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1.
J Cardiothorac Surg ; 19(1): 306, 2024 May 31.
Article in English | MEDLINE | ID: mdl-38822410

ABSTRACT

Peripheral venous catheter fracture with cardiovascular embolization is a rare but potentially serious complication. Herein, we report a case of peripheral venous catheter fracture with embolization in right ventricle in a preterm infant. The catheter fragment was successfully removed by surgical procedure via median sternotomy under cardiopulmonary bypass(CPB).We hope this case will increase awareness of this rare complication and improve cannulation safety.


Subject(s)
Catheterization, Peripheral , Device Removal , Infant, Premature , Humans , Infant, Newborn , Catheterization, Peripheral/methods , Device Removal/methods , Male , Equipment Failure , Heart Ventricles/surgery , Female
2.
Europace ; 26(6)2024 Jun 03.
Article in English | MEDLINE | ID: mdl-38833618

ABSTRACT

AIMS: Debulking of infective mass to reduce the burden if infective material is a fundamental principle in the surgical management of infection. The aim of this study was to investigate the validity of this principle in patients undergoing transvenous lead extraction in the context of bloodstream infection (BSI). METHODS AND RESULTS: We performed an observational single-centre study on patients that underwent transvenous lead extraction due to a BSI, with or without lead-associated vegetations, in combination with a percutaneous aspiration system during the study period 2015-22. One hundred thirty-seven patients were included in the final analysis. In patients with an active BSI at the time of intervention, the use of a percutaneous aspiration system had a significant impact on survival (log-rank: P = 0.0082), while for patients with a suppressed BSI at the time of intervention, the use of a percutaneous aspiration system had no significant impact on survival (log-rank: P = 0.25). CONCLUSION: A reduction of the infective burden by percutaneous debulking of lead vegetations might improve survival in patients with an active BSI.


Subject(s)
Device Removal , Prosthesis-Related Infections , Humans , Female , Male , Device Removal/methods , Aged , Prosthesis-Related Infections/surgery , Prosthesis-Related Infections/microbiology , Prosthesis-Related Infections/diagnosis , Prosthesis-Related Infections/mortality , Middle Aged , Treatment Outcome , Defibrillators, Implantable/adverse effects , Suction , Pacemaker, Artificial/adverse effects , Pacemaker, Artificial/microbiology , Endocarditis, Bacterial/surgery , Endocarditis, Bacterial/microbiology , Endocarditis, Bacterial/diagnosis , Endocarditis, Bacterial/mortality , Endocarditis, Bacterial/etiology , Retrospective Studies , Time Factors , Risk Factors , Aged, 80 and over
3.
Vasc Health Risk Manag ; 20: 245-250, 2024.
Article in English | MEDLINE | ID: mdl-38859874

ABSTRACT

Guidewire loss is a rare complication of central venous catheterization. A 65-year-old male was hospitalized in a high-dependency unit for exacerbation of chronic obstructive pulmonary disease, pneumonia, erythrocytosis, and clinical signs of heart failure. Upon admission, after an unsuccessful right jugular approach, a left jugular central venous catheter was placed. The next day, chest radiography revealed the catheter located in the left parasternal region, with suspected retention of the guidewire, visually confirmed by the presence of its proximal end inside the catheter. The left parasternal location of the catheter and the typical projection of the guidewire in the coronary sinus, later confirmed by echocardiography, raised suspicion of a persistent left superior vena cava (PLSVC). Agitated saline injected into the left antecubital vein confirmed bubble entry from the coronary sinus into the right atrium. After clamping the guidewire, the catheter was carefully retrieved along with the guidewire without any complications. This is the first reported case of guidewire retention in PLSVC and coronary sinus. It underscores the potential causes of guidewire loss and advocates preventive measures to avoid this potentially fatal complication.


