endothelium, Vascular/ultrastructure , Female , Guanylate Cyclase/analysis , Headache/metabolism , Male , Microscopy, Immunoelectron , Rats , Rats, Sprague-Dawley
20.
Biochem Biophys Res Commun ; 283(4): 883-7, 2001 May 18.
Article in English | MEDLINE | ID: mdl-11350067

ABSTRACT

Inhaled nitric oxide (NO) is known to influence the contractile state of pulmonary arteries most likely by activation of soluble guanylyl cyclase (sGC) in smooth muscle cells. However, the cellular distribution of sGC has not been determined empirically, due to a lack of specific antibodies. Here, we describe a novel antibody directed against the beta1 subunit of sGC to study the cellular distribution of sGC in lung during development. Using the novel antibody, the enzyme was demonstrated in fetal, neonatal, and adult lungs by Western blot, showing maximum expression in neonatal lung. These data were confirmed by measurements of sGC activity. In pulmonary arteries of fetal lung sGC-beta1 immunoreactivity was present in smooth muscle cells and absent in endothelial cells. With postnatal development an increase in immunoreactivity in endothelial cells and a reciprocal decrease in smooth muscle cells was apparent. The reported changes in sGC expression likely contribute to the known age-dependent differences in response to inhaled NO.


Subject(s)
Aging/metabolism , Guanylate Cyclase/metabolism , Nitric Oxide/metabolism , Pulmonary Artery/enzymology , Amino Acid Sequence , Animals , Antibody Specificity , Guanylate Cyclase/immunology , Immunohistochemistry , Molecular Sequence Data , Rats , Rats, Wistar
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