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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.]"

"Latar belakang. Komplikasi paru pascaoperasi merupakan salah satu penyebab penting morbiditas dan mortalitas pascaoperasi yang berkaitan dengan anestesia dan pembedahan. Pengaturan ventilasi mekanis berpengaruh terhadap munculnya komplikasi paru pascaoperasi. Penelitian ini bertujuan meneliti pengaruh volume tidal 6 mL/kg dan 10 mL/kg dengan menggunakan PEEP 6 cmH2O terhadap penanda fungsi paru yaitu PaO2/FiO2.Metode. Penelitian ini bersifat uji klinis acak senter tunggal terhadap pasien yang menjalani operasi abdominal mayor elektif di Rumah Sakit Cipto Mangunkusumo pada bulan November 2014 sampai April 2015. Sebanyak 52 subyek diambil dengan metode consecutive sampling. Subyek diacak dalam 2 kelompok yaitu kelompok yang medapat volume tidal 6 mL/kg dengan PEEP 6 cmH2O dan volume tidal 10 mL/kg dengan PEEP 6 cmH2O. Keluaran primer adalah pemeriksaan fungsi paru menggunakan rasio PaO2/FiO2. Keluaran sekunder adalah komplikasi paru (pneumonia, atelektasis, ARDS, gagal napas), komplikasi ekstraparu (SIRS, sepsis, sepsis berat), dan mortalitas dalam 28 hari pascaoperatif.Hasil. Kedua grup memiliki karakteristik dasar dan intraoperatif yang sama. Tidak ditemukan perbedaan yang bermakna rasio PaO2/FiO2 antara kelompok VT-6 mL/kg dengan VT-10 mL/kg, baik pada awal operasi (p=0,14), akhir operasi (p=0,44), hari pertama pascaoperasi (p=0,23), dan hari kedua pascaoperasi (p=0,39). Tidak ada perbedaan bermakna keluaran sekunder berupa kompikasi paru sampai hari ke-7 pascaoperasi, ekstraparu sampai hari ke-7 pascaoperasi, dan mortalitas dalam 28 hari pascaoperasi antara kedua kelompok.Simpulan. Volume tidal-6 sampai volume tidal-10 dengan PEEP6 cmH2O aman untuk dipakai pada pasien yang menjalani operasi abdominal mayor.

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Background. Postoperative pulmonary complications are one of the important causes of postoperative morbidity and mortality associated with anesthesia and surgery. Mechanical ventilation settings influence the emergence of postoperative pulmonary complications. The aim of this study is to investigate the influence of tidal volume 6 mL/kgBW and 10 mL/kgBW with PEEP 6cmH2O to pulmonary function which is measured by the ratio of PaO2 / FiO2.Methods. This study is a single center randomized clinical trial on patients undergoing elective major abdominal surgery at Cipto Mangunkusumo Hospital in November 2014 to April 2015. A total of 52 subjects were taken with consecutive sampling method. The subjects were randomized into two groups: the group receiving tidal volume 6 mL/kgBW with PEEP 6 cmH2O and the group receiving tidal volume of 10 mL/kgBW with PEEP 6 cmH2O. The primary output is the assessment of pulmonary function using the ratio of PaO2/FiO2. Secondary outputs are pulmonary complications (pneumonia, atelectasis, ARDS, respiratory failure), extrapulmonary complications (SIRS, sepsis, severe sepsis), and mortality within 28 days postoperative.Results. The two intervention groups had similar characteristics at baseline. There are no significant PaO2 / FiO2 ratio differences between the VT - 6 mL/kgBB with VT - 10 mL/kgBB, at the start of the operation (p=0,14), the end of surgery (p=0.44), the first postoperative day (p=0,23), and the second postoperative day (p=0,39) . There is no significant difference in the secondary outcomes in form of pulmonary complications until postoperative day 7, extrapulmonary complications until postoperative day 7, and in 28-days postoperative mortality between the two groups.Conclusions : Tidal volume of 6 to 10 mL/kg with PEEP 6 cmH2O are safe for use in patients undergoing major abdominal surgery."

