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"[ABSTRAKLatar Belakang. Manajemen jalan nafas merupakan salah satu tahap yang paling penting dalam bidang anestesiologi. Salah satu jenis Alat bantu jalan nafas yang telah dipergunakan secara luas adalah Laringeal Mask Airway (LMA/Sungkup Laring). Pada pemasangan sungkup laring tanpa menggunakan pelumpuh otot membutuhkan kedalaman anestesi yang cukup, Tes klinis yang mudah, akurat dan aplikatif diperlukan untuk menghindari terjadinya komplikasi. Penelitian ini bertujuan untuk membandingkan trapezius squeezing test dan jaw thrust sebagai indikator kedalaman anestesi pada pemasangan sungkup laring dengan propofol sebagai agen induksiMetode. Sebanyak 128 pasien di randomisasi ke dalam 2 kelompok yaitu jaw thrust dan trapezius squeezing test. Seluruh pasien mendapatkan premedikasi dengan midazolam 0.05 mg/kgBB dan Fentanyl 1 mcg/kgBB. Induksi menggunakan propofol titrasi. Manuver jaw thrust dan trapezius squeezing test dilakukan setiap 15 detik. Saat respon motorik hilang dilakukan pemasangan sungkup laring. Dicatat keberhasilan pemasangan, dosis propofol, tekanan darah, laju jantung, dan insiden apneu.Hasil. Keberhasilan pada kelompok jaw thrust 93.8%, sedangkan trapezius squeezing test yang 90.6%. Penggunaan rerata propofol pada kelompok jaw thrust yaitu sebesar 120.34 mg, sedangkan pada kelompok trapezius squeezing test yaitu sebesar 111,86 mg. Insiden apneu yang pada kelompok jaw thrust terjadi pada 10 (15.6%) pasien, sedangkan pada kelompok trapezius squeezing test sebesar 11 (17.2%) pasien. Tidak terdapat perubahan hemodinamik yang berarti pada kelompok jaw thrust sedangkan sedangkan pada kelompok trapezius squeezing test terdapat perubahan hemodinamik yang berarti di menit ke 3 dan ke 4Kesimpulan. Trapezius squeezing test tidak lebih baik daripada jaw thrust sebagai indikator klinis dalam menilai kedalaman anestesia pada insersi sungkup laring.

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ABSTRACTBackground. Airway management is one of the most important phase in anesthesiology. One of airway device that have been used generally is Laryngeal Mask Airway (LMA). Laryngeal mask insertion without muscle relaxant requires a level of depth anesthesia. An easy, accurate, an applicable clinical indicator were required to avoid complication. This study was determine the comparison trapezius squeezing test and jaw thrust as indicator of depth of anesthesia in laryngeal mask insertion with propofol as induction agent.Methods. 128 patient have been randomize in to 2 group that are jaw thrust and trapezius squeezing test. All patients were received premedication with midazolam 0.05 mg/kg and fentanyl 1 μg/kg. Induction were done by propofol titration. Jaw thrust and trapezius squeezing test maneuver were done in every 15 second. When motoric respond negative the laryngeal mask were inserted. The successful of laryngeal mask insertion was recorded, propofol consumption, blood pressure, heart rate, and incidence of apnea were also documented.Result. Laryngeal mask successfully inserted in 93.8% patients in jaw thrust group, and 90.6% in trapezius squeezing test group. Mean of propofol consumption in jaw thrust group is 120.34 mgs, and in trapezius squeezing test is 11.86 mgs. Incident of apnea in jaw thrust group happened in 10 patients (15.6%), and in trapezius squeezing test group happened in 11 patient (17.2%). Hemodynamic in jaw thrust group relatively stable but in trapezius squeezing test there is significant hemodynamic changing in minute third and fourth.Conclusion. Trapezius squeezing test is not better than jaw thrust as clinical indicators of depth of anesthesia for laryngeal mask insertion.;Background. Airway management is one of the most important phase in anesthesiology. One of airway device that have been used generally is Laryngeal Mask Airway (LMA). Laryngeal mask insertion without muscle relaxant requires a level of depth anesthesia. An easy, accurate, an applicable clinical indicator were required to avoid complication. This study was determine the comparison trapezius squeezing test and jaw thrust as indicator of depth of anesthesia in laryngeal mask insertion with propofol as induction agent.Methods. 128 patient have been randomize in to 2 group that are jaw thrust and trapezius squeezing test. All patients were received premedication with midazolam 0.05 mg/kg and fentanyl 1 μg/kg. Induction were done by propofol titration. Jaw thrust and trapezius squeezing test maneuver were done in every 15 second. When motoric respond negative the laryngeal mask were inserted. The successful of laryngeal mask insertion was recorded, propofol consumption, blood pressure, heart rate, and incidence of apnea were also documented.Result. Laryngeal mask successfully inserted in 93.8% patients in jaw thrust group, and 90.6% in trapezius squeezing test group. Mean of propofol consumption in jaw thrust group is 120.34 mgs, and in trapezius squeezing test is 11.86 mgs. Incident of apnea in jaw thrust group happened in 10 patients (15.6%), and in trapezius squeezing test group happened in 11 patient (17.2%). Hemodynamic in jaw thrust group relatively stable but in trapezius squeezing test there is significant hemodynamic changing in minute third and fourth.Conclusion. Trapezius squeezing test is not better than jaw thrust as clinical indicators of depth of anesthesia for laryngeal mask insertion., Background. Airway management is one of the most important phase in anesthesiology. One of airway device that have been used generally is Laryngeal Mask Airway (LMA). Laryngeal mask insertion without muscle relaxant requires a level of depth anesthesia. An easy, accurate, an applicable clinical indicator were required to avoid complication. This study was determine the comparison trapezius squeezing test and jaw thrust as indicator of depth of anesthesia in laryngeal mask insertion with propofol as induction agent.Methods. 128 patient have been randomize in to 2 group that are jaw thrust and trapezius squeezing test. All patients were received premedication with midazolam 0.05 mg/kg and fentanyl 1 μg/kg. Induction were done by propofol titration. Jaw thrust and trapezius squeezing test maneuver were done in every 15 second. When motoric respond negative the laryngeal mask were inserted. The successful of laryngeal mask insertion was recorded, propofol consumption, blood pressure, heart rate, and incidence of apnea were also documented.Result. Laryngeal mask successfully inserted in 93.8% patients in jaw thrust group, and 90.6% in trapezius squeezing test group. Mean of propofol consumption in jaw thrust group is 120.34 mgs, and in trapezius squeezing test is 11.86 mgs. Incident of apnea in jaw thrust group happened in 10 patients (15.6%), and in trapezius squeezing test group happened in 11 patient (17.2%). Hemodynamic in jaw thrust group relatively stable but in trapezius squeezing test there is significant hemodynamic changing in minute third and fourth.Conclusion. Trapezius squeezing test is not better than jaw thrust as clinical indicators of depth of anesthesia for laryngeal mask insertion.]"

