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1.
MMWR Morb Mortal Wkly Rep ; 64(13): 347-50, 2015 Apr 10.
Article in English | MEDLINE | ID: mdl-25856255

ABSTRACT

The Ebola virus disease (Ebola) epidemic in West Africa has so far produced approximately 25,000 cases, more than 40 times the number in any previously documented Ebola outbreak. Because of the risk for imported disease from infected travelers, in October 2014 CDC recommended that all travelers to the United States from Ebola-affected countries receive enhanced entry screening and postarrival active monitoring for Ebola signs or symptoms until 21 days after their departure from an Ebola-affected country. The state of Georgia began its active monitoring program on October 25, 2014. The Georgia Department of Public Health (DPH) modified its existing, web-based electronic notifiable disease reporting system to create an Ebola Active Monitoring System (EAMS). DPH staff members developed EAMS from conceptualization to implementation in 6 days. In accordance with CDC recommendations, "low (but not zero) risk" travelers are required to report their daily health status to DPH, and the EAMS dashboard enables DPH epidemiologists to track symptoms and compliance with active monitoring. Through March 31, 2015, DPH monitored 1,070 travelers, and 699 (65%) used their EAMS traveler login instead of telephone or e-mail to report their health status. Medical evaluations were performed on 30 travelers, of whom three were tested for Ebola. EAMS has enabled two epidemiologists to monitor approximately 100 travelers daily, and to rapidly respond to travelers reporting signs and symptoms of potential Ebola virus infection. Similar electronic tracking systems might be useful for other jurisdictions.


Subject(s)
Epidemics/prevention & control , Hemorrhagic Fever, Ebola/prevention & control , Population Surveillance/methods , Travel , Africa, Western/epidemiology , Georgia/epidemiology , Hemorrhagic Fever, Ebola/epidemiology , Humans
2.
J Oral Maxillofac Surg ; 68(2): 260-7, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20116693

ABSTRACT

PURPOSE: To establish a rat mandibular fracture model and investigate the short- and long-term effects of recombinant parathyroid hormone (PTH 1-34) on mandibular fracture healing in rats. MATERIALS AND METHODS: A controlled unilateral mandibular fracture was created surgically in 29 male Sprague-Dawley rats and then stabilized using an external fixation device. The rats were divided into 2 groups: 1 group received daily subcutaneous injections of 10 microg/kg of PTH(1-34) and 1 group served as the vehicle control. The rats were killed on postoperative days 7 and 21, and radiographic densitometry and histologic evaluation of new bone formation were performed. RESULTS: A novel unilateral mandibular fracture model was established that has significant differences from previously published models, both in the location of the osteotomy site and in the rigid external stabilization device. The PTH(1-34) treated rats showed a statistically significant difference (P < .05) in callous formation compared with the control animals. Radiographic densitometry evaluation of the injury site revealed an increase in bone density, apparent at day 7 in the experimental group. Visual inspection of the histologic sections stained with Masson's trichrome blue showed an apparent increase in new bone formation at 21 days in the PTH-treated group compared with the control group. CONCLUSIONS: Intermittent systemic administration of PTH(1-34) might enhance the healing of mandibular fractures in the early phase (7-day period). Long-term administration (21-day period) showed no statistically significant differences between the control and experimental group by radiographic densitometry.


Subject(s)
Bone Density Conservation Agents/administration & dosage , Fracture Healing/drug effects , Mandibular Fractures/surgery , Parathyroid Hormone/administration & dosage , Peptide Fragments/administration & dosage , Teriparatide/analogs & derivatives , Animals , Bone Density , Bone Regeneration/drug effects , Fracture Fixation, Internal , Humans , Male , Random Allocation , Rats , Rats, Sprague-Dawley , Recombinant Proteins/administration & dosage , Teriparatide/administration & dosage
3.
J Am Coll Surg ; 209(2): 278-83, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19632606

ABSTRACT

BACKGROUND: On the modern battlefield, the majority of injuries currently seen are to the extremities, often involving a large number of metallic fragments. Although they are typically left in place, the effects of these retained metal fragments on nerve healing have not been studied. STUDY DESIGN: In a rat model, the right peroneal nerve was surgically sectioned and reanastomosed (control group). In the study group, metal fragments from an artillery casing were placed around the reanastomosed peroneal nerve. Functional recovery in both groups was evaluated over a 4-week period by measuring maximum ankle dorsiflexion captured on video as the animals walked through a tunnel. Morphologic analyses included distal and proximal axon counts, measurement of nerve fiber and axon diameter ratios, and myelin thickness. RESULTS: A significant decrease (p < 0.05) in return toward baseline for the rats' ankle angle in the nerves exposed to metal fragments was noted at weeks 2 through 4. Distal axon counts were significantly less (p < 0.05) in the metal fragment group for weeks 1 through 4. Proximal axon counts were increased in both groups, with a greater (p < 0.05) increase in the metal fragment group. CONCLUSIONS: Functional recovery after rat peroneal nerve transection and repair is decreased when metal fragments are placed in and around the injury site. Select histologic indicators of nerve regeneration showed decreased healing when exposed to metal fragments. Further studies of functional recovery in patients sustaining penetrating injuries from bullets or explosive devices are indicated.