"ABSTRAK Latar Belakang. Optimalisasi hemodinamik perioperatif berkorelasi dengan peningkatan hasil terapi pascaoperasi. Alat pantau pulse contour analysis telah digunakan rutin pada operasi transplantasi ginjal di RSCM. Teknologi ini mahal dan harus dilakukan pemasangan akses kateter arteri. Terdapat alat ukur lain dengan kelebihan tidak invasif.Tujuan. Mengetahui kesesuaian hasil pengukuran hemodinamik antara teknik bio-impedance analysis dan pulse contour analysis pada pasien resipien transplantasi ginjal.Metode. Penelitian observasional statistik potong lintang terhadap 35 pasien resipien transplantasi ginjal di RSCM dan RSCM Kencana Jakarta periode Oktober 2017-Febuari 2018. Parameter hemodinamik pasien diukur menggunakan kedua alat uji yaitu ICONTM dan EV1000TM, pencatatan dilakukan pascainduksi, pascainsisi dan pascapelepasan klem arteri renalis. Analisis data menggunakan uji kesesuaian Bland-Altman dan korelasi.Hasil. Rerata perbedaan nilai indeks curah jantung dan indeks isi sekuncup antara kedua alat adalah 1,3 l/mnt/m2 dan 22,1 ml/denyut/m2 lebih tinggi pada EV1000TM. Rerata perbedaan hasil indeks tahanan vaskular sistemik dan stroke volume variation antara kedua alat adalah 973,3 dynes-detik-m2/cm5 dan 4,8 lebih rendah pada EV1000TM.Simpulan. Tidak terdapat kesesuaian hasil pengukuran curah jantung, tahanan vaskular sistemik dan stroke volume variation antara teknik bio-impedance analysis dengan teknik pulse contour analysis pada pasien resipien transplantasi ginjal.

Background. Hemodynamic optimization perioperative has strong correlation with improvement of post-operative outcome. Pulse contour analysis uses regularly for monitoring in renal transplantation surgery at RSCM hospital. This technology is expensive and need access to artery vascular. There is other monitoring device with excess non-invasive use. Purpose. Comparing hemodynamic measurement results between bio-impedance analysis and pulse contour analysis in renal transplant recipients.Method. Cross sectional observasional study to 35 renal transplantation recipient patients at RSCM and RSCM Kirana hospitals Jakarta during October 2017-February 2018. Each patient was measured with both devices ICONTM and EV1000TM. Data collected after induction, after incision and after renal artery release. All the data analyzed with Bland-Altmant agreement and corellation.Result. Mean difference of cardiac output index and stroke volume index are 1,3 l/mnt/m2 and 22,1 ml/denyut/m2 higher in EV1000TM. Mean difference of systemic vascular resistance index and stroke volume variation are 973,3 dynes-detik-m2/cm5 and 4,8 lower in EV1000TM. Conclusion. There is no agreement in measurement of cardiac output, systemic vascular resistance and stroke volume variation between bio-impedance analysis and pulse contour analysis in renal transplantation recipient patients. "

