ABSTRACT
Hyperthermia is thought to increase limb blood flow through the activation of thermosensitive mechanisms within the limb vasculature, but the precise vascular locus in which hyperthermia modulates perfusion remains elusive. We tested the hypothesis that local temperature-sensitive mechanisms alter limb hemodynamics by regulating microvascular blood flow. Temperature and oxygenation profiles and leg hemodynamics of the common (CFA), superficial (SFA) and profunda (PFA) femoral arteries, and popliteal artery (POA) of the experimental and control legs were measured in healthy participants during: (1) 3 h of whole leg heating (WLH) followed by 3 h of recovery (n = 9); (2) 1 h of upper leg heating (ULH) followed by 30 min of cooling and 1 h ULH bout (n = 8); and (3) 1 h of lower leg heating (LLH) (n = 8). WLH increased experimental leg temperature by 4.2 ± 1.2ºC and blood flow in CFA, SFA, PFA, and POA by ≥3-fold, while the core temperature essentially remained stable. Upper and lower leg blood flow increased exponentially in response to leg temperature and then declined during recovery. ULH and LLH similarly increased the corresponding segmental leg temperature, blood flow, and tissue oxygenation without affecting these responses in the non-heated leg segment, or perfusion pressure and conduit artery diameter across all vessels. Findings demonstrate that whole leg hyperthermia induces profound and sustained elevations in upper and lower limb blood flow and that segmental hyperthermia matches the regional thermal hyperemia without causing thermal or hemodynamic alterations in the non-heated limb segment. These observations support the notion that heat-activated thermosensitive mechanisms in microcirculation regulate limb tissue perfusion during hyperthermia.
Subject(s)
Blood Flow Velocity , Hemodynamics , Hyperemia/physiopathology , Hyperthermia, Induced/adverse effects , Leg/pathology , Muscle, Skeletal/pathology , Regional Blood Flow , Adult , Body Temperature Regulation , Female , Humans , Leg/blood supply , Male , Microcirculation , Muscle, Skeletal/blood supplyABSTRACT
INTRODUCTION: 22q13.3 deletion syndrome is a well-known syndrome characterized by typical clinical findings including neonatal hypotonia, absent or severely delayed speech, intellectual disability, and other various features, and detection of a heterozygous deletion of chromosome 22q13.3 with the involvement of at least part of SHANK3. It is reported that 10% to 29% of patients with 22q13.3 deletion syndrome present lymphedema. Protein-losing enteropathy (PLE) has never been reported in 22q13.3 deletion syndrome. PATIENT CONCERNS: The patient presented to our institution for refractory hypoalbuminemia and chronic lymphedema in both legs. DIAGNOSIS: The patient manifested intellectual disability, absent speech, tooth grinding, dysmorphic face, and abnormal hands and toenails. Copy-number variation sequencing confirmed the maternal deletion in 22q13.31-q13.33 (chr22:46285592-51244566, hg19). The patient was genetically diagnosed with 22q13.3 deletion syndrome. INTERVENTIONS: Low-fat diets and medium-chain triglycerides supplements were prescribed. The patient was recommended to wear compression garments and elevate legs. OUTCOMES: The symptom of diarrhea was resolved, but hypoalbuminemia persisted. Lower extremities lymphedema was gradually becoming severe. CONCLUSIONS: Primary lymphedema and PLE can occur simultaneously in a patient with 22q13.3 deletion syndrome. The 2 phenotypes could share the same genetic etiology of congenital lymphatic abnormalities. CELSR1 deletion may play a role in lymphatic dysplasia. The case also provides additional proof of the pathogenic effect of CELSR1 on hereditary lymphedema.
