• 제목/요약/키워드: Nausea and Vomiting of Pregnancy

검색결과 26건 처리시간 0.02초

A Case Report: Effect of Korean Medicine Including Distilled Form of Bosaeng-tang Gagambang on Moderate to Severe Hyperemesis Gravidarum.

  • Kim, Hae-Won;Baek, Seon-Eun;Yoo, Dong-Youl;Yoo, Jeong-Eun
    • 대한한의학회지
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    • 제41권4호
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    • pp.120-132
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    • 2020
  • Objectives: Hyperemesis gravidarum (HG) is defined as severe nausea and vomiting during pregnancy (NVP) with weight loss, ketonuria, and electrolyte imbalance. Many NVP or HG patients get hard to take herbal medicine since the smell and taste of it. Therefore, the distilled herbal medicines are often used in clinical practice. A 32-year-old, 14-week pregnant female was admitted for 3 weeks at a Korean medicine hospital. She was experiencing HG accompanied by 19.61% (10 kg) weight loss, ketonuria, and electrolyte imbalance. The patient received Bosaeng-tang gagambang in its distilled form, acupuncture, electro-acupuncture, sticker needles, cupping, moxibustion, and hydration during admission. The severity and frequency of NVP, weight loss, and ketonuria significantly improved without any side effects. Before the therapy, she admitted to two obstetrics and gynecology hospitals, 1 week each, with no improvement. This case presents the therapeutic potential of Korean medicine including herbal medicine in its diluted form for HG and NVP.

지속적인 쌀죽 섭취에 의한 각기병 1례 (A Case of Beriberi Because of Continuous Rice-soup Feeding during One and Half Years)

  • 양은석;윤영훈;노영일;문경래
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제7권2호
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    • pp.264-267
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    • 2004
  • 저자들은 1년 6개월간 지속적인 쌀죽의 섭취이후에 발등부터 시작하여, 전신적인 부종과 무관심, 걷지 못하는 증상을 주소로 입원한 환아가 티아민 투여 이후에 증상의 회복을 보인 beriberi 1례를 치험 하였기에 보고하는 바이다.

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Tapentadol: Can It Kill Two Birds with One Stone without Breaking Windows?

  • Chang, Eun Jung;Choi, Eun Ji;Kim, Kyung Hoon
    • The Korean Journal of Pain
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    • 제29권3호
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    • pp.153-157
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    • 2016
  • Tapentadol is a novel oral analgesic with a dual mode of action as an agonist of the ${\mu}$-opioid receptor (MOR), and as a norepinephrine reuptake inhibitor (NRI) all in a single molecule. Immediate release (IR) tapentadol shows its analgesic effect quickly, at around 30 minutes. Its MOR agonistic action produces acute nociceptive pain relief; its role as an NRI brings about chronic neuropathic pain relief. Absorption is rapid, with a mean maximal serum concentration at 1.25-1.5 h after oral intake. It is present primarily in the form of conjugated metabolites after glucuronidation, and excretes rapidly and completely via the kidneys. The most common adverse reactions are nausea, dizziness, vomiting, and somnolence. Constipation is more common in use of the ER formulation. Precautions against concomitant use of central nervous system depressants, including sedatives, hypnotics, tranquilizers, general anesthetics, phenothiazines, other opioids, and alcohol, or use of tapentadol within 14 days of the cessation of monoamine oxidase inhibitors, are advised. The safety and efficacy have not been established for use during pregnancy, labor, and delivery, or for nursing mothers, pediatric patients less than 18 years of age, and cases of severe renal impairment and severe hepatic impairment. The major concerns for tapentadol are abuse, addiction, seeking behavior, withdrawal, and physical dependence. The presumed problem for use of tapentadol is to control the ratio of MOR agonist and NRI. In conclusion, tapentadol produces both nociceptive and neuropathic pain relief, but with worries about abuse and dependence.

Medline 검색을 통한 임신오저에 대한 국외 침치료의 연구 동향 분석 (Investigation of Clinical Research of Acupuncture Treatment on Hyperemesis Gravidarum in Medline)

  • 김은경;황덕상;이진무;이창훈;장준복;이경섭
    • 대한한방부인과학회지
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    • 제25권4호
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    • pp.66-80
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    • 2012
  • Purpose: The purpose of this study is to examine acupuncture treatment suggested on the papers of hyperemesis gravidarum(HG) in medicine journals and to establish the future direction. Methods: The papers which were associated with acupuncture and HG published between 2000 and 2012 in Medline were searched. Results: 14 studies met the condition. They were 13 randomized controlled trial (RCT)s and 1 clinical study. 13 studies revealed that acupuncture has efficacies in HG. 1 study was shown to have no statistically significant efficacy. 2 studies revealed that acupuncture was safe treatment, and 1 study revealed that acupuncture was reliable treatment. Conclusions: From the paper research, acupuncture treatment seems to be effective on HG. However, due to the lack sufficient research of HG, it would be necessary to fulfill further study about the period of acupuncture treatment on HG and the selection of acupoint through well-designed study and establish standard of evidence of them.

