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1.
Acta Clin Belg ; 69(2): 120-1, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24724752

ABSTRACT

Cocaine abuse has been associated with a number of psychiatric, medical and neurological complications. Here we report the case of a male patient who suffered an episode of severe muscular weakness after cocaine abuse.


Subject(s)
Cocaine-Related Disorders/physiopathology , Muscle Weakness/chemically induced , Adult , Humans , Hypokalemia/chemically induced , Male , Muscle Weakness/diagnosis , Muscle Weakness/drug therapy , Muscle Weakness/physiopathology , Potassium Chloride/administration & dosage
2.
Eur J Cancer Care (Engl) ; 19(3): 413-6, 2010 May.
Article in English | MEDLINE | ID: mdl-19486124

ABSTRACT

This study presents a rare case of a patient who developed three different types of neoplasia in an 18-year period of time. The case presents a 31-year-old man with a history of treated Hodgkin's lymphoma in the neck region at the age of 13 years. The patient was admitted at the General Hospital of Nafplio for differential diagnosis of pain in the right subcostal region initiated 1 month before his admission and normochromic, normocytic anaemia. The laboratory examinations lead to the diagnosis of a sarcoma in the cardioesophageal junction. The patient was subjected to total gastrectomy. Nine months later he is admitted with a palpable firm lump in the nipple of the right breast, which suggested a malignant neoplasia. The patient was subjected to modified radical mastectomy. The appearance of three different types of neoplasia in three different organ systems in the same patient and the infrequency of the specific neoplasias individually and in combination present a special interest considering the patient's genetic background and the uniqueness of the case in the international literature.


Subject(s)
Breast Neoplasms, Male/diagnosis , Esophagogastric Junction , Hodgkin Disease/therapy , Neoplasms, Second Primary/diagnosis , Sarcoma/diagnosis , Stomach Neoplasms/diagnosis , Adult , Biopsy, Fine-Needle , Fatal Outcome , Gastrectomy , Humans , Male , Mastectomy , Nipples
3.
Anaesth Intensive Care ; 37(5): 733-9, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19775036

ABSTRACT

Sepsis is associated with abnormalities of muscle tissue oxygenation and of microvascular function. We investigated whether the technique of near-infrared spectroscopy can evaluate such abnormalities in critically ill patients and compared near-infrared spectroscopy-derived indices of critically ill patients with those of healthy volunteers. We studied 41 patients (mean age 58 +/- 22 years) and 15 healthy volunteers (mean age 49 +/- 13 years). Patients were classified into one of three groups: systemic inflammatory response syndrome (SIRS) (n = 21), severe sepsis (n = 8) and septic shock (n = 12). Near-infrared spectroscopy was used to continuously measure thenar muscle oxygen saturation before, during and after a three-minute occlusion of the brachial artery via pneumatic cuff. Oxygen saturation was significantly lower in patients with SIRS, severe sepsis or septic shock than in healthy volunteers. Oxygen consumption rate during stagnant ischaemia was significantly lower in patients with SIRS (23.9 +/- 7.7%/minute, P < 0.001), severe sepsis (16.9 +/- 3.4%/minute, P < 0.001) or septic shock (14.8 +/- 6%/minute, P < 0.001) than in healthy volunteers (35.5 +/- 10.6%/minute). Furthermore, oxygen consumption rate was significantly lower in patients with septic shock than patients with SIRS. Reperfusion rate was significantly lower in patients with SIRS (336 +/- 141%/minute, P < 0.001), severe sepsis (257 +/- 150%/minute, P < 0.001) or septic shock (146 +/- 101%/minute, P < 0.001) than in healthy volunteers (713 +/- 223%/minute) and significantly lower in the septic shock than in the SIRS group. Near-infrared spectroscopy can detect tissue oxygenation deficits and impaired microvascular reactivity in critically ill patients, as well as discriminate among groups with different disease severity.


Subject(s)
Critical Illness , Microcirculation , Oxygen/blood , Sepsis/blood , Systemic Inflammatory Response Syndrome/blood , APACHE , Brachial Artery/metabolism , Female , Humans , Ischemia/blood , Male , Middle Aged , Muscle, Skeletal/blood supply , Muscle, Skeletal/metabolism , Oxygen Consumption , Resuscitation/methods , Shock, Septic/blood , Spectroscopy, Near-Infrared , Treatment Outcome
4.
Eur J Cancer Care (Engl) ; 18(6): 653-6, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19552728

ABSTRACT

Patients with breast carcinoma often develop bone metastases that carry a high risk of complications. A randomized, placebo-controlled trial was conducted to evaluate the efficacy and safety of ibandronate in patients with metastatic bone disease following breast cancer. The primary efficacy end point of the study was the proportion of patients who developed skeletal-related events (SREs, defined as pathologic fracture, spinal cord compression, radiation therapy to bone, change in anti-neoplastic therapy and surgery to bone). Secondary end points included time to first skeletal event, skeletal morbidity rate (events/year) and time to progression of bone lesions. In 150 patients (148 [female symbol] / 2 [male symbol]) with breast carcinoma and bone metastases, treatment with intravenous ibandronate 6 mg over 15 min every 4 weeks for 24 months significantly reduced the proportion of patients who experienced an SRE compared with placebo (36% vs. 48%; P = 0.027). Time to first SRE was also delayed significantly (median 457 vs. 304 days; P = 0.007). Multiple event analysis showed that ibandronate reduced the risk of developing an SRE by 32% (hazard ratio = 0.69; 95% confidence interval 0.42-0.79; P = 0.003). In general, ibandronate was well tolerated with very rare grade 3 or 4 toxicity. In this study, ibandronate was shown to be significantly more effective than placebo as a treatment for metastatic bone disease from breast cancer using multiple end points.


