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1.
Ann Plast Surg ; 79(4): 410-414, 2017 Oct.
Article in English | MEDLINE | ID: mdl-28570457

ABSTRACT

The number of reduction mammoplasties performed in the United States continues to increase annually. Given the high incidence of breast cancer in women, it is routine practice for breast tissue excised during routine breast reductions procedures to be sent for pathology review. During pathology assessment, occult malignancy and on-occasion proliferative breast lesions of unknown and/or variable malignancy may also be present. We provide a review of commonly diagnosed atypical proliferative breast lesions in breast reduction specimens and a guide to plastic surgeons for further management.


Subject(s)
Breast Diseases/diagnosis , Incidental Findings , Mammaplasty , Breast/pathology , Breast/surgery , Breast Diseases/pathology , Breast Diseases/therapy , Female , Humans
2.
Plast Surg Nurs ; 36(2): 90-1, 2016.
Article in English | MEDLINE | ID: mdl-27254241

ABSTRACT

Breast reduction surgery is one of the most common procedures done by plastic surgeons. Although not detrimental to the final outcome, allergic reaction can negatively impact the postoperative course. This case presentation paints the classic picture of allergic reaction after breast surgery, likely due to skin glue. The typical signs of intense pruritus and erythematous rash surrounding incisions bilaterally are present. The patient was treated with our institutional protocol with good results. Our protocol is presented and further questions posed.


Subject(s)
Dermatitis, Allergic Contact/physiopathology , Mammaplasty/adverse effects , Adolescent , Dermatitis, Allergic Contact/drug therapy , Female , Humans , Mammaplasty/methods , Mammaplasty/standards , Triamcinolone/therapeutic use
3.
Neuromodulation ; 18(8): 754-6, 2015 Dec.
Article in English | MEDLINE | ID: mdl-25906677

ABSTRACT

OBJECTIVE: Implantable pulse generators for neurostimulation and other indications are becoming more widespread. Pain at the generator site, erosion through the subcutaneous issues, and migration of the generator are frequent post-operative complications that result in high rates of re-operation. We report a case where a submammary combined approach with plastic surgery for improved soft tissue coverage resulted in better esthetic and functional outcomes in a thin woman. MATERIALS AND METHODS: A 40-year-old thin woman presented for revision of spinal cord stimulator due to pain at the bilateral infraclavicular generator sites secondary to lack of soft tissue coverage. She underwent revision of the implantable generator site with placement of the generator in the submammary location and concurrent mastopexy with plastic surgery. RESULTS: At two-year follow-up she continues to be pain-free after surgery and is very satisfied by the cosmetic outcome. CONCLUSION: Submammary placement of implantable pulse generators in thin women combined with mastopexy may result in improved soft tissue coverage, decreased pain at the generator site, and a low rate of complications.


Subject(s)
Electric Stimulation Therapy/methods , Pain, Postoperative/therapy , Spinal Cord/physiology , Adult , Breast Implantation/adverse effects , Female , Humans , Longitudinal Studies , Mammaplasty/adverse effects , Mammaplasty/methods , Pain, Postoperative/etiology , Plastic Surgery Procedures/adverse effects , Treatment Outcome
4.
Plast Reconstr Surg ; 135(3): 682-689, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25719690