"ABSTRAKLatar belakang : Pemasangan sungkup laring tanpa menggunakan obat pelumpuh otot membutuhkan tingkat kedalaman anestesia yang cukup untuk mendepresi refleks jalan napas sehingga menghindari tersedak, batuk dan laryngospasm. Tes klinis yang mudah, akurat dan aplikatif diperlukan untuk menghindari terjadinya komplikasi seperti di atas. Tujuan penelitian ini adalah mengetahui keefektivan trapezius squeezing test sebagai indikator kedalaman anestesia saat pemasangan sungkup laring dihubungkan dengan Bispectral Index.Metode : Setelah lolos kaji etik dan mendapatkan persetujuan klinik, 105 pasien ASA 1-2 dilakukan pemasangan sungkup laring dengan trapezius squeezing test sebagai prediktor kedalaman anestesia. Semua pasien mendapatkan premedikasi midazolam 0,05mg/kgBB dan fentanyl 1 mcg/kgBB. Induksi dilakukan dengan propofol titrasi, dengan kedalaman anestesia diukur dengan trapezius squeezing test. Pemasangan sungkup laring dilakukan bila trapezius squeezing test negatif. Dicatat keberhasilan pemasangan sungkup laring. Tekanan darah, laju nadi dan nilai Bispectral Index juga didokumentasikan.Hasil : Sungkup laring berhasil dipasang pada 88 pasien sedangkan 14 pasien gagal dilakukan pemasangan sungkup laring walaupun trapezius squeezing test negatif. Nilai median Bispectral Index saat trapezius squeezing test negatif adalah 35.Kesimpulan : Trapezius squeezing test merupakan indikator klinis yang dapat diandalkan untuk menilai kedalaman anestesia saat pemasangan sungkup laring.

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ABSTRACTBackground : Laryngeal mask insertion without using muscle relaxant requires a level of depth of anesthesia sufficient to depress airway reflexes to avoid choking, coughing and laryngospasm. Easy, accurate and applicable clinical tests are required to avoid complications as above. The purpose of this study was to determine the effectiveness of the trapezius squeezing test as an indicator of the depth of anesthesia when inserting laryngeal mask airway associated with Bispectral Index. Methods : After ethical clearance and receive informed consent, 105 ASA 1-2 patients were done laryngeal mask insertion with trapezius squeezing test as a predictor of anesthesia depth. All the patient were receive premedication midazolam 0,05 mg/kg and fentanyl 1 mcg/kg. Induction were done by propofol titration with anesthesia depth is measured by trapezius squeezing test. Laryngeal mask were inserted when trapezius squeezing test negative. The successful of laryngeal mask insertion was recorded. Blood pressure, pulse rate and Bispectral Index score were also documented.Result :Larygeal mask successfully inserted in 88 patients while 14 patients failed despite the negative results of trapezius squeezing test. The median score of Bispectral Index when trapezius squeezing test negatif was 35.Conclusion : Trapezius squeezing test is a reliable clinical indicator to assess the depth of anesthesia during laryngeal mask insertion."