Subject(s)
Catheterization, Central Venous , Central Venous Catheters , Coronary Sinus , Device Removal , Persistent Left Superior Vena Cava , Humans , Male , Aged , Coronary Sinus/abnormalities , Coronary Sinus/diagnostic imaging , Catheterization, Central Venous/instrumentation , Catheterization, Central Venous/adverse effects , Persistent Left Superior Vena Cava/complications , Persistent Left Superior Vena Cava/diagnostic imaging , Persistent Left Superior Vena Cava/therapy , Treatment Outcome , Catheters, Indwelling , Vena Cava, Superior/abnormalities , Vena Cava, Superior/diagnostic imaging , Phlebography
4.
Ann Plast Surg ; 92(6S Suppl 4): S419-S422, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38857007

ABSTRACT

BACKGROUND: Tissue expander-based breast reconstruction is associated with high rates of infectious complications, often leading to tissue expander explants and delays in receipt of definitive breast reconstruction and adjuvant therapy. In this study, we describe a single-stage technique where deep inferior epigastric artery perforator (DIEP) flaps are used to salvage actively infected tissue expanders among patients originally planning for free flap reconstruction. METHODS: In this technique, patients with tissue expander infections without systemic illness are maintained on oral antibiotics until the day of their DIEP flap surgery, at which time tissue expander explant is performed in conjunction with aggressive attempt at total capsulectomy and immediate DIEP flap reconstruction. Patients are maintained on 1-2 weeks of oral antibiotics tailored to culture data. Patients undergoing this immediate salvage protocol were retrospectively reviewed, and complications and length of stay were assessed. RESULTS: In a retrospective series, a total of six consecutive patients with culture-proven tissue expander infections underwent tissue expander removal and DIEP flap reconstruction in a single stage and were maintained on 7-14 days of oral antibiotics postoperatively. Within this cohort, no surgical site infections, microvascular complications, partial flap losses, reoperations, or returns to the operating room were noted within a 90-day period. CONCLUSIONS: Among a select cohort of patients, actively infected tissue expanders may be salvaged with free flap breast reconstruction in a single surgery with a low incidence of postoperative complications. Prospective studies are needed to evaluate the influence of this treatment strategy on costs, number of surgeries, and dissatisfaction after staged breast reconstruction complicated by tissue expander infections.


Subject(s)
Epigastric Arteries , Mammaplasty , Perforator Flap , Salvage Therapy , Tissue Expansion Devices , Humans , Perforator Flap/blood supply , Female , Retrospective Studies , Mammaplasty/methods , Middle Aged , Epigastric Arteries/transplantation , Epigastric Arteries/surgery , Salvage Therapy/methods , Adult , Prosthesis-Related Infections/surgery , Anti-Bacterial Agents/therapeutic use , Anti-Bacterial Agents/administration & dosage , Tissue Expansion/methods , Breast Neoplasms/surgery , Treatment Outcome , Device Removal/methods
5.
Front Cell Infect Microbiol ; 14: 1373036, 2024.
Article in English | MEDLINE | ID: mdl-38873095

ABSTRACT

Serratia marcescens, as a Gram-negative opportunistic pathogen, is a rare cause of peritonitis and has worse clinical outcomes than Gram-positive peritonitis. In this case report, we describe a case of Serratia marcescens associated peritonitis that was successfully cured without catheter removal. A 40-year-old male patient with peritoneal dialysis who worked in the catering industry was admitted to the hospital for 16 hours after the discovery of cloudy peritoneal dialysate and abdominal pain. Ceftazidime and cefazolin sodium were immediately given intravenously as an empirical antibiotic regimen. After detecting Serratia marcescens in the peritoneal diasate culture, the treatment was switched to ceftazidime and levofloxacin. The routine examination of peritoneal dialysate showed a significant decrease in white blood cells, the peritoneal dialysate became clear, and the peritoneal dialysis catheter was retained. The patient was treated for 2 weeks and treated with oral antibiotics for 1 week. It is necessary to further strengthen the hygiene of work environment to prevent Serratia marcescens infection in peritoneal dialysis patients. We recommend that patients with Serratia marcescens associated peritonitis should be treated with a combination of antibiotics as early as possible empirically, and at the same time, the peritoneal dialysis fluid culture should be improved, and the antibiotic regimen should be timely adjusted according to the drug sensitivity results. For patients with clinical symptoms for more than 3 days, considering the strong virulence of Serratia marcescens, whether to use meropenem directly or not can provide a reference for clinical decision-making. Further clinical studies are needed to achieve more precise anti-infective treatment.