ABSTRACT

BACKGROUND: During breast reconstruction using the transverse rectus abdominis myocutaneous (TRAM) flap, the use of mesh for abdominal donor-site closure provides for a technology that potentially offers clinical benefit yet incurs an added cost. The authors' goal was to determine whether it is cost effective to use mesh during abdominal donor-site closure when performing a TRAM flap for breast reconstruction. METHODS: A literature review was conducted to identify and collect published hernia and bulge rates at abdominal TRAM flap donor sites closed either primarily or with mesh. A decision tree analysis was performed. Outcome probabilities, costs of complications, and expert utility estimates were populated into the decision tree model to evaluate the cost-utility of using mesh in TRAM abdominal donor-site closure. One-way sensitivity analyses were performed to verify the robustness of the results. RESULTS: The authors' literature review resulted in 10 articles describing 1195 patients who had TRAM abdominal donor-site closure primarily and 696 patients who had donor-site closure performed with mesh. Pooled hernia/bulge complication rates for these two groups were 7.87 percent and 4.45 percent, respectively. The use of mesh was more clinically effective based on total quality-adjusted life-years gained of 30.53 compared with 30.41 when performing primary fascial closure alone. The incremental additional cost incurred by the mesh arm when running the decision tree model was $693.14. This difference in cost, divided by the difference in clinical efficacy (0.12), results in an incremental cost-utility ratio value of $5776.17 per quality-adjusted life-year gained when using mesh, making it cost effective (when using a willingness-to-pay threshold of $50,000). One-way sensitivity analysis revealed the following: (1) using mesh was a cost effective option, provided that the price of mesh was less than or equal to $5970; (2) mesh was cost effective when its use led to a hernia/bulge rate less than or equal to 7.25 percent; and (3) primary facial closure was cost effective when its use led to a hernia/bulge rate less than or equal to 4.75 percent. CONCLUSION: The use of mesh when repairing the abdominal donor site during a pedicled or free TRAM flap breast reconstruction is cost effective compared with primary fascial closure alone.


Subject(s)
Cost-Benefit Analysis/methods , Fasciotomy , Mammaplasty/economics , Myocutaneous Flap , Rectus Abdominis/transplantation , Female , Humans , Mammaplasty/methods , Wound Healing
5.
Plast Reconstr Surg ; 133(1): 187-194, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24374678

ABSTRACT

BACKGROUND: Almost three times as many board-certified female plastic surgeons are unmarried compared with male colleagues. The purpose of this study was to determine why women in plastic surgery are less likely to be married. METHODS: A 52-question survey was sent to all female members of the American Society of Plastic Surgeons. Questions focused on type of training and practice; marital status; age at marriage; spousal education, financial, and professional status; relational goals, values, and satisfaction. A total of 729 questionnaires were sent via e-mail; responses were anonymous. RESULTS: Response rate was 34 percent (n = 250). Respondents were either married (64 percent), engaged (2 percent), in a "serious" relationship (11 percent), or not in a committed relationship (23 percent). Of unmarried respondents, 56 percent wanted to marry, 44 percent did not wish marriage at the time of the survey, and 42 percent had deliberatively postponed marriage. The most frequently cited reasons for being single were perceived lack of desirable partners (45 percent), job constraints (14 percent), and personality differences (13 percent). Female plastic surgeons who married later than 36 years of age were more likely to choose a spouse with a lower income, less education, and lower financial success compared with female plastic surgeons who married at a younger age. CONCLUSIONS: Women in surgical practice who marry later are less likely to find a partner with equal educational level, financial resources, and professional success. Hence, a shift occurs from hypergamy toward hypogamy. These findings are not unique to plastic surgery.


Subject(s)
Attitude of Health Personnel , Marriage/statistics & numerical data , Physicians, Women/psychology , Physicians, Women/statistics & numerical data , Surgery, Plastic/statistics & numerical data , Adult , Aged , Family , Female , Humans , Male , Middle Aged , Social Behavior , Surgery, Plastic/education , Surveys and Questionnaires
6.
Plast Reconstr Surg ; 132(5): 709e-723e, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24165623