"Berbagai studi dan penelitian telah dilakukan di berbagai negara untuk mengetahui pengetahuan pasien terhadap anestesia namun tidak ada instrumen kuesioner yang baku untuk menilai pengetahuan pasien tentang anestesia, dan hal ini belum pernah dilakukan di Indonesia khususnya di RSUPN Cipto Mangunkusumo. Kuesioner pengetahuan yang valid dan reliabel diharapkan menjadi standar untuk menilai pengetahuan masyarakat terhadap anestesia, dan dapat menjadi dasar bagi penelitian selanjutnya.Metode: Kuesioner pengetahuan anestesia sebelumnya telah melalui tahapan pretest oleh ahli dan uji pilot, hasil kuesioner uji pilot disempurnakan sehingga dianggap layak diujicobakan. Penelitian dilakukan pada bulan Januri 2014 sampai dengan Maret 2014 terhadap subyek secara consecutive sampling yang akan menjalani pembiusan dan diperiksa di klinik preoperatif RSUPN Cipto Mangunkusumo Jakarta. Teknik uji validitas menggunakan validitas konstruk dengan koefisien korelasi minimal 0,3 dapat dianggap valid dan uji reliabilitas menggunakan teknik konsistensi internal dengan nilai cronbach α minimal 0,4 dianggap reliabel.Hasil: Penelitian ini diikuti oleh 95 subyek dengan 1 subyek dikeluarkan dari penelitian karena tidak mengisi kuesioner secara lengkap. Kuesioner pengetahuan terdiri dari 20 pertanyaan, 8 pertanyaan diantaranya dinilai tidak valid dan reliabel yang dapat disebabkan oleh pertanyaan dan jawaban kuesioner yang tidak dapat dimengerti oleh subyek, pembahasan terlalu dalam dan penggunaan istilah medis yang tidak familiar. Beberapa jawaban pertanyaan memiliki kesamaan yang dapat membingungkan subyek, serta terdapat inkonsistensi jawaban yang diberikan oleh subyek. Tingkat penghasilan dan pendidikan subyek yang rendah serta pengalaman dan informasi yang kurang, sangat mempengaruhi pengetahuan subyek terhadap anestesia, tercermin dari rendahnya rerata tingkat pengetahuan subyek sebesar + 31,6%.Kesimpulan: Kuesioner penilaian pengetahuan tentang anestesia pada pasien di klinik preoperatif RSUPN Cipto Mangunkusumo tidak dapat dijadikan sebagai suatu standar instrumen yang baku oleh karena dinilai tidak valid dan reliabel.

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Various studies and researches have been conducted abroad to determine the patient?s anesthesia knowledge, although no standard questionnaires exist. Research on anesthesia?s knowledge questionnaires have never been done specifically in Cipto Mangunkusumo hospital. A valid and reliable questionnaire is aimed to be a standard instrument assessing the community?s knowledge on anesthesia, and as a foundation for future researches.Methods: The anesthesia knowledge questionnaires has been evaluated through a pre-test phase done by experts and pilot test, the results was then revised until it is acceptable and can be tested. Researches was conducted on January 2014 until March 2014 on subjects by consecutive sampling who are going to undergo anesthesia and evaluated at the preoperative clinic Cipto Mangunkusumo Hospital Jakarta. Validity test techniques using construct validity with the minimal correlation coefficient 0.3 is valid. Reliability tests using internal consistency techniques with minimal cronbach alpha value 0.4 is reliable.Results: Research was participated by 95 subjects with 1 subject excluded from the research because of not filling in the questionnaire completely. The knowledge questionnaire included 20 questions, whereas 8 questions was marked to be invalid and unreliable that may be caused by questions and answers were not fully understood by the subjects, the contents was too spesific, usage of medical terms that aren?t familiar. Some of the given answers have similarities that may confuse the subject, and also inconsistency from the subject?s answers. Low level of salary and education with lacking of experience and information from the subjects, has significant influence on the subjects knowledge on anesthesia which is reflected by the low average level of the subject`s knowledge which is + 31.6%.Conclusions: Anesthesia knowledge questionnaires on patients at preoperative clinic Cipto Mangunkusumo hospital is invalid and unreliable therefore fail to be a standard instrument."

