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1.
Transpl Infect Dis ; 25(6): e14140, 2023 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-37697912

RESUMEN

Rhodococcosis is an uncommon cause of pulmonary infection in thoracic organ transplant recipients. We describe a heart transplant recipient diagnosed with Rhodococcus equi left upper lung abscess with empyema thoracis complicated by bacteremia. The patient was successfully treated with appropriate antibiotics, adequate surgical resection, and optimization of immunosuppressants.


Asunto(s)
Infecciones por Actinomycetales , Empiema , Trasplante de Corazón , Absceso Pulmonar , Rhodococcus equi , Rhodococcus , Humanos , Absceso Pulmonar/tratamiento farmacológico , Infecciones por Actinomycetales/diagnóstico , Infecciones por Actinomycetales/tratamiento farmacológico , Trasplante de Corazón/efectos adversos
2.
Transpl Infect Dis ; 25(1): e13984, 2023 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-36305598

RESUMEN

The case discussed involves a 69-year-old Thai woman who underwent orthotopic heart transplantation 9 months before this event. She presented with fever without localizing signs or symptoms. However, her chest images revealed mass-like consolidation in the left upper lobe. Blood culture and lung tissue identified Rhodococcus equi. She was successfully treated with a combination of antimicrobial therapy, optimization of immunosuppressants, and surgical resection.


Asunto(s)
Empiema , Trasplante de Corazón , Absceso Pulmonar , Femenino , Humanos , Anciano , Tailandia , Pulmón
3.
J Med Assoc Thai ; 96(7): 819-23, 2013 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-24319853

RESUMEN

BACKGROUND: Although the public perceives video-assisted thoracic surgery (VATS) as advantageous because it is less invasive than a standard thoracotomy There are questioned the safety of VATS lobectomy and its adequacy as a cancer operation. This study is reviewed to assess this issue. MATERIAL AND METHOD: This retrospective study was performed between January 2009 and June 2011 in 58 patients who underwent VATS for a standard anatomic lobectomy with lymph node sampled or dissection for lung cancer 43 women (74%) and 15 men (26%) and mean age 60.28+/-11.14 years. None of this study group had any pleural effusion or pleural dissemination. RESULTS: The most symptom and sign of patients with lung cancer were normal [48 cases (83%), 54 cases (93%) respectively]. The most risk factor was smoking [12 cases (20%)]. The most lobectomy of VATS lobectomy was right upper lobectomy [17 cases (29%)] and the longest duration of VATS lobectomy was left upper lobectomy was 237.00+/-38.60 minutes. Thirty-one patients (53.4%) were adenocarcinoma. The VATS lobectomy was adequate for lung cancer surgery because malignant cells were not found from cytologic study of pleural lavages. The conversion rate from VATS to standard thoracotomy lobectomy was seven cases (12%), which the common causes were pleural symphysis and inadequate one lung ventilation. The postoperative courses showed minimal blood transfusion (0.11+/-0. 37u), intensive care unit (ICU) stay (0.61+/-0.56 days) and intercostal drainage (ICD) duration (6.10+/-5.79 days). There were no intra-and post-operative death. Seven cases (12%) had many complications; the most complication was bacteria pneumonia. A case needed re-thoracotomy due to medical treatment failure for chylothorax. CONCLUSION: VATS lobectomy (anatomic lobectomy and lymph nodes sampled or dissection)for lung cancer can be performed with low morbidity and no mortality.


Asunto(s)
Carcinoma/cirugía , Neoplasias Pulmonares/cirugía , Neumonectomía , Sarcoma/cirugía , Cirugía Torácica Asistida por Video , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Tailandia , Resultado del Tratamiento
4.
SAGE Open Med ; 10: 20503121221142171, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36568340

RESUMEN

Objectives: Anatomical lobectomy has always been the standard operative treatment of early-stage non-small cell lung cancer. However, there have been emerging evidences suggesting that a subanatomical resection, such as segmentectomy, may yield the same treatment results, even in patients with higher-stage non-small cell lung cancer. This study aimed to compare overall 5-year survival rate and disease-free survival between lobectomy and segmentectomy in patients with non-small cell lung cancer. Methods: The retrospective study included 380 patients who underwent surgery for non-small cell lung cancer at Ramathibodi Hospital between 1st January 2016 and 31st December 2020. Of 380 patients, 307 patients underwent lobectomy, while the other 73 patients underwent segmentectomy. Operative, admission, and follow-up data were collected from electronic medical records. Missing data were collected by telephone calls to patients or their relatives in deceased cases. Overall and disease-free survival were analyzed. Results: Median overall 5-year survival time after lobectomy and segmentectomy seemed to be different but not statistically significant (18.5 months versus 5.8 months, p = 0.127). Median disease-free survival time after lobectomy and segmentectomy was also similar (8.6 months versus 4.5 months, p = 0.511). Two deaths occurred during perioperative period, one from lobectomy group due to acute massive pulmonary embolism (0.3%) and the other from segmentectomy group due to acute exacerbation of chronic obstructive pulmonary disease with respiratory failure (1.4%). Conclusion: Lobectomy and segmentectomy result in similar overall 5-year survival rate and disease-free survival between these two comparison groups. Therefore, segmentectomy may be a potential alternative for operative treatment of non-small cell lung cancer. However, a larger and randomized-controlled trial may be needed to further validate these results.