Subject(s)
Cadherins/genetics , Chromosome Disorders/genetics , Lymphedema/genetics , Protein-Losing Enteropathies/genetics , Chromosome Deletion , Chromosomes, Human, Pair 22/genetics , DNA Copy Number Variations , Female , Humans , Hypoalbuminemia/genetics , Intellectual Disability/genetics , Leg/pathology , Young AdultABSTRACT
The role of rivaroxaban in the treatment of leg superficial venous thrombosis (SVT) is uncertain. This article aims to determine if rivaroxaban is an effective and safe treatment for leg SVT. Patients with symptomatic leg SVT of at least 5 cm length were randomized to 45 days of rivaroxaban 10 mg daily or to placebo, and followed for a total of 90 days. Treatment failure (required a nonstudy anticoagulant; had proximal deep vein thrombosis or pulmonary embolism; or had surgery for SVT) at 90 days was the primary efficacy outcome. Secondary efficacy outcomes included leg pain severity, and venous disease-specific and general health-related quality of life over 90 days. Major bleeding at 90 days was the primary safety outcome. Poor enrollment led to the trial being stopped after 85 of the planned 600 patients were randomized to rivaroxaban (n = 43) or placebo (n = 42). One rivaroxaban and five placebo patients had a treatment failure by 90 days (absolute risk reduction = 9.0%, 95% confidence interval: -22 to 5.9%). Leg pain improvement did not differ at 7 (p = 0.16) or 45 days (p = 0.89), but was greater with rivaroxaban at 90 days (p = 0.011). There was no difference in venous disease-specific (p = 0.99) or general health-related (p = 0.37) quality of life over 45 days. There were no major bleeds or deaths in either group. There were no identifiable differences in efficacy or safety between rivaroxaban and placebo in patients with symptomatic SVT but comparisons were undermined by a much smaller than planned sample size (NCT1499953).
Subject(s)
Factor Xa Inhibitors/therapeutic use , Leg/pathology , Rivaroxaban/therapeutic use , Venous Thrombosis/drug therapy , Adult , Aged , Aged, 80 and over , Factor Xa Inhibitors/pharmacology , Female , Humans , Male , Middle Aged , Randomized Controlled Trials as Topic , Rivaroxaban/pharmacology , Young AdultABSTRACT
OBJECTIVE: Aggressive fibromatosis (AF), also called desmoid tumor, is an uncommon soft-tissue neoplasm. Characteristically, it expands locally without metastatic potential. However, its tendency of relapse after curative resections has been well documented. Effective treatment options have been limited and there is a clear need for novel treatment strategies. METHODS: We used combination therapy including multikinase tyrosine kinase inhibitor for treating AF. RESULTS: We presented a case of an extra-abdominal AF who was successfully treated with meloxicam and sorafenib combination in our clinic. She tolerated this therapy well with only mild side effects. To our knowledge, this is the first case report of an extra-abdominal AF with a major partial response to sorafenib and meloxicam combination. CONCLUSION: Due to the favorable toxicity profile of sorafenib and meloxicam, this combination might be an effective treatment option for patients with locally aggressive and inoperable AF.
Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Fibromatosis, Aggressive/drug therapy , Muscle Neoplasms/drug therapy , Neoplasm Recurrence, Local/drug therapy , Adult , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Female , Fibromatosis, Aggressive/diagnostic imaging , Fibromatosis, Aggressive/pathology , Humans , Leg/pathology , Magnetic Resonance Imaging/methods , Meloxicam/administration & dosage , Muscle Neoplasms/diagnostic imaging , Muscle Neoplasms/pathology , Neoplasm Recurrence, Local/diagnostic imaging , Neoplasm Recurrence, Local/pathology , Protein Kinase Inhibitors/administration & dosage , Sorafenib/administration & dosage , Treatment OutcomeABSTRACT
Prolonged or unusual exercise may cause exercise-induced muscle damage (EIMD). To test whether Zynamite®, a mango leaf extract rich in the natural polyphenol mangiferin, administered in combination with quercetin facilitates recovery after EIMD, 24 women and 33 men were randomly assigned to two treatment groups matched by sex and 5 km running performance, and ran a 10 km race followed by 100 drop jumps to elicit EIMD. One hour before the competition, and every 8 hours thereafter for 24 hours, they ingested placebo (728 mg of maltodextrin) or 140 mg of Zynamite® combined with 140 mg of quercetin (double-blind). Although competition times were similar, polyphenol supplementation attenuated the muscle pain felt after the competition (6.8 ± 1.5 and 5.7 ± 2.2 a.u., p = 0.035) and the loss of jumping performance (9.4 ± 11.5 and 3.9 ± 5.2%, p = 0.036; p = 0.034) and mechanical impulse (p = 0.038) 24 hours later. The polyphenols attenuated the increase of serum myoglobin and alanine aminotransferase in men, but not in women (interaction p < 0.05). In conclusion, a single dose of 140 mg Zynamite® combined with 140 mg of quercetin, administered one hour before competition, followed by three additional doses every eight hours, attenuates muscle pain and damage, and accelerates the recovery of muscle performance.