"Latar belakang. Teknik Target Controlled Infusion untuk anestesia umum semakin banyak digunakan. Jumlah pasien geriatri yang harus menjalani prosedur operasi semakin bertambah, serta memerlukan pertimbangan khusus mengingat risiko operasi dan pembiusan yang lebih tinggi pada golongan ini. Penelitian ini bertujuan untuk membandingkan konsentrasi plasma (Cp) dan konsentrasi effect site (Ce) propofol menggunakan rumusan Marsh pada pasien geriatri ras Melayu di RSCM dengan dan tanpa pemberian premedikasi fentanil. Metode. Empat puluh pasien geriatri orang Indonesia Asli status fisik ASA 2, usia > 60 tahun dan BMI 18-30 kg/m2 dirandomisasi. Satu kelompok (20 pasien) mendapatkan Fentanil-Propofol, lainnya (20 pasien) mendapatkan NaCl-Propofol. Pemberian propofol menggunakan TCI rumusan Marsh dengan target konsentrasi plasma. Target Cp dimulai dari 1 µ/ml dinaikkan 1 µ/ml tiap menit sampai tercapai loss of consciousness (LoC) dan diteruskan sampai nilai BIS 45-60 selama 5 menit (steady state). Hasil. Pada kelompok Fentanil-Propofol saat LoC didapatkan Cp 3,15+0,35 µ/ml dan Ce 1,53+0,53 µ/ml dan saat BIS stabil didapatkan Cp 4,14+0,59 µ/ml dan Ce 2,63+0,60 µ/ml. Pada kelompok Nacl-Propofol saat LoC didapatkan Cp 4,20+0,61 µ/ml dan Ce 2,26+0,56 µ/ml dan saat BIS stabil didapatkan Cp 4,78+0,38 µ/ml dan Ce 3,30+0,52 µ/ml. Pasien-pasien yang mendapatkan fentanil terlebih dahulu memiliki Cp dan Ce yang lebih rendah baik saat LoC maupun saat nilai BIS stabil (P < 0,05). Kesimpulan. Terdapat perbedaan bermakna antara Cp dan Ce propofol yang diberikan premedikasi fentanil dan yang tidak.

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Background. The application of Target Controlled Infusion (TCI) technique in general anesthesia is progressively growing. Number of geriatric patients scheduled for operations increases every year, while this group needs special consideration following the higher risk of surgery and anesthesia. The purpose of our study was to compare the estimated plasma concentration (Cp) and the effect site concentration (Ce) of propofol using Marsh pharmacokinetic model for geriatric patients in Cipto Mangunkusumo Hospital with and without the administration of fentanyl premedication.

Methods. Forty patients, physical status ASA 2, aged > 60, BMI 18-30 kg/m2 randomly assigned to a fentanyl-propofol group or a saline-propofol group. TCI propofol was initiated using Marsh pharmacokinetic model. Initial plasma concentration in each group was 1 µ/ml and increased by 1 µ/ml every minute until there was no eyelash reflex, which defined as loss of consciousness (LoC). Propofol plasma concentration was increased and decreased to reach a stable BIS value between 45-60, considered as Cp and Ce at steady state.

Results. In the fentanyl-propofol group the estimated Cp at loss of consciousness was 3,15+0,35 µ/ml and Ce 1,53+0,53 µ/ml. At steady state, Cp was 4,14+0,59 µ/ml and Ce 2,63+0,60 µ/ml. In the saline-propofol group Cp 4,20+0,61 µ/ml and Ce 2,26+0,56 µ/ml. At steady state, Cp was 4,78+0,38 µ/ml and Ce 3,30+0,52 µ/ml. The estimated Cp and Ce in the fentanyl-propofol group were lower than saline-propofol group (p < 0.05).

Conclusion. There is a significant difference between Cp and Ce in the salinepropofol group and fentanyl-propofol group."

"ABSTRAKLatar Belakang: Quality of Recovery-40 (QoR-40) adalah salah satu instrumen yang telah digunakan luas di dunia untuk menilai kualitas pemulihan pascaanestesia umum. Saat ini belum ada instrumen spesifik yang menilai kualitas pemulihan pascaanestesia di Indonesia.Metode: Hasil terjemahan akan diujikan pada minimal 102 pasien yang menjalani anestesia umum satu hari praoperasi dan satu hari pascaoperasi. Uji kesahihan isi menggunakan koefisien Aiken v, uji kesahihan konstruksi (analisis faktor dan uji korelasi pearson), Konsitensi Internal ( Chronbach α), ketanggapan (responsiveness) dengan Standart respon mean (SRM) .Hasil: Uji kesahihan isi formula Aiken V didapatkan bahwa QoR-40 versi Indonesia sahih dengan nilai ≥ 0,5. Uji kesahihan konstruksi dengan analisis faktor menunjukan semua faktor memiliki korelasi yang tinggi (korelasi ≥ 0,5). Uji korelasi Pearson didapatkan 3 item pertanyaan dari dimensi dukungan tehadap pasien yang tidak sahih, (Mendapat dukungan dari dokter Rumah Sakit, ρ= 0,252), (Mampu memahami arahan dan nasehat ρ= 1,98), (Merasa bingung ρ= 0,202). Standart Respon Mean (SRM) pada Uji ketanggapan adalah 1,06. Terdapat hubungan negatif antara skor QoR-40 versi Indonesia dengan lama masa rawatanSimpulan: QoR - 40 versi Indonesia menunjukkan kesahihan dan keandalan yang memuaskan. Dimensi dukungan terhadap pasien dengan koefisien kesahihan terendah dan tiga pertanyaan yang tidak memiliki kesahihan konstruksi. Ada hubungan negatif antara skor QoR - 40 versi Indonesia dengan panjang pengobatan . Penelitian ini menghasilkan instrumen QoR - 40 versi Indonesia yang memiliki ketanggapan atau sensitif untuk menilai perubahan klinis pascanestesia umum.