Subject(s)
Anti-Bacterial Agents , Peritoneal Dialysis , Peritonitis , Serratia Infections , Serratia marcescens , Humans , Serratia marcescens/isolation & purification , Male , Peritonitis/microbiology , Peritonitis/drug therapy , Adult , Serratia Infections/microbiology , Anti-Bacterial Agents/therapeutic use , Anti-Bacterial Agents/administration & dosage , Peritoneal Dialysis/adverse effects , Treatment Outcome , Device Removal , Levofloxacin/therapeutic use , Ceftazidime/therapeutic use , Ceftazidime/administration & dosage , Cefazolin/therapeutic use
6.
JACC Cardiovasc Interv ; 17(11): 1340-1351, 2024 Jun 10.
Article in English | MEDLINE | ID: mdl-38866457

ABSTRACT

BACKGROUND: The etiology of transcatheter aortic valve (TAV) degeneration is poorly understood, particularly noncalcific mechanisms. OBJECTIVES: The authors sought to investigate noncalcific and calcific mechanisms of TAV degeneration and evaluate their impact on leaflet function by bench testing, imaging, and histology. METHODS: TAV explants were obtained from the EXPLANT THV registry and clinical institutions. Hydrodynamic assessment was performed using a heart valve pulse duplicator system under physiological conditions. Micro-computed tomography, high-resolution photography, high speed video, and hematoxylin and eosin staining were used to evaluate the morphological appearance, leaflet kinematics, and calcium burden of TAVs. RESULTS: A total of 14 explants were evaluated: 10 self-expanding CoreValve/Evolut TAVs (Medtronic), 3 balloon-expandable SAPIEN 3 TAVs (Edwards Lifesciences), and 1 mechanically expandable Lotus TAV (Boston Scientific). The median patient age at explantation was 73.0 years (Q1-Q3: 64.5-80.0 years), with a time to explantation of 4 years 1 month (1 year 5 months to 4 years 11 months). Six TAV explants were found to have leaflet calcification (162.4 mm3; 58.8-603.0 mm3), and 8 had no calcification detectable by micro-computed tomography and histology. All samples had impaired leaflet kinematics. There was no significant difference in the hydrodynamic mean gradient between calcified (47.2 mm Hg; 26.6-74.1 mm Hg) and noncalcified (27.6 mm Hg; 15.2-36.7 mm Hg; P = 0.28) TAVs. Leaflet calcification had a weak but nonsignificant association with the hydrodynamic mean gradient (r = 0.42; P = 0.14). CONCLUSIONS: TAV function can be severely impacted by noncalcific and calcific mechanisms of tissue degeneration. Importantly, functional stenosis can occur in TAVs in the absence of obvious and significant calcification.


Subject(s)
Aortic Valve , Calcinosis , Heart Valve Prosthesis , Hydrodynamics , Prosthesis Design , Prosthesis Failure , Registries , Transcatheter Aortic Valve Replacement , X-Ray Microtomography , Humans , Aged , Aortic Valve/physiopathology , Aortic Valve/diagnostic imaging , Aortic Valve/surgery , Aortic Valve/pathology , Calcinosis/physiopathology , Calcinosis/diagnostic imaging , Calcinosis/pathology , Calcinosis/surgery , Female , Aged, 80 and over , Male , Transcatheter Aortic Valve Replacement/instrumentation , Transcatheter Aortic Valve Replacement/adverse effects , Middle Aged , Time Factors , Device Removal , Aortic Valve Stenosis/physiopathology , Aortic Valve Stenosis/diagnostic imaging , Aortic Valve Stenosis/surgery , Hemodynamics , Biomechanical Phenomena , Materials Testing , Video Recording
7.
BMJ Case Rep ; 17(5)2024 May 28.
Article in English | MEDLINE | ID: mdl-38806399

ABSTRACT

Increasing use of tracheal expandable metallic hybrid stents will lead to common encounters with these devices in emergency airway management. The presence of these stents qualifies any patient as a challenge when an emergency tracheostomy is needed. We report an unorthodox technique of tracheostomy with concomitant removal of tracheal stent, without any major complications. Although the combined approach with bronchoscopy and tracheostomy has been reported in similar cases, we present a safe procedure when rigid bronchoscopy is not available.