Subject(s)
Exercise , Mangifera/chemistry , Muscle, Skeletal/pathology , Myalgia/therapy , Plant Extracts/pharmacology , Plant Leaves/chemistry , Quercetin/pharmacology , Biomarkers/metabolism , Body Composition/drug effects , Drug Therapy, Combination , Female , Humans , Lactic Acid/blood , Leg/pathology , Locomotion , Male , Muscle, Skeletal/drug effects , Myalgia/blood , Oxygen Consumption/drug effects , Physical Exertion , Range of Motion, Articular/drug effects , Running , Time FactorsABSTRACT
Lymphedema of the lower limbs often contributes to the mobility impairment of morbidly obese patients. Defining novel costeffective protocols is important for reducing treatment costs. The study aimed to assess if Capacitive and Resistive Energy Transfer (TECAR) can reduce edema and the minimum number of sessions needed to observe volume reduction. Forty-eight severely obese subjects (age range: 46-78 years; BMI >40 kg/m2) with bilateral lower limb lymphedema were divided into three groups undergoing either manual lymphatic drainage, pressure therapy, or TECAR, in addition to a multidisciplinary rehabilitation program. They were compared to a control group composed by 12 women (age: 67.4 ± 8.9 years, BMI: 44.6 ± 4.1 Kg/m2) undergoing only the rehabilitation program. A handheld laser scanner 3D system was used for volume measurements. In addition, patients were evaluated with a Timed Up and Go (TUG) test and pain/heaviness of the lower limbs with a Visual Analog Scale (VAS). A significant volume reduction was observed after 6 sessions of TECAR: specifically, in the whole limb (PRE: 9.7+2.8 dm3; POST: 9.4+2.8 dm3; p<0.05) and in the thigh (PRE: 3.5+1.3 dm3; POST: 3.3+1.2 dm3; p<0.05). The TUG and VAS for pain showed a significant improvement in all groups. Our preliminary results suggest that TECAR can provide a relatively early reduction of lower limb edema with improvement of patients' function and pain.
Subject(s)
Lymphedema/therapy , Physical Therapy Modalities , Pressure , Aged , Case-Control Studies , Diagnostic Imaging , Female , Humans , Leg/pathology , Lymphedema/diagnosis , Lymphedema/etiology , Lymphedema/rehabilitation , Male , Manual Lymphatic Drainage , Middle Aged , Obesity/complications , Organ Size , Treatment OutcomeABSTRACT
Calciphylaxis, also known as calcific uremic arteriolopathy, is a rare, life-threatening complication of end-stage renal disease. However, it may also occur in patients without renal failure, the nonuremic calciphylaxis. Most patients present with painful skin ulcers. Delayed diagnosis can lead to sepsis-related morbidity and mortality. Aberrations in calcium, phosphate, and parathyroid hormone physiology are common and biopsy is diagnostic. Early diagnosis and correction of vascular and metabolic aberrations may assist in healing as may the use of sodium thiosulfate and hyperbaric oxygen therapy. We report on successful treatment of a case of calciphylaxis in a renal transplant recipient with normal allograft function.