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ABSTRACTBackground: Quality of Recovery-40 (Qor-40) is one of the instruments that have been used widely in the world to assess the quality of recovery after general anesthesia. Currently there is no specific instrument that assesses the quality of recovery after general anesthesia in Indonesia.Methods: The translation will be tested on at least 102 patients undergoing general anesthesia preoperative one day and one day postoperative. Test the validity of the content using the coefficient Aiken V, Construction validity (factor analysis and Pearson correlation), Internal consistency (Chronbach α), responsiveness with Standard response mean (SRM).Results: Test the content validity of Aiken V formula found that Qor-40 Indonesian version valid with a value of ≥ 0.5. Test construction validity by factor analysis showed all the factors have a high correlation (correlation ≥ 0.5). Pearson correlation test item obtained 3 question in patient support dimension not valid, ( Getting support from Hospital doctors, ρ = 0.252), (Able to understand the direction and advice of ρ = 1.98), (Feeling confused ρ = 0.202). SRM on test responsiveness 1,06. There is a negative correlation between the scores Qor-40 version Indonesia with long term careConclusion: QoR-40 Indonesian version showed satisfactory validity and reliability. Dimensions support to patients with the lowest validity coefficient and three questions that do not have construction validity. There is a negative relationship between the score Qor-40 version of Indonesia with the length of treatment. This research resulted in the instrument Qor-40 Indonesia version (responsivness) or sensitive to assess clinical changes after general anesthesia."

"Latar Belakang: Penjadwalan operasi yang baik adalah yang mengoptimalkan workflow suatu kamar operasi, mengurangi kasus pembatalan operasi, dan ketidaktepatan prediksi waktu operasi. Unit Pelayanan Bedah Terpadu RSUPN Dr. Cipto Mangunkusumo memiliki peran besar terhadap berlangsungnya operational efficiency sehingga hal-hal terkait efisiensi kerja yang termasuk didalamnya penjadwalan pasien di kamar operasi menjadi fokus perhatian utama. Penelitian ini bertujuan untuk menilai korelasi waktu persiapan, induksi, dan pemulihan anestesi berdasarkan pemilihan teknik anestesi terhadap anesthesia-controlled time (ACT). Metode: Penelitian ini merupakan penelitian observasional yang dilaksanakan di Unit Pelayanan Bedah Terpadu RSUPN Dr. Cipto Mangunkusumo sejak Maret 2019 hingga Desember 2020, dengan total 1727 sampel yang memenuhi kriteria inklusi dan tidak memiliki kriteria eksklusi. Tim anestesi kamar operasi dengan menggunakan jam digital melakukan observasi, pengambilan, dan pencatatan data waktu secara manual kedalam lembar kuesioner yang disediakan di kamar operasi atau secara daring dengan mengakses tautan yang tersedia.Hasil: Terdapat hubungan linier positif yang bermakna antara waktu persiapan anestesi dengan ACT pada teknik anestesi umum-ETT (r=0.1, p 0.009), anestesi umum-ETT, CVC, ABP (r=0.253, p 0.028), dan anestesi umum-ETT/LMA, blok saraf perifer, CVC, ABP (r=0.489, p 0.013); waktu pemasangan monitor dengan ACT pada teknik anestesi umum-ETT (r=0.125, p 0.001), anestesi umum-ETT, CVC, ABP (r=0.502, p 0.000), anestesi umum-ETT/LMA, epidural (r=0.372, p 0.001), anestesi umum-ETT, epidural, CVC (r=0.436, p 0.006), sedasi (r=0.516, p 0.001), spinal (r=0.501, p 0.000), anestesi umum pediatrik-ETT/LMA, CVC, ABP (r=0.321, p 0.000), dan anestesi umum pediatrik-ETT/LMA, kaudal (r=0.445, p 0.001); waktu induksi anestesi dengan ACT pada teknik anestesi umum-ETT (r=0.513, p 0.000), anestesi umum-ETT, CVC, ABP (r=0.391, p 0.001), anestesi umum-LMA (r=0.312, p 0.017), anestesi umum-ETT/LMA, epidural (r=0.818, p 0.000), anestesi umum-ETT, epidural, CVC, ABP (r=0.559, p 0.000), spinal (r=0.503, p 0.000), kombinasi spinal-epidural (r=0.779, p 0.000), blok saraf perifer (r=0.729, p 0.000), anestesi umum pediatrik-ETT/LMA, CVC, ABP (r=0.511, p 0.000), dan anestesi umum pediatrik-ETT/LMA, kaudal (r=0.543, p 0.000); waktu insersi CVC dengan ACT pada teknik anestesi umum-ETT/LMA, CVC (r=0.553, p 0.002), anestesi umum-ETT, CVC, ABP (r=0.434, p 0.000), anestesi umum-ETT, epidural, CVC (r=0.415, p 0.010), dan anestesi umum-ETT, epidural CVC, ABP (r=0.288, p 0.023); waktu pemulihan anestesi dengan ACT pada teknik anestesi umum-ETT (r=0.157, p 0.000), anestesi umum-ETT/LMA, CVC (r=0.664, p 0.000), anestesi umum-ETT, CVC, ABP (r=0.374, p 0.001), anestesi umum-LMA (r=0.299, p 0.023), anestesi umum-ETT/LMA, epidural (r=0.557, p 0.000), anestesi umum-ETT, epidural, CVC (r=0.338, p 0.035), anestesi umum-ETT, epidural, CVC, ABP (r= 0.343, p 0.006), sedasi (r=0.351, p 0.033), anestesi umum pediatrik-ETT/LMA, CVC, ABP (r=0.424, p 0.000), dan anestesi umum pediatrik-ETT/LMA, kaudal (r=0.589, p 0.000). Simpulan: Waktu persiapan, induksi, dan pemulihan anestesi tidak berkorelasi dengan anesthesia-controlled time berdasarkan pemilihan teknik anestesi di Unit Pelayanan Bedah Terpadu Rumah Sakit Dr Cipto Mangunkusumo.