Subject(s)
Bronchoscopy , Device Removal , Tracheostomy , Humans , Tracheostomy/adverse effects , Tracheostomy/instrumentation , Tracheostomy/methods , Device Removal/methods , Bronchoscopy/methods , Stents/adverse effects , Trachea/surgery , Male , Tracheal Stenosis/surgery , Tracheal Stenosis/therapy , Tracheal Stenosis/etiology , Female
8.
Am J Otolaryngol ; 45(4): 104328, 2024.
Article in English | MEDLINE | ID: mdl-38733715

ABSTRACT

PURPOSE: To evaluate outcomes following explantation of percutaneous or transcutaneous bone conduction implants (pBCIs or tBCIs) and subsequent implantation of transcutaneous active bone conduction hearing devices (BCHDs); to provide guidance regarding staging of surgery and adjunctive procedures. MATERIALS AND METHODS: Retrospective chart review of eight adult subjects (ten ears) with pBCIs or tBCIs who underwent explantation of their device and subsequent implantation with a BCHD [MED-EL BONEBRIDGE™ (n = 7, 70 %) or Cochlear™ Osia® (n = 3, 30 %)]. RESULTS: Reasons for pBCI or tBCI explantation were pain (60 %, 6/10), infection (60 %, 6/10), skin overgrowth (50 %, 5/10), and inability to obtain new processors (20 %, 2/10). Median time between pBCI or tBCI removal and BCHD staged implant was 4.7 (IQR 2.2-8.1) months. Two subjects developed complications following BCHD implantation. One had a persistent wound overlying the osseointegrated screw after removal of the pBCI abutment, requiring removal and temporalis rotational flap. Staged Osia® implantation was performed, but ultimately wound dehiscence developed over the device. The second subject experienced an infection after BONEBRIDGE™ implantation (32 days after pBCI explant), necessitating washout and treatment with intravenous antibiotics. There was subsequent device failure. CONCLUSION: The transition from a pBCI or tBCI to a novel transcutaneous device is nuanced. Staged pBCI or tBCI explantation and novel BCHD implantation with sufficient time for wound healing is vital. Adjunctive procedures to augment soft tissue in cases of prior attenuation may be required to avoid complications with larger internal devices.


Subject(s)
Bone Conduction , Device Removal , Hearing Aids , Humans , Hearing Aids/adverse effects , Retrospective Studies , Male , Female , Middle Aged , Adult , Treatment Outcome , Aged , Bone-Anchored Prosthesis , Prosthesis Implantation/methods , Prosthesis Implantation/adverse effects , Hearing Loss, Conductive/surgery , Hearing Loss, Conductive/etiology
9.
Am J Case Rep ; 25: e943781, 2024 May 31.
Article in English | MEDLINE | ID: mdl-38816969

ABSTRACT

BACKGROUND Double-J (D-J) ureteric stents are widely applied in urological operations as they play a vital role in maintaining postoperative functionality of the patient's urinary system and thereby accelerating recovery. D-J stent encrustation may occur due to prolonged retention and lead to secondary complications. We report the case of a forgotten D-J stent that gradually formed into a bladder stone. CASE REPORT A 54-year-old man was referred to the Urology Department due to intermittent hematuria, left flank pain, and lower urinary tract symptoms that persisted for 2 weeks. His history was significant for undergoing left ureterolithotripsy followed by the implantation of an ipsilateral D-J stents 2 years ago in a local hospital. The patient did not follow-up regularly or actively seek medical attention for his urinary tract symptoms. Computed tomographic urography revealed a hyperdense tubular object protruding from the left distal ureter to the bladder. The patient underwent cystolithotripsy, left ureteric stent removal, and left ureteroscopy to clear away the bladder stone and its D-J stent core. CONCLUSIONS Formation of bladder stones secondary to prolonged indwelling D-J stent and its encrustation is not uncommon in developing countries where the level of public education is low. Prompt D-J stent removal can prevent complications associated with its retention and avoid unnecessary secondary procedures. Endoscopic urologic procedures are safe and feasible management options, and doctor-to-patient communication is vital for a better prognosis.