Subject(s)
Calciphylaxis , Kidney Transplantation/adverse effects , Leg Ulcer , Calciphylaxis/diagnosis , Calciphylaxis/etiology , Calciphylaxis/pathology , Calciphylaxis/therapy , Humans , Hyperbaric Oxygenation , Kidney Failure, Chronic/surgery , Leg/pathology , Leg Ulcer/diagnosis , Leg Ulcer/etiology , Leg Ulcer/pathology , Leg Ulcer/therapy , Male , Middle Aged , Thiosulfates/therapeutic useSubject(s)
Hypertension, Pulmonary/complications , Pain , Scurvy/complications , Adolescent , Ascorbic Acid/administration & dosage , Chest Pain/complications , Cholecalciferol/administration & dosage , Dietary Supplements , Echocardiography , Gingiva/pathology , Hemorrhage/complications , Humans , Iron/metabolism , Leg/pathology , Male , Wounds and Injuries/complicationsSubject(s)
Colitis, Ulcerative/complications , Colonoscopy/adverse effects , Fasciitis, Necrotizing/etiology , Administration, Intravenous , Aeromonas/isolation & purification , Aged, 80 and over , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/therapeutic use , Colitis, Ulcerative/diagnostic imaging , Debridement/methods , Fasciitis, Necrotizing/drug therapy , Fasciitis, Necrotizing/microbiology , Fasciitis, Necrotizing/surgery , Female , Humans , Hyperbaric Oxygenation/methods , Leg/diagnostic imaging , Leg/pathology , Pain/etiology , Skin Transplantation/methods , Tomography, X-Ray Computed/methods , Treatment OutcomeABSTRACT
Syringotropic mycosis fungoides (STMF) is an extremely rare form of cutaneous Tcell lymphoma with 51 published cases so far. Clinically STMF is manifested similarly to folliculotropic mycosis fungoides (MF), whereby the course of STMF is much milder. Histopathologically, it shows a prominent tropism of the Tcell lymphocytic infiltrate for the eccrine epithelium. We report the case of a 65-year-old woman with multiple small papules on the feet, shinbones and back.
Subject(s)
Mycosis Fungoides , Skin Neoplasms , Aged , Back/pathology , Female , Foot/pathology , Humans , Leg/pathology , Mycosis Fungoides/diagnosis , Mycosis Fungoides/physiopathology , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , T-Lymphocytes/pathologyABSTRACT
BACKGROUND The aim of this pragmatic study was to explore the intervention of acupuncture combined with hydrotherapy and perceived effects in type 2 diabetic patients with recently diagnosed, mild, lower-extremity arterial disease (LEAD) in comparison with a control group. MATERIAL AND METHODS One hundred twenty-six diabetes patients who were diagnosed mild LEAD according to ankle-brachial blood pressure index (ABPI) and peripheral neuropathy symptom were randomly assigned to either an experimental (n=64) or control group (n=62). The experimental group attended and completed (1) a 30-min session of acupuncture in certain selected points, and (2) a 30-min hydrotherapy exercise every 2 days for 15 weeks. The outcome parameters were assessed at baseline, after intervention, and at 6-week follow-up. RESULTS The intervention was associated with an improvement in leg flow conductance and partial physical capacities, including chair-sit-and-reach, the walking impairment questionnaire (WIQ), and physical component summary score (PCS), compared to the control group. The treatment benefits were sustained throughout the 6-week follow-up endpoint. There was no difference in fasting glucose levels, Hb1Ac, blood pressure, or BMI after the intervention. At the endpoint of 6-week follow-up, acupuncture plus hydrotherapy appeared to reduce inflammatory response by decreasing IL-6, TNF-α, malondialdehyde, and SOD, and increasing glutathione. CONCLUSIONS Acupuncture plus hydrotherapy, without significant glycemic-controlling effects in the type 2 diabetic patients with mild LEAD, exerts a measurable benefit in disease-specific physical functions and health-related quality of life. Our results suggest that the combined therapy regulates the inflammatory process and oxidative stress and contributes to immune protection.
Subject(s)
Acupuncture Therapy , Arteries/pathology , Diabetes Mellitus/therapy , Hydrotherapy , Leg/pathology , Vascular Diseases/therapy , Acupuncture Therapy/adverse effects , Case-Control Studies , Female , Follow-Up Studies , Glutathione/metabolism , Humans , Hydrotherapy/adverse effects , Male , Malondialdehyde/metabolism , Middle Aged , Superoxide Dismutase/metabolism , Treatment Outcome , Tumor Necrosis Factor-alpha/metabolismABSTRACT
Tattoo popularity continues to rise, with 3 in 10 Americans bearing at least one. Among tattoo complications, non-tuberculous mycobacteria (NTM) has emerged as a global public health concern. NTM infections associated with tattooing of immunocompetent individuals have occurred as sporadic cases and community outbreaks. Water sources are considered the major pathogenic reservoirs. Tattoo-related inoculation has been linked to contamination of ink, either during the manufacturing process or during dilution of black ink using non-sterile water. NTM infections have also been documented in a number of cosmetic and surgical procedures, including cutaneous surgery, Mohs micrographic surgery, mesotherapy, liposuction and laser resurfacing. NTM inoculation through exposure to contaminated water or non-sterile instruments remains a challenge for dermatologists and risk to patients. We reported a case of cutaneous Mycobacterium massiliense infection following tattoo placement. This report underscores the importance of clinicians to consider NTM infections in the differential diagnosis of procedure-related reactions.