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ackground: An ideal operating schedule is the one that optimizes the workflow of an operating room, reduces case cancellation and inaccurate prediction of total procedural time. Central Surgical Unit of Dr. Cipto Mangunkusumo Hospital has a major role of ensuring the continuity of operational efficiency so that matters related to work efficiency, including patient scheduling in the operating room, are the main focus of attention. This study aims to assess the correlation of time of preparation, anesthesia induction and recovery time with anesthesia-controlled time (ACT) based on the choice of anesthesia technique. Methodes: This observational research was done in Central Surgical Unit of Dr. Cipto Mangunkusumo Hospital from March 2019 to December 2020, with a total of 1727 samples that fulfilled inclusion criteria, without exclusion criteria. By means of using a digital clock, anesthesia team performs observations, retrieval, and recording of time data manually into a questionnaire sheet provided in the operating room or an online document by accessing the link provided.Results: There is a significant positive linear correlation between anesthesia preparation time and ACT on general anesthesia-ETT (r=0.1, p 0.009), general anesthesia-ETT, CVC, ABP (r=0.253, p 0.028), and general anesthesia-ETT/LMA, peripheral nerve block, CVC, ABP technique (r=0.489, p 0.013); basic monitoring placement time and ACT on general anesthesia-ETT (r=0.125, p 0.001), general anesthesia-ETT, CVC, ABP (r=0.502, p 0.000), general anesthesia-ETT/LMA, epidural (r=0.372, p 0.001), general anesthesia-ETT, epidural, CVC (r=0.436, p 0.006), sedation (r=0.516, p 0.001), spinal (r=0.501, p 0.000), pediatric general anesthesia-ETT/LMA, CVC, ABP (r=0.321, p 0.000), and pediatric general anesthesia-ETT/LMA, caudal technique (r=0.445, p 0.001); anesthesia induction time and ACT on general anesthesia-ETT (r=0.513, p 0.000), general anesthesia-ETT, CVC, ABP (r=0.391, p 0.001), general anesthesia-LMA (r=0.312, p 0.017), general anesthesia-ETT/LMA, epidural (r=0.818, p 0.000), general anesthesia-ETT, epidural, CVC, ABP (r=0.559, p 0.000), spinal (r=0.503, p 0.000), combined spinal-epidural (r=0.779, p 0.000), peripheral nerve block (r=0.729, p 0.000), pediatric general anesthesia-ETT/LMA, CVC, ABP (r=0.511, p 0.000), and pediatric general anesthesia -ETT/LMA, caudal technique (r=0.543, p 0.000); CVC insertion time and ACT on general anesthesia-ETT/LMA, CVC (r=0.553, p 0.002), general anesthesia-ETT, CVC, ABP (r=0.434, p 0.000), general anesthesia-ETT, epidural, CVC (r=0.415, p 0.010), and general anesthesia-ETT, epidural CVC, ABP technique (r=0.288, p 0.023); anesthesia recovery time and ACT on general anesthesia-ETT (r=0.157, p 0.000), general anesthesia-ETT/LMA, CVC (r=0.664, p 0.000), general anesthesia-ETT, CVC, ABP (r=0.374, p 0.001), general anesthesia-LMA (r=0.299, p 0.023), general anesthesia-ETT/LMA, epidural (r=0.557, p 0.000), general anesthesia-ETT, epidural, CVC (r=0.338, p 0.035), general anesthesia-ETT, epidural, CVC, ABP (r= 0.343, p 0.006), sedation (r=0.351, p 0.033), pediatric general anesthesia-ETT/L anesthesia-ETT/LMA, caudal technique(r=0.589, p 0.000). Conclusions: Time of anesthesia preparation, induction, and recovery do not correlate with ACT based on the anesthesia technique used to fascilitate surgery in Central Surgical Unit of Dr Cipto Mangunkusumo Hospital."