5.
J Pain Res ; 15: 2351-2361, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35996452

RESUMEN

Purpose: Thoracic paravertebral block (TPVB) is a recommended regional analgesia during video-assisted thoracoscopic surgery (VATS). However, single-injection TPVB does not last long enough to provide sufficient acute postoperative pain relief. Continuous TPVB through a catheter is technically challenging and often unreliable. Intravenous dexamethasone extends the analgesic duration with some peripheral nerve blocks. However, data on the effect of intravenous dexamethasone on pain relief with TPVB are limited. This study aimed to assess the analgesic efficacy of intravenous dexamethasone in patients who received TPVB for VATS. Patients and Methods: In this multicenter prospective randomized controlled trial, we recruited patients aged between 18 and 80 years with the American Society of Anesthesiologists of physical status class 1-3 and underwent elective VATS. Patients under general anesthesia randomly received 8 mg of intravenous dexamethasone (group D) or normal saline (group C). Ultrasound-guided TPVB (USG-TPVB) was performed at the T4-T5 and T6-T7 spaces. Multimodal analgesia was achieved via paracetamol, tramadol and intravenous morphine for both study groups. The primary outcome was time for the first analgesic requirement. Postoperative pain in terms of numeric rating score (NRS), total morphine consumption and postoperative nausea and vomiting (PONV) were assessed. Results: After excluding one patient, 59 patients were analyzed. There were no intergroup differences in baseline characteristics. The time to first analgesic requirement was longer in group D (305 [240, 510] minutes) than in group C (270 [180, 300] minutes) (P value = 0.02). The NRS at rest and on movement was lower in group D than in group C at 12 hours but did not differ at other time points. Postoperative morphine consumption was significantly lower in group D than in group C at 6,12,24 and 48 hours. Incidences of PONV were comparable between the groups. Conclusion: Intravenous dexamethasone, used as an adjunct to a single-injection USG-TPVB prolonged analgesic duration, had an opioid-sparing effect and provided better postoperative pain relief after VATS.

6.
J Med Assoc Thai ; 85(11): 1182-8, 2002 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-12546315

RESUMEN

OBJECTIVE: To determine early term results of the modified Cox maze procedure for curing atrial fibrillation (AF) associated with mitral valve disease. METHOD: Between January and December 2000, 10 consecutive patients with AF underwent the modified Cox maze procedure with mitral valve repair in 2 and replacement in 8. The associated procedure included 3 aortic valve replacements, 1 tricuspid annuloplasty, and 2 atrial septal defect closures. There were 5 males and 5 females, with ages ranging from 19 to 52 years (mean = 38.3 years). Pre-operative-existing AF time varied from 4 to 146 months (mean = 41.1 months), and left atrial dimension varied from 4.50 to 6.89 cm (mean 5.51 cm). The authors modified the maze atriotomies to preserve the sinus node artery and used cryoablation, incision and suture to simplify the procedures. RESULTS: Seven cases (70%) regained sinus rhythm and 3 cases (30%) still remained in AF. Two cases (double valve replacement) needed intraaortic balloon pump. Two of them developed cardiac tamponade 1 month post-operatively, (one in sinus rhythm case and another one in AF). Those 3 patients who remained in AF had a longer pre-operative existing AF-time and larger left atrial dimension but it was insignificant (p = 0.227 and p = 0.187 respectively). There was no early or late mortality. CONCLUSION: The pertaining results suggest that the modified Cox maze procedure has satisfactory effectiveness to cure atrial fibrillation, restore atrioventricular synchrony and preserve atrial transport function in the patients having AF associated with mitral valve disease.


Asunto(s)
Fibrilación Atrial/cirugía , Ablación por Catéter/métodos , Prótesis Valvulares Cardíacas , Insuficiencia de la Válvula Mitral/cirugía , Adulto , Fibrilación Atrial/complicaciones , Fibrilación Atrial/diagnóstico , Estudios de Cohortes , Electrocardiografía , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Insuficiencia de la Válvula Mitral/complicaciones , Insuficiencia de la Válvula Mitral/diagnóstico , Probabilidad , Medición de Riesgo , Muestreo , Índice de Severidad de la Enfermedad , Resultado del Tratamiento
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