Subject(s)
Bone Density Conservation Agents/administration & dosage , Bone Neoplasms/drug therapy , Breast Neoplasms , Diphosphonates/administration & dosage , Bone Neoplasms/secondary , Breast Neoplasms, Male , Double-Blind Method , Female , Humans , Ibandronic Acid , Infusions, Intravenous , Male , Middle Aged , Treatment Outcome
5.
Eur J Cancer Care (Engl) ; 17(6): 619-23, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18707619

ABSTRACT

Anaemia is common in patients receiving chemotherapy, causing symptoms that have a major impact on quality of life (QoL). Epoetin beta rapidly increases haemoglobin (Hb) levels and improves QoL in anaemic patients with a variety of tumours. This was a randomized, double-blind, parallel-group, dose-finding study assessing the efficacy and safety of once-weekly epoetin beta in patients with solid tumours receiving chemotherapy. Adult patients with anaemia (Hb < 11 g/dL) were randomized to receive epoetin beta 30,000 IU or 20,000 IU once weekly for 12 weeks. All patients received oral iron supplementation. Haemoglobin levels, transfusion need and QoL [Functional Assessment of Cancer Therapy-fatigue (FACT-F) subscale score] were assessed at regular intervals. Fifty patients were randomized; 30 patients received epoetin beta 30,000 IU once weekly and 20 received 20,000 IU once weekly. Mean (+/- SD) increase in Hb from baseline to week 12 was 1.75 +/- 2.15 g/dL in the 30,000 IU group (P = 0.008 vs. baseline) and 1.04 +/- 1.75 g/dL in the 20,000 IU group (non-significant). Haemoglobin response (increase in Hb >or=2 g/dL from baseline) was observed in 78.3% of patients receiving epoetin beta 30,000 IU and 66.7% receiving epoetin beta 20,000 IU. Improvements in FACT-F subscale score were significantly (P < 0.001) correlated with increases in Hb level. Transfusion use was low during the study in both groups. Both epoetin beta regiments were well tolerated and there were no dose-dependent adverse events. Epoetin beta 30,000 IU once weekly is an effective and well-tolerated treatment of anaemia in patients with solid tumours.


Subject(s)
Anemia/drug therapy , Erythropoietin/administration & dosage , Hematinics/administration & dosage , Hemoglobins/metabolism , Neoplasms/drug therapy , Adult , Aged , Anemia/chemically induced , Double-Blind Method , Drug Administration Schedule , Female , Hemoglobins/drug effects , Humans , Male , Middle Aged , Neoplasms/blood , Quality of Life , Recombinant Proteins , Treatment Outcome
6.
Acta Neurol Scand ; 118(3): 175-81, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18355395

ABSTRACT

OBJECTIVE: To investigate risk factors of critical illness polyneuromyopathy (CIPM) in a general multidisciplinary intensive care unit (ICU). PATIENTS AND METHODS: Prospective observational study in a 28-bed university multidisciplinary ICU. Four hundred and seventy-four (323 M/151 F, age 55 +/- 19) consecutive patients were prospectively evaluated. All patients were assigned admission Acute Physiology and Chronic Health Evaluation (APACHE II; 15 +/- 7) and Sequential Organ Failure Assessment (SOFA; 6 +/- 3) scores and were subsequently evaluated for newly developed neuromuscular weakness. Other potential causes of new-onset weakness after ICU admission were excluded before CIPM was diagnosed. RESULTS: Forty-four (23.8%) of 185 patients developed generalized weakness that met the criteria for CIPM. Patients with CIPM had higher APACHE II (18.9 +/- 6.6 vs 15.6 +/- 6.4, P = 0.004) and SOFA scores (8.4 +/- 2.9 vs 7.1 +/- 2.9, P = 0.013). According to multivariate logistic regression analysis, the following risk factors were independently associated with the development of CIPM: severity of illness at the time of ICU admission, administration of aminoglycoside antibiotics and high blood glucose levels. Analysis according to severity of illness stratification revealed the emergence of Gram (-) bacteremia as the most important independent predisposing factor for CIPM development in less severely ill patients. CONCLUSIONS: CIPM has a high incidence in the ICU setting. Our study revealed the association of aminoglycosides, hyperglycemia and illness severity with CIPM development, as well as the association between Gram (-) bacteremia and development of CIPM in less severely ill patient population.