"Latar belakang : Telah dilakukan penelitian untuk waktu optimal pemberian fentanil 2 .tg/kg BB dengan tujuan menekan respon kardiovaskuler akibat laringoskopi dan intubasi dengan membandingkan waktu pemberian fentanil 5 dan 7 menit sebelum dilakukan tindakan laringoskopi dan intubasi.Metode:Tiga puluh enam pasien ASA 1 dan ASA 2 dibagi dalam dua kelompok secara acak masing-masing tediri dari delapan belas pasien. Kelompok pertama diberikan fentanil dosis 2 µglkg BB waktu 5 menit sebelum laringoskopi dan intubasi, sedangkan kelompok kedua diberikan dosis yang sama dengan waktu 7 menit sebelum laringoskopi dan intubasi , data tekanan darah sistolik , diastolik, tekanan arteri rata-rata dan laju jantung dari kedua kelompok dibandingkan sampai 5 menit setelah intubasi.Hasil : Secara statistik tidak terdapat perbedaan bermakna antara kedua kelompok yang dibandingkan (p>0.05) dalam hal tekanan darah sistolik, tekanan darah diastolik, tekanan arteri rata-rata dan laju jantung akibat laringoskopi dan intubasi.Kesimpulan : Waktu optimal untuk injeksi fentanil 21tg kg BB-' untuk dapat menekan respon hemodinamik akibat laringoskopi dan intubasi adalah 5 dan 7 menit sebelum tindakan tersebut dilakukan.

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Background :This study was designed to examine the optimal time of injection of 2 gg/kg fentanyl to Attenuate circulatory responses due to laringoscopy and tracheal intubation that compared between 5 minute and 7 minute before laringoscopy and tacheal intubation.

Method : Thirty six patients ASA 1 and ASA 2 were randomly in two groups which each group eighteen patients. The patients in group 1 received fentanyl 2 pg/kg 5 minute and group 2 received the same dose 7 minute before laringoscopy and tracheal intubation.

Result : The result of this study were no statistical significant values both of groups in systolic, diastolic, mean arterial pressure and heart rate due to laringoscopy and intubation

Conclusion : The effective time to administer fentanyl 2pg kg _I to protect circulatory response to laringoscopy and tracheal intubation are 5 minute and 7 minute before intubation."

"Latar belakang : Hipotensi merupakan salah satu komplikasi akibat anestesia subarakhnoid pada seksio sesarea yang berpotensi membahayakan ibu dan janin. Kejadian hipotensi pada seksio sesarea dengan dosis bupivakain 8 - 12,5 mg berkisar antara 25 - 60%. Mengkombinasikan anestetika lokal dosis rendah dengan opioid lipofilik dan modifikasi posisi saat injeksi subarakhnoid mungkin dapat lebih menurunkan kejadian hipotensi. Tujuan penelitian ini adalah mengetahui efektivitas posisi Oxford dalam menurunkan kejadian hipotensi dibanding posisi lateral dengan regimen bupivakain 7,5 mg ditambah fentanil 25 mcg. Metode : Setelah lolos kaji etik dan mendapatkan persetujuan klinik 180 pasien yang akan menjalani seksio sesarea elektif dirandomisasi blok ke dalam kelompok posisi Oxford atau posisi lateral. Semua pasien mendapatkan dosis intratekal bupivakain 0,5% hiperbarik 7,5 mg ditambah fentanil 25 mcg. Coloading kristaloid diberikan 10 ml/ kgBB. Efedrin intravena diberikan sesuai standar. Kondisi hemodinamik dan profil blok sensorimotor dicatat. Penggunaan efedrin, efek samping dan nilai APGAR juga didokumentasikan. Hasil : Terdapat perbedaan yang secara statistik tidak bermakna pada kejadian hipotensi diantara kedua kelompok (p=0,121). Total jumlah penggunaan efedrin intravena diantara kedua kelompok berbeda dan dapat diperbandingkan. Profil blok sensorimotor diantara kedua kelompok dapat diperbandingkan. Kesimpulan : Modifikasi posisi Oxford pada anestesia subarakhnoid dengan dosis bupivakain 7,5 mg ditambah fentanil 25 mcg tidak memberikan hasil yang bermakna dalam menurunkan kejadian hipotensi.

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Background : Hypotension was one of the complications of subarachnoid anesthesia in caesarean section that potentially detrimental to the mother and baby. The insidens of hypotension in caesarean section with bupivacaine 8 - 12,5 mg were between 25 and 60%. Combining low dose of local anesthetics with lipofilic opioid and modification of position during subarachnoid injection might be more in lowering the hypotension insidens. The study was conducted to prove the effectiveness of Oxford position in lowering the hypotension insidens with regimen 7,5 mg bupivacaine added with 25 mcg fentanyl.