"Latar Belakang : Hipotermia merupakan salah satu strategi dalam manajemen neuroproteksi akibat terjadinya cedera iskemia selama pembedahan operasi jantung terbuka dengan mesin pintas jantung paru. Pendinginan bersifat lokal pada otak dengan menggunakan cooling helmet lebih dapat menekan proses kerusakan yang terjadi dibandingkan yang tidak menggunakan cooling helmet. Tujuan : Mengetahui hubungan antara penggunaan cooling helmet dengan perubahan kadar NSE yang lebih kecil dan delirium pascaoperasi jantung terbuka lebih rendah dibandingkan tidak menggunakan cooling helmet.Metode : Studi ini merupakan uji klinis acak tersamar ganda, dilakukan randomisasi pada 26 orang dimana dibagi menjadi 2 kelompok yaitu kelompok perlakuan n=13 (cooling helmet on) dan kelompok kontrol n=13 (cooling helmet off). Kriteria inklusi pasien yang terjadwal pertama kali menjalani operasi jantung terbuka dengan mesin pintas jantung paru, usia ≥ 18 tahun, ASA III, GCS 15, dan dapat berbahasa Indonesia.Hasil : Studi ini menunjukkan adanya perbedaan yang signifikan secara statistik pada kadar NSE antara kelompok perlakuan dan kelompok kontrol. Kadar NSE pada kelompok perlakuan (7.13 ± 7.63) lebih rendah dibandingkan kelompok kontrol (12.49 ± 6.81) (p<0.05). Namun, tidak terdapat perbedaan signifikan secara statistik pada kejadian delirium antara kedua kelompok (p>0.05).Kesimpulan : Cooling helmet berhubungan dengan penurunan kadara NSE namun tidak berpengaruh secara signifikan untuk mencegah terjadinya delirium setelah operasi jantung terbuka. Background: Hypothermia remains the most common neuroprotective management against ischemic injury during open heart surgery with cardiopulmonary bypass machine. Surface cooling in the brain delivered by cooling helmet provides more benefit to suppress cerebral injury compared to those who do not use cooling helmet. Objective: This study aimed to assess the effect of cooling helmet during surgery on NSE and delirium level after open-heart surgery patient with Cardiopulmonary Bypass (CPB) machine.Methods: This study is a double-blind, randomized, clinical trial, where 26 people were randomized into 2 groups, namely the treatment group n=13 (cooling helmet on) and the control group n=13 (cooling helmet off). The inclusion criteria were patients who are scheduled to undergo open heart surgery for the first time with cardiopulmonary bypass machine, age ≥18 years, ASA III, GCS 15, and can speak Indonesian. Results: The study was found significant differences in NSE levels between the treatment and the control group. NSE levels in the treatment group (7.13 ± 7.63) were lower than in the control group (12.49 ± 6.81) (p<0.05). There weren’t statistically significant differences in the outcome of delirium in both groups (p>0.05)Conclusion: The cooling helmet is associated with the decrease of NSE levels, but it did not significantly correlate to prevent the delirium after open-heart surgery."

"[ABSTRAKLatar Belakang : Laparoskopi kolesistektomi saat ini menjadi pilihan utama kasus batu kandung empedu simtomatik. Walaupun minimal, laporan mengenai nyeri abdomen dan nyeri bahu masih dirasakan pascalaparoskopi kolesistektomi. Nyeri ini muncul segera setelah operasi dan dapat bertahan selama 3 hari. Penelitian ini bertujuan untuk mengetahui efektivitas instilasi ropivakain 0.375% intraperitonium sebagai ajuvan terapi nyeri pascalaparoskopi kolesistektomi. Metode : Penelitian ini adalah uji klinik acak tersamar ganda yang dikerjakan di Instalasi Bedah Pusat RSCM pada bulan November 2014 sampai April 2015. Subjek yang memenuhi kriteria dibagi menjadi kelompok ropivakain (R) (n=35) mendapat 40 mL ropivakain 0.375% dan kelompok NaCl (N) (n=33) mendapat 40 mL NaCl 0.9%. Peracikan regimen dikerjakan oleh orang yang berbeda dengan operator dan penilai. Tingkat nyeri statis, dinamis dan nyeri rujuk dinilai pada jamke-1, 6 dan 24 pascaoperasi. Waktu meminta analgetik tambahan pertama (petidin) juga dicatat. Data regimen yang diterima baru dibuka setelah pengumpulan data selesai. Hasil : Secara statistik terdapat perbedaan bermakna pada proporsi nyeri statis jam pertama antara kelompok R dan N. Kelompok R cenderung memiliki nilai VAS lebih rendah (p=0.05;OR=0.453). Tidak terdapat perbedaan bermakna pada keseluruhan jenis nyeri yang dinilai dalam tiap-tiap waktu penilaian. Median waktu meminta petidin juga tidak berbeda antara kedua kelompok. Simpulan: Instilasi ropivakain 0.375% intraperitonium tidak lebih efektif sebagai ajuvan terapi nyeri pascalaparoskopi kolesistektomi dibandingkan tanpa ajuvan.