Subject(s)
Anti-Bacterial Agents/therapeutic use , Equipment Contamination , Fresh Water/microbiology , Ink , Leg/pathology , Mycobacterium Infections, Nontuberculous/microbiology , Mycobacterium abscessus/pathogenicity , Skin Diseases, Bacterial/microbiology , Tattooing/adverse effects , Adult , Disease Outbreaks , Humans , Male , Mycobacterium Infections, Nontuberculous/drug therapy , Public Health , Skin Diseases, Bacterial/drug therapy , Tattooing/standards , United StatesABSTRACT
BACKGROUND: The purpose of this study is to investigate the effects of the aqua-lymphatic therapy (ALT) on unilateral lower extremity lymphedema in the maintenance phase. MATERIALS AND METHODS: This is a randomized controlled trial with a blinded assessor. The study was completed with 30 ALT and 27 control group participants. Foot volume was assessed by a water displacement device, limb volume by circumference measurements, functional capacity by a 6-minute walk test, quality of life by Short Form-36, and social appearance by Social Appearance Anxiety Scale and hopeless by Beck Hopeless Scale. The ALT and the control group had group sessions twice in a week for 6 weeks directed by a physiotherapist. RESULTS: The mean age of ALT patients was 44.50 ± 13.69 years, whereas that of the control patients was 47.66 ± 16.82 years. After the intervention, both groups' measurement of edema, functional level, quality of life, as well as social and future concerns improved significantly but this improvement was higher in the ALT group (p < 0.05, p ≤ 0.001). CONCLUSIONS: ALT was found to be a safe effective method for unilateral lower extremity lymphedema patients during the maintenance phase of Complex Decongestive Physiotherapy.
Subject(s)
Leg/pathology , Lymphedema/therapy , Physical Therapy Modalities , Adult , Anxiety , Exercise Therapy , Female , Humans , Leg/physiopathology , Lymphedema/diagnosis , Lymphedema/psychology , Male , Middle Aged , Organ Size , Treatment OutcomeABSTRACT
The purpose of the study was to evaluate clinical efficacy of electromyostimulation (EMS) of the crural muscles as part of comprehensive therapy for post-thrombotic disease in patients with residual venous obstruction in the femoropopliteal segment. We carried out a prospective comparative clinical study enrolling patients having endured a fist episode of clinically unprovoked venous thrombosis of the femoropopliteal segment and completed the standard 6-month course of anticoagulant therapy and presenting with ultrasonographic signs of complete recanalization of the proximal venous segments (stenosis of 20% and more from the vessel's initial diameter), as well as scoring 5 points and more by the Villalta scale. The study included a total of 60 patients (38 men and 22 women, mean age 58.5±11.4 years) subdivided into two groups consisting of 30 patients each. Patients of both the Study and Control Groups underwent comprehensive therapy including wearing a compression knee sock (23-32 mmHg), a course phlebotrophic drugs, and dosed walking (not less than 5,000 steps a day). The Study Group patients were additionally subjected to daily electrical stimulation of the crural muscles with the "Veinoplus VI" unit (three 30-minute sessions a day). The duration of the follow up amounted to 12 months. The criteria for assessing therapeutic efficacy were as follows: severity of the disease by the VCSS and Villalta scales, quality of life as assessed by the CIVIQ-20 questionnaire, and lack of relapses of the venous thrombus. Clinical and instrumental assessment of the patients' condition was carried out monthly, with the disease's severity and quality of life assesses each 6 months. Relapses of venous thrombosis were registered in 7 (23.3%) patients from the Control Group and were not observed in patients undergoing EMS (p=0.011). In 5 cases, thrombosis was asymptomatic and in 4 cases it was presented by reocclusion of the involved venous segments. Patients of the Study Group were found to have a decrease in the disease's severity, reflected in points: VCSS (9.9±1.6 - 7.8 ± 1.6 - 6.1±1.5 (p <0.0001)); Villalta scale (18.9±3.9 - 12.8±4.0 - 8.3±2.7 (p<0.0001)); CIVIQ-20 score (67.8±8.4 - 51.3±8.4 - 40.0±10.5 (p<0.001)). The Control Group patients showed a similar tendency for the disease's severity: 8.1±2.8 - 7.3±2.1 - 7.2±2.1 points by the VCSS (p=0.014); 12.7±6.7 - 10.9±5.6 - 10.2±5.4 points by the Villalta scale (p=0.002), but not for quality of life: 48.2±19.3 - 46.7±17.3 - 47.4±16.2 points by the CIVIQ-20 (p>0.05). On the background of using EMS, the alterations in the studied parameters were characterized by higher velocity and intensity (p<0.05). The use of electromyostimulation as part of comprehensive treatment for post-thrombotic disease makes it possible to efficiently eliminate both subjective and objective signs of venous insufficiency, improve patients' quality of life and decrease the risk for the development of relapsing venous thrombosis.