Methods : After ethical clearance and receive informed consent 180 elective caesarean section patient were randomized into Oxford group or lateral group. All the patient were receive the same dose of intrathecal 7,5 mg 0,5% hyperbaric bupivacaine added with 25 mcg fentanyl. Coloading of 10 ml/ kgBW with cristaloid was given. Intravenous ephedrine was given according to a standard. Hemodynamic changes and sensorimotor block profile were documented. Epedhrine consumption, side effect and APGAR score were also documented.

Result : There is a difference that statistically not significant in hypotension insidens between two groups (p=0,121). The total intravenous ephedrine consumption between two groups was different and comparable. The profile of sensorimotor block between two groups could be compared.

Conclusion : Modification of Oxford position in subarachnoid anesthesia with 7,5 mg bupivacaine added with 25 mcg fentanyl was not more effective in lowering insidens of hypotension."

"Latar belakang dan tujuan: Anastasia subarahnoid adalah salah satu tindakan anestesia regional yang sexing dilakukan untuk bedah sesar. Bupivakain hiperbarik 0,5% adalah obat anestetik lokal yang lazim dipakai untuk tehnik pembiusan tersebut. Posisi tubuh dan gaya gravitasi memiliki efek dan mempengaruhi penyebaran dari obat yang bersifat hiperbarik. Penelitian ini dilakukan untuk mengetahui pengaruh posisi tubuh saat penyuntikan obat bupivakain hiperbarik 0,5% terhadap efek hipotensi yang ditimbulkan.Metode : Penelitian dilakukan terhadap 90 wanita hamil berstatus ASA I-II usia 17-50 tahun yang menjalani bedah sesar, dibagi secara arak menjadi 2 kelompok duduk dan lateral dekubitus kiri. Setelah dilakukan penyuntikan obat, setelah 2 menit pasien dikembalikan ke posisi terlentang miring kiri 15 derajat, dan dilakukan co loading kristaloid 10 mllkgBB selama 10 menit Dilakukan pencatatan tekanan darah selama operasi setiap 2 menit selama 20 menit pertama clan selanjutnya tiap 5 menit. Ketinggian hambatan sensorik clan ketinggian maksimal hambatan, jumlah total efedrin dan cairan kristaloid yang diberikan selama operasi juga dicatat. Data hasil penelitian diolah dengan menggunakan uji t, uji Mann Whitneydan uji Chi kuadrat.Hasil : Kekerapan hipotensi antara kelompok posisi duduk dan lateral dekubitus kiri tidak berbeda secara statistik meskipun lebih banyak terjadi pada kelompok lateral dekubitus kiri (67%) dibandingkan posisi duduk (51%). Posisi duduk mengalami hipotensi lebih lambat, derajat hipotensinya lebih rendah dan pemakaian efedrin yang lebih sedikit.Kesimpulan: Posisi tubuh saat penyuntikan that bupivakain hiperbarik 0,5% pada anestesia subarahnoid mempengaruhi derajat hipotensi yang terjadi pada kasus bedah sesar.

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Backgrounds and objectives . Spinal anesthesia is one of the regional anesthesia technique frequently performed for cesarean section. Hyperbaric bupivacaine 0.5% is the most frequent local anesthetic used for this technique. Spread of the hyperbaric local anesthetics is affected by the position of the patient and gravity. In the present study we evaluated the effect of maternal posture whether sitting position during the induction of spinal anesthesia using 05% hyperbaric bupivacaine would induce less hypotension as compared with the left lateral position.

Methods. Ninety pregnant women underwent cesarean delivery were randomly assigned to receive a spinal injection consisting of 12.5 mg 0.5% hyperbaric bupivacaine in either sitting or left lateral position. After 2 minutes, patients were turned to a 15 degrees left lateral position and intravenous infusion of 10 mllkgbodyweigh t of crystalloids was started for 10 minutes along with the induction of spinal anesthesia. Intraoperative blood pressure were recorded , in this study hypotension is defined as a decrease in systolic blood pressure less than 100 mmHg or 20% below baseline values. The height of sensory block was measured, time to T6 spread of the sensory block and the highest level of sensory blockade were noted. Total given of ephedrine and crystalloids rntraopertive were also noted. Statistical evaluation was performed using t?test, Mann Whitney test and Chi square as appropriate.

Result : The incidence of hypotension was not significantly different between sitting and left lateral position but more often in lateral position (51% vs 67%). Sitting position group has longer interval of the first hypotension (p=0.008),less severe of hypotension (p=0.042), less ephedrine supplementation (p=0.014), and longer interval for reaching the T6 dermatome blockade (p <0,0001).

Conclusion: Maternal posture during induction of spinal anesthesia using 0.5% hyperbaric bupivacaine has influence to severity of hypotension for cesarean section."