임부의 수면양상 (Sleep Patterns of Pregnant Women)

  • 최병선;윤진상
    • 수면정신생리
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    • 제5권1호
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    • pp.45-53
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    • 1998
  • 연구배경 : 본 연구는 정상 단태 임부에서 임신 경과에 따른 수면양상의 변화 및 그 원인을 알아보고자 하였다. 방법 : 임신 제1 삼분기에 수면설문지를 작성한 임부를 대상으로, 임신 제2 및 제3 삼분기에도 동일한 수면 설문지를 가지고 추적조사를 하였다. 조사내용은 각 임신 시기에서의 수면 잠복기, 총 수면시간, 수면중 깨는 횟수, 각성시 회복감, 주간의 상태, 수면 자세, 수면 양상변화의 원인 등이었다. 결과 : 다음은 총 3회의 설문조사를 성실히 수행했던 26명의 임부에 대한자료분석의 결과이다. 1. 각 임신 시기와 임신전과의 비교 결과, 수면 잠복기는 임신 제1 및 제2 삼분기에서 감소하였고, 총 수면시간은 임신 제1, 제2 및 제3 삼분기에서 모두 증가하였다. 임신 제3 삼분기에는 수면 중 깨는 횟수가 증가하였고, 각성시 회복감이 감소하였다. 임신 제1, 제2 및 제3 삼분기 모두에서 주간에 피곤감과 졸리움이 증가하였다. 2. 각 임신 시기간의 비교 결과, 임신 제3 삼분기에는 수면 잠복기 및 수면중 깨는 횟수가 임신 제1 및 제2 삼분기보다 증가하였다. 또한 임신 제3 삼분 기에는 제1 및 제2 삼분기보다 각성시 회복감이 더 적었고, 주간의 졸리움도 더 심하였다. 3. 수면 자세는 임신 제1 및 제2 삼분기에 복와위 또는 앙와위를 취했던 임부도 제3 삼분기에는 모든 임부가 측와위를 취했다. 4. 수면양상변화의 원인으로서 임신제1 삼분기에는 오심과 구토, 속쓰림과 소화불량 및 빈뇨, 제2 삼분기에는 빈뇨, 태아의 움직임 및 둔부의 통증, 제3 삼분기에서는 빈뇨, 태아의 움직임, 하지의 경련과 요통순으로 많았다. 결론 : 이상의 결과는 정상 단태임신과 관련한 수면 변화의 자료로서, 향후 임부에서 수면위생의 향상과 수면장애의 치료를 위한 기초적 자료로 활용할 가치가 있다고 생각된다.

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Study on the Acceptability and Effectiveness of an Oral Contraceptive Among Iud Drop-outs in Rural Korea

  • Yang, J.M.;Bang, S.;Song, S.W.;Youn, B.B.
    • Journal of Preventive Medicine and Public Health
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    • 제1권1호
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    • pp.51-66
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    • 1968
  • During a period of about one year(November '66 to December '67), the Yonsei University College of Medicine conducted a field trial of the oral contraceptive(Ovulen) in order to study its acceptability and use-effectiveness among IUD drop-outs in Koyang county. We can summarize the outstanding findings from this investigation as follows; 1. 61.4% of the IUD drop-outs interviewed (911 women) wanted to use the pill. Most of the reasons for not wanting to use it(352 women) pertained to either use of other contraceptive methods(98) or subfecundity(150) following IUD terminations. Only 83 out of 911 women gave reasons related to the difficulty of obtaining pills. Therefore, we can state that most IUD drop-outs if still in need of a contraceptive methods are in favor of trying the pill, and especially so if this method is conveniently available. 2. The 467 women or 37% of those who terminated IUD use actually visited the clinic for medical screening, and only 11 of them or 2.4% were rejected because of pregnancy and other medical reasons such as cervical erosion, myoma, breast mass, etc. 5.5% or 25 of the 456 women who received the first cycle did not take a single pill during the study period. 3. When we defined those 431 women who accepted and took one or more tablets we found that women over age 30, with 4 or more children, and/or with a higher educational level were the best prospects for recruitment. 4. In accuracy of use, about two thirds of the users started taking the pill on the 5 th day as directed for the first three cycles, but the percentages rose sharply to about 80% in later cycles. Tardiness in starting pill use in the first cycle may have occurred partly because they had to return to the clinic monthly to get each new cycle. Among acceptors who did not quit between cycles, 80 to 90% were regular users, missing two or less tablets in each cycle. 5) More than 60% of the users felt well and sometimes lost their pre-acceptance symptoms. especially dysmenorrhea. However, 27.4% (58 women) had side effects attributable to the pill compund as nausea, vomiting, indigestion, breast tenderness, decreased lactation or breakthrough bleeding. 25.0% (53 women) also complained of medical diseases or symptoms not related to the pill, especially during the first three cycles. However, as the confidence and experience of the client and the field workers grew, the incidence of unrelated medical complaints quickly fell to a lower level in the later cycles. 6. As of the end of this study, on December 31, 1967, 49.2% (212 women) had discontinued the use of the pill for medical reasons as well as for the non medical reasons. Only one case terminated use due to a pregnancy after taking pills. The cumulative continuation rates (by the life table method), were 58.9%, 51.9%, 41.0% at the end of 3 months, 6 months and one year, respectively. These rates are lower than in the U.S. studies. Even when we add the retaking group to the first segment, the continuation rate goes up only about 5% above the first segment rates mentioned above. Possible explanations are different dosages, the newerness of the method and the use of only one point for pill distribution in the country together with a monthly return for cycle 1, 2, 3, and 4-6.

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