Subject(s)
Anticoagulants/therapeutic use , Electric Stimulation Therapy/methods , Leg , Physical Therapy Modalities , Quality of Life , Stockings, Compression , Venous Thrombosis/complications , Aged , Combined Modality Therapy/methods , Female , Femoral Vein/diagnostic imaging , Femoral Vein/pathology , Humans , Leg/blood supply , Leg/pathology , Male , Middle Aged , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Postthrombotic Syndrome/diagnosis , Postthrombotic Syndrome/physiopathology , Postthrombotic Syndrome/psychology , Postthrombotic Syndrome/therapy , Secondary Prevention/methods , Treatment Outcome , Ultrasonography/methodsABSTRACT
STUDY DESIGN: Randomized two-group parallel. OBJECTIVES: The objective of this study was to analyze the adaptations on the popliteal artery (mean blood velocity (MBV), peak blood velocity (PBV), arterial resting diameter (RD) and blood flow (BF)) induced by 12 weeks of simultaneous application of whole-body vibration and electromyostimulation (WBV+ES) in patients with spinal cord injury (SCI). Secondarily, the musculoskeletal effects of this therapy on the gastrocnemius muscle thickness (MT) and femoral neck bone mineral density (BMD) were analyzed. SETTING: Valladolid, Spain. METHODS: Seventeen SCI patients (American Spinal Injury Association (ASIA) A or B) were randomly assigned to the experimental group (EG=9) or the control group (CG=8). Each subject was assessed in four different occasions: at baseline, after 6 weeks (Post-6) and 12 weeks of the treatment (Post-12) and 8 weeks after the end of the treatment (Post-20). Subjects in the EG performed 30 10-min sessions of WBV+ES during 12 weeks. RESULTS: In the EG, RD increased compared with the baseline value at Post-6 (9.5%, P<0.01), Post-12 (19.0%, P<0.001) and Post-20 (16.7%, P<0.001). Similarly, in the EG, BF increased compared with the baseline value and with CG only at Post-12 ((33.9%, P<0.01) and (72.5%, P<0.05), respectively). Similarly, WBV+ES increased the MT of the gastrocnemius. BMD of both hips remained invariable during the study. CG showed no change at any point. CONCLUSIONS: WBV+ES improved popliteal artery BF, RD and MT after 12 weeks in SCI patients. This increase in RD remained above baseline after 8 weeks. The combination of WBV and ES could be considered a promising alternative to reverse the musculoskeletal atrophy and improve peripheral vascular properties in SCI patients.