ABSTRACT

BACKGROUND: The purpose of this study was to assess the cost-effectiveness of five standardized procedures for breast reconstruction to delineate the best reconstructive approach in postmastectomy patients in the settings of nonirradiated and irradiated chest walls. METHODS: A decision tree was used to model five breast reconstruction procedures from the provider perspective to evaluate cost-effectiveness. Procedures included autologous flaps with pedicled tissue, autologous flaps with free tissue, latissimus dorsi flaps with breast implants, expanders with implant exchange, and immediate implant placement. All methods were compared with a "do-nothing" alternative. Data for model parameters were collected through a systematic review, and patient health utilities were calculated from an ad hoc survey of reconstructive surgeons. Results were measured in cost (2011 U.S. dollars) per quality-adjusted life-year. Univariate sensitivity analyses and Bayesian multivariate probabilistic sensitivity analysis were conducted. RESULTS: Pedicled autologous tissue and free autologous tissue reconstruction were cost-effective compared with the do-nothing alternative. Pedicled autologous tissue was the slightly more cost-effective of the two. The other procedures were not found to be cost-effective. The results were robust to a number of sensitivity analyses, although the margin between pedicled and free autologous tissue reconstruction is small and affected by some parameter values. CONCLUSIONS: Autologous pedicled tissue was slightly more cost-effective than free tissue reconstruction in irradiated and nonirradiated patients. Implant-based techniques were not cost-effective. This is in agreement with the growing trend at academic institutions to encourage autologous tissue reconstruction because of its natural recreation of the breast contour, suppleness, and resiliency in the setting of irradiated recipient beds.


Subject(s)
Breast Neoplasms/surgery , Breast/surgery , Mammaplasty/economics , Mammaplasty/methods , Breast Neoplasms/radiotherapy , Cost-Benefit Analysis , Decision Trees , Female , Humans , Mastectomy , Surgical Flaps/economics
7.
Plast Reconstr Surg ; 131(5): 693e-701e, 2013 May.
Article in English | MEDLINE | ID: mdl-23629108

ABSTRACT

BACKGROUND: Laser-assisted indocyanine green angiography is a U.S. Food and Drug Administration-approved technology used to assess tissue viability and perfusion. Its use in plastic and reconstructive surgery to assess flap perfusion in autologous breast reconstruction is relatively new. There have been no previous studies evaluating the cost-effectiveness of this new technology compared with the current practice of clinical judgment in evaluating tissue perfusion and viability in free autologous breast reconstruction in patients who have undergone mastectomy. METHODS: A comprehensive literature review was performed to identify the complication rate of the most common complications with and without laser-assisted indocyanine green angiography in free autologous breast reconstruction after mastectomy. These probabilities were combined with Medicare Current Procedural Terminology provider reimbursement codes (cost) and utility estimates for common complications from a survey of 10 plastic surgeons to fit into a decision model to evaluate the cost-effectiveness of laser-assisted indocyanine green angiography. RESULTS: The decision model revealed a baseline cost difference of $773.66 and a 0.22 difference in the quality-adjusted life-years, yielding an incremental cost-utility ratio of $3516.64 per quality-adjusted life year favoring laser-assisted indocyanine green angiography. Sensitivity analysis showed that using laser-assisted indocyanine green angiography was more cost-effective when the complication rate without using laser-assisted indocyanine green angiography (clinical judgment alone) was 4 percent or higher. CONCLUSIONS: The authors' study demonstrates that laser-assisted indocyanine green angiography is a cost-effective technology under the most stringent acceptable thresholds when used in immediate free autologous breast reconstruction.


Subject(s)
Angiography/economics , Angiography/methods , Indocyanine Green , Mammaplasty/economics , Mammaplasty/methods , Coloring Agents , Cost-Benefit Analysis , Female , Free Tissue Flaps/blood supply , Free Tissue Flaps/economics , Health Care Surveys , Humans , Mammaplasty/adverse effects , Postoperative Complications/economics , Postoperative Complications/prevention & control
8.
Plast Reconstr Surg ; 131(5): 820e-826e, 2013 May.
Article in English | MEDLINE | ID: mdl-23629121

ABSTRACT

The Practice Advisory on Liposuction published by the American Society of Plastic Surgeons provides a thorough review of anesthetic techniques and guidelines for surgeons who perform liposuction. However, there is evidence to support several changes to the anesthetic infiltrate guidelines that will improve patient safety. These proposed recommendations will have the most impact on patients undergoing office-based procedures, where dedicated anesthesia providers may not be present, but they should also guide practice in both ambulatory care centers and hospitals. The primary foci of the proposed changes include restrictions on bupivacaine use and creation of lidocaine concentration guidelines.