Subject(s)
Stents , Urinary Bladder Calculi , Humans , Male , Middle Aged , Stents/adverse effects , Urinary Bladder Calculi/surgery , Urinary Bladder Calculi/therapy , Ureter/surgery , Device Removal , Foreign Bodies/surgery , Ureteroscopy , Lithotripsy
10.
BMC Public Health ; 24(1): 1458, 2024 May 31.
Article in English | MEDLINE | ID: mdl-38822304

ABSTRACT

BACKGROUND/AIMS: The dapivirine vaginal ring is a self-administered, women-initiated, discreet, long-acting HIV-1 prevention option for women. It was found to be safe and effective in healthy HIV-negative women who adhered to product use instructions, and has been approved for use in women aged 18 and older in some African countries. A qualitative study was conducted to explore participants' and their male partners' discussions on accidental/purposeful vaginal ring removals during The Ring Study (IPM 027 clinical trial). METHODS: Data were collected via in-depth interviews and focus group discussions with female trial participants and their male partners, from seven research centres in South Africa and Uganda. Data were thematically analysed using NVivo. RESULTS: More participants reported purposeful ring removals than accidental expulsions. Various factors influenced purposeful ring removal - including individual (discomfort during use/sex and to clean it), partner (to show them, because of discomfort during sex, to test if partners could feel it, and concerns of harm), organisational (doctor's request), and socio-cultural (rumours about sickness and infertility). Some described their own ring use removal, others discussed why other participants removed their rings. CONCLUSIONS: Vaginal ring adherence is critical to improve and support product efficacy. Counselling on vaginal anatomy, vaginal ring insertion and importance of adherence is important to minimise vaginal ring removal. Couples counselling is also important to facilitate support and long-term vaginal ring adherence behaviour. Understanding factors influencing vaginal ring adherence is important for tailoring and targeting messages to support correct and consistent vaginal ring use as it is made available to the public.


Subject(s)
Contraceptive Devices, Female , HIV Infections , Pyrimidines , Qualitative Research , Sexual Partners , Humans , Female , Male , Adult , South Africa , Pyrimidines/administration & dosage , Uganda , HIV Infections/prevention & control , Sexual Partners/psychology , Young Adult , Self Report , Focus Groups , Device Removal , Middle Aged , Interviews as Topic , Adolescent , Anti-HIV Agents/administration & dosage , Anti-HIV Agents/therapeutic use
11.
Jt Dis Relat Surg ; 35(2): 439-442, 2024 Apr 26.
Article in English | MEDLINE | ID: mdl-38727126

ABSTRACT

Tension band wiring (TBW) is one of the most commonly used fixation techniques to fix olecranon osteotomies. Hardware prominence has been the most commonly reported complication of TBW. However, distal migration of Kirschner (K)-wire after TBW fixation for olecranon osteotomy has not been reported. In this case report, we presented distal migration of K-wire detected nine months after initial surgery in a 46-year-old male patient. The patient was operated on for an intraarticular distal humerus fracture using an olecranon osteotomy. The osteotomy was fixed with TBW fixation. The patient missed routine follow-ups and presented to the outpatient clinic with a complaint of skin irritation at the elbow nine months after the surgery. On radiological examination, distal migration of one K-wire was detected. The K-wire was surgically removed without any complication. Physicians should be aware of possible complications of TBW and remove fixation after fracture union to avoid unexpected complications.