Subject(s)
Ankle Joint/physiopathology , Metals , Nerve Regeneration/physiology , Peripheral Nerve Injuries , Peroneal Nerve/surgery , Wounds, Gunshot/complications , Analysis of Variance , Animals , Ankle Joint/innervation , Male , Rats , Rats, Sprague-Dawley , Recovery of Function
4.
Aesthetic Plast Surg ; 32(4): 624-31, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18443849

ABSTRACT

BACKGROUND: Distal ischemic necrosis of surgical flaps remains a challenging problem for the reconstructive surgeon. Recent studies have shown that either sildenafil or vascular endothelium growth factor (VEGF) treatment significantly improves ischemic skin flap viability. In this study, the effect of the combination of sildenafil and VEGF165 was evaluated on a rat skin flap model using orthogonal polarization spectral imaging and histologic analysis. METHODS: Rats were assigned to either a sham (n = 31), vehicle (n = 24), sildenafil (n = 24), VEGF (n = 23), or sildenafil and VEGF combination treatment (n = 21) groups. Distances from the distal end of the flap to avascular, stasis, and normal capillary blood flow zones were determined using orthogonal polarization spectral imaging on a skin flap model. Vessel density assessment was done at 7 days post surgery. RESULTS: Imaging analysis showed significant reduction in avascular and stasis areas in sildenafil and VEGF combination-treated groups at 7 days post surgery (p < 0.05). The combination-treated group, however, was not significantly different when compared to the group treated with sildenafil only. The sildenafil-treated group showed a significant (p < 0.05) reduction in both areas at day 7 compared to the VEGF and control groups. Histologic analysis showed no significant differences in vessel density between the groups. CONCLUSION: The combination of sildenafil and VEGF decreases the extent of avascular and stasis zones in skin flaps. The skin flap improvement seen with the combination treatment was similar to the sildenafil treatment alone suggesting that enhanced flap survival was due solely to the effect of sildenafil.


Subject(s)
Angiogenesis Inducing Agents/administration & dosage , Graft Survival/drug effects , Piperazines/administration & dosage , Sulfones/administration & dosage , Surgical Flaps/blood supply , Vascular Endothelial Growth Factor A/administration & dosage , Vasodilator Agents/administration & dosage , Animals , Capillaries/anatomy & histology , Male , Purines/administration & dosage , Rats , Rats, Sprague-Dawley , Sildenafil Citrate , Surgical Flaps/pathology
5.
Laryngoscope ; 116(4): 522-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16585853

ABSTRACT

OBJECTIVE: Distal ischemic necrosis of the flap remains an unsolved, challenging problem. Phosphodiesterase (PDE) inhibitors, which include the drug sildenafil, are a relatively new class of U.S. Food and Drug Administration-approved medications whose effect on tissue viability has not been widely explored. The vasodilatory effects of these drugs have the potential to enhance blood flow to flaps and increase their survivability. The purpose of this study was to examine the short- and long-term effects of sildenafil, administered intraperitoneally at a dose of 9 mg/kg per day, on the survival of surgical skin flaps in rats. METHODS: A McFarlane-type random pattern skin (3 x 10-cm) flap model was used to evaluate the effect of sildenafil on necrosis at multiple time points. Rats were assigned to sildenafil-treated (9 mg/kg per day intraperitoneally; n = 34), vehicle control (n = 35), or sham (no injection; n = 40) groups. In each group, caudally based, dorsal, rectangular (3 x 10-cm) flaps were created. Flap necrosis was determined using orthogonal polarization spectral imaging and digital photography analysis on days 1, 3, 5, and 7 postsurgery. RESULTS: Orthogonal polarization spectral imaging results showed a significant decrease in necrosis and stasis in rats treated with sildenafil on days 1 and 3. Although reductions observed at days 5 and 7 were not as dramatic as days 1 and 3, digital photography analysis confirmed a decrease in the area of necrosis at all time points evaluated. CONCLUSIONS: These results suggest that PDE 5 inhibitors may play a more important role in early postoperative skin flap viability rather than at later time points and may be beneficial for skin flap viability as shown in the rat model. PDE 5 inhibitors may reduce the extent of necrosis after reconstructive surgeries.


Subject(s)
Dermatologic Surgical Procedures , Microcirculation/drug effects , Phosphodiesterase Inhibitors/pharmacology , Piperazines/pharmacology , Surgical Flaps/blood supply , 3',5'-Cyclic-GMP Phosphodiesterases/antagonists & inhibitors , Animals , Blood Flow Velocity/drug effects , Disease Models, Animal , Follow-Up Studies , Male , Necrosis/pathology , Necrosis/prevention & control , Purines , Rats , Rats, Sprague-Dawley , Sildenafil Citrate , Sulfones , Surgical Flaps/pathology , Time Factors , Treatment Outcome
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