Subject(s)
Ambulatory Surgical Procedures/standards , Anesthesia, Local/standards , Anesthetics, Local/administration & dosage , Lipectomy/standards , Practice Guidelines as Topic , Anesthetics, Local/adverse effects , Anesthetics, Local/pharmacokinetics , Bupivacaine/administration & dosage , Bupivacaine/adverse effects , Bupivacaine/pharmacokinetics , Humans , Lidocaine/administration & dosage , Lidocaine/adverse effects , Lidocaine/pharmacokinetics , Patient Safety
9.
10.
Neurosurgery ; 71(1 Suppl Operative): 15-20; discussion 21, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22899488

ABSTRACT

BACKGROUND: Hemicraniectomy is an established neurosurgical procedure. However, before cranial vault reconstruction, it is imperative that sufficient scalp soft tissue is available for coverage of the reconstructed skull. OBJECTIVE: To present 2 complex cases of posttraumatic patients requiring soft tissue expansion of the scalp before definite cranioplasty with use of a synthetic polyethylene graft. METHODS: Two patients underwent decompressive hemicraniectomy for trauma and required delayed cranioplasty. Both patients had developed significant scalp contraction and presented with a paucity of soft tissue. These patients underwent a staged cranioplasty in which we first achieved scalp-tissue expansion adjacent to the craniectomy site over a prolonged interval. In a second stage, the patient underwent definite reconstructive surgery in which the subgaleal expanders were removed and polyethylene allograft cranioplasty was performed. RESULTS: Cutaneous coverage of the underlying defect could be achieved in this setting without causing tension on the incision line secondary to the now available excess scalp tissue. CONCLUSION: Repair of a cranial defect requires detailed attention to the available scalp and its size relationship to the skull defect to achieve a successful outcome with an aesthetically pleasing, reliable, and lasting result. Preoperative scalp tissue expansion is a valuable step in taking care of patients presenting with scalp soft tissue defect. This technique reduces the morbidity associated with conventional rotational and free-flap techniques.


Subject(s)
Craniotomy/methods , Plastic Surgery Procedures/methods , Scalp/surgery , Tissue Expansion/methods , Adult , Female , Humans , Skull/injuries , Skull/surgery , Transplantation, Homologous , Young Adult
12.
Semin Plast Surg ; 26(4): 164-9, 2012 Nov.
Article in English | MEDLINE | ID: mdl-24179449

ABSTRACT

Our understanding of cleft palates has come a long way over the last few decades. A better understanding of the long-term consequences of a cleft palate and its effect on speech development challenges surgeons to not only effectively repair the cleft, but to also restore function of the palate for adequate speech. Coordination with speech pathologists is integral for effective management of cleft palate patients, particularly as children begin to develop language. In this article, the authors review and summarize the various challenges and goals of cleft palate management.