Subject(s)
Intensive Care Units/statistics & numerical data , Polyneuropathies/epidemiology , Polyneuropathies/etiology , APACHE , Aminoglycosides/adverse effects , Anti-Bacterial Agents/adverse effects , Bacteremia/complications , Blood Glucose , Female , Gram-Negative Bacterial Infections/complications , Humans , Hyperglycemia/complications , Male , Middle Aged , Polyneuropathies/physiopathology , Risk Factors
7.
Anaesth Intensive Care ; 35(6): 920-3, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18084983

ABSTRACT

This study examined the incidence of hyperamylasaemia, in the absence of other plausible causes of pancreatic dysfunction, in intensive care unit (ICU) patients who received propofol. One-hundred-and-seventy-two consecutive patients of a general ICU who stayed for more than 24 hours were studied. Patients with a diagnosis consistent with elevated serum amylase levels at admission were excluded from the study, as were patients who had received medications known to raise serum amylase levels. Forty-four patients 53 +/- 20 years of age and median duration of ICU stay of five days (range two to 55) were eligible. Thirty of those, aged 54 +/- 21 years and median duration of ICU stay of five days (range two to 27) received continuous infusion of propofol for sedation (maximum dose 45 microg/kg/min). Of the 30 patients who received propofol, 16 (53%) developed hyperamylasaemia (125 to 466 IU/l) after two to nine days of continuous infusion. Liver and kidney function remained normal throughout the observation period. Of the 14 patients who did not receive propofol (aged 51 +/- 18 years), only two (14%) developed hyperamylasaemia, a significantly lower incidence (P = 0.021). Propofol infusion is associated with biochemical evidence of pancreatic injury. Amylase levels monitoring of propofol-sedated patients is warranted.


Subject(s)
Hyperamylasemia/chemically induced , Hypnotics and Sedatives/adverse effects , Propofol/adverse effects , Cohort Studies , Humans , Intensive Care Units , Length of Stay , Middle Aged
8.
Eur J Cancer Care (Engl) ; 16(6): 539-42, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17944770

ABSTRACT

Patients with metastatic colorectal carcinoma (CRC) often develop bone metastases with a high risk of complications. Ibandronate is a novel single-nitrogen bisphosphonate that has been shown to be effective for treating bone metastases from breast cancer. A randomized, placebo-controlled trial was conducted to evaluate the efficacy and safety of ibandronate in patients with bone metastases from CRC. The primary efficacy end point was the proportion of patients with skeletal-related events (defined as pathologic fracture, spinal cord compression, radiation therapy to bone, change in antineoplastic therapy or surgery to bone). Secondary end points included time to first skeletal event, skeletal morbidity rate (events/year) and time to progression of bone lesions. In 73 patients with CRC, treatment with intravenous ibandronate 6 mg administered via a 15-min infusion significantly reduced the proportion of patients with skeletal events (39% vs. 78% with placebo; P = 0.019) and prolonged the time to first event by at least 6 months (median >279 vs. 93 days with placebo; P = 0.009). Ibandronate also significantly reduced the skeletal morbidity rate (mean 2.36 vs. 3.14 with placebo; P = 0.018) and prolonged time to progression of bone lesions (214 days vs. 81 days with placebo; P = 0.018). Ibandronate was well tolerated with very rare grade 3 or 4 toxicity. Furthermore, the incidence of renal adverse events was comparable with placebo and there were no clinically relevant changes in serum creatinine. Ibandronate provided significant clinical benefits for patients with bone metastases secondary to CRC. These results indicate that ibandronate may be an effective treatment for patients with metastatic bone disease following CRC. Larger studies are required for further assessment.


Subject(s)
Bone Density Conservation Agents/administration & dosage , Bone Neoplasms/prevention & control , Bone Neoplasms/secondary , Colorectal Neoplasms , Diphosphonates/administration & dosage , Adult , Bone Density Conservation Agents/therapeutic use , Diphosphonates/therapeutic use , Female , Humans , Ibandronic Acid , Infusions, Intravenous , Male , Middle Aged , Pilot Projects
9.
Langenbecks Arch Chir ; 353(1): 19-33, 1980.
Article in German | MEDLINE | ID: mdl-7206977

ABSTRACT

Clinical findings, diagnosis, and pathology of heart myxoma are discussed on the basis of personal experience with nine patients. There was a striking variety of signs and symptoms caused by tumor embolization, hemodynamic obstruction, and autoimmunologic reactions. Echocardiography is the method of choice, although angiography may still be necessary in atypical or negative echocardiographic findings. The tumor should be removed as soon as possible after diagnosis. There is danger of tumor embolization in the course of the operation. Long-term results are good, if resection of the tumors is performed before catastrophic complications occur. Morphologically, myxomas are genuine tumors characterized by myxomatous stromata and cells.


Subject(s)
Heart Neoplasms/diagnosis , Myxoma/diagnosis , Adult , Angiography , Echocardiography , Female , Heart Neoplasms/pathology , Heart Neoplasms/surgery , Humans , Male , Middle Aged , Myxoma/pathology , Myxoma/surgery
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