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ABSTRACTBackground: Laparoscopy cholecystectomy has been the preferred procedure for symptomatic cholelithiasis. Although less minimal, abdominal and shoulder pain are still reported. The pain rises after operation and persists for 3 days. The aim of this study was to determine the effect of intraperitoneal ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy.Method: This was a randomized, double blinded, clinical control trial that held in central operating theater Ciptomangunkusumo hospital during November 2014 until April 2015. Subjects divided into two groups. The ropivacaine (R) group (n=35) got 40 mL ropivacain 0.375% and the control (N) group (n=33) got NaCl 0.9% in same volume. Regiment was prepared by different personel from the operator and evaluator. Pain at rest, cough and shoulder pain were recorded in VAS at 1st, 6th and 24th hours postoperative. Time to get the first petidine dose was also recorded.Result: Ropivacaine had higher proportion of mild pain at rest (VAS<4) at 1st hour (p=0.050; OR=0.453). There were no statistically significant difference for other pain proportions in any time measured. Median time to get first petidine dose did not differ between the two groups.Conclusion: Intraperitoneal instillation of ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy is not more effective than without adjuvant.;Background: Laparoscopy cholecystectomy has been the preferred procedure for symptomatic cholelithiasis. Although less minimal, abdominal and shoulder pain are still reported. The pain rises after operation and persists for 3 days. The aim of this study was to determine the effect of intraperitoneal ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy.Method: This was a randomized, double blinded, clinical control trial that held in central operating theater Ciptomangunkusumo hospital during November 2014 until April 2015. Subjects divided into two groups. The ropivacaine (R) group (n=35) got 40 mL ropivacain 0.375% and the control (N) group (n=33) got NaCl 0.9% in same volume. Regiment was prepared by different personel from the operator and evaluator. Pain at rest, cough and shoulder pain were recorded in VAS at 1st, 6th and 24th hours postoperative. Time to get the first petidine dose was also recorded.Result: Ropivacaine had higher proportion of mild pain at rest (VAS<4) at 1st hour (p=0.050; OR=0.453). There were no statistically significant difference for other pain proportions in any time measured. Median time to get first petidine dose did not differ between the two groups.Conclusion: Intraperitoneal instillation of ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy is not more effective than without adjuvant., Background: Laparoscopy cholecystectomy has been the preferred procedure for symptomatic cholelithiasis. Although less minimal, abdominal and shoulder pain are still reported. The pain rises after operation and persists for 3 days. The aim of this study was to determine the effect of intraperitoneal ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy.Method: This was a randomized, double blinded, clinical control trial that held in central operating theater Ciptomangunkusumo hospital during November 2014 until April 2015. Subjects divided into two groups. The ropivacaine (R) group (n=35) got 40 mL ropivacain 0.375% and the control (N) group (n=33) got NaCl 0.9% in same volume. Regiment was prepared by different personel from the operator and evaluator. Pain at rest, cough and shoulder pain were recorded in VAS at 1st, 6th and 24th hours postoperative. Time to get the first petidine dose was also recorded.Result: Ropivacaine had higher proportion of mild pain at rest (VAS<4) at 1st hour (p=0.050; OR=0.453). There were no statistically significant difference for other pain proportions in any time measured. Median time to get first petidine dose did not differ between the two groups.Conclusion: Intraperitoneal instillation of ropivacaine 0.375% as adjuvant in postlaparoscopy cholecystectomy pain therapy is not more effective than without adjuvant.]"