13.
J Craniofac Surg ; 22(5): 1822-6, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21959443

ABSTRACT

BACKGROUND: Our protocol for closure of unilateral complete or severe incomplete cleft lip begins with active dentofacial orthopedics (Latham device) followed by nasolabial adhesion and alveolar gingivoperioplasty. We have observed that preliminary adhesion provides more orbicularis oris muscle for the second-stage labial repair. METHODS: A quantitative prospective assessment of all patients undergoing nasolabial adhesion by the senior author between November of 2009 and July of 2010 was undertaken to assess whether there is an increase in lateral orbicularis oris muscle mass by the time of formal repair. Standard anthropometric points were placed before nasolabial adhesion and again at the second-stage closure. Ultrasonographic measurements of orbicularis muscle thickness were made on both lateral labial elements along a line drawn between sbal and cphi. The mean interval increase in thickness of lateral orbicularis oris was determined. RESULTS: Sixteen patients underwent nasolabial adhesion during the study period. Four patients with asymmetric bilateral cleft lip patients and 2 patients who did not have a second ultrasonographic study were excluded. The remaining 10 patients in the study had a nasolabial adhesion at a mean age of 3.9 months (range, 3.1-4.3 months). Mean orbicularis oris thickness before adhesion was 0.7 mm on the cleft side and 1.2 mm on the noncleft side. The increase in orbicularis thickness after the mean interoperative interval of 2.9 months (range, 2.6-3.5 months) was calculated. On the cleft side, there was 0.8 mm (138%) mean increase in orbicularis oris muscle thickness compared with 0.4 mm (32%) mean increase on the noncleft side. CONCLUSIONS: Labial adhesion in preparation for repair of unilateral complete or severe incomplete cleft lip results in a measurable increased thickness of lateral orbicularis oris. This additional muscular bulk is useful in construction of the philtral ridge.


Subject(s)
Cleft Lip/surgery , Facial Muscles/surgery , Lip/surgery , Oral Surgical Procedures/methods , Cleft Lip/diagnostic imaging , Cleft Lip/pathology , Facial Muscles/diagnostic imaging , Female , Humans , Infant , Lip/diagnostic imaging , Lip/pathology , Male , Prospective Studies , Rhinoplasty/methods , Treatment Outcome , Ultrasonography
14.
Neurosurg Focus ; 31(2): E5, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21806344

ABSTRACT

OBJECT The primary goals of treatment in the infant with craniosynostosis are to correct the deformity and allow for adequate brain growth in as safe and effective a manner as possible. Herein, the authors present the results of treating craniosynostosis using an endoscope-assisted strip craniectomy and postoperative helmet therapy (EASC + PHT) in the hopes of providing further evidence of its role in the treatment of multiple different forms of craniosynostosis. This is a retrospective review of the patients treated with this technique at Children's Hospital Boston. METHODS The electronic medical records of all children with craniosynostosis treated using this technique were reviewed retrospectively. A priori, data were collected for deformity type, patient age at surgery, number of transfusions, operative time, length of hospital stay, and anthropometric measurements. RESULTS One hundred seventy-three patients (61 females and 112 males) were treated at our institution between July 2004 and March 2011 with EASC + PHT. The mean operative time was 46.30 minutes. Eight (4.6%) of the 173 patients received blood transfusions. The average length of hospital stay was 1.35 days, with the majority of patients being discharged the day after surgery. All complications and any patient who required additional craniofacial reconstructions are discussed. In addition, a subgroup analysis was done for patients who had undergone surgery and had longer than 1 year of follow-up. CONCLUSIONS The authors' growing database of patients supports the experiences described by others that early treatment of craniosynostosis with an EASC + PHT is a safe and efficacious technique. In addition, cost reduction due to decreased hospital stay and limitation of blood transfusions are demonstrable benefits associated with the use of this technique.


Subject(s)
Craniosynostoses/surgery , Decompressive Craniectomy/methods , Endoscopy/methods , Head Protective Devices , Postoperative Care/instrumentation , Craniosynostoses/pathology , Craniosynostoses/therapy , Decompressive Craniectomy/instrumentation , Endoscopy/instrumentation , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Male , Postoperative Care/methods , Retrospective Studies , Treatment Outcome
15.
J Craniofac Surg ; 22(4): 1219-24, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21772212

