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1.
Ophthalmic Plast Reconstr Surg ; 37(5): e172-e173, 2021.
Article En | MEDLINE | ID: mdl-33795608

Suction aspiration, which has not yet been described in the treatment for myiasis in the periorbital and facial regions, was used to achieve rapid resolution of maggot burden in a 78-year-old patient who presented with a large ulcerated squamous cell carcinoma of the face. This technique also facilitates submission of parasite samples for further analysis. Suction aspiration had no complications, such as significant residual ruptured maggots in the wound or eye injury. Suction aspiration is a safe and efficient technique to reduce maggot burden that has advantages over classic myiasis treatments, especially near the eyes and airway.


Carcinoma, Squamous Cell , Myiasis , Aged , Animals , Face , Humans , Larva , Myiasis/diagnosis , Myiasis/therapy
2.
Laryngoscope ; 131(3): E792-E799, 2021 03.
Article En | MEDLINE | ID: mdl-32516508

OBJECTIVES: We implement a novel enhanced recovery after surgery (ERAS) protocol with pre-operative non-opioid loading, total intravenous anesthesia, multimodal peri-operative analgesia, and restricted red blood cell (pRBC) transfusions. 1) Compare differences in mean postoperative peak pain scores, opioid usage, and pRBC transfusions. 2) Examine changes in overall length of stay (LOS), intensive care unit LOS, complications, and 30-day readmissions. METHODS: Retrospective cohort study comparing 132 ERAS vs. 66 non-ERAS patients after HNC tissue transfer reconstruction. Data was collected in a double-blind fashion by two teams. RESULTS: Mean postoperative peak pain scores were lower in the ERAS group up to postoperative day (POD) 2. POD0: 4.6 ± 3.6 vs. 6.5 ± 3.5; P = .004) (POD1: 5.2 ± 3.5 vs. 7.3 ± 2.3; P = .002) (POD2: 4.1 ± 3.5 vs. 6.6 ± 2.8; P = .000). Opioid utilization, converted into morphine milligram equivalents, was decreased in the ERAS group (POD0: 6.0 ± 9.8 vs. 10.3 ± 10.8; P = .010) (POD1: 14.1 ± 22.1 vs. 34.2 ± 23.2; P = .000) (POD2: 11.4 ± 19.7 vs. 37.6 ± 31.7; P = .000) (POD3: 13.7 ± 20.5 vs. 37.9 ± 42.3; P = .000) (POD4: 11.7 ± 17.9 vs. 36.2 ± 39.2; P = .000) (POD5: 10.3 ± 17.9 vs. 35.4 ± 45.6; P = .000). Mean pRBC transfusion rate was lower in ERAS patients (2.1 vs. 3.1 units, P = .017). There were no differences between ERAS and non-ERAS patients in hospital LOS, ICU LOS, complication rates, and 30-day readmissions. CONCLUSION: Our ERAS pathway reduced postoperative pain, opioid usage, and pRBC transfusions after HNC reconstruction. These benefits were obtained without an increase in hospital or ICU LOS, complications, or readmission rates. LEVEL OF EVIDENCE: 3 Laryngoscope, 131:E792-E799, 2021.


Enhanced Recovery After Surgery , Otorhinolaryngologic Surgical Procedures/rehabilitation , Perioperative Care/methods , Plastic Surgery Procedures/rehabilitation , Tissue Transplantation/rehabilitation , Aged , Analgesia/methods , Analgesics, Opioid/therapeutic use , Blood Transfusion/statistics & numerical data , Double-Blind Method , Female , Head/surgery , Humans , Length of Stay/statistics & numerical data , Male , Middle Aged , Neck/surgery , Otorhinolaryngologic Surgical Procedures/methods , Pain Management/statistics & numerical data , Pain Measurement/statistics & numerical data , Pain, Postoperative/epidemiology , Pain, Postoperative/therapy , Patient Readmission/statistics & numerical data , Retrospective Studies , Surgical Flaps , Treatment Outcome
3.
Laryngoscope ; 130(11): 2663-2666, 2020 11.
Article En | MEDLINE | ID: mdl-31904874

OBJECTIVES: To compare flexible distal-chip laryngoscopy (FDL) versus rigid telescopic laryngoscopy (RTL) in regard to examinees' pain level, comfort, satisfaction, and preference, and to evaluate the clinician's assessment of the examinees' experience with both exam types. STUDY DESIGN: Randomized crossover study. METHODS: Twenty-three normal adult subjects were recruited to undergo both FDL and RTL; the initial exam type was randomized. Subjects and clinicians completed corresponding questionnaires after each exam. Differences in participant characteristics and questionnaire scores between the two exam types were assessed via Pearson χ2 and paired t tests, respectively. RESULTS: Overall, participants reported that FDL was more uncomfortable than RTL (4.22 vs. 2.91, P = .003) and scored higher on the pain scale for FDL compared to RTL (2.91 vs. 1.70, P = .006). However, there was no significant difference in number of participants who preferred FDL versus RTL (10 [43%] vs. 13 [57%]). Poor correlation was seen between clinicians' assessment of participants' discomfort and actual reported discomfort for FDL (2.70 vs. 4.22, P = .001). CONCLUSIONS: Subjects undergoing FDL experience greater discomfort and pain compared to RTL, but do not demonstrate a differential preference of exam. Overall, clinicians underestimate the discomfort of patients undergoing FDL, but participants maintain high satisfaction with both exams nonetheless. LEVEL OF EVIDENCE: 1 Laryngoscope, 130:2663-2666, 2020.


Equipment Design/adverse effects , Laryngoscopes/adverse effects , Laryngoscopy/instrumentation , Pain, Postoperative/epidemiology , Adult , Cross-Over Studies , Female , Humans , Laryngoscopy/psychology , Male , Middle Aged , Pain Measurement , Pain, Postoperative/etiology , Patient Satisfaction/statistics & numerical data , Treatment Outcome
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