"Latar Belakang: Kecemasan praoperasi selalu menjadi perhatian bagi pasien maupun dokter anestesiologis dan dokter bedah. Pasien-pasien yang dihadapkan pada kenyataan harus menjalani operasi khususnya operasi jantung mungkin akan mengalami kecemasan yang lebih tinggi karena keadaan jantung mereka yang tidak baik, konsep operasi jantung yang menakutkan dan ketidakpastian terhadap hasilnya. Kecemasan akan mengaktifkan stres respon yang menyebabkan stimulasi sistem saraf simpatis yang kemudian akan menstimulasi kardiovaskular dengan meningkatkan jumlah katekolamin darah yang menyebabkan takikardi, hipertensi, iskemik dan infark miokardial. Respon tersebut mungkin mempunyai efek merugikan pada sirkulasi koroner, yang menyebabkan peningkatan morbiditas dan mortalitas. Berbagai penanganan telah dikembangkan, salah satunya adalah dengan pemberian informasi (edukasi). Dengan pemberian edukasi melalui komunikasi efektif, informatif dan empati diharapkan terjadi penurunan tingkat kecemasan pasien sebelum menjalani pembiusan dan pembedahan. Penelitian ini secara umum ingin mengetahui pengaruh edukasi pra-anestesia terhadap tingkat kecemasan pasien dewasa yang akan menjalani operasi jantung terbuka di Instalasi PJT RSUPN Cipto Mangunkusumo.Metode: Penelitian ini menggunakan uji kuasi eksperimen pada pasien dewasa yang akan menjalani operasi jantung terbuka di Instalasi PJT RSUPN Cipto Mangunkusumo. Setelah mendapatkan ijin komite medik dan informed consent, sebanyak 36 subyek didapatkan dengan consecutive sampling pada bulan Maret 2016. Sebelum dilakukan penilaian tingkat kecemasan sebelum edukasi dengan menggunakan instrumen APAIS, terlebih dahulu dilakukan pengukuran tanda vital, kemudian dilanjutkan dengan pemberian edukasi dan diskusi. Jika subyek tidak mengalami gaduh gelisah dan atau tanda bahaya kardiovaskular, maka keesokan hari sebelum subyek dibawa ke ruang operasi, akan dilakukan penilaian ulang tingkat kecemasan subyek dengan menggunakan instrumen yang sama. Hasil: Uji Wilcoxon menunjukkan terdapat penurunan bermakna rerata tingkat kecemasan sebelum edukasi dibandingkan dengan sesudah edukasi (p<0,001). Simpulan: Edukasi pra-anestesia menurunkan tingkat kecemasan pasien dewasa yang akan menjalani operasi jantung terbuka di Instalasi PJT RSUPN Cipto Mangunkusumo.

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Background: Preoperative anxiety is always a concern for patients, anesthetist and surgeon. Patients are faced with the reality had to undergo surgery, especially heart surgery may experience higher anxiety because their heart condition is not good, scary concept of heart surgery and uncertainty of the results. Anxiety will activate the stress response that causes stimulation of the sympathetic nervous system, which then stimulates the cardiovascular by increasing the amount of blood catecholamines that cause tachycardia, hypertension, ischemia and myocardial infarction. The response may have detrimental effects on the coronary circulation, which leads to increase morbidity and mortality. Various handling have been developed, one of which is the provision of information (education). With the provision of education through effective and informative communication with empathy are expected to decline the level of anxiety of patients before undergoing anesthesia and surgery. The objective of this study is to determine the effect of preanesthesia education to the level of anxiety in adult patients undergoing open heart surgery in the Installation of PJT Cipto Mangunkusumo.

Methods: This study used a quasi-experimental trials of adult patients undergoing open heart surgery in the Installation of PJT Cipto Mangunkusumo. After getting permission from the medical committee and getting informed consent, a total of 36 subjects is obtained by consecutive sampling in March 2016. Prior to the assessment of the level of anxiety before education using APAIS instrument, first performed measurements of vital signs, and then continued with education and discussion. If the subject is not experiencing restless and rowdy or cardiovascular distress signal, then the next day before the subject is taken to the operating room, the level of anxiety of the subject will be reassessed using the same instrument.

Results: Wilcoxon test showed that there was a significant decrease in the average level of anxiety before education compared with after education (p<0.001).

Conclusion: Preanesthesia education lowers the level of anxiety in adult patients undergoing open heart surgery in the Installation of PJT Cipto Mangunkusumo."