ABSTRACT

BACKGROUND: Since 1995, the senior surgeon has straightened the deviated anterocaudal septum in all infants undergoing primary repair of unilateral complete cleft lip/palate. METHODS: A retrospective assessment was done on 17 patients who did not have septal correction and 17 patients who did have septal correction at the time of nasolabial repair. Operative reports were reviewed, and secondary procedures on the nose were documented.Posterior-anterior cephalograms were used to measure septal deviation from the midline, angle of septal deviation, and width of the inferior turbinate on the noncleft side. The angle subtended by the superior and inferior segments of the cartilaginous septum was measured at the point of maximal septal deviation. RESULTS: The uncorrected group had a mean maximal septal deviation from the midline of 5.8 mm compared with 4.1 mm in the corrected group (P < 0.01). The uncorrected group had a mean width of the contralateral inferior turbinate of 12.7 mm compared with 10.2 mm in the corrected group (P < 0.01). The uncorrected group had a mean subtended angle of 137.8 degrees compared with 147.9 degrees in the corrected group (P < 0.01). CONCLUSIONS: Positioning the anterior caudal septum during primary repair of unilateral complete cleft lip results in less septal deviation and a smaller contralateral turbinate as documented by posteroanterior cephalometry in adolescence.


Subject(s)
Cleft Lip/surgery , Nasal Septum/surgery , Adolescent , Cephalometry/methods , Child , Cleft Lip/classification , Cleft Palate/surgery , Female , Follow-Up Studies , Humans , Lip/surgery , Male , Nasal Bone/surgery , Nasal Cartilages/pathology , Nasal Obstruction/surgery , Nasal Septum/abnormalities , Nasal Septum/pathology , Reoperation , Retrospective Studies , Surgical Flaps/classification , Turbinates/pathology
16.
J Neurosurg Pediatr ; 7(6): 620-6, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21631199

ABSTRACT

OBJECT: Suturectomy as a treatment for craniosynostosis was largely replaced in the late twentieth century by more extensive, but predictable, cranial remodeling procedures. Recent technical innovations, such as using the endoscope combined with postoperative orthotic reshaping, have led to a resurgence of interest in suturectomy as a safer, less invasive method. METHODS: A retrospective chart review was performed for all cases of sagittal synostosis treated with endoscopic sagittal suture strip craniectomy and helmet therapy between 2004 and 2008. Data collected included gestational age, genetic evaluations and syndromic status, age at operation, duration of procedure, need for blood transfusions, length of hospital stay, preoperative and postoperative head circumference percentile and cranial index, duration of helmet use, length of follow-up, complications, and revisions. RESULTS: Fifty-six patients with isolated sagittal synostosis were treated using endoscopic suturectomy and completed helmet therapy. Mean age at time of procedure was 3.24 months. Mean operative duration was 45.32 minutes. Mean hospital stay was 1.39 days. There were 2 transfusions and no deaths. The mean length of follow-up was 2.34 years. Helmet therapy was instituted for a mean of 7.47 months. Head circumference percentile increased from 61.42% to 89.27% over 2 years of follow-up. Cranial index increased from a preoperative mean of 0.69 to 0.76 over 2 years of follow-up. Reoperations for synostosis included 1 sagittal suture refusion and 2 cases in which other sutures fused. CONCLUSIONS: Sagittal synostosis can be safely treated with endoscopic suturectomy and helmet therapy. Improvements in cranial volume and shape are comparable to open procedures and are enduring.


Subject(s)
Craniosynostoses/surgery , Endoscopy/instrumentation , Head Protective Devices , Orthopedic Procedures/methods , Postoperative Care/methods , Skull/surgery , Cephalometry , Female , Humans , Infant , Male , Suture Techniques/instrumentation , Treatment Outcome
17.
Plast Reconstr Surg ; 127(5): 2045-2053, 2011 May.
Article in English | MEDLINE | ID: mdl-21532431