Subject(s)
Bone Wires , Foreign-Body Migration , Olecranon Process , Osteotomy , Humans , Bone Wires/adverse effects , Male , Middle Aged , Olecranon Process/injuries , Olecranon Process/surgery , Olecranon Process/diagnostic imaging , Osteotomy/adverse effects , Osteotomy/methods , Osteotomy/instrumentation , Foreign-Body Migration/surgery , Foreign-Body Migration/diagnostic imaging , Foreign-Body Migration/etiology , Humeral Fractures/surgery , Humeral Fractures/diagnostic imaging , Fracture Fixation, Internal/adverse effects , Fracture Fixation, Internal/methods , Fracture Fixation, Internal/instrumentation , Device Removal/methods , Elbow Joint/surgery , Elbow Joint/diagnostic imaging , Intra-Articular Fractures/surgery , Intra-Articular Fractures/diagnostic imaging
12.
Jt Dis Relat Surg ; 35(2): 404-409, 2024 Apr 26.
Article in English | MEDLINE | ID: mdl-38727121

ABSTRACT

OBJECTIVES: This study aimed to compare the course of anxiety change in children who used headphones during cast removal with controls in midterm follow-up. PATIENTS AND METHODS: Sixty-six patients who underwent forearm fracture treatment with closed reduction and long arm casting between June 2021 and March 2023 were retrospectively reviewed. Patients were divided into two groups based on the use of headphones (n=27; 21 males, 6 females; mean age: 8.0±1.8 years; range, 6 to 12 years) or not (n=39; 27 males, 12 females; mean age: 8.9±1.8 years; range, 6 to 12 years) during cast removal with an oscillating saw. Primary outcome measures included preprocedure, postprocedure, and six-month anxiety assessments with the State-Trait Anxiety Inventory. RESULTS: There was an acute increase in the mean state anxiety scores after the procedure, which returned to below baseline at the six-month follow-up in the headphone (31.4±8.3, 33.3±8.7, and 25.1±4.1, respectively) and control groups (34.9±11.1, 37.4±9.5, and 27.3±5.3, respectively). The mean trait anxiety scores before the procedure, after the procedure, and at six months remained similar in the headphone (33.6±3.0, 34.6±3.2, and 32.4±2.8; p>0.05) and control groups (34.1±2.7, 33.7±3.0, and 33.7±3.0, p>0.05). CONCLUSION: This study suggests that the acute anxiety during cast removal did not create anxiety sequelae in the sixth month regardless of headphone use.


Subject(s)
Anxiety , Casts, Surgical , Humans , Female , Male , Child , Retrospective Studies , Anxiety/psychology , Anxiety/etiology , Device Removal/psychology , Forearm Injuries/surgery , Forearm Injuries/psychology , Closed Fracture Reduction/methods
13.
Eur J Contracept Reprod Health Care ; 29(3): 115-130, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38712717

ABSTRACT

INTRODUCTION: Migration is a rare but serious complication of the etonogestrel contraceptive implant, and little is known about its extent. PURPOSE: To document and characterise cases of etonogestrel contraceptive implant migration in the scientific literature. METHODS: A systematic review of Medline, Embase and Global Health databases was carried out between January 2000 and January 2023 to identify articles presenting implant migrations. Narrative reviews, conference abstracts and articles not written in English or French were excluded. RESULTS: Forty-five articles, mostly published since 2016, were identified (eight case series and 37 case reports), for a total of 148 independent cases of migration: in pulmonary blood vessels (n = 74), in non-pulmonary blood vessels (n = 16) and extravascular (n = 58). Many patients are asymptomatic and migration is often an incidental finding. A non-palpable implant and symptoms related to implant location (intra- or extra-vascular) may be indicative of migration. Inadequate insertion and normal or underweight appear to increase the risk of migration. Scientific societies and authors offer practical strategies to deal with implant migration. CONCLUSION: Professionals who insert and remove contraceptive implants must be adequately trained. They need to be on the lookout for implant migration, and promptly refer patients to appropriate care if migration is suspected.


This systematic review documents and characterises 148 cases of vascular and extravascular etonogestrel contraceptive implant migration. Healthcare professionals must be aware of this rare but serious complication and be adequately trained to insert and remove contraceptive implants.