"Latar Belakang : Akumulasi cairan yang telah terjadi pasien sepsis dan diperberat oleh resusitasi cairan memiliki dampak buruk terhadap organ ginjal (sepsis related kidney injury). Oleh karena itu, tujuan penelitian ini ingin menilai efektivitas deresusitasi dini menggunakan furosemide terhadap kejadian AKI pada pasien sepsis dengan menggunakan pNGAL sebagai parameter AKI. Metode : Penelitian ini menggunakan desain uji klinis acak tersamar ganda, yang dilakukan pada pasien sepsis di ICU RSUPN Dr. Cipto Mangunkusumo (RSCM) pada periode Juli – Desember 2023. Kadar pNGAL diperiksa pada jam ke-0 dan ke-48 jam perawatan ICU. Sebanyak 40 subjek dibagi menjadi 2 kelompok yaitu 20 pasien pada kelompok perlakuan diberikan injeksi furosemide kontinyu 2 mg/jam, dan 20 pasien pada kelompok kontrol diberikan injeksi placebo 2 mL/jam. Hasil : Ditemukan kadar pNGAL telah meningkat sejak awal perawatan di ICU pada semua subjek. Tidak terdapat perbedaan bermakna selisih kadar pNGAL jam ke-0 dan ke-48 (p=0,146). Ditemukan penurunan kadar pNGAL yang cukup besar pada kelompok intervensi dibandingkan dengan kelompok kontrol. Kadar laktat, TVS, lama perawatan ICU, lama penggunaan ventilator pada kedua kelompok tidak ditemukan berbeda bermakna. Rerata balans cairan pada jam ke-24 ditemukan lebih rendah pada kelompok intervensi (-391,01 ± 871,59 mL vs. 586,90 ± 1382 mL, p=0,016). Proporsi subjek yang menerima terapi pengganti ginjal dan mengalami kematian dalam 28 hari juga tidak berbeda signifikan. Simpulan : Penggunaan furosemide bermanfaat untuk mengurangi akumulasi cairan dalam 24 jam pertama perawatan sehingga menghambat progresifitas kerusakan tubulus ginjal pada pasien SAKI.

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Background: Fluid accumulation occurs in septic patients and is increased by fluid resuscitation, causing kidney damage. This study aimed to determine the effectiveness of early deresuscitation with furosemide on the incidence of AKI in sepsis patients using pNGAL as an AKI parameter. Methods: This study used a double-blind, randomized clinical trial design conducted on sepsis patients in the ICU at RSUPN Dr. Cipto Mangunkusumo (RSCM) in July – December 2023. pNGAL levels were measured at the first and 48th hours of ICU care. A total of 40 participants were divided into two groups: 20 patients in the treatment group were given continuous furosemide injections at a rate of 2 mg/hour, while 20 patients in the control group were given placebo injections of 2 mL/hour. Results: pNGAL levels had increased since all subjects started treatment in the ICU. There was no difference in changes of pNGAL levels at 0 and 48 hours (p=0.146). A trend of reduction in pNGAL levels was found in the intervention group compared to the control group. Lactate levels, TVS, length of ICU stay, and length of ventilator use in the two groups were not found to be significantly different. Fluid at 24 hours was lower in the intervention group (-391.01 ± 871.59 mL vs. 586.90 ± 1382 mL, p=0.016). The proportion of participants who underwent renal replacement therapy and died within 28 days showed no significant difference. Conclusion: Furosemide effectively lowers fluid accumulation in the first 24 hours of therapy, slowing the course of renal tubular injury in SAKI patients."