Subject(s)
Arteries/physiopathology , Electric Stimulation Therapy/methods , Leg/physiopathology , Spinal Cord Injuries/physiopathology , Spinal Cord Injuries/therapy , Vibration/therapeutic use , Adult , Aged , Arteries/pathology , Blood Flow Velocity , Bone Density , Female , Femur/chemistry , Humans , Leg/pathology , Male , Middle Aged , Muscle, Skeletal/pathology , Muscle, Skeletal/physiopathology , Organ Size , Regional Blood Flow , Spinal Cord Injuries/pathology , Treatment OutcomeSubject(s)
Folic Acid/therapeutic use , Hyperhomocysteinemia/complications , Hyperhomocysteinemia/drug therapy , Skin Diseases, Vascular/drug therapy , Skin Diseases, Vascular/etiology , Vitamin B 12/therapeutic use , Vitamin B 6/therapeutic use , Adult , Female , Humans , Leg/blood supply , Leg/pathology , Male , Middle AgedABSTRACT
Results of treatment of 71 patients, suffering an acute idiopathic deep veins thrombo' sis (DVT) of lower extremities,were analyzed. In 32 (45.1%) patients rivaroxaban was applied, in 39 (54.9%) varfarin. The term of anticoagulant therapy was determined in accordance to the Ddimers level. Recurrence of the DVT, of massive hemorrhage or pulmonary thromboembolism in the followup groups were absent. In 29 (74.4%) patientsa constant dose of varfarin was lined up during minimal recommended period. For reduction of the DVT occurrence risk a rivaroxaban may serve as an alternative to varfarin.
Subject(s)
Anticoagulants/therapeutic use , Femoral Vein/drug effects , Fibrin Fibrinogen Degradation Products/metabolism , Rivaroxaban/therapeutic use , Venous Thrombosis/drug therapy , Warfarin/therapeutic use , Adult , Aged , Biomarkers/blood , Drug Administration Schedule , Female , Femoral Vein/metabolism , Femoral Vein/pathology , Humans , Leg/blood supply , Leg/pathology , Male , Middle Aged , Prospective Studies , Pulmonary Embolism/prevention & control , Venous Thrombosis/blood , Venous Thrombosis/pathologyABSTRACT
INTRODUCTION: Exon-skipping drugs in Duchenne muscular dystrophy (DMD) aim to restore truncated dystrophin expression, which is present in the milder Becker muscular dystrophy (BMD). MRI skeletal muscle T2 relaxation times as a representation of edema/inflammation could be quantitative outcome parameters for such trials. METHODS: We studied T2 relaxation times, adjusted for muscle fat fraction using Dixon MRI, in lower leg muscles of DMD and BMD patients and healthy controls. RESULTS: T2 relaxation times correlated significantly with fat fractions in patients only (P < 0.001). After adjusting for muscle fat, T2 relaxation times were significantly increased in 6 muscles of DMD patients (P < 0.01), except for the extensor digitorum longus. In BMD, T2 relaxation times were unchanged. CONCLUSIONS: T2 relaxation times could be a useful outcome parameter in exon-skipping trials in DMD but are influenced by fat despite fat suppression. This should be accounted for when using quantitative T2 mapping to investigate edema/inflammation.
Subject(s)
Magnetic Resonance Imaging , Muscle, Skeletal/pathology , Muscular Dystrophy, Duchenne/pathology , Relaxation , Adolescent , Adult , Child , Female , Humans , Leg/pathology , Male , Middle Aged , Young AdultABSTRACT
OBJECTIVE: Na+ can be stored in muscle and skin without commensurate water accumulation. The aim of this study was to assess Na+ and H2O in muscle and skin with MRI in acute heart failure patients before and after diuretic treatment and in a healthy cohort. METHODS: Nine patients (mean age 78 years; range 58-87) and nine age and gender-matched controls were studied. They underwent 23Na/1H-MRI at the calf with a custom-made knee coil. Patients were studied before and after diuretic therapy. 23Na-MRI gray-scale measurements of Na+-phantoms served to quantify Na+-concentrations. A fat-suppressed inversion recovery sequence was used to quantify H2O content. RESULTS: Plasma Na+-levels did not change during therapy. Mean Na+-concentrations in muscle and skin decreased after furosemide therapy (before therapy: 30.7±6.4 and 43.5±14.5 mmol/L; after therapy: 24.2±6.1 and 32.2±12.0 mmol/L; pË0.05 and pË0.01). Water content measurements did not differ significantly before and after furosemide therapy in muscle (p = 0.17) and only tended to be reduced in skin (p = 0.06). Na+-concentrations in calf muscle and skin of patients before and after diuretic therapy were significantly higher than in healthy subjects (18.3±2.5 and 21.1±2.3 mmol/L). CONCLUSIONS: 23Na-MRI shows accumulation of Na+ in muscle and skin in patients with acute heart failure. Diuretic treatment can mobilize this Na+-deposition; however, contrary to expectations, water and Na+-mobilization are poorly correlated.