Subject(s)
Contraceptive Agents, Female , Desogestrel , Drug Implants , Foreign-Body Migration , Humans , Desogestrel/administration & dosage , Desogestrel/adverse effects , Female , Drug Implants/adverse effects , Contraceptive Agents, Female/administration & dosage , Contraceptive Agents, Female/adverse effects , Device Removal , Contraceptive Agents, Hormonal/adverse effects , Contraceptive Agents, Hormonal/administration & dosage
14.
Card Electrophysiol Clin ; 16(2): 139-142, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38749632

ABSTRACT

This case report discusses a 42-year-old male with dextro-transposition of the great arteries (D-TGA) status post Mustard repair and sick sinus syndrome status post dual-chamber pacemaker implant, who developed symptomatic superior vena cava (SVC) baffle stenosis. He was treated with a combined pacemaker extraction and subsequent SVC baffle stenting. The case highlights the complexities of treating SVC baffle stenosis in the presence of cardiac implantable devices and demonstrates the efficacy of this combined approach. Furthermore, the authors delve into the intricacies of D-TGA, its surgical history, and the long-term complications associated with atrial switch procedures.


Subject(s)
Device Removal , Pacemaker, Artificial , Stents , Transposition of Great Vessels , Humans , Transposition of Great Vessels/surgery , Male , Adult , Pacemaker, Artificial/adverse effects , Superior Vena Cava Syndrome/surgery , Superior Vena Cava Syndrome/etiology , Sick Sinus Syndrome/therapy , Sick Sinus Syndrome/surgery
15.
Card Electrophysiol Clin ; 16(2): 143-147, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38749633

ABSTRACT

We present a complex case of cardiac implantable electronic device infection and extraction in the setting of bacteremia, large lead vegetation, and patent foramen ovale. Following a comprehensive preprocedural workup including transesophageal echocardiogram and computed tomography lead extraction protocol, in addition to the involvement of multiple subspecialties, an open chest approach to extraction was deemed a safer option for eradication of the patient's infection. Despite percutaneous techniques having evolved as the preferred extraction method during the last few decades, this case demonstrates the importance of a thorough evaluation at an experienced center to determine the need for open chest extraction.


Subject(s)
Defibrillators, Implantable , Device Removal , Pacemaker, Artificial , Prosthesis-Related Infections , Humans , Device Removal/methods , Defibrillators, Implantable/adverse effects , Prosthesis-Related Infections/surgery , Prosthesis-Related Infections/diagnostic imaging , Pacemaker, Artificial/adverse effects , Male , Echocardiography, Transesophageal , Tomography, X-Ray Computed , Aged , Foramen Ovale, Patent/surgery , Foramen Ovale, Patent/diagnostic imaging , Female , Middle Aged
16.
Card Electrophysiol Clin ; 16(2): 117-124, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38749629

ABSTRACT

Transvenous laser lead extraction poses a risk of major complications (0.19%-1.8%), notably injury to the superior vena cava (SVC) in 0.19% to 0.96% of cases. Various factors contribute to SVC injury, which can be categorized as patient-related (such as female gender, low body mass index, diabetes, renal problems, anemia, and reduced ejection fraction), device-related (including the number, dwell time, and type of leads), or procedural-related (such as reason for extraction, venous obstructions, and bilateral lead placements).


Subject(s)
Device Removal , Laser Therapy , Vena Cava, Superior , Humans , Vena Cava, Superior/injuries , Vena Cava, Superior/surgery , Female , Device Removal/adverse effects , Male , Laser Therapy/adverse effects , Middle Aged , Aged , Defibrillators, Implantable/adverse effects , Pacemaker, Artificial/adverse effects
17.
Card Electrophysiol Clin ; 16(2): 149-155, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38749634

ABSTRACT

Leadless pacemaker systems (LPs) were developed as an alternative to traditional transvenous permanent pacemakers (TV-PPM) due to increasing rates of device and procedural related complications, leading to a high-cost burden to our health-care system. LPs were initially indicated for single-chamber ventricular pacing; however, recent developments have allowed for dual-chamber pacing too. These systems have demonstrated highly successful implant rates with stable pacing performance. This article describes the retrieval techniques of the Micra LPs and ways to mitigate challenges encountered during the retrieval process.