ABSTRACT

BACKGROUND: Velocardiofacial syndrome is the most common defined disorder associated with palatal insufficiency. The authors' purpose is to evaluate one surgeon's experience with correction of velopharyngeal insufficiency in velocardiofacial syndrome using a tailored pharyngeal flap. METHODS: The authors reviewed the records of all children with velocardiofacial syndrome and velopharyngeal insufficiency who were managed with a pharyngeal flap between 1983 and 2009. Data collected included age at operation, preoperative videofluoroscopic findings, speech outcomes, complications, and need for a secondary operation. RESULTS: The authors identified 33 patients with velocardiofacial syndrome and velopharyngeal insufficiency who had postoperative speech evaluations. Velopharyngeal insufficiency was diagnosed at a median age of 5 years. Palatal findings were: Veau type I (n = 4), overt submucous (n = 6), or occult submucous (n = 23). Median preoperative lateral pharyngeal wall movement was 22 percent (range, 0 to 90 percent). Successful correction of velopharyngeal insufficiency was achieved in 29 of 33 patients (88 percent). One patient had a medially displaced right internal carotid artery, and evidenced intraoperative bleeding and required a blood transfusion. One patient developed obstructive sleep apnea. CONCLUSION: A tailored pharyngeal flap is highly effective for correction of velopharyngeal insufficiency in velocardiofacial syndrome with few complications.


Subject(s)
DiGeorge Syndrome/physiopathology , Nasal Mucosa/transplantation , Pharynx/surgery , Plastic Surgery Procedures/methods , Speech/physiology , Surgical Flaps , Velopharyngeal Insufficiency/physiopathology , Adolescent , Child , Child, Preschool , DiGeorge Syndrome/complications , DiGeorge Syndrome/surgery , Female , Follow-Up Studies , Humans , Male , Retrospective Studies , Treatment Outcome , Velopharyngeal Insufficiency/etiology , Velopharyngeal Insufficiency/surgery , Young Adult
18.
Plast Reconstr Surg ; 127(4): 1631-1642, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21460669

ABSTRACT

BACKGROUND: Autogenous particulate cranial bone graft has been proven to be effective for inlay cranioplasty but does not provide structural contour. This limitation can be overcome using an exchange cranioplasty technique. This study probes the effectiveness of this method for large (>5 cm(2)) or complicated cranial defects. METHODS: The authors conducted a retrospective review of patients managed with autologous exchange cranioplasty between 2005 and 2010. Full-thickness calvarial bone was removed from the intact cranium; particulate bone graft was harvested from the graft endocortex or ectocortex of intact cranium. The original defect was repaired with the full-thickness graft and the donor site was covered with particulate graft. Patient records were reviewed for age at cranioplasty, operative indication, size and location of defect, operative time, blood loss, and length of follow-up. Outcome variables included complications, osseous defects, and need for revision cranioplasty. RESULTS: Twenty patients underwent exchange cranioplasty at a mean age of 8.3 ± 6.2 years. Average values for the group included length of procedure, 4.7 hours; estimated blood loss, 288 ml; hospital stay, 3.1 days; and follow-up, 1.57 years (range, 24 weeks to 3.7 years). Eighty-five percent of patients underwent postoperative computed tomographic scanning to document healing. Fifteen patients had complete healing; five patients had residual bone defects (four by computed tomography and palpation, and one by computed tomography only). The cranial defect area decreased 96 percent on average from a preoperative mean of 85.2 cm(2) to a postoperative combined defect size (donor plus recipient) of 3.3 cm(2). CONCLUSION: Autologous exchange cranioplasty using particulate bone graft is safe and highly effective for reconstructing even large cranial defects.