"Latar Belakang: Disfungsi ginjal prabedah meningkatkan risiko gagal ginjal dan kematian pada pasien bedah jantung. Studi yang meneliti efek proteksifurosemid pada bedah jantung sebagian besar dilakukan pada pasien dengan fungsi ginjal normal. Penelitian ini bertujuan mengevaluasi efek furosemid dosis rendah profilaksis pada pasien bedah jantung dengan disfungsi ginjal ringan-sedang.Metode: Delapan puluh tujuh pasien bedah jantung elektif dengan disfungsi ginjal ringan -sedang (LFGe30-89 mL/min/1,73 m2), terdaftar dalam kelompok furosemid (n = 43) atau kontrol (n = 44). Furosemid (2 mg/jam) atau NaCl 0,9% 2 cc/jam diberikan setelah induksi dan dilanjutkan selama total 12 jam. Kami memeriksa sampel darah pada 12, 24, 48, dan 120 jam setelah infus mulai mengukur perubahan LFGe. Penurunan LFGe>20% dianggap sebagai perburukan fungsi ginjal, sedangkan peningkatan LFGe>20% dianggap sebagai pemulihan fungsi ginjal. Kami membandingkan kebutuhan infus furosemid terapeutik dan terapi penggantian ginjal pada kedua kelompok.Hasil: Dari 90 subjek yang direkrut, 3 subjek drop out(1 subjek data tidak lengkap dan 2 subjek dipasangintra-aortic balloon pump/IABPsaat pembedahan), hanya 87 subjek yang diikutsertakan dalam analisis. Insiden penurunan LFGepada jam ke-12, ke-24 dan ke-48 lebih banyak terjadi pada kelompok kontrol, berbedasignifikan pada sampel jam ke-48 (p value0,047). Proporsi peningkatan LFGe>20% pada sampel 120 jam hampir sama pada kedua kelompok. Subyek dalam kelompok furosemid membutuhkan lebih sedikit pemberian infus furosemid dosis terapeutik (p<0,05). Namun, penggunaan terapi pengganti ginjal lebih banyak ditunjukkan pada kelompok furosemid daripada kelompok kontrol meskipun tidak signifikan. Lama rawat di ICU dan rumah sakit lebih lama pada kelompok furosemid dibandingkan dengan kontrol, sedangkan angka kematian ditunjukkan sama antara kedua kelompok.Simpulan: Furosemid dosis rendah dapat mengurangi kejadian perburukan fungsi ginjal, dan kebutuhan infus terapeutik furosemid, tetapi tidak mencegah kebutuhanuntuk terapi pengganti ginjal. Penggunaan infus furosemid dosis rendah perioperatif dapat dipertimbangkan karena menunjukkan efek yang menguntungkan.

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Background: Preoperative renal dysfunction increases the risk of postoperative renal failure and mortality in cardiac surgery patients. Studies investigated the protective effect of furosemide in cardiac surgery mostly conducted in patients with normal renal function. This study aim to evaluate the effect of prophylactic low-dose furosemide in cardiac surgery patients with mild to moderate renal dysfunction.

Methods: Eighty-seven patients of elective cardiac surgery with mild to moderate renal dysfunction (eGFR 30-89 mL/min/1.73 m2), were enrolled in either furosemide (n = 43) or control (n = 44) groups. Furosemide (2 mg/h) or 0.9% NaCl is administered after induction and continued for a total of 12 hours. We examined blood samples on 12, 24, 48, and 120 hours after infusion started to measure the change in eGFR. A >20% decrease in eGFR was considered as worsening of renal function, while >20% increase in eGFR as recovering of renal function. We compared the requirement for therapeutic furosemide infusion and renal replacement therapy in both groups. 

Results: 90 subjects recruited, 3 were dropped out (1 subject's data incomplete and 2 subjects underwent intraoperativeintraaortic balloon pump/IABP installation), only 87 subjects were included in the analysis. The incidence of decreasing of GFR at the 12th, 24th and 48th hour was shown more likely in control group, more significantin 48 hours (p value 0.047). The proportion of >20% GFR increase in the 120-hour sample was almost the same in both groups. Subjects in furosemide group required less administration of therapeutic dose furosemide infusion (p<0.05). However, use of renal replacement therapy was shown more in the furosemide group than the control group although is not significant. The length of stay in ICU and hospital were longer in the furosemide group compared to  control, while the mortality rate were shown to be equal between two groups.

Conclusions: Low-dose furosemide can reduce the incidence of  worsening renal function, and the need for a therapeutic furosemide infusion, but does not prevent the usage for renal replacement therapy. Continuous low-dose furosemide perioperative can be considereddue to beneficial effects proven."