Subject(s)
Device Removal , Pacemaker, Artificial , Humans , Cardiac Pacing, Artificial/methods
19.
Ann Plast Surg ; 92(6): 621-624, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38717197

ABSTRACT

ABSTRACT: The unique dual-lumen and baffle design of the IDEAL IMPLANT Structured Saline breast implant gives it specific advantages over both silicone gel-filled and the original saline-filled implants. This internal baffle structure also gives it an appearance on various radiologic imaging studies that may be misinterpreted as a rupture because of similarities to the well-known radiologic appearance of a ruptured silicone gel implant. Patients may present with various misinterpreted imaging studies, highlighting the need for plastic surgeons and radiologists to be familiar with the normal appearance of the intact IDEAL IMPLANT and be able to distinguish it from a ruptured IDEAL IMPLANT. The radiology findings must be correlated with the clinical findings, or an intact IDEAL IMPLANT misdiagnosed as ruptured, may cause unnecessary patient worry, and may prompt unnecessary surgery for removal or replacement.


Subject(s)
Breast Implants , Device Removal , Diagnostic Errors , Prosthesis Failure , Humans , Breast Implants/adverse effects , Female , Unnecessary Procedures , Breast Implantation/adverse effects , Breast Implantation/methods , Adult , Prosthesis Design , Silicone Gels , Saline Solution , Middle Aged
20.
J Med Case Rep ; 18(1): 234, 2024 May 02.
Article in English | MEDLINE | ID: mdl-38698425

ABSTRACT

BACKGROUND: Nexplanon implants are a common hormonal contraceptive modality. Though rare, these devices can embolize into the injured wall of the basilic vein, through the right heart, and finally wedge itself into a pulmonary artery. With adherence to the arterial wall over time, it becomes less amenable to endovascular retrieval. Patients may present with symptoms mimicking a pulmonary embolism, or without any symptoms at all. In asymptomatic cases, endovascular retrieval and/or surgery is required when patients wish to begin having children prior to biological inactivity. The current literature showed as little as nine case reports detailing lung tissue removal in the aim of reversing a patient's implanted contraceptive device. CASE PRESENTATION: A 22-year-old asymptomatic active-duty Caucasian female presented for elective outpatient Nexplanon removal. The suspicion of possible implant migration arose when it was discovered to be non-palpable in her left arm. After plain film x-rays failed to localize the implant, a chest x-ray and follow-up Computed Tomography (CT) scan revealed that the Nexplanon had migrated to a distal branch of the left pulmonary artery. Due to the patient's strong desires to begin having children, the decision was made for removal. Initial endovascular retrieval failed due to Nexplanon encapsulation within the arterial wall. Ultimately, the patient underwent a left video-assisted thoracoscopic surgery (VATS) for exploration and left lower lobe basilar S7-9 segmentectomy, which successfully removed the Nexplanon. CONCLUSIONS: Implanted contraceptive devices can rarely result in migration to the pulmonary vasculature. These radiopaque devices are detectable on imaging studies if patients and clinicians are unable to palpate them. An endovascular approach should be considered first to spare lung tissue and avoid chest-wall incisions, but can be complicated by encapsulation and adherence to adjacent tissue. A VATS procedure with single-lung ventilation via a double-lumen endotracheal tube allows surgeons to safely operate on an immobilized lung while anesthesiologists facilitate single-lung ventilation. This patient's case details the uncommon phenomenon of Nexplanon migration, and the exceedingly rare treatment resolution of lung resection to remove an embolized device.


Subject(s)
Desogestrel , Device Removal , Foreign-Body Migration , Humans , Female , Device Removal/methods , Desogestrel/administration & dosage , Foreign-Body Migration/surgery , Foreign-Body Migration/diagnostic imaging , Young Adult , Contraceptive Agents, Female/administration & dosage , Drug Implants , Pulmonary Artery/surgery , Pulmonary Artery/diagnostic imaging , Tomography, X-Ray Computed , Pulmonary Embolism/etiology , Treatment Outcome , Pneumonectomy
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