Subject(s)
Bone Transplantation , Skull/surgery , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Male , Plastic Surgery Procedures , Skull/pathology , Tissue and Organ Harvesting , Transplantation, Autologous , Young Adult
19.
J Craniofac Surg ; 22(2): 455-61, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21403567

ABSTRACT

BACKGROUND: The facial features of children with FGFR3Pro250Arg mutation (Muenke syndrome) differ from those with the other eponymous craniosynostotic disorders. We documented midfacial growth and position of the forehead after fronto-orbital advancement (FOA) in patients with the FGFR3 mutation. METHODS: We retrospectively reviewed all patients who had an FGFR3Pro250Arg mutation and craniosynostosis. Only patients who had FOA in infancy or early childhood were included. The clinical records were evaluated for type of sutural fusion; midfacial hypoplasia and other clinical data, including age at operation; type of procedures and fixation (wire vs resorbable plate); frequency of frontal readvancement, forehead augmentation, midfacial advancement; and complications. Preoperative and postoperative sagittal orbital-globe relationship was measured by direct anthropometry. Outcome of FOA was graded according to the Whittaker classification as category I, no revision; category II, minor revisions, that is, foreheadplasty; category III, alternative bony work; category IV; redo of initial procedure (ie, secondary FOA). Midfacial position was determined by clinical examination and lateral cephalometry. RESULTS: A total of 21 study patients with Muenke syndrome (8 males and 13 females) were analyzed. The types of craniosynostosis were bilateral coronal (n=15), of which 3 also had concurrent sagittal fusion, and unilateral coronal (n=5). Two patients had early endoscopic suturectomy, but later required FOA. Mean age at FOA was 22.9 months (range, 3-128 months). Secondary FOA was necessary in 40% of patients (n=8), and secondary foreheadplasty in 25% (n=5) of patients. No frontal revisions were needed in the remaining 35% of patients (n=7). Mean age at initial FOA was significantly younger in the group requiring repeat FOA or foreheadplasty compared with patients who did not require revision (P<0.05). Location of synostosis, type of fixation, and bone grafting did not significantly affect the need for revision. Only 30% (n=6) of patients developed midfacial retrusion. CONCLUSIONS: The frequency of frontal revision in patients with Muenke syndrome who had FOA in infancy and early childhood is lower than previously reported. Age at forehead advancement inversely correlated with the incidence of relapse and need for secondary frontal procedures. Midfacial retrusion is relatively uncommon in FGFR3Pro250Arg patients.


Subject(s)
Craniosynostoses/genetics , Craniosynostoses/surgery , Forehead/surgery , Frontal Bone/surgery , Orbit/surgery , Receptor, Fibroblast Growth Factor, Type 3/genetics , Abnormalities, Multiple , Arginine/genetics , Cephalometry , Endoscopy , Female , Forehead/abnormalities , Forehead/growth & development , Frontal Bone/abnormalities , Frontal Bone/growth & development , Humans , Infant , Male , Orbit/abnormalities , Orbit/growth & development , Proline/genetics , Reoperation , Retrospective Studies
20.
Plast Reconstr Surg ; 127(1): 131-141, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21200207

ABSTRACT

BACKGROUND: Loss of hair-bearing regions of the face caused by trauma, tumor resection, or burn presents a difficult reconstructive task for plastic surgeons. The ideal tissue substitute should have the same characteristics as the facial area affected, consisting of thin, pliable tissue with a similar color match and hair-bearing quality. METHODS: This is a retrospective study of 34 male patients who underwent reconstruction of hair-bearing facial regions performed by the senior author (J.J.P.). Local and pedicled flaps were used primarily to reconstruct defects after tumor extirpation, trauma, infections, and burns. Two patients had irradiation before reconstruction. Two patients had prior facial reconstruction with free flaps. RESULTS: The authors found that certain techniques of reconstructing defects in hair-bearing facial regions were more successful than others in particular facial regions and in different sizes of defects. CONCLUSION: The authors were able to develop a simple algorithm for management of facial defects involving the hair-bearing regions of the eyebrow, sideburn, beard, and mustache that may prospectively aid the planning of reconstructive strategy in these cases.


Subject(s)
Face/surgery , Hair , Humans , Male , Plastic Surgery Procedures/methods , Retrospective Studies , Surgical Flaps
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